Possible mechanisms of spasmolytic action of bile salts on the isolated guinea-pig gallbladder.

N Sunagane, T Kobori, T Urono, K Kubota
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引用次数: 4

Abstract

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.

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胆盐对离体豚鼠胆囊解痉作用的可能机制。
胆盐对胆囊平滑肌的解痉作用可以解释胆酸治疗中胆绞痛的缓解。研究了胆盐、熊去氧胆酸盐和去氧胆酸盐在离体豚鼠胆囊中的解痉作用机制。胆盐加速了45ca从胆囊流出的同步松弛,抑制了去极化肌肉准备的细胞对45ca的摄取。此外,它们敏感地抑制cacl2诱导的去极化肌肉收缩。胆盐可显著提高胆囊组织环AMP含量。二丁基环AMP模拟了胆盐对钙外排和肌肉松弛的影响,但对细胞钙摄取没有影响。这些结果表明,胆盐通过加速钙的外排产生松弛作用,这可能与细胞循环AMP水平的升高有关,并通过抑制钙在细胞膜上的内流产生松弛作用。
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