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丙戊酸的发育毒性。

Developmental toxicity of valproic acid.

作者信息

Cotariu D, Zaidman J L

机构信息

Department of Biochemical Pathology, Assaf Harofeh Medical Center, Sackler School of Medicine, Tel Aviv University, Zerifin, Israel.

出版信息

Life Sci. 1991;48(14):1341-50. doi: 10.1016/0024-3205(91)90430-j.

Abstract

Valproic acid is a very effective anticonvulsant agent widely used in the management of various forms of epilepsy. Administration of the drug during pregnancy results in increased incidence of congenital abnormalities in both humans and experimental animals. In recent years, a significant number of research efforts have attempted to define the contributory role of valproic acid to the impairment of normal prenatal growth and development. The present report summarizes current knowledge that has emerged from clinical and research studies. The specific topics include: the placental transfer of valproic acid; the teratogenic potential; structure-teratogenicity and dose-response relationships; species and strain differences; biochemical changes evoked by the drug in the fetus.

摘要

丙戊酸是一种非常有效的抗惊厥药物,广泛用于治疗各种形式的癫痫。孕期服用该药物会导致人类和实验动物先天性异常的发生率增加。近年来,大量研究致力于确定丙戊酸对正常产前生长发育受损的作用。本报告总结了临床和研究中出现的现有知识。具体主题包括:丙戊酸的胎盘转运;致畸潜力;结构-致畸性和剂量反应关系;物种和品系差异;药物在胎儿体内引起的生化变化。

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