二乙基二硫代氨基甲酸酯,而非双硫仑,抑制离体小鼠胰岛β细胞四氧嘧啶诱导的染料积累。

Medical biology Pub Date : 1986-01-01
L Norlund, K Grankvist, H A Hansson, R Norlund
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引用次数: 0

摘要

四氧嘧啶对胰腺β细胞的致糖尿病作用被认为是由羟基自由基介导的。自由基的初始攻击可能在质膜水平。二乙基二硫代氨基甲酸酯(DDTC)及其二聚体二硫醚(Antabuse)最近被证明可以防止自由基产生剂的损害。因此,研究了DDTC和双硫仑抑制四氧嘧啶诱导的离体ob/ob小鼠胰岛β细胞染料积累的能力。Evans蓝作为质膜通透性指标。DDTC (100 μ m 1 mM)抑制四氧嘧啶诱导的β细胞对染料的摄取,而双硫仑(100 μ m 1 mM)没有抑制作用。用clark型氧电极研究了DDTC对还原性谷胱甘肽(GSH)、四氧胺和FeSO4混合物耗氧量的影响。DDTC(20、100微米)对混合液耗氧量无影响。这表明,DDTC对四氧嘧啶诱导的离体β细胞染料摄取的抑制作用发生在自由基产生之外的一个步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diethyldithiocarbamate, but not disulfiram, inhibits alloxan-induced dye accumulation of isolated mouse islet beta-cells.

The diabetogenic action of alloxan on pancreatic beta-cells is thought to be mediated by hydroxyl radicals. The initial attack of the radicals is probably at the plasma membrane level. Diethyldithiocarbamate (DDTC) and its dimer disulfiram (Antabuse) have recently been shown to protect against damage by free radical generating agents. The ability of DDTC and disulfiram to inhibit alloxan-induced dye accumulation of isolated ob/ob mice islet beta-cells was therefore studied. Evans blue was used as an indicator of plasma membrane permeability. DDTC (100 microM 1 mM) but not disulfiram (100 microM 1 mM) inhibited alloxan-induced dye uptake of beta-cells. The effect of DDTC on oxygen consumption in a mixture of reduced glutathione (GSH), alloxan and FeSO4 was studied with a Clark-type oxygen electrode. DDTC (20, 100 microM) had no effect on the oxygen consumption of this mixture. It is suggested that the DDTC inhibition of alloxan-induced dye uptake of isolated beta-cells takes place at a step beyond the generation of free radicals.

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