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二甲基噻嗪在分离的大鼠肝细胞中的主动转运。

Active transport of dimethialium in isolated rat hepatocytes.

作者信息

Yoshioka K, Nishimura H, Iwashima A

出版信息

Biochim Biophys Acta. 1983 Jul 13;732(1):308-11. doi: 10.1016/0005-2736(83)90217-1.

Abstract

The uptake of dimethialium, a thiamine analog having a methyl group in place of the hydroxyethyl group in the thiazole moiety, was studied in freshly isolated rat hepatocytes. In an Na+-medium, dimethialium at 10 microM was accumulated rapidly by the cells and an almost steady intra- to extracellular distribution ratio of 4.2 was attained in 5 min of incubation. The Kt and the Vmax for the saturable component were estimated to be 27 microM and 19 pmol/10(5) cells per min, respectively. In a K+ medium, the uptake of dimethialium was decreased to 58% of that of control. Ouabain and 2,4-dinitrophenol significantly lowered the rate of dimethialium uptake. Both phenylthiazinothiamine and oxythiamine were inhibitory on the uptake of dimethialium, which uptake was also inhibited by choline. These data indicate that dimethialium transport in liver cells proceeds via a carrier-mediated active process dependent on Na+ and biological energy. Furthermore, these results also suggest that thiamine transport in liver is dissociable from thiamine phosphorylation.

摘要

在新鲜分离的大鼠肝细胞中研究了二甲噻啶的摄取情况,二甲噻啶是一种硫胺类似物,在噻唑部分用甲基取代了羟乙基。在含Na⁺的培养基中,10微摩尔的二甲噻啶被细胞迅速积累,孵育5分钟后细胞内与细胞外的分布比达到4.2,接近稳定状态。饱和成分的转运常数(Kt)和最大转运速率(Vmax)分别估计为27微摩尔和每分钟19皮摩尔/10⁵个细胞。在含K⁺的培养基中,二甲噻啶的摄取量降至对照的58%。哇巴因和2,4 - 二硝基苯酚显著降低了二甲噻啶的摄取速率。苯噻嗪硫胺和氧硫胺均抑制二甲噻啶的摄取,胆碱也能抑制其摄取。这些数据表明,肝细胞中二甲噻啶的转运是通过依赖于Na⁺和生物能量的载体介导的主动过程进行的。此外,这些结果还表明肝脏中硫胺的转运与硫胺磷酸化是可分离的。

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