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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0005456,
umls-concept:C0012984,
umls-concept:C0026820,
umls-concept:C0040300,
umls-concept:C0080103,
umls-concept:C0178587,
umls-concept:C0806909,
umls-concept:C0871261,
umls-concept:C1152723,
umls-concept:C1167622,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1801960,
umls-concept:C2911692
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pubmed:issue |
3
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pubmed:dateCreated |
1989-10-17
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pubmed:abstractText |
In microsomal fractions from dog aorta, saphenous veins, mesenteric arteries and veins, both [3H]prazosin and [3H]rauwolscine displayed monophasic saturation in binding. The Kd for [3H] rauwolscine binding was similar for all these blood vessels, but the maximum number of [3H]rauwolscine binding sites was 3 to 7 times higher in veins compared to arteries. The Kd for [3H] prazosin was higher in saphenous vein than that in the arteries. The maximum number of binding sites for [3H]prazosin was similar, except for that in aorta, which was 3 times greater. Phenylephrine (alpha-1 adrenoceptor selective agonist) or norepinephrine (nonselective adrenoceptor agonist) produced similar maximal responses in all vessels. The alpha-2 adrenoceptor selective agonist, B-HT 920 (2-amino-6-allyl-3,4,7,8-tetrahydro-6H-thiazolo[5,4-d]-azepine)-induced contraction in veins but not in arteries. Prazosin (10(-6) M) inhibited completely the contractions to norepinephrine (3 x 10(-6) M) in mesenteric arteries and to phenylephrine (3 x 10(-6) M) in arteries and veins. Contractile responses of mesenteric artery were unaffected by rauwolscine. Rauwolscine (10(-7) M) caused a greater parallel rightward shift of the concentration-response curve to norepinephrine than did prazosin (10(-7) M) in saphenous veins, and a further rightward shift of responses to norepinephrine after 10(-7) M prazosin in mesenteric vein and saphenous vein and abolished B-HT 920-induced responses at alpha-2 adrenoceptors. The tissues responding to B-HT-920 correspond to those having the highest alpha-2 receptor density as measured by [3H]rauwolscine binding. The density of such sites required for contraction to be initiated in veins was much higher than with alpha-1 adrenoceptor sites.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Azepines,
http://linkedlifedata.com/resource/pubmed/chemical/Norepinephrine,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylephrine,
http://linkedlifedata.com/resource/pubmed/chemical/Prazosin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Adrenergic, alpha,
http://linkedlifedata.com/resource/pubmed/chemical/Yohimbine,
http://linkedlifedata.com/resource/pubmed/chemical/talipexole
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0022-3565
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
250
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1119-24
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2550616-Animals,
pubmed-meshheading:2550616-Aorta,
pubmed-meshheading:2550616-Azepines,
pubmed-meshheading:2550616-Dogs,
pubmed-meshheading:2550616-Mesenteric Arteries,
pubmed-meshheading:2550616-Mesenteric Veins,
pubmed-meshheading:2550616-Norepinephrine,
pubmed-meshheading:2550616-Phenylephrine,
pubmed-meshheading:2550616-Prazosin,
pubmed-meshheading:2550616-Receptors, Adrenergic, alpha,
pubmed-meshheading:2550616-Vasomotor System,
pubmed-meshheading:2550616-Veins,
pubmed-meshheading:2550616-Yohimbine
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pubmed:year |
1989
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pubmed:articleTitle |
Relation between density (maximum binding) of alpha adrenoceptor binding sites and contractile response in four canine vascular tissues.
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pubmed:affiliation |
Department of Neurosciences, Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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