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前列腺素与抗炎药物的副作用——肾脏

Prostaglandins and the side effects of anti-inflammatory drugs--the kidney.

作者信息

Crowshaw K

出版信息

Agents Actions Suppl. 1979(6):213-23. doi: 10.1007/978-3-0348-7232-4_24.

Abstract

The most important renal side effect of non-steroidal anti-inflammatory therapy in man is analgesic nephropathy. One possible mechanism for this effect is inhibition of renal prostaglandin synthesis. However, an understanding of the regional biosynthesis of renal prostaglandins, of their pharmacological, physiological and pathological properties in the kidney and an understanding of the consequences of their inhibition by drugs is required in order to assess whether such a mechanism is involved. These aspects are reviewed, using much of the early work of the author as a basis for the discussion. The following conclusions can be drawn form a review of published work. "The consequences of the inhbiition of renal prostaglandin synthesis do not seem to bear much relationship to the renal side effects of anti-inflammatory therapy in man". It is further suggested that impaired renomedullary blood flow arising from decreased renomedullary PGE2 synthesis results in increased accumulation of drug in the renal medulla leading to direct toxic damage. Finally, examples of diseases associated with increased or decreased renal PGE2 synthesis are discussed and some examples of drug interactions are presented.

摘要

非甾体抗炎治疗对人体最重要的肾脏副作用是镇痛剂肾病。这种作用的一种可能机制是抑制肾脏前列腺素的合成。然而,为了评估是否涉及这样一种机制,需要了解肾脏前列腺素的区域生物合成、它们在肾脏中的药理、生理和病理特性,以及了解药物对它们的抑制作用的后果。本文以作者的许多早期工作为讨论基础,对这些方面进行了综述。从已发表的工作综述中可以得出以下结论:“抑制肾脏前列腺素合成的后果似乎与抗炎治疗对人体的肾脏副作用没有太大关系”。进一步表明,肾髓质前列腺素E2合成减少导致肾髓质血流受损,从而导致药物在肾髓质中积累增加,进而导致直接毒性损伤。最后,讨论了与肾脏前列腺素E2合成增加或减少相关的疾病实例,并列举了一些药物相互作用的例子。

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