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体外实验中,磺脲类药物不会改变胰岛素与大鼠肝细胞的结合情况,也不会改变胰岛素对氨基酸转运的作用。

Sulphonylureas in vitro do not alter insulin binding or insulin effect on amino acid transport in rat hepatocytes.

作者信息

Dolais-Kitabgi J, Alengrin F, Freychet P

出版信息

Diabetologia. 1983 Jun;24(6):441-4. doi: 10.1007/BF00257344.

Abstract

The effects of four sulphonylureas (gliclazide, glibenclamide, chlorpropamide and glipizide) on insulin binding and insulin action were studied in vitro using primary cultured rat hepatocytes. Cells were cultured for 20 h in the absence or presence of the sulphonylurea. The binding of insulin to rat hepatocyte monolayers was not altered in cells previously exposed to gliclazide at 0.7, 7.0 or 70 micrograms/ml; and to glibenclamide, chlorpropamide, or glipizide at 0.1, 1.0 and 10 micrograms/ml. Insulin-induced down regulation was not affected by a simultaneous exposure of hepatocyte monolayers to any of the four agents. The stimulatory effect of insulin on alpha-aminoisobutyric acid uptake by the cells was not modified following exposure to the drugs. These studies indicate that the sulphonylureas tested do not have a direct effect on insulin receptors in hepatocytes; and that, in vitro, they do not alter the post-receptor events involved in the insulin-induced stimulation of amino acid transport in these cells.

摘要

使用原代培养的大鼠肝细胞在体外研究了四种磺酰脲类药物(格列齐特、格列本脲、氯磺丙脲和格列吡嗪)对胰岛素结合及胰岛素作用的影响。细胞在不存在或存在磺酰脲类药物的情况下培养20小时。胰岛素与大鼠肝细胞单层的结合在先前暴露于0.7、7.0或70微克/毫升格列齐特以及0.1、1.0和10微克/毫升格列本脲、氯磺丙脲或格列吡嗪的细胞中未发生改变。胰岛素诱导的下调不受肝细胞单层同时暴露于这四种药物中任何一种的影响。细胞暴露于这些药物后,胰岛素对细胞摄取α-氨基异丁酸的刺激作用未被改变。这些研究表明,所测试的磺酰脲类药物对肝细胞中的胰岛素受体没有直接作用;并且在体外,它们不会改变这些细胞中胰岛素诱导的氨基酸转运刺激所涉及的受体后事件。

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