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心脏对氯丙嗪、丙咪嗪和阿米替林抑制黄素形成作用的敏感性。

Cardiac sensitivity to the inhibitory effects of chlorpromazine, imipramine and amitriptyline upon formation of flavins.

作者信息

Pinto J, Huang Y P, Pelliccione N, Rivlin R S

出版信息

Biochem Pharmacol. 1982 Nov 1;31(21):3495-9. doi: 10.1016/0006-2952(82)90632-3.

Abstract

Chlorpromazine, imipramine and amitriptyline, drugs structurally related to riboflavin, each inhibited the formation in vivo of flavin adenine dinucleotide (FAD) from riboflavin in rat heart at 2-5 mg/kg body weight, doses comparable on a weight basis to those used clinically. All three drugs inhibited FAD formation in heart within 5 hr after a single dose of 25 mg/kg. Chlorpromazine under these conditions also inhibited FAD formation in liver, cerebrum and cerebellum. A series of psychoactive agents structurally unrelated to riboflavin did not inhibit flavin formation in the organs tested. These findings indicate that the inhibitory effects of the drugs studied have organ specificity with respect to FAD formation.

摘要

氯丙嗪、丙咪嗪和阿米替林,这些在结构上与核黄素相关的药物,在大鼠心脏中,每千克体重2至5毫克的剂量下(按体重计算,这些剂量与临床使用剂量相当),均抑制了体内核黄素形成黄素腺嘌呤二核苷酸(FAD)的过程。单次给予25毫克/千克剂量后,这三种药物在5小时内均抑制了心脏中FAD的形成。在这些条件下,氯丙嗪还抑制了肝脏、大脑和小脑中FAD的形成。一系列在结构上与核黄素无关的精神活性药物并未抑制所测试器官中黄素的形成。这些发现表明,所研究药物对FAD形成的抑制作用具有器官特异性。

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