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烟酸和阿西莫司对脂肪分解的抑制作用。

Inhibition of lipolysis by nicotinic acid and by acipimox.

作者信息

Fuccella L M, Goldaniga G, Lovisolo P, Maggi E, Musatti L, Mandelli V, Sirtori C R

出版信息

Clin Pharmacol Ther. 1980 Dec;28(6):790-5. doi: 10.1038/clpt.1980.236.

Abstract

Acipimox (5-methylpyrazinecarboxylic acid 4-oxide) is a new lipolysis inhibitor that has a distant chemical relationship with nicotinic acid (NA). The tritiated compound (100 mg) is rapidly absorbed, peak plasma radioactivity being reached after 2 hr, with an almost total elimination unchanged in urine. A comparison of th antilipolytic activity of three doses of acipimox and three doses of NA showed acipimox to be 20 times as potent as NA. There was a correlation between intensity and duration of effect for acipimox, but not for NA. Plasma acipimox levels correlated with inhibition of lipolysis. In consideration of the very good subjective tolerability of acipimox at all doses tested, this drug may be suitable for control of lipolysis in hyperlipidemias.

摘要

阿西莫司(5-甲基吡嗪羧酸4-氧化物)是一种新型脂肪分解抑制剂,与烟酸(NA)在化学结构上关系较远。标记有氚的化合物(100毫克)吸收迅速,2小时后达到血浆放射性峰值,几乎全部以原形从尿液中排出。对三剂阿西莫司和三剂NA的抗脂解活性进行比较,结果显示阿西莫司的效力是NA的20倍。阿西莫司的效应强度和持续时间之间存在相关性,而NA则不然。血浆阿西莫司水平与脂肪分解抑制相关。鉴于在所有测试剂量下阿西莫司都具有非常好的主观耐受性,该药可能适用于控制高脂血症中的脂肪分解。

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