Hypertension, Vol 5, 887-892, Copyright © 1983 by American Heart Association
T Kanbe, Y Nara, M Tagami and Y Yamori
Mechanisms of vascular hypertrophy induced by hypertension were studied in
cultured aortic smooth muscle cells from spontaneously hypertensive rats
(SHR) and stroke-prone SHR (SHRSP) and compared with those from
normotensive Wistar-Kyoto (WKY) rats. Fetal calf serum-stimulated ornithine
decarboxylase (ODC) activity of cultured smooth muscle cells was greater in
SHR and SHRSP than in WKY. Beta- but not alpha- adrenergic agonist
stimulated ODC activity acutely in cultured smooth muscle cells from WKY,
and isoprenaline-induced activation was blocked by the beta-blocker,
propranolol, and enhanced by the phosphodiesterase inhibitor,
1-methyl-3-isobutylxanthine. These results indicate that cultured vascular
smooth muscle cells from SHR and SHRSP are more prone to increase the
protein synthesis than those from WKY through the trophic induction of ODC
activity and that the regulation of ODC activity by catecholamines is
mediated through beta-agonistic effect in cultured smooth muscle cells.
ARTICLES
Studies of hypertension-induced vascular hypertrophy in cultured smooth muscle cells from spontaneously hypertensive rats
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