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维生素K缺乏大鼠经口服和结肠直肠给药后叶绿醌和甲萘醌的生物利用度。

Bioavailability of phylloquinone and menaquinones after oral and colorectal administration in vitamin K-deficient rats.

作者信息

Groenen-van Dooren M M, Ronden J E, Soute B A, Vermeer C

机构信息

Department of Biochemistry, University of Limburg, Maastricht, The Netherlands.

出版信息

Biochem Pharmacol. 1995 Sep 7;50(6):797-801. doi: 10.1016/0006-2952(95)00202-b.

Abstract

Rats were made vitamin K-deficient by feeding them a diet devoid of vitamin K and by rigorously preventing coprophagy. After one week, circulating prothrombin concentrations were between 5 and 10% of initial values, and various amounts of phylloquinone, menaquinone-4, and menaquinone-9 were given in a single dose either subcutaneously, orally, or colorectally. The relative 'vitamin K activities' of these compounds were assessed by comparing their ability to support prothrombin synthesis after subcutaneous injection. Intestinal and colonic absorption were deduced from the difference between subcutaneous and either oral or colorectal administration of the vitamers. It is concluded that the colonic absorption of all three forms of vitamin K is extremely poor, suggesting that physiological menaquinones in the colon do not contribute substantially to vitamin K status in rats. Furthermore, the stimulation of prothrombin synthesis by menaquinone-9 lasted much longer than that by the two other K-vitamers, resulting in a substantially higher 'vitamin K activity' of menaquinone-9.

摘要

通过给大鼠喂食缺乏维生素K的饲料并严格防止其食粪,使其维生素K缺乏。一周后,循环凝血酶原浓度为初始值的5%至10%,然后将不同量的叶绿醌、甲萘醌-4和甲萘醌-9以单剂量分别皮下、口服或经结直肠给予。通过比较皮下注射后它们支持凝血酶原合成的能力来评估这些化合物的相对“维生素K活性”。从维生素类物质皮下给药与口服或经结直肠给药之间的差异推断肠道和结肠的吸收情况。得出的结论是,三种形式的维生素K在结肠的吸收都极差,这表明结肠中的生理性甲萘醌对大鼠的维生素K状态贡献不大。此外,甲萘醌-9对凝血酶原合成的刺激持续时间比其他两种维生素K更长,导致甲萘醌-9的“维生素K活性”显著更高。

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