<?xml version="1.0" encoding="utf-8"?>
<XML>
<JOURNAL>
<YEAR>2017</YEAR>
<VOL>21</VOL>
<NO>4</NO>
<MOSALSAL>67</MOSALSAL>
<PAGE_NO>350</PAGE_NO>


<ARTICLES>

	<ARTICLE> 
		<TitleF>The controllability of cardiac rhythm in elderly</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Recent reports have shown that rare fluctuations in cardiac cycles are &#8216;forgotten&#8217; quickly in healthy individuals and it is possible to quantify the &#8220;memory length&#8221; of a physiological time-series using an inverse statistical approach. Methods: In the present study, we assessed the effect of aging on memory length in cardiac rhythm. Results: There was a longer memory length in cardiac time-series of elderly subjects in comparison with younger adults for both decelerating and accelerating rare fluctuations in cardiac rhythm. Conclusion: The increased memory length of the cardiac time-series in elderly subjects may indicate reduced controllability of cardiovascular regulatory system.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>260</FPAGE>
			<TPAGE>265</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/8
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1396/5/17
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/16
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/8/25
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Tara</Name>
				<MidName></MidName>
				<Family>Ghafari</Family>
				<NameE>Tara</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghafari</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Medical School, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>t.ghafari@sbmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ava</Name>
				<MidName></MidName>
				<Family>Ghafari</Family>
				<NameE>Ava</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ghafari</FamilyE>
				<Organizations>
				<Organization>Department of Electronic, Information and Bioengineering, Politecnico di Milano University, Milan, Italy</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>ava.ghafari@mail.polimi.it</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ali R.</Name>
				<MidName></MidName>
				<Family>Mani</Family>
				<NameE>Ali R.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mani</FamilyE>
				<Organizations>
				<Organization>Division of Medicine, UCL, London, UK</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>a.r.mani@ucl.ac.uk</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohammad Reza</Name>
				<MidName></MidName>
				<Family>Raoufy</Family>
				<NameE>Mohammad Reza</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Raoufy</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>raoufy@modares.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Heart rate variability</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Memory length</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Controllability</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Elderly</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>[1]. Guevara, M.R., Glass, L., Shrier, A., Phase locking, period-doubling bifurcations, and irregular dynamics in periodically stimulated cardiac cells. Science.  1981; Dec 18; 214(4527):1350–1353.##[2]. Glass, L., Shrier, A., Belair, J., Chaotic cardiac rhythms. Chaos. 1986:236–256.##[3]. Goldberger, A.L., Chaos and fractals in human physiology. Sci. Am. 1990; 262(2):42–49.##[4]. Ivanov, P.Ch., Rosenblum, M., Peng, C. K., et al. Scaling behavior of heartbeat intervals obtained by wavelet-based time series analysis. Nature (London). 1996; 383:323±327.##[5]. Goldberger, A.L., Heartbeats, Hormones, and Health Is Variability the Spice of Life? Am. J. Respir. Crit. Care. Med. 2001; 163(6):1289–1290. ##[6]. Goldberger, A.L., Peng, C.K., Lipsitz, L.A., What is physiologic complexity and how does it change with aging and disease? Neurobiol. Aging. 2002; Jan-Feb; 23(1):23-6.##[7]. Goldberger, A.L., Amaral, L.A.N., Hausdorff, J.M., Ivanov, P.C., Peng, C.K., Stanley, H.E. Fractal dynamics in physiology: alterations with disease and aging. Proc. Natl. Acad. Sci. 2002; 99(90001):2466–2472.##[8]. Buchman, T.G., The community of the self. Nature. 2002; 420(6912):246–251.##[9]. Buchman, T.G., Nonlinear dynamics, complex systems, and the pathobiology of critical illness. Curr. Opin. Crit. Care. 2004; 10(5):378.##[10]. Mani, A.R., Montagnese, S., Jackson, C.D., et al. Decreased heart rate variability in patients with cirrhosis relates to the presence and degree of hepatic encephalopathy. Am. J. Physiol. Gastrointest. Liver. Physiol. 2009; Feb;296(2):G330-8. doi: 10.1152/ajpgi.90488.2008. ##[11]. Ahmad, S., Ramsay, T., Huebsch, L., et al. Continuous multi-parameter heart rate variability analysis heralds onset of sepsis in adults. PLoS One., 2009; Aug 14; 4(8):e6642. doi:10.1371/journal.pone.0006642.##[12]. Moss, T.J., Lake, D.E., Moorman, J.R., Local dynamics of heart rate: detection and prognostic implications. Physiol. Meas. 2014; Oct; 35(10):1929-42. doi:10.1088/0967-3334/35/10/1929.##[13]. Ebadi, H., Shirazi, A.H., Mani, A.R., Jafari, G.R., Inverse statistical approach in heartbeat time series. J. Stat. Mech. 2011; Aug P08014.##[14]. Shirazi, A.H., Raoufy, M.R., Ebadi, H., et al. Quantifying memory in complex physiological time-series. PLoS One. 2013; Sep 5: 8(9):e72854.##[15]. Mazloom, R., Shirazi, A.H., Hajizadeh, S., Dehpour, A.R., Mani, A.R., The effect of endotoxin on the controllability of cardiac rhythm in rats. Physiol. Meas. 2014; Mar: 35(3):339-49.##[16]. Goldberger, A.L., Findley, L.J., Blackburn, M.R., Mandell, A.J., Nonlinear dynamics of heart failure: implications of long-wavelength cardiopulmonary oscillations. Am. Heart J. 1984; 107:612-615.##[17]. Lipsitz, L.A., Mietus, J., Moody, G.B., Goldberger, A.L., Spectral characteristics of heart rate variability before and during postural tilt. Relations to aging and risk of syncope. Circulation. 1990; Jun; 81(6):1803-10.##[18]. Lipsitz, L.A., Goldberger, A.L., Loss of 'complexity' and aging. Potential applications of fractals and chaos theory to senescence. JAMA. 1992; Apr 1; 267(13):1806-9.##[19]. Lipsitz ,L.A., Age-related changes in the “complexity” of cardiovascular dynamics: a potential marker of vulnerability to disease. Chaos. 1995; 5:102–9.##[20]. Goldberger, A.L., Non-linear dynamics for clinicians: chaos theory, fractals, and complexity at the bedside. Lancet. 1996; 347:1312–1314.##[21]. Iyengar, N., Peng, C.K., Morin, R., Goldberger, A.L., Lipsitz, L.A., Age-related alterations in the fractal scaling of cardiac interbeat interval dynamics. Am. J. Physiol. 1996; 271: R1078–84.##[22]. Goldberger, A.L., Fractal variability versus pathologic periodicity: complexity loss and stereotypy in disease. Perspect. Biol. Med. 40:543–561.##[23]. Pikkujamsa, S.M., Makikallio, T.H., Sourander, L.B., et al. Cardiac interbeat interval dynamics from childhood to senescence: comparison of conventional and new measures based on fractals and chaos theory. Circulation. 1999; 100:393–9.##[24]. Beckers, F., Verheyden, B., Aubert, A.E., Aging and nonlinear heart rate control in a healthy population. Am. J. Physiol. Heart. Circ. Physiol. 2006; 290:H2560–70.##[25]. Goldberger, A.L., Amaral, L.A.N., Glass, L., Hausdorff, J.M., et al. PhysioBank., PhysioToolkit., and PhysioNet: Components of a New Research Resource for Complex Physiologic Signals. Circulation. 2000; 101(23):e215-e220##[26]. Peng, C.K., Mietus, J.E., Liu, Y., et al. Quantifying Fractal Dynamics of Human Respiration: Age and Gender Effects. Ann. Biomed. Eng. May; 2002; 30(5):683-92.##[27]. Kaplan, D.T., Biophys, J., Furman, M.I., et al. Aging and the complexity of cardiovascular dynamics. 1991; Apr 59(4): 945–949.##[28]. Wei, J.Y., Gersh, B.J. Heart disease in the elderly. Curr. Probl. Cardiol. 1987; 12:7-65.##[29]. Lipsitz, L.A., Clinical physiology of aging. In: Textbook of Internal Medicine. 2004; 3rd edition. Philadelphia. PA: Lippincott.##[30]. Liu, Y.Y., Slotine, J.J., Barab´asi, A.L., Controllability of complex networks. Nature. 2011; 473:167–73.##[31]. Raoufy MR, Ghafari T, Mani AR., Complexity Analysis of Respiratory Dynamics. Am J Respir Crit Care Med. 2017; Jul 15;196(2):247-248. ##[32]. Schmidt H.,  Saworski, J., Werdan, K., Müller-Werdan, U., Decreased beating rate variability of spontaneously contracting cardiomyocytes after co-incubation with endotoxin.  J. Endotoxin. Res. 2007; 13(6):339-42. doi:10.1177/0968051907086233.##[33]. Gholami, M., Mazaheri, P., Mohamadi, A., Endotoxemia is associated with partial uncoupling of cardiac pacemaker from cholinergic neural control in rats. Shock. 2012; Feb;37(2):219-27. doi:10.1097/SHK.0b013e318240b4be. ## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Renin-angiotensin system and unilateral ureteral obstruction</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Unilateral ureteral obstruction (UUO) is a clinical scenario that leads to obstructive nephropathy. UUO alters the expression of many mediators in the ipsilateral kidney. Renin-angiotensin system (RAS) is involved in UUO. Angiotensin II (Ang II) and angiotensin 1-7 (Ang 1-7) as the main arms of RAS influence kidney function which may alter by UUO. Ang II via Ang II receptor subtypes I (AT1R) reduces renal blood flow and glomerular filtration rate and induces oxidative stress, apoptosis as well as inflammation in renal tissue and contributes to renal fibrosis in UUO model. Also, Ang 1-7 receptor (MasR) and Ang II receptor subtype II (AT2R) may have a protective effect against UUO-induced renal injury. In addition, there is crosstalk among RAS with the main vasodilator factors (prostaglandins E2 and I2, bradykinin, atrial natriuretic factor, nitric oxide and adenosine) and the main vasoconstrictor factors (endothelin and vasopressin) in the ipsilateral kidney with UUO. In this review, the roles of the RAS on renal function and its interactions with the other factors in the kidney with UUO were discussed.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>266</FPAGE>
			<TPAGE>278</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/1
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1396/5/10
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/29
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/8/7
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Jalal</Name>
				<MidName></MidName>
				<Family>Hassanshahi</Family>
				<NameE>Jalal</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hassanshahi</FamilyE>
				<Organizations>
				<Organization>Water &#38; Electrolytes research Center, Isfahan University of Medical Sciences, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>hasanshahij@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Maleki</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Maleki</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, Ilam University of Medical Sciences, Ilam, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>maryammaleki777@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mehdi</Name>
				<MidName></MidName>
				<Family>Nematbakhsh</Family>
				<NameE>Mehdi</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Nematbakhsh</FamilyE>
				<Organizations>
				<Organization>Water &#38; Electrolytes research Center, Isfahan University of Medical Sciences, Isfahan, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>nematbakhsh@med.mui.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Renin-angiotensin system</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Unilateral ureteral obstruction</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Kidney injury</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Angiotensin II</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Angiotensin 1-7</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Alan C, Kurt HA, Topaloğlu N, Ersay AR, Cakir D, Baştürk G. Nitric oxide and asymmetric dimethyl arginine (adma) levels in an experimental hydronephrotic kidney caused by unilateral partial ureteral obstruction. International braz j urol: official journal of the Brazilian Society of Urology 2016; 42: 614.##Amann B, Tinzmann R, Angelkort B. Ace inhibitors improve diabetic nephropathy through suppression of renal mcp-1. Diabetes Care 2003; 26: 2421-2425.##Armando I, Jezova M, Juorio AV, Terrón JA, Falcón-Neri A, Semino-Mora C, et al. Estrogen upregulates renal angiotensin ii at2receptors. American Journal of Physiology-Renal Physiology 2002; 283: F934-F943.##Bae EH, Kim IJ, Park JW, Ma SK, Choi K, Lee J, et al. Altered regulation of renin-angiotensin, endothelin and natriuretic peptide systems in rat kidney with chronic unilateral ureteral obstruction. Urologia internationalis 2007; 79: 170-176.##Baiardi G, Macova M, Armando I, Ando H, Tyurmin D, Saavedra JM. Estrogen upregulates renal angiotensin ii at 1 and at 2 receptors in the rat. Regulatory peptides 2005; 124: 7-17.##Bascands J-L, Schanstra JP. Obstructive nephropathy: Insights from genetically engineered animals. Kidney international 2005; 68: 925-937.##Benndorf RA, Krebs C, Hirsch-Hoffmann B, Schwedhelm E, Cieslar G, Schmidt-Haupt R, et al. Angiotensin ii type 2 receptor deficiency aggravates renal injury and reduces survival in chronic kidney disease in mice. Kidney international 2009; 75: 1039-1049.##Bhaskaran M, Reddy K, Radhakrishanan N, Franki N, Ding G, Singhal PC. Angiotensin ii induces apoptosis in renal proximal tubular cells. American Journal of Physiology-Renal Physiology 2003; 284: F955-F965.##Bosnyak S, Jones ES, Christopoulos A, Aguilar M-I, Thomas WG, Widdop RE. Relative affinity of angiotensin peptides and novel ligands at at1 and at2 receptors. Clinical science 2011; 121: 297-303.##Brewster UC, Perazella MA. The renin-angiotensin-aldosterone system and the kidney: Effects on kidney disease. The American journal of medicine 2004; 116: 263-272.##Bürgelová M, Kramer HJ, Teplan V, Thumová M, Červenka L. Effects of angiotensin-(1–7) blockade on renal function in rats with enhanced intrarenal ang ii activity. Kidney international 2005; 67: 1453-1461.##Burns WC, Velkoska E, Dean R, Burrell LM, Thomas MC. Angiotensin ii mediates epithelial-to-mesenchymal transformation in tubular cells by ang 1–7/mas-1-dependent pathways. American Journal of Physiology-Renal Physiology 2010; 299: F585-F593.##Campbell DJ. The renin–angiotensin and the kallikrein–kinin systems. The international journal of biochemistry &#38; cell biology 2003; 35: 784-791.##Canals M, Jenkins L, Kellett E, Milligan G. Up-regulation of the angiotensin ii type 1 receptor by the mas proto-oncogene is due to constitutive activation of gq/g11 by mas. Journal of Biological Chemistry 2006; 281: 16757-16767.##Carey R, Jin X, Wang Z, Siragy H. Nitric oxide: A physiological mediator of the type 2 (at2) angiotensin receptor. Acta physiologica scandinavica 2000; 168: 65-71.##Carlström M, Brown RD, Edlund J, Sällström J, Larsson E, Teerlink T, et al. Role of nitric oxide deficiency in the development of hypertension in hydronephrotic animals. American Journal of Physiology-Renal Physiology 2008a; 294: F362-F370.##Carlström M, Lai EY, Steege A, Sendeski M, Ma Z, Zabihi S, et al. Nitric oxide deficiency and increased adenosine response of afferent arterioles in hydronephrotic mice with hypertension. Hypertension 2008b; 51: 1386-1392.##Ceravolo GS, Montezano AC, Jordão MT, Akamine EH, Costa TJ, Takano AP, et al. An interaction of renin-angiotensin and kallikrein-kinin systems contributes to vascular hypertrophy in angiotensin ii-induced hypertension: In vivo and in vitro studies. PloS one 2014; 9: e111117.##Chappel M, Ferrario C. 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Role of methoxyestradiols in the growth inhibitory effects of estradiol on human glomerular mesangial cells. Hypertension 2002; 39: 418-424.##Eddy AA, López-Guisa JM, Okamura DM, Yamaguchi I. Investigating mechanisms of chronic kidney disease in mouse models. Pediatric nephrology 2012; 27: 1233-1247.##Eltzschig HK, Ibla JC, Furuta GT, Leonard MO, Jacobson KA, Enjyoji K, et al. Coordinated adenine nucleotide phosphohydrolysis and nucleoside signaling in posthypoxic endothelium role of ectonucleotidases and adenosine a2b receptors. The Journal of experimental medicine 2003; 198: 783-796.##Eltzschig HK, Thompson LF, Karhausen J, Cotta RJ, Ibla JC, Robson SC, et al. Endogenous adenosine produced during hypoxia attenuates neutrophil accumulation: Coordination by extracellular nucleotide metabolism. Blood 2004; 104: 3986-3992.##Eskild-Jensen A, Paulsen LF, Wogensen L, Olesen P, Pedersen L, Frøkiær J, et al. At1 receptor blockade prevents interstitial and glomerular apoptosis but not fibrosis in pigs with neonatal induced partial unilateral ureteral obstruction. American Journal of Physiology-Renal Physiology 2007; 292: F1771-F1781.##Esteban V, Lorenzo O, Rupérez M, Suzuki Y, Mezzano S, Blanco J, et al. Angiotensin ii, via at1 and at2 receptors and nf-κb pathway, regulates the inflammatory response in unilateral ureteral obstruction. Journal of the American Society of Nephrology 2004; 15: 1514-1529.##Felsen D, Schulsinger D, Gross SS, Kim FY, Marion D, Vaughan ED. Renal hemodynamic and ureteral pressure changes in response to ureteral obstruction: The role of nitric oxide. The Journal of urology 2003; 169: 373-376.##Fernandes L, Fortes ZB, Nigro D, Tostes RC, Santos RA, de Carvalho MHC. Potentiation of bradykinin by angiotensin-(1-7) on arterioles of spontaneously hypertensive rats studied in vivo. 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			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Ferulic acid, a phenolic phytochemical with neuroprotective, anti-inflammatory, and antioxidant properties, has shown promising antidepressant-like effects in behavioral studies; however, its mechanism(s) of action have not been fully understood. Based on the contribution of nerve growth factor (NGF) and endocannabinoid signaling (eCBs) to the emotional or antidepressant activity and their interaction, we aimed to evaluate whether ferulic acid affects NGF or eCB contents in the brain regions involved in the modulation of emotions. Methods: Following single and four-week once-daily intraperitoneal injections of ferulic acid (50, 100, 130 and 150 mg/kg), amitriptyline (2.5, 5, 8 and 10 mg/kg) or lorazepam (2, 5, 8 and 10 mg/kg) into male Wistar rats, NGF and eCB levels were quantified by Bio-Rad protein assay and isotope-dilution liquid chromatography/mass spectrometry. In the case of significant alteration of brain NGF or eCB content, the effects of pre-treatment with cannabinoid CB1 or CB2 receptor antagonist (AM251 or SR144528) were investigated. Results: Four-week treatment with the highest doses of ferulic acid or amitriptyline led to a significant and sustained enhancement of eCB and NGF contents in brain region-specific fashion. Neither acute nor four-week treatment with lorazepam affected NGF or eCB levels. Pre-treatment with AM251 (3 mg/kg), but not SR144528, prevented the elevation of NGF levels. AM251 showed no effect by itself. Conclusion: Ferulic acid similar to the conventional antidepressant, amitriptyline, affects brain eCB and NGF signaling. CB1 receptors mediate the production of brain NGF.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>279</FPAGE>
			<TPAGE>294</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/12017/02/5
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1395/11/17
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/292017/09/7
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/6/16
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Parichehr</Name>
				<MidName></MidName>
				<Family>Hassanzadeh</Family>
				<NameE>Parichehr</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hassanzadeh</FamilyE>
				<Organizations>
				<Organization>Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>p-hassanzadeh@razi.tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Elham</Name>
				<MidName></MidName>
				<Family>Arbabi</Family>
				<NameE>Elham</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Arbabi</FamilyE>
				<Organizations>
				<Organization>Research Center for Gastroenterology and Liver Disease, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>arbabiavalelham@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Atyabi</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Atyabi</FamilyE>
				<Organizations>
				<Organization>Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>atyabifa@tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Rassoul</Name>
				<MidName></MidName>
				<Family>Dinarvand</Family>
				<NameE>Rassoul</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Dinarvand</FamilyE>
				<Organizations>
				<Organization>Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>Dinarvand@tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Ferulic acid</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Nerve growth factor</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Endocannabinoids</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>CB1 receptors</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Brain</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Prof. Abolhassan Ahmadiani##Prof. Mohammad-Reza Zali##Prof. Fatemeh Atyabi##Prof. Rassoul Dinarvand## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Effect of Ocimum basilicum hydro-alcoholic extract on oxidative damage of brain tissue following seizures induced by pentylenetetrazole in mice</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: A relationship between epileptic seizures and brain tissue oxidative damage has been suggested. Ocimum basilicum (O. basilicum) has been shown to have beneficial effects including hypnotic and protective against tissue oxidative damage. The present study was designed to evaluate the effects of O. basilicum hydro-alcoholic extract on oxidative damage of brain tissue following seizures induced by pentylenetetrazole (PTZ) in mice. Methods: The animals were grouped and treated as follows: 1- control group which received saline; 2- PTZ group (90 mg/kg, ip); 3 to 5- three groups which received 25, 50 or 100 mg/kg of a hydro-ethanolic extract of O. basilicum before PTZ. First minimal clonic seizure (MCS) and the first generalized tonic-clonic seizure (GTCS) latencies were analyzed. The brains of the animals were then collected and stored to use for biochemical evaluation. Results: The plant extract in 50 and 100 mg/kg doses, significantly postponed the MCS and GTCS seizures onsets (P&#60;0.05-P&#60;0.01) when administered before PTZ. PTZ - induced seizures also increased lipid-peroxidation in the brain tissue which was presented by a high level of malondialdehyde (MDA) in the brain tissue compared to the control group (P&#60;0.001). O. basilicum extract attenuated MDA levels in the brain (P&#60;0.05-P&#60;0.001). PTZ - induced seizures also decreased brain tissue total thiols compared to the control group (P&#60;0.001). Pretreatment with all doses of O. basilicum extract improved thiol content in the brain tissue (P&#60;0.05). Conclusion: The current study revealed that hydro-ethanolic extract of O. basilicum possesses significant antioxidant and anticonvulsant activities.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>295</FPAGE>
			<TPAGE>303</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/12017/02/52017/06/23
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1396/4/2
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/292017/09/72017/10/4
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/7/12
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Tayebeh</Name>
				<MidName></MidName>
				<Family>Khodabakhshi</Family>
				<NameE>Tayebeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Khodabakhshi</FamilyE>
				<Organizations>
				<Organization>Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>khodabakhsht921@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Farimah</Name>
				<MidName></MidName>
				<Family>Beheshti</Family>
				<NameE>Farimah</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Beheshti</FamilyE>
				<Organizations>
				<Organization>Department of Basic Science and Neuroscience Research Center, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>beheshtif931@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mahmoud</Name>
				<MidName></MidName>
				<Family>Hosseini</Family>
				<NameE>Mahmoud</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hosseini</FamilyE>
				<Organizations>
				<Organization>Division of Neurocognitive Sciences, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>hosseinim@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Seyed Mojtaba</Name>
				<MidName></MidName>
				<Family>Mousavi</Family>
				<NameE>Seyed Mojtaba</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mousavi</FamilyE>
				<Organizations>
				<Organization>Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>mousavism911@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hassan</Name>
				<MidName></MidName>
				<Family>Rakhshandeh</Family>
				<NameE>Hassan</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rakhshandeh</FamilyE>
				<Organizations>
				<Organization>Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>rakhshandehh@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Hamid Reza</Name>
				<MidName></MidName>
				<Family>Sadeghnia</Family>
				<NameE>Hamid Reza</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sadeghnia</FamilyE>
				<Organizations>
				<Organization>Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>sadeghniahr@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Azita</Name>
				<MidName></MidName>
				<Family>Aghaei</Family>
				<NameE>Azita</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Aghaei</FamilyE>
				<Organizations>
				<Organization>Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>aghaeia@mums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Ocimum basilicum</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Hydro-alcoholic extract</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pentylenetetrazole</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Seizures</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Mice</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Oxidative damage</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Brain</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>1.	Sander JW. The epidemiology of epilepsy revisited. Curr Opin Neurol. 2003;16(2):165-70.##2.	Meador KJ. Cognitive outcomes and predictive factors in epilepsy. Neurology. 2002;58(8 Suppl 5):S21-6.##3.	Kudin AP, Kudina TA, Seyfried J, Vielhaber S, Beck H, Elger CE, et al. Seizure-dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus. Eur J Neurosci. 2002;15(7):1105-14.##4.	Mehla J, Reeta KH, Gupta P, Gupta YK. Protective effect of curcumin against seizures and cognitive impairment in a pentylenetetrazole-kindled epileptic rat model. Life Sci. 2010;87(19-22):596-603.##5.	Hosseini M, Harandizadeh F, Niazamand S, Soukhtanloo M, Mahmoudabady M. Antioxidant effect of Achillea wilhelmsii extract on pentylenetetrazole (seizure model)-induced oxidative brain damage in Wistar rats. Indian J Physiol Pharmacol. 2013;57(4):418-24.##6.	Rosche J, Uhlmann C, Froscher W. [Cognitive deficits and psychiatric disorders in patients with new-onset epilepsy]. Fortschr Neurol Psychiatr. 2010;78(1):18-26.##7.	Gupta YK, Briyal S. Protective effect of vineatrol against kainic acid induced seizures, oxidative stress and on the expression of heat shock proteins in rats. Eur Neuropsychopharmacol. 2006;16(2):85-91.##8.	Ramesh KV, Padmavathi K. Assessment of Immunomodulatory Activity of Euphorbia hirta L. Indian J Pharm Sci. 2010;72(5):621-5.##9.	Singh HP, Mittal S, Kaur S, Batish DR, Kohli RK. Characterization and antioxidant activity of essential oils from fresh and decaying leaves of Eucalyptus tereticornis. J Agric Food Chem. 2009;57(15):6962-6.##10.	Muralidharan A, Dhananjayan R. Cardiac stimulant activity of Ocimum basilicum Linn. extracts. 2004.##11.	Bilal A, Jahan N, Ahmed A, Bilal SN, Habib S, Hajra S. Phytochemical and pharmacological studies on Ocimum basilicum Linn-A review. Int J Curr Res Rev. 2012;4:73-83.##12.	Dashputre NL, Naikwade NS. Preliminary immunomodulatory activity of aqueous and ethanolic leaves extracts of Ocimum basilicum Linn. in mice. Int J Pharm Tech Res. 2010;2:1342-9.##13.	Kaya I, Yiğit N, Benli M. Antimicrobial activity of various extracts of Ocimum basilicum L. and observation of the inhibition effect on bacterial cells by use of scanning electron microscopy. African Journal of Traditional, Complementary and Alternative Medicines. 2008;5(4):363-9.##14.	Agrawal R, Tyagi E, Saxena G, Nath C. Cholinergic influence on memory stages: A study on scopolamine amnesic mice. Indian J Pharmacol. 2009;41(4):192-6.##15.	Di Stasi L, Oliveira G, Carvalhaes M, Queiroz-Junior M, Tien O, Kakinami S, et al. Medicinal plants popularly used in the Brazilian Tropical Atlantic Forest. Fitoterapia. 2002;73(1):69-91.##16.	Oliveira JS, Porto LA, Estevam CS, Siqueira RS, Alves PB, Niculau ES, et al. Phytochemical screening and anticonvulsant property of Ocimum basilicum leaf essential oil. Boletín Latinoamericano y del Caribe de Plantas Medicinales y Aromáticas. 2009;8(3):195-202.##17.	Bora KS, Arora S, Shri R. Role of Ocimum basilicum L. in prevention of ischemia and reperfusion-induced cerebral damage, and motor dysfunctions in mice brain. Journal of ethnopharmacology. 2011;137(3):1360-5.##18.	Mehri S, Meshki MA, Hosseinzadeh H. Linalool as a neuroprotective agent against acrylamide-induced neurotoxicity in Wistar rats. Drug and chemical toxicology. 2014:1-5.##19.	Askari VR, Baradaran Rahimi V, Ghorbani A, Rakhshandeh H. Hypnotic Effect of Ocimum basilicum on Pentobarbital-Induced Sleep in Mice. Iran Red Crescent Med J. 2016;18(7):e24261.##20.	Ebrahimzadeh Bideskan AR, Hosseini M, Mohammadpour T, Karami R, Khodamoradi M, Nemati Karimooy H, et al. Effects of soy extract on pentylenetetrazol-induced seizures in ovariectomized rats. Zhong Xi Yi Jie He Xue Bao.9(6):611-8.##21.	Farrokhi E, Hosseini M, Beheshti F, Vafaee F, Hadjzadeh MA-R, Dastgheib SS. Brain Tissues Oxidative Damage as A Possible Mechanism of Deleterious Effects of Propylthiouracil-Induced Hypothyroidism on Learning and Memory in Neonatal and Juvenile Growth in Rats. Basic and clinical neuroscience. 2014;5(4):285.##22.	Beheshti F, Hosseini M, Shafei MN, Soukhtanloo M, Ghasemi S, Vafaee F, et al. The effects of Nigella sativa extract on hypothyroidism-associated learning and memory impairment during neonatal and juvenile growth in rats. Nutritional Neuroscience. 2017;20(1):49-59.##23.	Hosseini M, Harandizadeh F, Niazmand S, Soukhtanloo M, Faizpour A, Ghasemabady M. The role for nitric oxide on the effects of hydroalcoholic extract of Achillea wilhelmsii on seizure. Avicenna J Phytomed. 2014;4(4):251-9.##24.	Hosseini M, Pkan P, Rakhshandeh H, Aghaie A, Sadeghnia HR, Rahbardar MG. The Effect of Hydro-Alcoholic Extract of Citrus Flower on Pentylenetetrazole and Maximal Electroshock-Induced Seizures in Mice. World Applied Sciences Journal. 2011;15(8):1104-9.##25.	Hosseini M, Sadeghnia HR, Salehabadi S, Alavi H, Gorji A. The effect of L-arginine and L-NAME on pentylenetetrazole induced seizures in ovariectomized rats, an in vivo study. Seizure. 2009;18(10):695-8.##26.	Pourganji M, Hosseini M, Soukhtanloo M, Zabihi H, Hadjzadeh MA. Protective role of endogenous ovarian hormones against learning and memory impairments and brain tissues oxidative damage induced by lipopolysaccharide. Iran Red Crescent Med J. 2014;16(3):e13954.##27.	Sakina M, Dandiya P, Hamdard M, Hameed A. Preliminary psychopharmacological evaluation of&#60; i&#62; Ocimum sanctum&#60;/i&#62; leaf extract. J Ethnopharmacol. 1990;28(2):143-50.##28.	Patel M. Mitochondrial dysfunction and oxidative stress: cause and consequence of epileptic seizures. Free Radic Biol Med. 2004;37(12):1951-62.##29.	Costello DJ, Delanty N. Oxidative injury in epilepsy: potential for antioxidant therapy? Expert Rev Neurother. 2004;4(3):541-53.##30.	Zhen J, Qu Z, Fang H, Fu L, Wu Y, Wang H, et al. Effects of grape seed proanthocyanidin extract on pentylenetetrazole-induced kindling and associated cognitive impairment in rats. Int J Mol Med. 2014;34(2):391-8.##31.	Porter RJ. Antiepileptic drug development program. Prog Clin Biol Res. 1983;127:53-66.##32.	Hosseinzadeh H, Sadeghnia HR. Protective effect of safranal on pentylenetetrazol-induced seizures in the rat: involvement of GABAergic and opioids systems. Phytomedicine. 2007;14(4):256-62.##33.	Loscher W, Fassbender CP, Nolting B. The role of technical, biological and pharmacological factors in the laboratory evaluation of anticonvulsant drugs. II. Maximal electroshock seizure models. Epilepsy Res. 1991;8(2):79-94.##34.	Xie T, Wang WP, Mao ZF, Qu ZZ, Luan SQ, Jia LJ, et al. Effects of epigallocatechin-3-gallate on pentylenetetrazole-induced kindling, cognitive impairment and oxidative stress in rats. Neurosci Lett. 2012;516(2):237-41.##35.	Liu SH, Chang CD, Chen PH, Su JR, Chen CC, Chaung HC. Docosahexaenoic acid and phosphatidylserine supplementations improve antioxidant activities and cognitive functions of the developing brain on pentylenetetrazol-induced seizure model. Brain Res. 2012;1451:19-26.##36.	Sudha K, Rao AV, Rao A. Oxidative stress and antioxidants in epilepsy. Clin Chim Acta. 2001;303(1-2):19-24.##37.	Reilly C, Agnew R, Neville BG. Depression and anxiety in childhood epilepsy: a review. Seizure. 2011;20(8):589-97.##38.	Maldonado A, Ramos W, Perez J, Huaman LA, Gutierrez EL. [Convulsive status epilepticus: clinico-epidemiologic characteristics and risk factors in Peru]. Neurologia. 2010;25(8):478-84.##39.	Liang LP, Beaudoin ME, Fritz MJ, Fulton R, Patel M. Kainate-induced seizures, oxidative stress and neuronal loss in aging rats. Neuroscience. 2007;147(4):1114-8.##40.	Vafaee F, Hosseini M, Sadeghinia HR, Hadjzadeh MA, Soukhtanloo M, Rahimi M. The effects of soy extract on spatial learning and memory damage induced by global ischemia in ovariectomised rats. Malays J Med Sci. 2014;21(3):19-30.##41.	Burdock GA, Carabin IG. Safety assessment of coriander (Coriandrum sativum L.) essential oil as a food ingredient. Food Chem Toxicol. 2009;47(1):22-34.##42.	Ghasemi Pirbalouti A, Mahdad E, Craker L. Effects of drying methods on qualitative and quantitative properties of essential oil of two basil landraces. Food Chem. 2013;141(3):2440-9.##43.	Bakkali F, Averbeck S, Averbeck D, Idaomar M. Biological effects of essential oils--a review. Food Chem Toxicol. 2008;46(2):446-75.##44.	Oxenham SK, Svoboda KP, Walters DR. J Phytopathol. 2005;153:174-80.##45.	Farag M. Utilization of Basil Extract as a Radioprotector in Male Rats. 2013.##46.	Chiang LC, Ng LT, Cheng PW, Chiang W, Lin CC. Antiviral activities of extracts and selected pure constituents of Ocimum basilicum. Clin Exp Pharmacol Physiol. 2005;32(10):811-6.##47.	Quintans-Junior LJ, Barreto RS, Menezes PP, Almeida JR, Viana AF, Oliveira RC, et al. beta-Cyclodextrin-complexed (-)-linalool produces antinociceptive effect superior to that of (-)-linalool in experimental pain protocols. Basic Clin Pharmacol Toxicol. 2013;113(3):167-72.##48.	Sakurada T, Kuwahata H, Katsuyama S, Komatsu T, Morrone LA, Corasaniti MT, et al. Intraplantar injection of bergamot essential oil into the mouse hindpaw: effects on capsaicin-induced nociceptive behaviors. Int Rev Neurobiol. 2009;85:237-48.##49.	Okoli CO, Ezike AC, Agwagah OC, Akah PA. Anticonvulsant and anxiolytic evaluation of leaf extracts of Ocimum gratissimum, a culinary herb. Pharmacognosy Res. 2010;2(1):36-40.##50.	Muscat R, Willner P. Suppression of sucrose drinking by chronic mild unpredictable stress: a methodological analysis. Neuroscience &#38; Biobehavioral Reviews. 1992;16(4):507-17.##51.	Golechha M, Bhatia J, Arya DS. Hydroalcoholic extract of Emblica officinalis Gaertn. affords protection against PTZ-induced seizures, oxidative stress and cognitive impairment in rats. Indian J Exp Biol. 2010;48(5):474-8.##52.	Soszynski M, Bartosz G. Decrease in accessible thiols as an index of oxidative damage to membrane proteins. Free Radic Biol Med. 1997;23(3):463-9.##53.	Jayasinghe C, Gotoh N, Aoki T, Wada S. Phenolics composition and antioxidant activity of sweet basil (Ocimum basilicum L.). Journal of Agricultural and Food Chemistry. 2003;51(15):4442-9.##54.	Politeo O, Jukic M, Milos M. Chemical composition and antioxidant capacity of free volatile aglycones from basil (Ocimum basilicum L.) compared with its essential oil. Food Chemistry. 2007;101(1):379-85.##55.	Bayala B, Bassole IHN, Gnoula C, Nebie R, Yonli A, Morel L, et al. Chemical Composition, Antioxidant, Anti-Inflammatory and Anti-Proliferative Activities of Essential Oils of Plants from Burkina Faso. PloS one. 2014;9(3):e92122.##56.	Khanna N, Bhatia J. Antinociceptive action of Ocimum sanctum (Tulsi) in mice: possible mechanisms involved. J Ethnopharmacol. 2003;88(2-3):293-6.##57.	Elisabetsky E, Brum LF, Souza DO. Anticonvulsant properties of linalool in glutamate-related seizure models. Phytomedicine. 1999;6(2):107-13.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>A distinct serum protein pattern in patients with paranoid schizophrenia</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Schizophrenia is a chronic mental illness, whose aetiology is still unclear; therefore, information about differences in serum protein patterns may improve the understanding of the pathophysiology of schizophrenia. The goal of this study was to use the proteomic approach to identify altered protein levels in the serum samples from patients with schizophrenia. Methods: Blood was collected from 10 patients with paranoid schizophrenia and 10 healthy volunteers matched by sex and age. Serum proteins were isolated by 2D gel electrophoresis. Proteins with altered levels were identified by matrix-assisted laser desorption ionisation time-of-flight mass spectrometry. Results: We uncovered major changes in the expression of such proteins as apolipoproteins of classes A4 and C3, transthyretin (TTR) and serum amyloid A1. An increase in expression was found only for apolipoprotein A4, whereas the expression of apolipoprotein C3, TTR and serum amyloid A1 was decreased. The observed differences in the expression of serum proteins (TTR and serum amyloid) are in good agreement with the results obtained by other research groups during analyses of cerebrospinal fluid or post-mortem brain tissues by other methods. Conclusion: Such alterations of the expression of these proteins may indicate problems with regulation, for example, in the synthesis. On the other hand, the altered protein expression may simply reflect the pathophysiological status of patients, where these proteins could be candidates for biomarkers. Further research is needed to confirm the significance of the altered levels of these proteins in the pathogenesis of schizophrenia and to determine their suitability as biomarkers of schizophrenia.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>304</FPAGE>
			<TPAGE>311</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/12017/02/52017/06/232017/04/10
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1396/1/21
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/292017/09/72017/10/42017/09/22
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/6/31
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Irina V.</Name>
				<MidName></MidName>
				<Family>Alekseeva</Family>
				<NameE>Irina V.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Alekseeva</FamilyE>
				<Organizations>
				<Organization>Institute of Chemical Biology and Fundamental Medicine SB RAS, Novosibirsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>irina.alekseeva@niboch.nsc.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Nadezhda A.</Name>
				<MidName></MidName>
				<Family>Timofeyeva</Family>
				<NameE>Nadezhda A.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Timofeyeva</FamilyE>
				<Organizations>
				<Organization>Institute of Chemical Biology and Fundamental Medicine SB RAS, Novosibirsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>na_timof@niboch.nsc.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Svetlana A.</Name>
				<MidName></MidName>
				<Family>Ivanova</Family>
				<NameE>Svetlana A.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ivanova</FamilyE>
				<Organizations>
				<Organization>Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>svetlana@mail.tomsknet.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>German G.</Name>
				<MidName></MidName>
				<Family>Simutkin</Family>
				<NameE>German G.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Simutkin</FamilyE>
				<Organizations>
				<Organization>Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>simutkin@niboch.nsc.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Arkadiy V.</Name>
				<MidName></MidName>
				<Family>Semke</Family>
				<NameE>Arkadiy V.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Semke</FamilyE>
				<Organizations>
				<Organization>Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>redo@mail.tomsknet.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Innokentiy S.</Name>
				<MidName></MidName>
				<Family>Losenkov</Family>
				<NameE>Innokentiy S.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Losenkov</FamilyE>
				<Organizations>
				<Organization>Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>losenkov@niboch.nsc.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Nikolay A.</Name>
				<MidName></MidName>
				<Family>Bokhan</Family>
				<NameE>Nikolay A.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bokhan</FamilyE>
				<Organizations>
				<Organization>Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>mental@tnimc.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Olga S.</Name>
				<MidName></MidName>
				<Family>Fedorova</Family>
				<NameE>Olga S.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Fedorova</FamilyE>
				<Organizations>
				<Organization>Institute of Chemical Biology and Fundamental Medicine SB RAS, Novosibirsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>fedorova@niboch.nsc.ru</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Alexander A.</Name>
				<MidName></MidName>
				<Family>Chernonosov</Family>
				<NameE>Alexander A.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Chernonosov</FamilyE>
				<Organizations>
				<Organization>Institute of Chemical Biology and Fundamental Medicine SB RAS, Novosibirsk, Russia</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>alexander.chernonosov@niboch.nsc.ru</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Psychiatric disorder</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Schizophrenia</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Proteomics</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Biomarker</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Alekseeva IV, Timofeeva NA, Chernonosov AA, Ivanova SA, Bokhan NA, Fedorova OS. Use of two-dimensional electrophoresis for proteomic studies of serum from patients with mental disorders. Vestnik of Novosibirsk State University. Series: Biology, Clinical Medicine 2013; 11: 56–60.##Baumann H, Gauldie J. The acute phase response. Immunology Today 1994; 15: 74–80.##Bramon E, Dempster E, Frangou S, Shaikh M, Walshe M, Filbey FM, et al. Neuregulin-1 and the p300 waveform--a preliminary association study using a psychosis endophenotype. Schizophrenia research 2008; 103: 178–185.##Brauner JM, Groemer TW, Stroebel A, Grosse-Holz S, Oberstein T, Wiltfang J, et al. Spot quantification in two dimensional gel electrophoresis image analysis: Comparison of different approaches and presentation of a novel compound fitting algorithm. BMC bioinformatics 2014; 15: 181.##Bystritsky A. Treatment-resistant anxiety disorders. Molecular psychiatry 2006; 11: 805–814.##Candiano G, Bruschi M, Musante L, Santucci L, Ghiggeri GM, Carnemolla B, et al. Blue silver: A very sensitive colloidal coomassie g-250 staining for proteome analysis. Electrophoresis 2004; 25: 1327–1333.##Chattopadhyay A, Paila YD. Lipid-protein interactions, regulation and dysfunction of brain cholesterol. Biochemical and biophysical research communications 2007; 354: 627–633.##Chow TJ, Loh HC. Altered levels of serum haptoglobin and apo a-i in schizophrenia. Sains Malaysiana 2011; 40: 1319–1323.##Davalieva K, Maleva Kostovska I, Dwork AJ. Proteomics research in schizophrenia. Frontiers in cellular neuroscience 2016; 10: 18.##Eckel RH. Lipoprotein lipase. A multifunctional enzyme relevant to common metabolic diseases. The New England journal of medicine 1989; 320: 1060–1068.##Geyer MA, Vollenweider FX. Serotonin research: Contributions to understanding psychoses. Trends in pharmacological sciences 2008; 29: 445–453.##Giuliano S, Agresta AM, Palma Ad, Viglio S, Mauri P, Fumagalli M, et al. Proteomic analysis of lymphoblastoid cells from nasu-hakola patients: A step forward in our understanding of this neurodegenerative disorder. PloS one 2014; 9: e110073.##Guest PC, Guest FL, Martins-de Souza D. Making sense of blood-based proteomics and metabolomics in psychiatric research. The international journal of neuropsychopharmacology 2016; 19: 1–10.##Huang JT-J, Leweke FM, Oxley D, Wang L, Harris N, Koethe D, et al. Disease biomarkers in cerebrospinal fluid of patients with first-onset psychosis. PLoS medicine 2006; 3: e428.##Huang TL. Decreased serum albumin levels in taiwanese patients with schizophrenia. Psychiatry Clin Neurosci 2002; 56: 627-30.##Ivanova SA, Fedorenko OY, Smirnova LP, Semke AV. Biomarker discovery and development of pharmacogenetic approaches to personalized therapy of patients with schizophrenia. Siberian vestnik of psychiatry and narcology 2013: 12–16.##Kessler RC, Demler O, Frank RG, Olfson M, Pincus HA, Walters EE, et al. Prevalence and treatment of mental disorders, 1990 to 2003. The New England journal of medicine 2005; 352: 2515–2523.##Lepedda AJ, Nieddu G, Zinellu E, Muro Pd, Piredda F, Guarino A, et al. Proteomic analysis of plasma-purified vldl, ldl, and hdl fractions from atherosclerotic patients undergoing carotid endarterectomy: Identification of serum amyloid a as a potential marker. Oxidative medicine and cellular longevity 2013; 2013: 385214.##Moore H, West AR, Grace AA. The regulation of forebrain dopamine transmission: Relevance to the pathophysiology and psychopathology of schizophrenia. Biological Psychiatry 1999; 46: 40–55.##Pae CU, Paik IH, Lee C, Lee SJ, Kim JJ, Lee CU. Decreased plasma antioxidants in schizophrenia. Neuropsychobiology 2004; 50: 54-6.##Perkins DN, Pappin DJC, Creasy DM, Cottrell JS. Probability-based protein identification by searching sequence databases using mass spectrometry data. Electrophoresis 1999; 20: 3551–3567.##Pesic I, Dihazi GH, Muller GA, Jahn O, Hoffmann M, Eltoweissy M, et al. Short-term increase of glucose concentration in pds results in extensive removal and high glycation level of vital proteins during continuous ambulatory peritoneal dialysis. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2011; 26: 2674–2683.##Ranjekar PK, Hinge A, Hegde MV, Ghate M, Kale A, Sitasawad S, et al. Decreased antioxidant enzymes and membrane essential polyunsaturated fatty acids in schizophrenic and bipolar mood disorder patients. Psychiatry research 2003; 121: 109–122.##Turck CW, Maccarrone G, Sayan-Ayata E, Jacob AM, Ditzen C, Kronsbein H, et al. The quest for brain disorder biomarkers*. The Journal of Medical Investigation 2005; 52: 231–235.##van Os J, Kapur S. Schizophrenia. The Lancet 2009; 374: 635–645.##Vohnout B, Gaetano Gd, Donati MB, Iacoviello L. The relationship between dyslipidemia and inflammation. In: Mancini M, editor. Nutritional and metabolic bases of cardiovascular disease. Chichester, West Sussex, UK: Wiley-Blackwell, 2011: 202–210.##Wan C, Yang Y, Li H, La Y, Zhu H, Jiang L, et al. Dysregulation of retinoid transporters expression in body fluids of schizophrenia patients. Journal of proteome research 2006; 5: 3213–3216.##Wang H, Eckel RH. Lipoprotein lipase: From gene to obesity. American journal of physiology. Endocrinology and metabolism 2009; 297: E271-88.##Yang Y, Wan C, Li H, Zhu H, La Y, Xi Z, et al. Altered levels of acute phase proteins in the plasma of patients with schizophrenia. Analytical chemistry 2006; 78: 3571–3576.##Zheng P, Gao HC, Li Q, Shao WH, Zhang ML, Cheng K, et al. Plasma metabonomics as a novel diagnostic approach for major depressive disorder. Journal of proteome research 2012; 11: 1741–1748.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Anti-diabetic effect of aqueous extract Crocus sativus L. in tartrazine induced diabetic male rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: In this study, we evaluated the antidiabetic and antidiabetogenic effect of saffron against diabetes induced by artificial dye tartrazine on normal male rats. 

Methods: Dried saffron was macerated for 12 hours in distilled water before usage and crude extract was used to treat male rats. Rats were divided into 5 groups consisted of 6 rats and treatment was performed daily and orally. Group-1 treated with distilled water, group-2 with tartrazine 10mg/kg followed by saffron 120mg/kg until the last day of treatment, group-3 administered with tartrazine, group-4 treated with saffron for 60 days and administered with tartrazine, group-5 with saffron for 105 days. Levels of blood glucose and body weight have been evaluated every 10 days and clinical demonstrations and metabolic parameters were evaluated at the end of the experiment. Results: Levels of blood glucose and body weight have been evaluated every 10 days and clinical demonstrations and metabolic parameters were evaluated at the end of the experiment. Results showed that treatment with tartrazine and saffron did not affect body weights, metabolic parameters but changed the blood glucose levels after 105 days of administration. The levels of glucose and creatinine were significantly increased in group-2 and group-3 compared to control group (P&#60;0.05). There was no significant difference in the level of glucose, creatinine in group4 (P&#62;0.05). Treatment with saffron decreases creatinine level. Conclusion: The outcomes suggest that saffron has curative (antidiabetic) and protective (antidiabetogenic) effect against diabetes induced by tartrazine via reducing blood glucose level and creatinine. Therefore, it should be considered in future therapeutic researches.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>312</FPAGE>
			<TPAGE>321</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/12017/02/52017/06/232017/04/102017/03/1
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1395/12/11
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/292017/09/72017/10/42017/09/222017/10/29
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/8/7
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Iliass</Name>
				<MidName></MidName>
				<Family>Lahmass</Family>
				<NameE>Iliass</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Lahmass</FamilyE>
				<Organizations>
				<Organization>Université Mohamed Premier, Faculty of Sciences, Department of Biology, Laboratory of Biochemistry, Oujda, Morocco</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>i.lahmass@ump.ac.ma</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Assia</Name>
				<MidName></MidName>
				<Family>Sabouni</Family>
				<NameE>Assia</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sabouni</FamilyE>
				<Organizations>
				<Organization>Université Mohamed Premier, Faculty of Sciences, Department of Biology, Laboratory of Biochemistry, Oujda, Morocco</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>a.sabouni@ump.ac.ma</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohammed</Name>
				<MidName></MidName>
				<Family>Elyoubi</Family>
				<NameE>Mohammed</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Elyoubi</FamilyE>
				<Organizations>
				<Organization>Université Mohamed Premier, Faculty of Sciences, Department of Biology, Laboratory of Biochemistry, Oujda, Morocco</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>m.elyoubi@ump.ac.ma</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Redouane</Name>
				<MidName></MidName>
				<Family>Benabbes</Family>
				<NameE>Redouane</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Benabbes</FamilyE>
				<Organizations>
				<Organization>Université Mohamed Premier, Faculty of Sciences, Department of Biology, Laboratory of Biochemistry, Oujda, Morocco</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>r.benabbes@ump.ac.ma</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Slimane</Name>
				<MidName></MidName>
				<Family>Mokhtari</Family>
				<NameE>Slimane</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Mokhtari</FamilyE>
				<Organizations>
				<Organization>Regional Laboratory of Medical Analysis, Hôpital Al Farabi, Oujda, Morocco</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>s.moukhtari@ump.ac.ma</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ennouamane</Name>
				<MidName></MidName>
				<Family>Saalaoui</Family>
				<NameE>Ennouamane</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Saalaoui</FamilyE>
				<Organizations>
				<Organization>Université Mohamed Premier, Faculty of Sciences, Department of Biology, Laboratory of Biochemistry, Oujda, Morocco</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>e.saalaoui@ump.ac.ma</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Crocus sativus L.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antidiabetic effect</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Antidiabetogenic effect</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Tartrazine</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Saffron</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Abdullaev FI, Espinosa-Aguirre JJ. Biomedical properties of saffron and its potential use in cancer therapy and chemoprevention trials. Cancer detection and prevention 2004; 28: 426-432.##Akhondzadeh S, Fallah-Pour H, Afkham K, Jamshidi A-H, Khalighi-Cigaroudi F. Comparison of crocus sativus l. And imipramine in the treatment of mild to moderate depression: A pilot double-blind randomized trial [isrctn45683816]. BMC complementary and alternative medicine 2004; 4: 1.##Amin KA, Abdel Hameid H, 2nd, Abd Elsttar AH. Effect of food azo dyes tartrazine and carmoisine on biochemical parameters related to renal, hepatic function and oxidative stress biomarkers in young male rats. Food Chem Toxicol 2010; 48: 2994-9.##Arasteh A, Aliyev A, Khamnei S, Delazar A, Mesgari M, Mehmannavaz Y. Effects of hydromethanolic extract of saffron (crocus sativus) on serum glucose, insulin and cholesterol levels in healthy male rats.  2010.##Ashour AA, Abdelaziz I. Role of fast green on the blood of rats and the therapeutic action of vitamins c or e. Int. J. Integr. Biol 2009; 6: 6-11.##Assimopoulou AN, Sinakos Z, Papageorgiou VP. Radical scavenging activity of crocus sativus l. Extract and its bioactive constituents. Phytother Res 2005; 19: 997-1000.##Bhandari PR. Crocus sativus l. (saffron) for cancer chemoprevention: A mini review. J Tradit Complement Med 2015; 5: 81-7.##Borzelleca J, Hallagan J. A chronic toxicity/carcinogenicity study of fd &#38; c yellow no. 5 (tartrazine) in mice. Food and chemical toxicology 1988; 26: 189-194.##Caballero-Ortega H, Pereda-Miranda R, Abdullaev FI. Hplc quantification of major active components from 11 different saffron (&#60; i&#62; crocus sativus&#60;/i&#62; l.) sources. Food Chemistry 2007; 100: 1126-1131.##Chan JC, Ng MC, Critchley JA, Lee SC, Cockram CS. Diabetes mellitus--a special medical challenge from a chinese perspective. Diabetes Res Clin Pract 2001; 54 Suppl 1: S19-27.##Chen Y, Zhang H, Tian X, Zhao C, Cai L, Liu Y, et al. Antioxidant potential of crocins and ethanol extracts of gardenia jasminoides ellis and crocus sativus l.: A relationship investigation between antioxidant activity and crocin contents. Food Chem 2008; 109: 484-492.##Collins TFX, Black TN, Brown LH, Bulhack P. Study of the teratogenic potential of fd &#38; c yellow no. 5 when given by gavage to rats. Food and Chemical Toxicology 1990; 28: 821-827.##Committee of the Japan Diabetes Society on the Diagnostic Criteria of Diabetes M, Seino Y, Nanjo K, Tajima N, Kadowaki T, Kashiwagi A, et al. Report of the committee on the classification and diagnostic criteria of diabetes mellitus. J Diabetes Investig 2010; 1: 212-28.##Devlin J, David TJ. Tartrazine in atopic eczema. Arch Dis Child 1992; 67: 709-11.##Eidi A, Eidi M, Esmaeili E. Antidiabetic effect of garlic (allium sativum l.) in normal and streptozotocin-induced diabetic rats. Phytomedicine 2006; 13: 624-9.##Elgazar AF, Rezq AA, Bukhari HM. Anti-hyperglycemic effect of saffron extract in alloxan-induced diabetic rats. Eur J Biol Sci 2013; 5: 14-22.##Evans JL. Antioxidants: Do they have a role in the treatment of insulin resistance? Indian Journal of Medical Research 2007; 125: 355.##Fabiny DL, Ertingshausen G. Automated reaction-rate method for determination of serum creatinine with the centrifichem. Clinical chemistry 1971; 17: 696-700.##Hemmati M, Asghari S, Zohoori E, Karamian M. Hypoglycemic effects of three iranian edible plants; jujube, barberry and saffron: Correlation with serum adiponectin level. Pak J Pharm Sci 2015; 28: 2095-9.##Himri I, Bellahcen S, Souna F, BELMEKKI F, Aziz M, Bnouham M, et al. A 90-day oral toxicity study of tartrazine, a synthetic food dye, in wistar rats. Group 2011; 300: 00.##Hosseinzadeh H, Younesi HM. Antinociceptive and anti-inflammatory effects of crocus sativus l. Stigma and petal extracts in mice. BMC Pharmacol 2002; 2: 7.##Hosseinzadeh H, Ziaee T, Sadeghi A. The effect of saffron, crocus sativus stigma, extract and its constituents, safranal and crocin on sexual behaviors in normal male rats. Phytomedicine 2008; 15: 491-5.##Jorns A, Tiedge M, Lenzen S, Munday R. Effect of superoxide dismutase, catalase, chelating agents, and free radical scavengers on the toxicity of alloxan to isolated pancreatic islets in vitro. Free Radic Biol Med 1999; 26: 1300-4.##Kanakis CD, Tarantilis PA, Tajmir-Riahi HA, Polissiou MG. Crocetin, dimethylcrocetin, and safranal bind human serum albumin: Stability and antioxidative properties. J Agric Food Chem 2007; 55: 970-7.##Kianbakht S, Hajiaghaee R. Anti-hyperglycemic effects of saffron and its active constituents, crocin and safranal, in alloxan-induced diabetic rats. Journal of Medicinal Plants 2011; 3: 82-89.##Koutsogeorgopoulou L, Maravelias C, Methenitou G, Koutselinis A. Immunological aspects of the common food colorants, amaranth and tartrazine. Vet Hum Toxicol 1998; 40: 1-4.##Liu Y, Sun J, Rao S, Su Y, Yang Y. Antihyperglycemic, antihyperlipidemic and antioxidant activities of polysaccharides from catathelasma ventricosum in streptozotocin-induced diabetic mice. Food Chem Toxicol 2013; 57: 39-45.##Mohajeri D, Mousavi G, Doustar Y. Antihyperglycemic and pancrease-protective effects of croucus sativus l.(saffron) stigma ethano j. Cardivasc. Pharmacol lic extract on rat with alloxan-induced diabetes. J. Biol. Sci 2009; 9: 302-310.##Mohajeri D, Tabrizi BA, Mousavi G, Mesgari M. Anti-diabetic activity of crocus sativus l.(saffron) stigma ethanolic extract in alloxan-induced diabetic rats. Res. J. Biol. Sci 2008; 3: 102-1108.##Morris J, Bubenik G. Seasonal levels of minerals, enzymes, nutrients and metabolic products in plasma of intact and castrated adult male white-tailed deer (odocoileus virginianus). Comparative Biochemistry and Physiology Part A: Physiology 1983; 74: 21-28.##Naghizadeh B, Mansouri MT, Ghorbanzadeh B, Farbood Y, Sarkaki A. Protective effects of oral crocin against intracerebroventricular streptozotocin-induced spatial memory deficit and oxidative stress in rats. Phytomedicine 2013; 20: 537-42.##Neuman I, Elian R, Nahum H, Shaked P, Creter D. The danger of ‘yellow dyes’(tartrazine) to allergic subjects. Clinical &#38; Experimental Allergy 1978; 8: 65-68.##Ríos JL, Recio MC, Giner RM, Máñez S. An update review of saffron and its active constituents. Phytotherapy Research 1996; 10: 189-193.##Sampathu SR, Shivashankar S, Lewis YS, Wood AB. Saffron (crocus sativus linn.) — cultivation, processing, chemistry and standardization. C R C Critical Reviews in Food Science and Nutrition 1984; 20: 123-157.##Sasaki YF, Kawaguchi S, Kamaya A, Ohshita M, Kabasawa K, Iwama K, et al. The comet assay with 8 mouse organs: Results with 39 currently used food additives. Mutation Research/Genetic Toxicology and Environmental Mutagenesis 2002; 519: 103-119.##Smyth S, Heron A. Diabetes and obesity: The twin epidemics. Nat Med 2006; 12: 75-80.##Srivastava R, Ahmed H, Dixit RK, Dharamveer, Saraf SA. Crocus sativus l.: A comprehensive review. Pharmacogn Rev 2010; 4: 200-8.##Subramanian SP, Prasath GS. Antidiabetic and antidyslipidemic nature of trigonelline, a major alkaloid of fenugreek seeds studied in high-fat-fed and low-dose streptozotocin-induced experimental diabetic rats. Biomedicine &#38; Preventive Nutrition 2014; 4: 475-480.##Teuscher E, Anton R, Lobstein A. Plantes aromatiques: Épices, aromates, condiments et huiles essentielles: Tec &#38; Doc, 2005.##Trinder P. Determination of glucose in blood using glucose oxidase with an alternative oxygen acceptor. Annals of Clinical Biochemistry: An international journal of biochemistry in medicine 1969; 6: 24-27.##Walton K, Walker R, van de Sandt JJ, Castell JV, Knapp AG, Kozianowski G, et al. The application of in vitro data in the derivation of the acceptable daily intake of food additives. Food Chem Toxicol 1999; 37: 1175-97.##Winterhalter P, Straubinger M. Saffron—renewed interest in an ancient spice. Food Reviews International 2000; 16: 39-59.##c #### ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Changes in vascular reactivity of the coronary artery and thoracic aorta in the delta sarcoglycan null mutant mice</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Mutations in the delta sarcoglycan gene (d-SG) cause limb-girdle muscular dystrophy type 2F with structural and functional alterations in cardiac, smooth and skeletal muscle. The objective of the present study was to improve information about changes in vascular reactivity of the thoracic aorta and the coronary artery in the perfused heart of the d-SG-null mutant mouse model. Methods: Female knockout (KO) and wild-type (WT) mice (5 months old) with and without nitric oxid and prostanoids antagonist were used. Curves doses response to phenylephrine, angiotensin II and acetylcholine were constructed. Results: The results shows an increment in the contractile response to angiotensin II in the aorta and the isolated heart from the KO mice, and it seems due to a major participation of prostanoids. On the other hand the relaxant effect of acetylcholine is less in the KO than in the WT mice. Conclusion: Changes in vascular reactivity in KO mice seems due to the participation of prostanoids instead of nitric oxide.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>322</FPAGE>
			<TPAGE>330</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/12017/02/52017/06/232017/04/102017/03/12017/05/13
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1396/2/23
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/292017/09/72017/10/42017/09/222017/10/292017/10/4
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/7/12
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Maria C.</Name>
				<MidName></MidName>
				<Family>Castillo-Hernandez</Family>
				<NameE>Maria C.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Castillo-Hernandez</FamilyE>
				<Organizations>
				<Organization>Instituto Politécnico Nacional, Escuela Superior de Medicina, Sección de Estudios de Posgrado e Investigación, México</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>rcoral@ipn.mx</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Gustavo</Name>
				<MidName></MidName>
				<Family>Guevara-Balcazar</Family>
				<NameE>Gustavo</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Guevara-Balcazar</FamilyE>
				<Organizations>
				<Organization>Instituto Politécnico Nacional, Escuela Superior de Medicina, Sección de Estudios de Posgrado e Investigación, México</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>gguevarab@ipn.mx</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Alexandre</Name>
				<MidName></MidName>
				<Family>Kormanovski</Family>
				<NameE>Alexandre</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kormanovski</FamilyE>
				<Organizations>
				<Organization>Instituto Politécnico Nacional, Escuela Superior de Medicina, Sección de Estudios de Posgrado e Investigación, México</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email></Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ivan</Name>
				<MidName></MidName>
				<Family>Rubio Gayosso</Family>
				<NameE>Ivan</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rubio Gayosso</FamilyE>
				<Organizations>
				<Organization>Instituto Politécnico Nacional, Escuela Superior de Medicina, Sección de Estudios de Posgrado e Investigación, México</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>aiorubio@ipn.mx</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Ramon M.</Name>
				<MidName></MidName>
				<Family>Coral-Vazquez</Family>
				<NameE>Ramon M.</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Coral-Vazquez</FamilyE>
				<Organizations>
				<Organization>Instituto Politécnico Nacional, Escuela Superior de Medicina, Sección de Estudios de Posgrado e Investigación, México</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>ccastillohe@ipn.mx</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Delta sarcoglycan gene</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Vascular reactivity</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Aorta</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Heart</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Castillo-Hernández MC; Martinez-Godinez MA; Guevara-Balcazar G; Miliar-Garcia A;  Mancilla J; Lopez-Mayorga RM;  Castillo-Henkel EF; Castillo-Henkel C. Extraendothelial and constitutive COX-2 expression is involved in the contractile effect of angiotensin II in the rat aorta. Autonomic &#38; autacoid pharmacology 2010;30(4):205-11##Chadwick JA, Bhattacharyas S, Lowe J, Weisleder N, Rafael-Fortney JA. Renin-angiotensin-aldosterona system inhibitors improve membrane stability and change expression profiles in dystrophic skeletal muscles. Am J Physiol Cell Physiol, 2017;312(2):C155-C168.##Cohn RD, Durbeej M, Steve M, Coral-Vázquez R, Sally P, Campbell KP. Prevention of cardiomyophaty in mouse models lacking the smoothmuscle sarcoglycan-sarcospan complex. J Clin Invest 2001;107-R1-R7.##Coral-Vázquez R, Cohn RD, Moore SA, Hill JA, Weiss RM, Davisson RL, Straub V, Barresi R, Bansal D, Hrstka RF, Williamson R, Campbell KP. Disruption of the sarcoglycansarcospan complex in vascular smooth muscle: A novel mechanism for cardiomyopathy and muscular dystrophy. Cell 1999;98:465–474.##Dikalov SI and  Nazarewicz R.Angiotensin II-Induced Production of Mitochondrial Reactive Oxygen Species: Potential Mechanisms and Relevance for Cardiovascular Disease. Antioxidants &#38; redox signaling. 2013;  19(10): 1985-1094.##Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP. Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E. Mol Cell. 2000;5:141–151.##Guimaraes S and Moura D. Vascular Adrenoceptors: An Update. Pharmacol Rev  2001;53:319-356.##Heydemann A, Huber JM , Kakkar R, Wheeler MT, McNally EM. Functional nitric oxide synthase mislocalization in cardiomyopathy. Journal of Molecular and Cellular Cardiology 2004;36:213–223.##Moncada S, Palmer RM, and Higgs EA. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol Rev 1991;43:109-142.##Pérez-Diaz Iván, Hiriart Marcia, Olivares-Reyes, Robles Diaz. Receptores para la angiotensina II diferentes a los clásicos receptores membranales AT1 y AT2:características y su papel en el funcionamiento celular. Revista de educación bioquímica, 2006, 25(2). ;55-60.  ##Pueyo ME, Michel JB. Angiotensin II receptors in endothelial sells. Gen Pharmacol, 1997; 29(5):695-696.##Ramírez-Sánchez I, Rosas-Vargas H, Ceballos-Reyes G, Salamanca F, Coral-Vázquez RM. Expression Analysis of the SG-SSPN Complex in Smooth Muscle and Endothelial Cells of Human Umbilical Cord Vessels. J Vasc Res 2005;42:1–7##Ramirez-Sanchez I, Ceballos-Reyes G, Rosas-Vargas H, Cerecedo-Mercado D, Zentella-Dehesa A, Salamanca F, Coral-Vazquez RM. Expression and function of utrophin associated protein complex in stretched endothelial cells: dissociation and activation of eNOS. Frontiers in Bioscience 2007;12:1956-1962.##Sabharwal R, Weiss RM, Zimerman K, Domening O, Cicha MZ, Chapleau MW.Angiotensin-dependent autonomic dysregulation precedes dilated cardiomyiopathy in a mouse model of muscular dystrophy. Exp. Physiol, 2015;100(7):776-795.##Sandona D and Betto R. Sarcoglycanopathies: molecular pathogenesis and therapeutic prospects. Expert reviews 2009;11(e28):1-27.##Santeliz CH, Estrada L, Chávez A. El sistema renina-angiotensina-aldosterona y su papel funcional más allá del control de la presión arterial. Rev Mex Cardiol 2008; 19 (1):21-29.##Shin J, Jo H, and Park H. Caveolin-1 is transiently dephosphorylated by shear stress activated protein tyrosine phosphatase mu. Biochem Biophys Res Comm 2006; 339:737-741##Straub V, Ettinger AJ, Durbeej M,  Venzke DP, Cutshall S, Sanes JR and Campbell KP. ε-Sarcoglycan Replaces α-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex. J Biol Chem 1999;274(39):27989-27996##Toda N and Okamura T. The Pharmacology of Nitric Oxide in the Peripheral Nervous System of Blood Vessels. Pharmacol Rev 2003;55:271-324.##Wheeler MT, Zarnegar S, McNally EM.. Sarcoglycan,a novel component of the sarcoglycan complex, is reduced in muscular dystrophy. Hum Mol Genet 2002;11: 2147–2154.##Yoshida M, Hama H,  Ishikawa-Sakurai M,  Imamura M,  Mizuno Y,  Araishi K, Wakabayashi-Takai E, Noguchi S, Sasaoka T and Ozawa E. Biochemical evidence for association of dystrobrevin with the sarcoglycansarcospan complex as a basis for understanding sarcoglycanopathy. Human Molecular Genetics 2000;9:1033-1040.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Aerosol delivery of ferulic acid-loaded nanostructured lipid carriers: A promising treatment approach against the respiratory disorders</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: Treatment of lung diseases is one of the major healthcare challenges. Ferulic acid (FA), a phenolic compound with well-established antioxidant and anti-inflammatory properties, has shown promising therapeutic potential against the pulmonary disorders; however, low bioavailability may negatively affect its efficiency. This, prompted us to incorporate FA into the nanostructured lipid carriers (FA-NLCs) and evaluate the toxicity of this nanoformulation in human lung adenocarcinoma cell line (A549) and its suitability for pulmonary drug delivery. Methods: FA-NLCs were prepared by high-pressure homogenization followed by assessment of the physicochemical properties of nanoparticles, in vitro release profile, aerosol characteristics, in vitro cytotoxicity, pharmacokinetic parameters and lung deposition of the nanoparticles after nebulization in Balb/c mice. Results: Formation of FA-NLCs which exhibited a controlled release profile, was confirmed by scanning electron microscope and differential scanning calorimetry. FA-NLCs exhibited toxic effects on A549 cells for longer time periods as compared to FA solution. Following the aerosolization, suitable aerodynamic properties were obtained and FA-NLCs formulation provided significantly increased residence time and slower lung clearance for FA. Further confocal microscopy visualization confirmed the lung deposition of nanoparticles. Encapsulation of FA into the NLCs resulted in the improved pharmacokinetic parameters in plasma or lung tissue samples. Conclusion: Application of the aerosolized FA-NLCs formulation which improves the pulmonary bioavailability of FA might result in the increased efficiency and reduced dosing frequency of this phytochemical. In this respect, development of inhalable nano-based drug delivery systems appears as a promising therapeutic approach against the lung disorders.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>331</FPAGE>
			<TPAGE>342</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/12017/02/52017/06/232017/04/102017/03/12017/05/132017/04/29
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1396/2/9
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/292017/09/72017/10/42017/09/222017/10/292017/10/42017/09/11
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/6/20
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Parichehr</Name>
				<MidName></MidName>
				<Family>Hassanzadeh</Family>
				<NameE>Parichehr</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Hassanzadeh</FamilyE>
				<Organizations>
				<Organization>Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>p-hassanzadeh@razi.tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Elham</Name>
				<MidName></MidName>
				<Family>Arbabi</Family>
				<NameE>Elham</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Arbabi</FamilyE>
				<Organizations>
				<Organization>Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>arbabiavalelham@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Rostami</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rostami</FamilyE>
				<Organizations>
				<Organization>Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>frostamii@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fatemeh</Name>
				<MidName></MidName>
				<Family>Atyabi</Family>
				<NameE>Fatemeh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Atyabi</FamilyE>
				<Organizations>
				<Organization>Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>atyabifa@tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Rassoul</Name>
				<MidName></MidName>
				<Family>Dinarvand</Family>
				<NameE>Rassoul</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Dinarvand</FamilyE>
				<Organizations>
				<Organization>Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>Dinarvand@tums.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Ferulic acid</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Nanostructured lipid carriers</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Lung deposition</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Nebulization</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Balb/c mice</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Prof. Ahmadiani##Prof. Zali##Prof. Dehpour## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Effect of Syzygium aromaticum (clove) extract on seminiferous tubules and oxidative stress after testicular torsion in adult rats</TitleF>
		<TitleE></TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Introduction: The aim was to investigate the protective effect of the Syzygium aromaticum extract on damaged tissues and the oxidative stress after testicular torsion.&#160;Methods: Rats were randomly divided into a control group subjected to a sham procedure and three treatment groups comprising testicular torsion followed by detorsion (TD), testicular torsion detorsion followed by the treatment with an extract of Syzygium aromaticum (TDSA) and treatment done by extract of Syzygium aromaticum alone. Testicular torsion was induced by 720 degrees of counterclockwise rotation of the left testis for 4h. After the duration of the induction of the torsion, detorsion was done. The animals were given daily oral administrations of just Syzygium aromaticum (4 mg/kg) for seven days. The measurement of the oxidative stress and testosterone levels, as well as assessments of histomorphometry were conducted seven days after detorsion. Results: The Johnsen score, along with the thickness of the epithelium and diameter of the seminiferous tubules, significantly increased in the testicular torsion group after receiving treatment with the extract of Syzygium aromaticum as compared to TD group. The levels of testosterone and glutathione peroxidase activity also increased significantly in the TDSA compared to TD group. The MDA levels decreased in TDSA compared to TD group. Conclusion: The findings of the current study suggested that Syzygium aromaticum might have provided a protective effect against testicular torsion detorsion injury.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>343</FPAGE>
			<TPAGE>350</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2017/08/82017/08/12017/02/52017/06/232017/04/102017/03/12017/05/132017/04/292017/01/23
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1395/11/4
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2017/11/162017/10/292017/09/72017/10/42017/09/222017/10/292017/10/42017/09/112017/08/31
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1396/6/9
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Moghimian</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Moghimian</FamilyE>
				<Organizations>
				<Organization>Department of Basic Sciences, School of Medicine, Gonabad University of Medical Sciences, Gonabad, Islamic Republic of Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>moghimian.m@gmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Seyd-Hosein</Name>
				<MidName></MidName>
				<Family>Abtahi-Evari</Family>
				<NameE>Seyd-Hosein</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Abtahi-Evari</FamilyE>
				<Organizations>
				<Organization>Department of Basic Sciences, School of Medicine, Gonabad University of Medical Sciences, Gonabad, Islamic Republic of Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>abtahi.h@gmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Majid</Name>
				<MidName></MidName>
				<Family>Shokoohi</Family>
				<NameE>Majid</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Shokoohi</FamilyE>
				<Organizations>
				<Organization>Department of Basic Sciences, School of Medicine, Gonabad University of Medical Sciences, Gonabad, Islamic Republic of Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>a.shokooh@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mostafa</Name>
				<MidName></MidName>
				<Family>Amiri</Family>
				<NameE>Mostafa</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Amiri</FamilyE>
				<Organizations>
				<Organization>Department of Basic Sciences, School of Medicine, Gonabad University of Medical Sciences, Gonabad, Islamic Republic of Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>amiri.m@gmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Malihe</Name>
				<MidName></MidName>
				<Family>Soltani</Family>
				<NameE>Malihe</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Soltani</FamilyE>
				<Organizations>
				<Organization>Department of Basic Sciences, School of Medicine, Gonabad University of Medical Sciences, Gonabad, Islamic Republic of Iran</Organization>
				</Organizations>
				<Countries>
				<Country></Country>
				</Countries>
				<EMAILS>
				<Email>m.soltani@gmu.ac.ir</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Syzygium  aromaticum</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Clove</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Oxidative stress</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Testicular torsion</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Department of Basic Sciences, School of Medicine, Gonabad University of Medical Science, Gonabad, Islamic Republic of Iran## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>

</ARTICLES>

</JOURNAL>
</XML>
