<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Journal of Advances in Medical and Biomedical Research</title>
<title_fa>Journal of Advances in Medical and Biomedical Research</title_fa>
<short_title>J Adv Med Biomed Res</short_title>
<subject>Medical Sciences</subject>
<web_url>http://journal.zums.ac.ir</web_url>
<journal_hbi_system_id>52</journal_hbi_system_id>
<journal_hbi_system_user>journal52</journal_hbi_system_user>
<journal_id_issn>1606-9366</journal_id_issn>
<journal_id_issn_online>2676-6264</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.30699/jambr</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>1388</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2009</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<volume>17</volume>
<number>67</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>fa</language>
	<article_id_doi></article_id_doi>
	<title_fa>بررسی تداخل اثر بی دردی حاصل از JWH133 و دوزهای معمول و بسیار ناچیز سلکوکسیب در موش سوری</title_fa>
	<title>Interaction between JWH133-induced Antinociception and two extreme Doses of Celecoxib</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa>مقاله پژوهشی</content_type_fa>
	<content_type>Original Research Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;Background and Objective: JWH133 is known to have cannabinoid-2 (CB2) receptor agonist properties. Celecoxib, a selective cyclooxygenase-2 (COX-2) inhibitor, is also known to have antinociceptive properties. Endocannabinoids produce analgesia possibly through cyclooxygenase (COX) pathway. The aim of the present work was: to study the effect of celecoxib on JWH133 induced antinociception and to compare the effects of two different dose ranges of celecoxib (mg/kg and nano g/kg) on the JWH133 antiniciceptive effect. Materials and Methods: We have studied the possible interaction of administration of mg/kg (50-200 mg/kg) and Ultra-Low Dose (ULD) (25 and 50 ng/kg) of celecoxib on the antinociceptive effect of intraperitoneal (i.p.) injection of JWH133 using formalin test in mice. Results: JWH133 (0.01, 0.1 and 1 mg/kg) induced antinociceptive effect just in phase I of the formalin test. Celecoxib (50-200 mg/kg) and its ULD (25 and 50 ng/kg) attenuated and potentiated, JWH133 induced antinociception, respectively. Conclusions: It is concluded that JWH-133 induced antinociception is modulated by celecoxib and mg/kg doses of celecoxib showed opposite effects compare to its ultra-low doses.&lt;/p&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Key words: JWH133, Antinociception, Celecoxib, Ultra-Low Dose (ULD), Mice</keyword>
	<start_page>11</start_page>
	<end_page>22</end_page>
	<web_url>http://journal.zums.ac.ir/browse.php?a_code=A-10-4-486&amp;slc_lang=fa&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Zahra</first_name>
	<middle_name></middle_name>
	<last_name>Ghahremani</last_name>
	<suffix></suffix>
	<first_name_fa>زهرا</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>قهرمانی</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>5200319475328460060478</code>
	<orcid>5200319475328460060478</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Physiology and Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Soudeh</first_name>
	<middle_name></middle_name>
	<last_name>Rezaee- Kalaj</last_name>
	<suffix></suffix>
	<first_name_fa>سوده</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>رضائی کلج</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>5200319475328460060479</code>
	<orcid>5200319475328460060479</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Physiology and Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohammad Reza</first_name>
	<middle_name></middle_name>
	<last_name>Zarrindast</last_name>
	<suffix></suffix>
	<first_name_fa>محمد رضا</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>زرین دست</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>5200319475328460060480</code>
	<orcid>5200319475328460060480</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Bizhan</first_name>
	<middle_name></middle_name>
	<last_name>Jahanguiri</last_name>
	<suffix></suffix>
	<first_name_fa>بیژن</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>جهانگیری</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>5200319475328460060481</code>
	<orcid>5200319475328460060481</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dept. of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohammad Reza</first_name>
	<middle_name></middle_name>
	<last_name>jafari</last_name>
	<suffix></suffix>
	<first_name_fa>محمد رضا</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>جعفری</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>jafarimrj@yahoo.com</email>
	<code>5200319475328460060482</code>
	<orcid>5200319475328460060482</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Dept. of Physiology and Pharmacology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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