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磺酰脲类药物对大鼠离体子宫自发运动及诱发收缩的影响。

Effects of sulphonylureas on spontaneous motility and induced contractions in rat isolated uterus.

作者信息

Villar A, Ivora M D, D'Ocon M P, Anselmi E

出版信息

J Pharm Pharmacol. 1986 Oct;38(10):778-80. doi: 10.1111/j.2042-7158.1986.tb04493.x.

Abstract

To clarify the action of sulphonylureas on calcium, the effect of tolbutamide and glibenclamide has been investigated on a Ca-dependent process, the contractile activity of uterine smooth muscle. Both sulphonylureas antagonized the contractions evoked by CaCl2 in a non-competitive manner when the uterus was maintained in depolarizing solution and did not affect the spontaneous contractions of rat uterus. The capacity of tolbutamide and glibenclamide to relax vanadate-induced contraction of rat uterus in Ca-free medium suggests that sulphonylureas may have an intracellular site of action related to cytosolic free Ca levels, or effect a reduction in Ca action.

摘要

为阐明磺脲类药物对钙的作用,研究了甲苯磺丁脲和格列本脲对一种钙依赖性过程——子宫平滑肌收缩活性的影响。当子宫处于去极化溶液中时,两种磺脲类药物均以非竞争性方式拮抗氯化钙诱发的收缩,且不影响大鼠子宫的自发收缩。甲苯磺丁脲和格列本脲在无钙培养基中使钒酸盐诱导的大鼠子宫收缩舒张的能力表明,磺脲类药物可能有一个与胞浆游离钙水平相关的细胞内作用位点,或能降低钙的作用。

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