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肾脏和肝脏中维生素K依赖的γ-谷氨酰羧化酶底物对华法林和维生素K治疗的反应。

Responses of renal and hepatic vitamin K dependent gamma-glutamyl carboxylase substrates to warfarin and vitamin K treatments.

作者信息

Karl P I, Friedman P A

出版信息

Int J Biochem. 1985;17(12):1313-6. doi: 10.1016/0020-711x(85)90053-9.

Abstract

A single intraperitoneal injection of warfarin (5 mg/kg) in the rat causes maximal accumulation of hepatic vitamin K dependent carboxylase substrate by 8 hr. In the kidney accumulation is slower with maximal amounts of the substrate appearing at about 16 hr. Vitamin K administered intravenously to warfarin-treated rats causes the complete disappearance of the hepatic substrate in 2 hr. In contrast, neither a single nor multiple injections of the vitamin decrease the renal substrate level by more than 30%. However, this decrease can be augmented by inhibition of protein synthesis with cycloheximide.

摘要

给大鼠腹腔内单次注射华法林(5毫克/千克),8小时时肝脏维生素K依赖性羧化酶底物的积累达到最大值。在肾脏中,底物积累较慢,大约16小时时出现最大量。给经华法林处理的大鼠静脉注射维生素K,2小时时肝脏底物完全消失。相比之下,单次或多次注射该维生素,肾脏底物水平的降低均不超过30%。然而,用环己酰亚胺抑制蛋白质合成可增强这种降低作用。

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