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角鲨对钾的升压反应被镁和酚妥拉明阻断。

Dogfish pressor response to potassium blocked by magnesium and phentolamine.

作者信息

Carroll R G, Opdyke D F, Keller N E

出版信息

Am J Physiol. 1982 Mar;242(3):R185-8. doi: 10.1152/ajpregu.1982.242.3.R185.

Abstract

In vivo infusion of MgCl2 blocks the dogfish pressor response to K+. This action of Mg2+ was contrasted to phentolamine in in vivo and in vitro experiments. Mg2+ blocks the spontaneous release of catecholamines from dogfish chromaffin tissue but does not alter the norepinephrine-induced contraction of the isolated dogfish artery. In vivo infusion of Mg2+ causes a significant decrease in resting catecholamine levels and diminishes the catecholamine release caused by K+ challenge. Both Mg2+ and phentolamine block the pressor action of K+, Mg2+ by preventing the K+-induced release of catecholamines and phentolamine by preventing the circulating catecholamines from interacting with alpha-adrenergic receptor sites.

摘要

在体输注氯化镁可阻断角鲨对钾离子的升压反应。在体内和体外实验中,将镁离子的这一作用与酚妥拉明进行了对比。镁离子可阻断角鲨嗜铬组织中儿茶酚胺的自发释放,但不改变去甲肾上腺素诱导的离体角鲨动脉收缩。在体输注镁离子会导致静息儿茶酚胺水平显著降低,并减少钾离子刺激引起的儿茶酚胺释放。镁离子和酚妥拉明均可阻断钾离子的升压作用,镁离子通过阻止钾离子诱导的儿茶酚胺释放,酚妥拉明则通过阻止循环中的儿茶酚胺与α-肾上腺素能受体部位相互作用来实现。

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