<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Basic and Clinical Neuroscience Journal</title>
<title_fa>مجله علوم اعصاب پایه و بالینی</title_fa>
<short_title>BCN</short_title>
<subject>Medical Sciences</subject>
<web_url>http://bcn.iums.ac.ir</web_url>
<journal_hbi_system_id>137</journal_hbi_system_id>
<journal_hbi_system_user>journal137</journal_hbi_system_user>
<journal_id_issn>2008-126X</journal_id_issn>
<journal_id_issn_online>2228-7442</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.32598/bcn</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1390</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2011</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<volume>2</volume>
<number>4</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>Capsazepine, a Transient Receptor Potential Vanilloid Type 1 (TRPV1) Antagonist, Attenuates Antinociceptive Effect of CB1 Receptor agonist, WIN55,212-2, in the Rat Nucleus Cuneiformis</title>
	<subject_fa>Clinical Neuroscience</subject_fa>
	<subject>Clinical Neuroscience</subject>
	<content_type_fa>Original</content_type_fa>
	<content_type>Original</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p align=&quot;left&quot;&gt;&lt;b&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;Introduction: &lt;/font&gt;&lt;/font&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;Nucleus cuneiformis (NCF), as part of descending pain inhibitory system, cooperates with periaqueductal gray (PAG) and rostral ventromedial medulla (RVM) in supraspinal modulation of pain. Cannabinoids have analgesic effects in the PAG, RVM and NCF. The transient receptor potential vanilloid type 1(TRPV1) can be activated by anandamide and WIN55,212-2 as a cannabinoid receptor agonist. The aim of the current study is to investigate the possible interplay between the cannabinoid and vanilloid systems for modulation of pain at the NCF. &lt;/font&gt;&lt;/font&gt;&lt;/font&gt;&lt;b&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;&lt;p align=&quot;justify&quot;&gt;Methods: &lt;/p&gt;&lt;/font&gt;&lt;/font&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;In this study, a cannabinoid receptor agonist, WIN55,212-2 ( 15 μg/0.3 μl DMSO), and selective TRPV1 receptor antagonist, capsazepine (10, 25, 50 and100 nmol/0.3 μl DMSO), were microinjected bilaterally into the NCF, and tail-flick and formalin tests were used to assess the animal’s pain-related behaviors at 5-min intervals for a 60-min period. &lt;/font&gt;&lt;/font&gt;&lt;/font&gt;&lt;b&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;&lt;p align=&quot;justify&quot;&gt;Results: &lt;/p&gt;&lt;/font&gt;&lt;/font&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;Our findings demonstrated that analgesic effect of WIN55,212-2 were dose-dependently attenuated by capsazepine in both tests. In the tail-flick test, capsazepine at both doses of 50 (P&lt;0.01) and 100 (P&lt;0.001) nmol could significantly prevent the antinociceptive effect of WIN55,212-2 while capsazepine, in formalin test, could decreased its antinociceptive effect at the dose of 50 nmol (P&lt;0.05) as well. On the other hand, solely administration of the highest dose of capsazepine in both tests did not alter the pain-related behaviors. &lt;/font&gt;&lt;/font&gt;&lt;/font&gt;&lt;b&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot;&gt;&lt;p&gt;Discussion: &lt;/p&gt;&lt;/font&gt;&lt;/font&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;&lt;font color=&quot;#221e1f&quot; size=&quot;2&quot; face=&quot;Times New Roman,Times New Roman&quot;&gt;It suggests a possible role for TRPV1 receptors in NCF-mediated cannabinoid-induced antinociception. &lt;/font&gt;&lt;/font&gt;&lt;/font&gt;&lt;/b&gt;&lt;/b&gt;&lt;/b&gt;&lt;/b&gt;&lt;/p&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Nucleus Cuneiformis,TRPV1 Receptor,Cannabinoids,Tail-Flick,Formalin Test,Rat</keyword>
	<start_page>19</start_page>
	<end_page>26</end_page>
	<web_url>http://bcn.iums.ac.ir/browse.php?a_code=A-10-1-72&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Asghar</first_name>
	<middle_name></middle_name>
	<last_name>Parvishan</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></email>
	<code>1370031947532846001192</code>
	<orcid>1370031947532846001192</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Zahra</first_name>
	<middle_name></middle_name>
	<last_name>Taslimil</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></email>
	<code>1370031947532846001193</code>
	<orcid>1370031947532846001193</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohammad</first_name>
	<middle_name></middle_name>
	<last_name>Ebrahimzadeh</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></email>
	<code>1370031947532846001194</code>
	<orcid>1370031947532846001194</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Abbas</first_name>
	<middle_name></middle_name>
	<last_name>Haghparast</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></email>
	<code>1370031947532846001195</code>
	<orcid>1370031947532846001195</orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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