<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Pharmaceutical and Biomedical Research</title>
<title_fa></title_fa>
<short_title>Pharm Biomed Res</short_title>
<subject>Medical Sciences</subject>
<web_url>http://pbr.mazums.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2423-4486</journal_id_issn>
<journal_id_issn_online>2423-4494</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.29252/pbr</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1398</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>4</month>
	<day>1</day>
</pubdate>
<volume>5</volume>
<number>2</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>Effects of ethanol extract of the resin exudate of boswellia dalzielii hutch on pain in mice</title>
	<subject_fa>سم شناسی</subject_fa>
	<subject>Toxicology</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Original Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>This study aimed to determine the analgesic properties and the acute toxicity of Ethanol Extract of the Resin Exudate of &lt;em&gt;Boswellia dalzielii&lt;/em&gt; (EERBD) in mice animal model. We used the writhing or acetic acid abdominal constriction, tail-immersion, and hot plate tests to assess the analgesic effect of EERBD at three doses (100, 200, and 400 mg/kg). To study the acute toxicity of EERBD, 24 female mice were divided into four groups (n=6) and were orally treated with EERBD at the doses of 0, 2000, 4000, and 5000 mg/kg, as per OECD (Organization for Economic Co-operation and Development) guidelines No. 420.&lt;br&gt;
In the acetic acid-induced writhing reflex model, the EERBD ministration decreased the mean total number of writhes at the two doses (100 and 400 mg/kg), which were found highly significant (&lt;em&gt;P&lt;/em&gt;&lt;0.001) compared to control group. In the tail immersion model, the EERBD administration at the dose of 400 mg/kg significantly increased the pain reaction time (&lt;em&gt;P&lt;/em&gt;&lt;0.001 as compared to control) at 30 min, but another tested sample had no significant latency. In the hot-plate model, the drug extract created significant (&lt;em&gt;P&lt;/em&gt;&lt;0.001) increase in the latency period compared to the control group at oral doses of 100 and 400 mg/kg when compared to initial time and control group (4.5 &amp;plusmn; 1.29 s) with protective effect from 4.25 &amp;plusmn; 1.50 s after 30 min.&amp;nbsp; Administration of EERBD at the dose of 200 mg/kg showed no significant analgesic activity based on writing, tail immersion, and hot-plate tests. The extract did not show toxicity signs or death at dose of less than 5000 mg/kg per oral. The results suggest that EERBD contain bioactive substances with analgesics effects; hence, it might be a better alternative to conventional drug therapy for pain management.</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Writing, hot plate,tail immersion, acute toxicity, resins, Boswellia dalzielii</keyword>
	<start_page>32</start_page>
	<end_page>37</end_page>
	<web_url>http://pbr.mazums.ac.ir/browse.php?a_code=A-10-670-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Jeweldai</first_name>
	<middle_name></middle_name>
	<last_name>Vedekoi</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>jeweldai2014@yahoo.fr</email>
	<code>10031947532846006193</code>
	<orcid>10031947532846006193</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Biological Sciences, Faculty of Science, University of Ngaoundéré, Ngaoundéré, Cameroon</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Sokeng</first_name>
	<middle_name></middle_name>
	<last_name>Dongmo Selestin</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>10031947532846006194</code>
	<orcid>10031947532846006194</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Biological Sciences, Faculty of Science, University of Ngaoundéré, Ngaoundéré, Cameroon</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Koubé</first_name>
	<middle_name></middle_name>
	<last_name>Juliette</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>10031947532846006195</code>
	<orcid>10031947532846006195</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Departments of Animal Biology and Physiology, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Kamtchouing</first_name>
	<middle_name></middle_name>
	<last_name>Pierre</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>10031947532846006196</code>
	<orcid>10031947532846006196</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Departments of pharmaceutical sciences, University of Douala, Douala, Cameroon</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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