Sunagane N, Kobori T, Urono T, Kubota K
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Science University of Tokyo, Japan.
Nihon Heikatsukin Gakkai Zasshi. 1990 Jun;26(3):143-50. doi: 10.1540/jsmr1965.26.143.
The spasmolytic action of bile salts on gallbladder smooth muscle could explain the alleged relief of biliary colic seen during bile acid therapy. The mechanisms of spasmolytic action of bile salts, ursodeoxycholate and deoxycholate were studied in the isolated gallbladder of guinea-pigs. The bile salts accelerated the 45Ca-efflux from the gallbladder with synchronous relaxation and inhibited the cellular 45Ca-uptake by the depolarized muscle preparation. Further, they sensitively inhibited CaCl2-induced contraction of the depolarized muscle. The tissue cyclic AMP content of the gallbladder was significantly elevated by the bile salts. Dibutyryl cyclic AMP mimicked the effects of bile salts on the Ca-efflux and the muscle relaxation, but showed no effect on the cellular Ca-uptake. From these results, it is suggested that the bile salts produce the relaxant action through accelerating Ca-efflux, which is probably coupled with the elevation of the cellular cyclic AMP level, and through suppressing the Ca-influx across the cell membrane.
胆盐对胆囊平滑肌的解痉作用可以解释在胆汁酸治疗期间所声称的胆绞痛缓解现象。在豚鼠的离体胆囊中研究了胆盐、熊去氧胆酸和脱氧胆酸的解痉作用机制。胆盐加速了胆囊中45Ca的外流,同时伴有松弛,并且抑制了去极化肌肉标本对细胞内45Ca的摄取。此外,它们能敏感地抑制氯化钙诱导的去极化肌肉收缩。胆盐使胆囊组织中的环磷酸腺苷(cAMP)含量显著升高。二丁酰环磷酸腺苷模拟了胆盐对钙外流和肌肉松弛的作用,但对细胞内钙摄取没有影响。从这些结果表明,胆盐通过加速钙外流产生松弛作用,这可能与细胞内环磷酸腺苷水平的升高有关,并且通过抑制钙跨细胞膜内流来实现。