Klebanov B M, Chernoshtan K A
Farmakol Toksikol. 1977 Jul-Aug;40(4):428-30.
The influence exerted by a number of non-steroid antiphlogistic agents on the fermentative mechanism responsible for the formation and decomposition of kininines in an inflammation focus and on the permeability of vessels in a skin changed under the effect of exogenous bradykininine was studied. Bradykininine, chigamin, sodium salicylate and mephenaminate are shown to inhibit "in vitro" the kininogenic and intensify the kininase activity of the exudate in rats with turpentine-induced pleuritis, while indometacin affects only the activity of kininogenases. Butadion, chingamin and sodium mephenaminate merely reduce the reactivity of the skin with respect to exogenous bradykininine.
研究了多种非甾体抗炎药对炎症灶中激肽原形成和分解的发酵机制以及在外源性缓激肽作用下发生变化的皮肤血管通透性的影响。结果表明,缓激肽、奇加明、水杨酸钠和甲灭酸在“体外”可抑制松节油诱导胸膜炎大鼠渗出液中的激肽原生成并增强激肽酶活性,而吲哚美辛仅影响激肽原酶的活性。布他酮、奇加明和甲灭酸仅降低皮肤对外源性缓激肽的反应性。