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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4 Pt 2
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pubmed:dateCreated |
1991-11-20
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pubmed:abstractText |
Chronic treatment with estrogens enhances some endothelium-dependent relaxations. Whether or not progesterone would exert a similar effect is unknown. Experiments were designed to determine the effect of chronic treatment with progesterone on endothelium-dependent responses. Adult female dogs were ovariectomized and pellets containing carrier substance, estrogen, progesterone, or estrogen plus progesterone were implanted subcutaneously. After 14-21 days coronary arteries were removed, cut into rings, and suspended for the measurement of isometric force in organ chambers in the presence of indomethacin. Endothelium-dependent relaxations to ADP, bradykinin, or the calcium ionophore did not differ among groups. However, relaxations to acetylcholine and to the alpha 2-adrenergic agonist BHT-920 were greater in the estrogen-treated group than in the estrogen plus progesterone-treated group. In rings without endothelium, relaxations to nitric oxide and isoproterenol did not differ among groups. However, relaxations of the smooth muscle to ADP were greater in the progesterone-treated group than in the progesterone plus estrogen group. These results suggest that progesterone alone minimally affects endothelium-dependent responses. However, progesterone seems to antagonize the stimulatory effects of estrogen on two endothelium-dependent responses that are associated with pertussis toxin-sensitive guanine nucleotide regulatory proteins and the production of nitric oxide. These studies suggest that a specific receptor/second messenger system can be modulated by female reproductive steroid hormones.
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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/Acetylcholine,
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Diphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Adrenergic alpha-Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Azepines,
http://linkedlifedata.com/resource/pubmed/chemical/Estrogens,
http://linkedlifedata.com/resource/pubmed/chemical/Progesterone,
http://linkedlifedata.com/resource/pubmed/chemical/talipexole
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0002-9513
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
261
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
R1022-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1681744-Acetylcholine,
pubmed-meshheading:1681744-Adenosine Diphosphate,
pubmed-meshheading:1681744-Adrenergic alpha-Agonists,
pubmed-meshheading:1681744-Animals,
pubmed-meshheading:1681744-Arteries,
pubmed-meshheading:1681744-Azepines,
pubmed-meshheading:1681744-Coronary Vessels,
pubmed-meshheading:1681744-Dogs,
pubmed-meshheading:1681744-Endothelium, Vascular,
pubmed-meshheading:1681744-Estrogens,
pubmed-meshheading:1681744-Female,
pubmed-meshheading:1681744-Progesterone,
pubmed-meshheading:1681744-Vasodilation
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pubmed:year |
1991
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pubmed:articleTitle |
Progesterone and modulation of endothelium-dependent responses in canine coronary arteries.
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pubmed:affiliation |
Department of Physiology and Biophysics, Mayo Clinic and Foundation, Rochester, Minnesota 55905.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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