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泻药在体外对肠上皮细胞蛋白激酶C的刺激作用。

Stimulation of enterocyte protein kinase C by laxatives in-vitro.

作者信息

Beubler E, Schirgi-Degen A

机构信息

Department of Experimental and Clinical Pharmacology, Karl-Franzens-University, Graz, Austria.

出版信息

J Pharm Pharmacol. 1993 Jan;45(1):59-62. doi: 10.1111/j.2042-7158.1993.tb03680.x.

Abstract

To elucidate the role of protein kinase C in the mechanism of action of stimulatory laxatives, experiments were performed with preparations of rat lysed enterocytes. The phorbol ester 4-beta-phorbol 12-myristate 13-acetate (PMA) concentration-dependently (2-200 micrograms mL-1) stimulated the activity of protein kinase C in this preparation. Ricinoleic acid, the active principle of castor oil, deacetylbisacodyl, the active principle of bisacodyl, and deoxycholic acid exerted the same effect, although less efficiently. This reflects their potency for inducing intestinal fluid secretion and prostaglandin release, effects that are also induced more potently by PMA. Accordingly, the potency of the three C18 fatty acids, ricinoleic acid, stearic acid and oleic acid on protein kinase C activity in-vitro, on prostaglandin E2 release and on net fluid secretion in-vivo runs in parallel. It is therefore concluded that stimulatory laxatives activate protein kinase C, leading to prostaglandin E2 release, thus resulting in net fluid secretion.

摘要

为阐明蛋白激酶C在刺激性泻药作用机制中的作用,利用大鼠裂解肠上皮细胞制剂进行了实验。佛波酯4-β-佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)在该制剂中浓度依赖性地(2 - 200微克/毫升)刺激蛋白激酶C的活性。蓖麻油的活性成分蓖麻油酸、比沙可啶的活性成分去乙酰比沙可啶和脱氧胆酸也有相同作用,尽管效率较低。这反映了它们诱导肠液分泌和前列腺素释放的能力,PMA也更有效地诱导这些作用。因此,三种C18脂肪酸(蓖麻油酸、硬脂酸和油酸)对体外蛋白激酶C活性、体内前列腺素E2释放和净液体分泌的效力是平行的。因此得出结论,刺激性泻药激活蛋白激酶C,导致前列腺素E2释放,从而引起净液体分泌。

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