Russell J, Spickett C M, Reglinski J, Smith W E, McMurray J, Abdullah I B
Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, UK.
FEBS Lett. 1994 Jun 27;347(2-3):215-20. doi: 10.1016/0014-5793(94)00548-6.
The effect of the thiol containing compounds N-acetylcysteine and captopril on glutathione metabolism in human erythrocytes has been investigated non-invasively using 1H spin echo NMR. N-Acetylcysteine was found to increase the reduced form of glutathione while captopril increased the oxidized form, but no changes in the total glutathione concentration were observed. Incubation of the cells with buthionine sulphoximine to inhibit de novo glutathione synthesis did not affect the response. The results show that these compounds act by altering the redox balance of glutathione rather than by stimulating its synthesis, and that their mechanisms of action are different, and not simply due to the presence of the thiol group.
已使用氢质子自旋回波核磁共振技术对含硫醇化合物N-乙酰半胱氨酸和卡托普利对人体红细胞中谷胱甘肽代谢的影响进行了非侵入性研究。结果发现,N-乙酰半胱氨酸可增加还原型谷胱甘肽,而卡托普利可增加氧化型谷胱甘肽,但未观察到总谷胱甘肽浓度有变化。用丁硫氨酸亚砜胺孵育细胞以抑制谷胱甘肽的从头合成,并不影响该反应。结果表明,这些化合物是通过改变谷胱甘肽的氧化还原平衡而非刺激其合成来发挥作用的,且它们的作用机制不同,并非仅仅是由于硫醇基团的存在。