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一种新型生物活性有机硒化合物——IV. PZ 51(依布硒啉)对离体肝细胞中ADP-铁诱导的脂质过氧化的谷胱甘肽依赖性保护作用。

A novel biologically active selenoorganic compound--IV. Protective glutathione-dependent effect of PZ 51 (ebselen) against ADP-Fe induced lipid peroxidation in isolated hepatocytes.

作者信息

Müller A, Gabriel H, Sies H

出版信息

Biochem Pharmacol. 1985 Apr 15;34(8):1185-9. doi: 10.1016/0006-2952(85)90493-9.

Abstract

PZ 51 (Ebselen) is capable of inhibiting ADP-Fe-induced lipid peroxidation in isolated hepatocytes, assessed by generation of low-level chemiluminescence, and the formation of alkanes (ethane, n-pentane) and malondialdehyde. The sulphur analog PZ 25 is much less active. PZ 51 is ineffective in glutathione-depleted hepatocytes that were obtained after phorone pretreatment of the animals. However, other antioxidants, like (+)-cyanidanol-3 or diethyldithiocarbamate are effective in inhibiting lipid peroxidation also in glutathione-depleted cells. The results are attributed to a GSH peroxidase-like activity of PZ 51. Addition of the chemically synthetized compound, PZ 51-SG, a glutathione adduct of PZ 51, does not provide extra protection in GSH-depleted cells in comparison to the parent compound, PZ 51. Dithioerythritol exhibits a protective effect, and PZ 51 is more efficient than in the absence of this thiol reductant. Dithioerythritol also exerts an effect in glutathione-depleted cells. A peroxidase-like activity using DTE as reductant is demonstrated in vitro.

摘要

PZ 51(依布硒啉)能够抑制分离肝细胞中由ADP-铁诱导的脂质过氧化,这通过低水平化学发光的产生以及烷烃(乙烷、正戊烷)和丙二醛的形成来评估。硫类似物PZ 25的活性则低得多。PZ 51对经佛波醇预处理的动物所获得的谷胱甘肽耗竭的肝细胞无效。然而,其他抗氧化剂,如(+)-氰定醇-3或二乙基二硫代氨基甲酸盐,在谷胱甘肽耗竭的细胞中也能有效抑制脂质过氧化。这些结果归因于PZ 51的谷胱甘肽过氧化物酶样活性。与母体化合物PZ 51相比,添加化学合成的化合物PZ 51-SG(PZ 51的谷胱甘肽加合物)在谷胱甘肽耗竭的细胞中并不能提供额外的保护。二硫赤藓糖醇具有保护作用,且PZ 51在此情况下比没有这种硫醇还原剂时更有效。二硫赤藓糖醇在谷胱甘肽耗竭的细胞中也发挥作用。体外实验证明了以二硫赤藓糖醇作为还原剂的过氧化物酶样活性。

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