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人脐动脉中收缩性肾上腺素能受体的特性研究

Characterization of contractile adrenoceptors in the human umbilical artery.

作者信息

Bodelsson G, Stjernquist M

机构信息

Department of Obstetrics and Gynecology, University Hospital, Malmö, Sweden.

出版信息

Eur J Pharmacol. 1995 Aug 25;282(1-3):95-101. doi: 10.1016/0014-2999(95)00277-r.

Abstract

Adrenoceptors mediating contraction in ring segments of human umbilical arteries from normal term pregnancies were investigated in vitro. Contraction was elicited by (order of potency indicated): noradrenaline = the alpha 2-adrenoceptor agonist oxymetazoline >> the alpha 1-adrenoceptor agonist phenylephrine. The alpha 1-adrenoceptor antagonist prazosin antagonized the contraction elicited by noradrenaline and phenylephrine. The alpha 2-adrenoceptor antagonist rauwolscine antagonized the contraction elicited by noradrenaline and oxymetazoline. Oxymetazoline had an efficacy 5 times higher than that of noradrenaline and the 5-hydroxytryptamine receptor antagonist methysergide antagonized the contraction elicited by oxymetazoline. It is suggested that the contractile adrenoceptors in the human umbilical artery consist of both alpha 1 and alpha 2 subtypes. Furthermore, the contractile effect of oxymetazoline seems to be mediated via both alpha 2-adrenoceptors and 5-hydroxytryptamine receptors.

摘要

体外研究了足月正常妊娠人脐动脉环段中介导收缩的肾上腺素能受体。收缩由以下物质引发(按效力顺序):去甲肾上腺素 = α2肾上腺素能受体激动剂羟甲唑啉 >> α1肾上腺素能受体激动剂去氧肾上腺素。α1肾上腺素能受体拮抗剂哌唑嗪可拮抗去甲肾上腺素和去氧肾上腺素引发的收缩。α2肾上腺素能受体拮抗剂育亨宾可拮抗去甲肾上腺素和羟甲唑啉引发的收缩。羟甲唑啉的效力比去甲肾上腺素高5倍,5-羟色胺受体拮抗剂麦角新碱可拮抗羟甲唑啉引发的收缩。提示人脐动脉中的收缩性肾上腺素能受体由α1和α2两种亚型组成。此外,羟甲唑啉的收缩作用似乎是通过α2肾上腺素能受体和5-羟色胺受体介导的。

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