Hypoxic contractile response in isolated rat thoracic aorta: role of endothelium, extracellular calcium and endothelin
Hypoxic contractile response in isolated rat thoracic aorta: role of endothelium, extracellular calcium and endothelin
复制标题
离体大鼠胸主动脉缺氧收缩反应:内皮、细胞外钙和内皮素的作用
DOI:
10.1111/j.1472-8206.1997.tb00178.x
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发表时间:
1997
影响因子:
2.9
通讯作者:
É. Bellissant
中科院分区:
文献类型:
--
作者:
D. Pape;J. Beuchard;P. Guillo;H. Allain;É. Bellissant
Summary— The effects of hypoxia on isolated arteries remain controversial, depending on the species, vascular beds and protocols. The aims of the study were to characterize the response of rat thoracic aorta to hypoxia and to examine the roles of endothelium, extracellular calcium and endothelin in this response. Hypoxia was induced by bubbling Krebs solution with 95% N2 and 5% CO2 instead of 95% O2 and 5% CO2. Experiments were performed during 1 h in norepinephrine (0.01 μM) precontracted rings. Hypoxia produced a biphasic response consisting of an initial transient partial relaxation (67% at 14 min) followed by a slow but sustained contraction (27% from 40 to 60 min). After endothelium removal, relaxation appeared faster with increased magnitude (82% at 12 min) and was followed by a weak transient contraction (16% at 25 min). In endothelium‐intact rings, Ca2+ free medium (EGTA, 0.1 mM) and Ca2+ channel blockers, verapamil (0.05, 0.5 and 5 μM) or nicardipine (0.1, 1 and 10 μM), had no effect on relaxation but inhibited the contraction, the effects of both calcium antagonists being concentration‐dependent. Similarly, the ETA/ETB receptor antagonist, bosentan (0.1, 10 and 1,000 nM), induced a concentration‐dependent decrease in the contraction. We conclude that 1) the response of rat thoracic aorta during 1 h of hypoxia is biphasic (relaxation followed by contraction); 2) the endothelium is involved in the contraction whereas its role in the relaxation remains to be elucidated; 3) extracellular calcium is involved in the contraction; and 4) endothelin may play a role in the contraction.
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影响因子:
5.5
作者:
RUBANYI, GM;VANHOUTTE, PM
通讯作者:
VANHOUTTE, PM
影响因子:
3.3
作者:
Chen, SJ;Chen, YF;Oparil, S
通讯作者:
Oparil, S
影响因子:
--
作者:
GRASER, T;VANHOUTTE, PM
通讯作者:
VANHOUTTE, PM
DOI:
10.1152/ajpheart.1990.259.2.h281
发表时间:
1990
期刊:
The American journal of physiology
影响因子:
--
作者:
Yuan,XJ;Tod,ML;Rubin,LJ;Blaustein,MP
通讯作者:
Blaustein,MP
DOI:
10.1152/jappl.1991.71.1.30
发表时间:
1991
期刊:
Journal of applied physiology (Bethesda, Md. : 1985)
影响因子:
--
作者:
Mathew,R;Burke-Wolin,T;Gewitz,MH;Wolin,MS
通讯作者:
Wolin,MS