CYTOSOLIC FREE CALCIUM OF AORTA IN HYPERTENSIVE RATS - CHRONIC INHIBITION OF ANGIOTENSIN CONVERTING ENZYME

被引:94
作者
SADA, T
KOIKE, H
IKEDA, M
SATO, K
OZAKI, H
KARAKI, H
机构
[1] SANKYO CO LTD, BIOL RES LABS,DIV CARDIOVASC,1-2-58 HIROMACHI, SHINAGAWA KU, TOKYO 140, JAPAN
[2] UNIV TOKYO, FAC AGR, DEPT VET PHARMACOL, TOKYO 113, JAPAN
关键词
Calcium; Converting enzyme inhibition; Fluorescent indicators; Spontaneously hypertensive rats; Vascular smooth muscle;
D O I
10.1161/01.HYP.16.3.245
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Cytosolic free calcium concentration ([Ca2+]i) and muscle tension were simultaneously measured in aortic tissue isolated from spontaneously hypertensive rats (SHR), normotensive Wistar-Kyoto (WKY) rats, and SHR chronically treated with a novel angiotensin converting enzyme inhibitor, CS-622. In the presence of 2.5 mM Ca2+ in the bathing solution, aortic [Ca2+], measured with fura-2 was higher in SHR than in WKY rats, and it was almost the same in CS-622-treated SHR and untreated WKY rats. Increase of external Ca2+ concentration from zero to 2.5 mM elicited a contraction in SHR aortas but not in aortas from both CS-622-treated SHR and untreated WKY rats. When the aortas were contracted by 60 mM K+, however, [Ca2+]i as well as developed tension was similar in the three groups. CGP-28392 (10-6 M), a Ca2+ channel activator, induced a rhythmic activity superimposed on a gradual increase of [Ca2+]i and tension in SHR aortas but not in the aortas of CS-622-treated SHR or untreated WKY rats. Nicardipine (10-7 M) decreased the resting [Ca2+]i and the resting tone in SHR aortas, but not in WKY rat aortas. These results suggest that SHR aortas have a higher myogenic tone due to increased [Ca2+]i than WKY rat aortas and that the increased [Ca2+]i is attributed to alterations of dihydropyridine-sensitive Ca2+ channels in SHR aortas. Further, the decrease of the vascular tone induced by long-term administration of the angiotensin converting enzyme inhibitor may be due to a reduction of increased [Ca2+], in SHR.
引用
收藏
页码:245 / 251
页数:7
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