Source:http://linkedlifedata.com/resource/pubmed/id/10756122
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2000-6-13
|
pubmed:abstractText |
The aim of the present study was to assess the status of ET-1 receptor subtypes (ET(A)and ET(B)) in ventricular myocytes and fibroblasts and to determine the role of PKC-dependent pathways in ET-1-stimulated cardiac cells in deoxycorticosterone acetate (DOCA)-salt hypertensive rats. Systolic blood pressure and relative heart to body weight were significantly increased in DOCA-salt rats. In unilaterally nephrectomized (Uni-Nx) control rats, more than 90% of cardiomyocyte ET receptors were of the ET(A)subtype, whereas in fibroblasts ET(A)and ET(B)receptors were present in a 1:3 ratio. In DOCA-salt rats, the density of the ET(A)receptor subtype was reduced by 31% in cardiomyocytes and in cardiac fibroblasts only ET(B)receptor density was decreased by 29%. Affinity was unchanged. The relative expression of immunoreactive PKC alpha, gamma and epsilon was significantly increased, whereas PKC delta was not altered in cardiac extracts of DOCA-salt rats. In cardiac fibroblasts from DOCA-salt rats PKC delta was significantly increased and PKC epsilon was not translocated after ET-1 stimulation. The hearts of DOCA-salt hypertensive rats are thus characterized by: (1) decreased density of cardiomyocyte ET(A)receptors and fibroblast ET(B)receptors; (2) cell-specific enhanced expression of some PKC isoenzymes (alpha, gamma, delta and epsilon); and (3) unresponsiveness of PKC epsilon to translocate in the presence of ET-1. Together with alterations of ET-1-induced Ca(2+)handling in cardiac myocytes and fibroblasts, which we previously reported, results from the present study indicate a marked modification of the cardiac ET-1 system of DOCA-salt hypertensive rats.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Desoxycorticosterone,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Endothelin A,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Endothelin B,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Endothelin
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0022-2828
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright 2000 Academic Press.
|
pubmed:issnType |
Print
|
pubmed:volume |
32
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
665-76
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:10756122-Animals,
pubmed-meshheading:10756122-Biological Transport,
pubmed-meshheading:10756122-Blood Pressure,
pubmed-meshheading:10756122-Body Weight,
pubmed-meshheading:10756122-Cells, Cultured,
pubmed-meshheading:10756122-Desoxycorticosterone,
pubmed-meshheading:10756122-Heart,
pubmed-meshheading:10756122-Hypertension,
pubmed-meshheading:10756122-Isoenzymes,
pubmed-meshheading:10756122-Male,
pubmed-meshheading:10756122-Myocardium,
pubmed-meshheading:10756122-Organ Size,
pubmed-meshheading:10756122-Protein Kinase C,
pubmed-meshheading:10756122-Rats,
pubmed-meshheading:10756122-Rats, Sprague-Dawley,
pubmed-meshheading:10756122-Receptor, Endothelin A,
pubmed-meshheading:10756122-Receptor, Endothelin B,
pubmed-meshheading:10756122-Receptors, Endothelin
|
pubmed:year |
2000
|
pubmed:articleTitle |
Altered cardiac endothelin receptors and protein kinase C in deoxycorticosterone-salt hypertensive rats.
|
pubmed:affiliation |
MRC Multidisciplinary Research Group on Hypertension, Clinical Research Institute of Montreal, Montreal, Quebec, H2W 1R7, Canada.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|