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[泛酸衍生物对急性乙醇中毒的保护作用及乙酰辅酶A代谢系统的变化]

[The protective effect of pantothenic acid derivatives and changes in the system of acetyl CoA metabolism in acute ethanol poisoning].

作者信息

Moiseenok A G, Dorofeev B F, Omel'ianchik S N

出版信息

Farmakol Toksikol. 1988 Sep-Oct;51(5):82-6.

PMID:2905277
Abstract

Calcium pantothenate (CaP), calcium 4'-phosphopantothenate (CaPP), pantethine, panthenol, sulfopantetheine and CoA decrease acute toxicity of acetaldehyde in mice. All studied compounds diminish duration of the narcotic action of ethanol--ET (3.5 g/kg intraperitoneally) in mice and rats. In the latter this effect is realized at the expense of "long sleeping" and "middle sleeping" animals. CaP (150 mg/kg subcutaneously) and CaPP (100 mg/kg subcutaneously) prevent hypothermia and a decrease of oxygen consumption in rats induced by ET administration. Combined administration of ET, CaP and CaPP leads to a characteristic increase of acid-soluble CoA fractions in the rat liver and a relative decrease of acetyl CoA synthetase and N-acetyltransferase reactions. The antitoxic effect of preparations of pantothenic acid is not mediated by CoA-dependent reactions of detoxication, but most probably is due to intensification of ET oxidation and perhaps to its elimination from the organism.

摘要

泛酸钙(CaP)、4'-磷酸泛酸钙(CaPP)、泛硫乙胺、泛醇、磺基泛酰乙胺和辅酶A可降低乙醛对小鼠的急性毒性。所有研究的化合物均可缩短乙醇(ET,3.5 g/kg腹腔注射)对小鼠和大鼠的麻醉作用持续时间。在大鼠中,这种作用是以“长时间睡眠”和“中等时间睡眠”的动物为代价实现的。皮下注射CaP(150 mg/kg)和CaPP(100 mg/kg)可预防ET给药诱导的大鼠体温过低和耗氧量降低。ET、CaP和CaPP联合给药导致大鼠肝脏中酸溶性辅酶A组分显著增加,乙酰辅酶A合成酶和N-乙酰转移酶反应相对减少。泛酸制剂的抗毒作用不是由依赖辅酶A的解毒反应介导的,很可能是由于ET氧化增强,也许还由于其从机体中消除。

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