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降血糖药物2-(3-甲基肉桂酰腙基)丙酸酯(BM 42.304)的作用机制研究

Studies on the mechanism of action of the hypoglycemic agent, 2-(3-methylcinnamylhydrazono)-propionate (BM 42.304).

作者信息

Deaciuc I V, Kühnle H F, Strauss K M, Schmidt F H

出版信息

Biochem Pharmacol. 1983 Nov 15;32(22):3405-12. doi: 10.1016/0006-2952(83)90369-6.

Abstract

A new hypoglycemic agent, 2-(3-methylcinnamylhydrazono)-propionate MCHP (BM 42.304) was shown to be an inhibitor of the transfer of long-chain fatty acids across the mitochondrial inner membrane. The following data support this conclusion: the drug, at already 5 microM, inhibited ketogenesis from oleate but not from octanoate in the perfused guinea-pig liver; likewise, ketogenesis from L-(-)-palmitoylcarnitine and palmitoyl-CoA + L-(-)-carnitine, but not from octanoate, was depressed in isolated guinea-pig liver mitochondria. Oxigraphic measurements of the oxygen uptake by isolated mitochondria showed that the drug impaired oxygen uptake with the long-chain fatty acid derivatives but not with octanoate. Finally, in vivo effects of the drug such as hypoketonemia and an increased concentration of free fatty acids in blood are in agreement with the above formulated mechanism of action. A comment is given on the relationships between fatty acid oxidation and gluconeogenesis in the guinea-pig liver.

摘要

一种新型降糖药2-(3-甲基肉桂酰腙基)-丙酸酯MCHP(BM 42.304)被证明是长链脂肪酸跨线粒体内膜转运的抑制剂。以下数据支持这一结论:在灌注的豚鼠肝脏中,该药物在5微摩尔浓度时就抑制了油酸生成酮体,但不抑制辛酸生成酮体;同样,在分离的豚鼠肝脏线粒体中,L-(-)-棕榈酰肉碱和棕榈酰辅酶A+L-(-)-肉碱生成酮体受到抑制,但辛酸生成酮体不受影响。对分离线粒体耗氧量的氧摄取描记测量表明,该药物损害了长链脂肪酸衍生物的氧摄取,但不影响辛酸的氧摄取。最后,该药物的体内效应,如低酮血症和血液中游离脂肪酸浓度升高,与上述作用机制相符。文中对豚鼠肝脏中脂肪酸氧化与糖异生之间的关系进行了评论。

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