Mechanisms of hypoxic pulmonary vasoconstriction: can anyone be right?

被引:100
作者
Ward, JPT
Aaronson, PI
机构
[1] Kings Coll London, Dept Resp Med & Allergy, Guys Hosp, London SE1 7EH, England
[2] Kings Coll London, Dept Pharmacol, Guys Hosp, London SE1 7EH, England
[3] Kings Coll London, St Thomas Hosp, Sch Med & Dent, London SE1 7EH, England
来源
RESPIRATION PHYSIOLOGY | 1999年 / 115卷 / 03期
基金
英国惠康基金;
关键词
Ca2+; stores; hypoxic pulmonary vasoconstriction; channels; K+; endothelium; pulmonary vessels; hypoxia; pulmonary vasoconstriction; mediators; endothelium-derived constricting; factor; pulmonary circulation;
D O I
10.1016/S0034-5687(99)00025-0
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Despite extensive studies over many years, there is still no real consensus regarding the mechanisms responsible for hypoxic pulmonary vasoconstriction (HPV). This is partially related to extensive variation between preparations. species, and the length of the hypoxic challenge, but also to an apparent abundance of potential mechanisms. Whereas there is good evidence that hypoxia causes inhibition of K+ channels in pulmonary artery smooth muscle, with subsequent depolarisation and Ca2+ influx through voltage-activated Ca2+ channels, there is also strong support for a critical role for Ca2+ release from intracellular stores. Moreover other studies suggest that the endothelium provides an essential component of the overall response. We suggest in this review that sustained HPV, as seen in the intact animal. is multi-factorial in origin and requires activation of more than one process for the full response to develop. Fundamental issues that remain unresolved are outlined. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:261 / 271
页数:11
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