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缓激肽通过高亲和力受体抑制大鼠子宫肌层腺苷酸环化酶活性。

Bradykinin inhibits rat myometrial adenylate cyclase activity via a high-affinity receptor.

作者信息

Liebmann C, Reissmann S

机构信息

Department of Biology, Friedrich Schiller University, Jena.

出版信息

Biomed Biochim Acta. 1990;49(11):1231-4.

PMID:1965565
Abstract

Bradykinin (BK) which contracts the rat uterus inhibited at subnanomolar concentrations rat myometrial adenylate cyclase stimulated by NaF or guanyl nucleotides by about 40%. The effect was maximal at about 10 to 100 pM. At a higher concentration (100 nM), bradykinin was ineffective. Together with recently presented results these data suggest that in rat myometrium the adenylate cyclase may be coupled by a G12/G13-type G-protein to a high-affinity BK receptor.

摘要

使大鼠子宫收缩的缓激肽(BK)在亚纳摩尔浓度时,可抑制由氟化钠或鸟苷酸刺激的大鼠子宫肌层腺苷酸环化酶,抑制率约为40%。该效应在约10至100皮摩尔时达到最大。在较高浓度(100纳摩尔)时,缓激肽无效。结合最近公布的结果,这些数据表明,在大鼠子宫肌层中,腺苷酸环化酶可能通过G12/G13型G蛋白与高亲和力的BK受体偶联。

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