<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Medical Journal of the Islamic Republic Of Iran</title>
<title_fa>مجله پزشکی جمهوری اسلامی ایران</title_fa>
<short_title>Med J Islam Repub Iran</short_title>
<subject>Medical Sciences</subject>
<web_url>http://mjiri.iums.ac.ir</web_url>
<journal_hbi_system_id>2</journal_hbi_system_id>
<journal_hbi_system_user>journal2</journal_hbi_system_user>
<journal_id_issn>1016-1430</journal_id_issn>
<journal_id_issn_online>2251-6840</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>10.18869/mjiri</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1379</year>
	<month>11</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2001</year>
	<month>2</month>
	<day>1</day>
</pubdate>
<volume>14</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>SUBTYPES OF α1-ADRENOCEPTORS IN RABBIT SAPHENOUS VEIN</title>
	<subject_fa>Physiology</subject_fa>
	<subject>Physiology</subject>
	<content_type_fa>Original Research: Basic Science in Medicine</content_type_fa>
	<content_type>Original Research: Basic Science in Medicine</content_type>
	<abstract_fa></abstract_fa>
	<abstract>We investigated the a,-adrenoceptor subtypes of rabbit saphenous vein which
has a mixed functional population of α1 and α2 -adrenoceptors. Lateral saphenous
veins were obtained from male rabbits weighing 3.20-4 kg, which were killed by
overdose with pentobarbitone sodium (i.v. injection). They were easily dissected
out and placed in cold, oxygenated modified Krebs-Henselite solution (Krebs).
Each preparation was cut transversely into 3-4 mm rings and suspended between
thick wire supports. The vein rings were mounted in 10 mL isolated organ bath,
bathed in Krebs maintained at 37°C and gassed with 95% 02 plus 5% CO2, Cumulative
concentration-response curves (CCRC) were constructed by increasing
the concentration of the agonists in half-log increments. The preparations were
left for a further period of 45-60 min before re-exposure to the agonist. Competitive
antagonists like prazosin and rauwolscine were incubated in preparations at
least for 45 minutes prior to the onset of a second CCRC. The strategy was based
on using the a1-adrenoceptor selective agonist, phenylephrine (PE). Prazosin, an
α1 -adrenoceptor selective antagonist, competitively inhibited contractile responses
to phenylephrine with a pA2 value of 8, WB-41 0 1 had a pA2 of 8.6 but a low
Schild plot slope, while low potency was found with 5MU (PA2 7.2) and HV -723
(pA2 7.97). This data is not consistent with a definitive for αlA or αlN and taken
alone the evidence from prazosin is in favour of αIL' However the selective α2-
adrenoceptor antagonist delequamine inhibited phenylephrine-induced contractions.
Overall the data is consistent with phenylephrine-induced contractions being
mediated by a,- and a2 -adrenoceptors. The best estimate of the subtype of ajadrenoceptor
mediating contraction is aiL due to the relatively low absolute pA2
values for prazosin.
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>α1-adrenoceptor subtypes, phenylephrine, prazosin, delequamine, WB-4101, SMU, HV-723.</keyword>
	<start_page>363</start_page>
	<end_page>367</end_page>
	<web_url>http://mjiri.iums.ac.ir/browse.php?a_code=A-10-298-293&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>M</first_name>
	<middle_name></middle_name>
	<last_name>MOHAMMADI NAGHADEH </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>20031947532846004293</code>
	<orcid>20031947532846004293</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>From the Department of Physiology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, I.R. Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>JC</first_name>
	<middle_name></middle_name>
	<last_name>McGRATH</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>20031947532846004294</code>
	<orcid>20031947532846004294</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>the Clinical Research Initiative in Heart Failure, West Medical Building, University of Glasgow, Glasgow G21 8QQ, U.K.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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