[缓激肽结合细胞组分的研究。1. 大鼠子宫微粒体和膜组分激肽酶活性的特性]
[Studies on bradykinin-binding cell fractions. 1. Characterization of kininase activity of the microsomal and membrane fraction from the rat uterus].
作者信息
Jankova T, Paegelow I, Reissmann S, Arold H
出版信息
Acta Biol Med Ger. 1975;34(1):9-13.
PMID:241185
Abstract
In the membrane fraction of rat uterus, kinin-destroying activity was found and characterized as kininase II by means of several kininase inhibitors. It could be shown that sudies of bradykinin-receptor interactions requires the use of kininase inhibitors like phenanthroline or the use of a stable bradykinin analogue like [8-erythro-alpha-amino-beta-phenylbutyric acid]-bradykinin.
摘要
在大鼠子宫的膜部分中，发现了激肽破坏活性，并通过几种激肽酶抑制剂将其鉴定为激肽酶II。可以证明，缓激肽受体相互作用的研究需要使用菲咯啉等激肽酶抑制剂，或者使用[8-赤藓糖-α-氨基-β-苯基丁酸]-缓激肽等稳定的缓激肽类似物。
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