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首页> 外文期刊>Japanese Journal of Pharmacology >Effects of the New Anti-Ulcer Drug Ecabet Sodium (TA-2711) on Pepsin Activity I. Inactivation of Enzyme Protein
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Effects of the New Anti-Ulcer Drug Ecabet Sodium (TA-2711) on Pepsin Activity I. Inactivation of Enzyme Protein

机译:新型抗溃疡药物依卡比特钠(TA-2711)对胃蛋白酶活性的影响I.酶蛋白的失活

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References(19) Cited-By(21) To investigate the mechanism of the anti-peptic action of ecabet sodium (TA-2711) observed in pylorus-ligated rats, effects of this drug on the peptic activity of rat gastric juice, purified hog pepsin and pepsinogen were studied in vitro. After incubation with or without ecabet at acidic pH, the reaction mixture was centrifuged, and the peptic activity of the supernatant was measured. Ecabet depressed the peptic activity of pepsin and pepsinogen in parallel with a decrease in the protein concentration of the respective super natant. Depression was greatest with pepsinogen (97% at 2.5 mg/ml of the drug) followed by gastric juice (about 60% at 10 mg/ml), and inhibition of the peptic activity of pepsin was weakest (about 10% at 10 mg/ml). When a fraction of the rat gastric juice containing substances with molecular weights below 10, 000 was added to the pepsin solution, the anti-peptic activity of ecabet was potentiated. These results suggest that oral dosing of ecabet reduces the peptic activity of gastric juice by precipitating pepsin, which is facilitated by an unknown component(s) of gastric juice, and that the inactivation of pepsinogen may also contribute to the anti-peptic activity of ecabet.
机译:参考文献(19)Cited-By(21)研究幽门结扎大鼠中依卡倍特钠(TA-2711)的抗消化作用机制,该药物对大鼠胃液,纯化猪的消化活性的影响对胃蛋白酶和胃蛋白酶原进行了体外研究。在有或没有依卡倍特的酸性pH条件下温育后,将反应混合物离心,并测量上清液的消化活性。 Ecabet降低了胃蛋白酶和胃蛋白酶原的消化活性,同时降低了相应上清液的蛋白质浓度。胃蛋白酶原引起的抑郁感最大(2.5 mg / ml时为97%),其次是胃液(10 mg / ml时为60%),胃蛋白酶的消化活性抑制作用最弱(10 mg / ml时约为10%)。毫升)。当将一部分大鼠胃液中分子量低于10、000的物质添加到胃蛋白酶溶液中时,依卡贝特的抗消化活性增强。这些结果表明口服依卡贝特的剂量通过沉淀胃蛋白酶降低胃液的消化活性,而胃蛋白酶的未知成分促进了胃蛋白酶的消化,胃蛋白酶原的失活也可能有助于依卡贝特的抗消化活性。

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