<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Physiology and Pharmacology</title>
<title_fa></title_fa>
<short_title>Physiol Pharmacol</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ppj.phypha.ir</web_url>
<journal_hbi_system_id>32</journal_hbi_system_id>
<journal_hbi_system_user>journal32</journal_hbi_system_user>
<journal_id_issn>24765236</journal_id_issn>
<journal_id_issn_online>24765244</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.22034</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>(previous ISSN: 17350581)</journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1398</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<volume>23</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Neuroprotective effects of caffeine against beta-amyliod neurotoxicity: The involvement of glycogen synthase kinase-3β protein</title>
	<subject_fa>Neurophysiology/Pharmacology</subject_fa>
	<subject>Neurophysiology/Pharmacology</subject>
	<content_type_fa>Short communication</content_type_fa>
	<content_type>Short communication</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The reduction of glycogen synthase kinase-3&amp;beta; protein level may correlate to the neuroprotective effects of antioxidant agents like caffeine. Therefore, we aimed to evaluate the impact of GSK-3&amp;beta; protein on neuroprotective effects of caffeine in the SHSY5Y cells exposed to beta-amyloid. &lt;strong&gt;Methods:&lt;/strong&gt; We incubated SHSY5Ycells with beta-amyloid 25&amp;ndash;35 and caffeine (0.6 and 1mM) for 24h. Cell viability was determined using MTT test. We used the western blotting technique to measure the glycogen synthase kinase-3&amp;beta; and phosphorylated glycogen synthase kinase-3&amp;beta; protein levels.&lt;strong&gt; Results:&lt;/strong&gt; Caffeine (0.6 and 1mM) diminished beta-amyloid neurotoxicity and attenuated the beta-amyloid effects on the glycogen synthase kinase-3&amp;beta; protein level in a neuronal culture. &lt;strong&gt;Conclusion: &lt;/strong&gt;Caffeine neuroprotective effects against beta-amyloid may correlate to glycogen synthase kinase-3&amp;beta; protein.&lt;/div&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Caffeine, Amyloid-beta peptide, Glycogen synthase kinase, Neuroprotection.</keyword>
	<start_page>150</start_page>
	<end_page>153</end_page>
	<web_url>http://ppj.phypha.ir/browse.php?a_code=A-10-1178-2&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Majid Reza</first_name>
	<middle_name></middle_name>
	<last_name>Farrokhi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>farokhim@sums.ac.ir</email>
	<code>3200319475328460029589</code>
	<orcid>3200319475328460029589</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Shiraz Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Masoumeh</first_name>
	<middle_name></middle_name>
	<last_name>Emamghoreishi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>emamm@sums.ac.ir</email>
	<code>3200319475328460029590</code>
	<orcid>3200319475328460029590</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Pharmacology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Atena</first_name>
	<middle_name></middle_name>
	<last_name>Amiri</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>neuroscien@sums.ac.ir</email>
	<code>3200319475328460029591</code>
	<orcid>3200319475328460029591</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Shiraz Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mojtaba</first_name>
	<middle_name></middle_name>
	<last_name>Keshavarz</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mkeshavar@sums.ac.ir</email>
	<code>3200319475328460029592</code>
	<orcid>3200319475328460029592</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Shiraz Neuroscience Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
