Source:http://linkedlifedata.com/resource/pubmed/id/15347843
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2004-9-6
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pubmed:abstractText |
Mesenteric arteries (230-290 microm) were isolated from virgin female rats at diestrous and proestrous phases of the estrous cycle and from ovariectomized (OVX) rats with or without estrogen (E2) replacement (17beta-estradiol, 7.5 + 5 mg pellets, 21 d release). Arteries were mounted in a pressurized myograph system. Angiotensin-(1-7) [Ang-(1-7)] concentration-dependent responses (10(-10)-10(-5) M) were determined in arteries preconstricted with endothelin-1 (10(-7) M). Mesenteric arteries were pretreated with the specific Ang-(1-7) antagonist, D-[Ala7]-Ang-(1-7) (10(-7) M) to assess the Ang-(1-7) receptor-mediated dilator effect. Ang-(1-7) did not dilate mesenteric arteries from virgin rats at diestrus and placebo-treated OVX female rats as compared to the time control; however, Ang-(1-7) elicited a modest dilation at proestrus as compared to diestrus, which reached statistical significance at 10(-8) M concentrations. Ang-(1-7) caused a concentration-dependent vasodilation in mesenteric arteries of females with E2 replacement, with an EC50 of 21 nM. D-[Ala7]-Ang-(1-7) blocked the vasodilator effect of Ang-(1-7). Our results demonstrate that during proestrus Ang-(1-7) elicits modest vasodilation as compared to diestrus, but lacks vasodilatory properties in vessels from diestrous and ovariectomized rats. Estrogen replacement restores a significant dilator response to Ang-(1-7) in OVX rats that is mediated by a D-[Ala7]-Ang-(1-7) sensitive site.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Angiotensin I,
http://linkedlifedata.com/resource/pubmed/chemical/Endothelin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Estradiol,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Placebos,
http://linkedlifedata.com/resource/pubmed/chemical/angiotensin I (1-7)
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1355-008X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
161-5
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pubmed:dateRevised |
2010-6-24
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pubmed:meshHeading |
pubmed-meshheading:15347843-Angiotensin I,
pubmed-meshheading:15347843-Animals,
pubmed-meshheading:15347843-Diestrus,
pubmed-meshheading:15347843-Dose-Response Relationship, Drug,
pubmed-meshheading:15347843-Endothelin-1,
pubmed-meshheading:15347843-Estradiol,
pubmed-meshheading:15347843-Estrous Cycle,
pubmed-meshheading:15347843-Female,
pubmed-meshheading:15347843-Mesenteric Arteries,
pubmed-meshheading:15347843-Ovariectomy,
pubmed-meshheading:15347843-Peptide Fragments,
pubmed-meshheading:15347843-Placebos,
pubmed-meshheading:15347843-Proestrus,
pubmed-meshheading:15347843-Rats,
pubmed-meshheading:15347843-Rats, Sprague-Dawley,
pubmed-meshheading:15347843-Vasodilation
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pubmed:year |
2004
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pubmed:articleTitle |
Vascular responses to Angiotensin-(1-7) during the estrous cycle.
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pubmed:affiliation |
The Hypertension and Vascular Disease Center, Wake Forest University School of Medicine, Winston-Salem, NC 27157-1032, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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