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药物性吸收不良

Drug-induced malabsorption.

作者信息

Longstreth G F, Newcomer A D

出版信息

Mayo Clin Proc. 1975 May;50(5):284-93.

PMID:1127993
Abstract

Pharmacologic agents of diverse types may alter gastrointestinal absorption of nutrients and other substances. Mechanisms underlying drug-induced absorptive defects that have been documented include: (1) a direct toxic effect causing morphologic changes in the mucosa of the small intestine; (2) inhibition of mucosal enzymes with or without morphologic evidence of mucosal damage; (3) binding and precipitation of micellar components, such as bile acids and fatty acids; and (4) alteration of the physicochemical state of another drug or dietary ion. The malabsorptive effect generally is dose-related, rather than an idiosyncratic reaction, and usually involves multiple nutrients. Certain clinical states, such as in the malnourished alcoholic may predipose the gastrointestinal tract to a drug-induced absorptive defect. For this review we discuss in detail nine commonly used drugs or types of drugs that cause malabsorption of dietary nutrients or other medications.

摘要

不同类型的药物制剂可能会改变营养物质和其他物质的胃肠道吸收。已被证实的药物诱导吸收缺陷的潜在机制包括:(1)直接毒性作用导致小肠黏膜形态改变;(2)抑制黏膜酶,无论有无黏膜损伤的形态学证据;(3)结合并沉淀胶束成分,如胆汁酸和脂肪酸;(4)改变另一种药物或膳食离子的物理化学状态。吸收不良效应通常与剂量相关,而非特异反应,且通常涉及多种营养素。某些临床状态,如营养不良的酗酒者,可能使胃肠道易发生药物诱导的吸收缺陷。在本综述中,我们详细讨论九种常用药物或药物类型,它们会导致膳食营养素或其他药物的吸收不良。

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