IDENTIFICATION OF A NONENDOTHELIAL CELL THROMBOXANE-LIKE CONSTRICTOR RESPONSE AND ITS INTERACTION WITH THE RENIN-ANGIOTENSIN SYSTEM IN THE AORTA OF SPONTANEOUSLY HYPERTENSIVE RATS

Citation
Sm. Dyer et al., IDENTIFICATION OF A NONENDOTHELIAL CELL THROMBOXANE-LIKE CONSTRICTOR RESPONSE AND ITS INTERACTION WITH THE RENIN-ANGIOTENSIN SYSTEM IN THE AORTA OF SPONTANEOUSLY HYPERTENSIVE RATS, Journal of vascular research, 31(1), 1994, pp. 52-60
Citations number
34
Categorie Soggetti
Hematology,"Medicine, General & Internal",Physiology
ISSN journal
10181172
Volume
31
Issue
1
Year of publication
1994
Pages
52 - 60
Database
ISI
SICI code
1018-1172(1994)31:1<52:IOANCT>2.0.ZU;2-S
Abstract
Aortic ring preparations from spontaneously hypertensive rats (SHR) an d normotensive Wistar Kyoto (WKY) rats were treated with N-omega-nitro -L-arginine (NOLA, 10(-4) M). This produced a sustained contraction in preparations from SHR but not WKY rats. A similar contraction in aort ic ring preparations from the SHR was produced with methylene blue (10 (-5) M) and N-G-monomethyl-L-arginine (10(-5) M). The NOLA-induced con traction was reversed with indomethacin (8 x 10(-6) M), ridogrel (10(- 5) M) and SQ 29548 (10(-6) M) thus confirming the involvement of throm boxane A(2)/prostaglandin H-2 processes. Subsequent experiments demons trated that the thromboxane-like contraction was not dependent upon th e presence of endothelial cells and occurred in preparations from youn g, prehypertensive (5 week) and older (17 week) SHRs. The thromboxane- like contraction was markedly suppressed with chronic captopril treatm ent and reinstated 4 weeks after withdrawal from captopril. The additi on of saralasin (10(-6) M) or captopril (10(-6) M) to; aortic ring pre parations did not suppress the thromboxane-like contractions. The fore going findings support the presence of a nonendothelial cell thromboxa ne-like constrictor agent in the aorta of the SHR that is revealed aft er impairment of nitric oxide production. The activity of the thrombox ane-like constrictor process is not tightly linked to prevailing blood pressure, but is reduced with chronic in vivo inhibition of the angio tensin-converting enzyme.