Volume 23, Issue 2 (June 2019)                   Physiol Pharmacol 2019, 23(2): 129-139 | Back to browse issues page

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Roshankhah S, Jalili C, Salahshoor M R. Protective effects of Petroselinum crispum on ischemia/reperfusion-induced acute kidney injury in rats. Physiol Pharmacol. 2019; 23 (2) :129-139
URL: http://phypha.ir/ppj/article-1-1433-en.html
Abstract:   (401 Views)
Introduction: Petroselinum crispum (P. crispum) is an associate of Umbelliferae family that has several therapeutic attributes. Ischemia/reperfusion (I/R) is one of the main challenges in acute kidney damage. This study was designed to assess the anti-inflammatory and protective effects of P. crispum extract against I/R-induced renal disorders. Methods: Forty male rats were randomly divided into five groups (n=8) namely normal control (saline) and I/R control group, and three groups of I/R intraperitoneally pretreated with various doses of P. crispum (100, 150 and 200mg/kg). The I/R-induced renal inflammation was evaluated by determining leukocyte infiltration and mRNA expression level of intercellular adhesion molecule-1 and tumor necrotic factor-alpha. Antioxidant capacity of kidneys and thiobarbituric acid reactive species were measured in kidneys for the evaluation of oxidative stress. In addition, the diameters of renal glomeruli, kidney function indicators and serum nitrite oxide levels were respectively determined by morphometric analysis, autoanalyzer device and Griess technique. Results: The I/R increased all measured parameters except for the tissue ferric reducing/antioxidant power (FRAP) level, which was decreased compared to the normal control group. However, pretreatment with P. crispum extract in all doses significantly reduced blood urea nitrogen, kidney malondialdehyde, creatinine, glomerular diameter, leukocyte infiltration, levels of tumor necrotic factor-alpha, adhesion molecule-1 expression, and nitrite oxide as well as increased tissue FRAP compared to the I/R control group. Conclusion: It seems that P. crispum administration improves I/R-induced acute kidney injury.
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Types of Manuscript: Original Research | Subject: Kidney