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长春质碱:一种新型的胰腺酶释放刺激剂。

Catharanthine: a novel stimulator of pancreatic enzyme release.

作者信息

Williams J A

出版信息

Cell Tissue Res. 1978 Sep 5;192(2):277-84. doi: 10.1007/BF00220745.

Abstract

The plant alkaloid, catharanthine, was shown to stimulate release of amylase from pancreatic fragments and to cause extensive degranulation of pancreatic acinar cells with accumulation of membrane material in the Golgi region. The extent and time course of maximal catharanthine stimulation was comparable to that induced by the cholinergic analog bethanechol. Antimycin inhibited the action of catharanthine while atropine did not. Removal of Ca2+ from the incubation medium inhibited amylase release induced by catharanthine but did not affect release induced by bethanechol. Catharanthine induced a delayed release of 45Ca2+ from prelabeled pancreatic fragments as compared to bethanechol. It is suggested therefore that catharanthine activates the physiological pathway controlling amylase release by causing a rise in cytoplasmic Ca2+ but the mechanism by which this occurs is different from that caused by physiological secretagogues.

摘要

植物生物碱长春质碱可刺激胰腺碎片释放淀粉酶,并导致胰腺腺泡细胞广泛脱颗粒,高尔基体区域出现膜物质积聚。长春质碱最大刺激的程度和时间进程与胆碱能类似物氨甲酰甲胆碱诱导的情况相当。抗霉素可抑制长春质碱的作用,而阿托品则无此作用。从孵育培养基中去除Ca2+可抑制长春质碱诱导的淀粉酶释放,但不影响氨甲酰甲胆碱诱导的释放。与氨甲酰甲胆碱相比,长春质碱诱导预先标记的胰腺碎片延迟释放45Ca2+。因此,有人提出长春质碱通过引起细胞质Ca2+升高来激活控制淀粉酶释放的生理途径,但发生这种情况的机制与生理性促分泌剂引起的机制不同。

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