Source:http://linkedlifedata.com/resource/pubmed/id/11465653
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7 Pt 1
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pubmed:dateCreated |
2001-7-23
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pubmed:abstractText |
To evaluate the potential contribution of endothelin-1 (ET-1) toward the cardiovascular complications of diabetes, the present study examined the effects of chronic ET receptor blockade with bosentan on heart function and vascular reactivity in streptozotocin (STZ)-induced diabetic rats. Wistar rats were divided into four groups: control, control bosentan-treated, diabetic, and diabetic bosentan-treated. After chronic bosentan treatment, cardiac function and vascular reactivity were assessed. Exvivo working heart function was determined in terms of rate of contraction (+dP/dt), rate of relaxation (-dP/dt), and left ventricular developed pressure (LVDP). Contractile responses to ET-1 were determined in isolated superior mesenteric arteries. In addition, ET-1-like immunoreactivity was determined in ventricular and vascular tissues by immunohistochemistry. Cardiac function was depressed in the untreated-diabetic group. Bosentan treatment improved working heart function; hearts from the diabetic bosentan-treated group exhibited improved LVDP and -dP/dt. The contractile responses of mesenteric arteries to ET-1 were exaggerated in the untreated-diabetic group. Long-term bosentan treatment normalized these responses. Immunohistochemical analyses revealed increased ET-1-like immunoreactivity in ventricular and vascular tissues from untreated diabetic rats. These data show the beneficial effects of ET(A/B) receptor blockade on cardiovascular function in STZ-diabetic rats. An altered ET-1 system may contribute toward the pathogenesis of cardiovascular dysfunction in diabetes.
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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/Antihypertensive Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Endothelin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Endothelin,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfonamides,
http://linkedlifedata.com/resource/pubmed/chemical/bosentan
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0895-7061
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
679-87
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pubmed:dateRevised |
2009-2-24
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pubmed:meshHeading |
pubmed-meshheading:11465653-Animals,
pubmed-meshheading:11465653-Antihypertensive Agents,
pubmed-meshheading:11465653-Atrial Function, Left,
pubmed-meshheading:11465653-Diabetes Mellitus, Experimental,
pubmed-meshheading:11465653-Endothelin-1,
pubmed-meshheading:11465653-Male,
pubmed-meshheading:11465653-Mesenteric Arteries,
pubmed-meshheading:11465653-Myocardial Contraction,
pubmed-meshheading:11465653-Rats,
pubmed-meshheading:11465653-Rats, Wistar,
pubmed-meshheading:11465653-Receptors, Endothelin,
pubmed-meshheading:11465653-Sulfonamides,
pubmed-meshheading:11465653-Vasoconstriction
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pubmed:year |
2001
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pubmed:articleTitle |
Long-term endothelin receptor blockade improves cardiovascular function in diabetes.
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pubmed:affiliation |
Division of Pharmacology and Toxicology, Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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