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N-(膦酰甲基)甘氨酸对大鼠肝脏线粒体“体内”琥珀酸连接的吡啶核苷酸还原的抑制作用。

Inhibition of succinate-linking reduction of pyridine nucleotide in rat liver mitochondria 'in vivo' by N-(phosphonomethyl)glycine.

作者信息

Olorunsogo O O, Bababunmi E A

出版信息

Toxicol Lett. 1980 Dec;7(2):149-52. doi: 10.1016/0378-4274(80)90048-x.

Abstract

The pattern of the interaction of N-(phosphonomethyl)glycine (PMG), a broad-spectrum and non-selective herbicide with succinate-linked reduction of pyridine nucleotide, was investigated in liver mitochondria isolated 5 h after albino rats were given i.p. injections of PMG. Although there was no appreciable inhibition of the reduction of pyridine nucleotide at dosage levels less than 150 mg PMG/kg, the extent of inhibition increased as the dose was raised to 240 mg PMG/kg. Maximal inhibition of 34.5% and 45.4% were obtained at 240 mg PMG/kg when externally added ATP and high-energy intermediate, respectively, were used as the source of energy. These findings suggest that the inhibitory effect of PMG may be due to its uncoupling effect on oxidative phosphorylation.

摘要

在白化大鼠腹腔注射N-(膦酰基甲基)甘氨酸(PMG)5小时后分离出的肝线粒体中,研究了广谱非选择性除草剂PMG与琥珀酸连接的吡啶核苷酸还原反应的相互作用模式。虽然在剂量水平低于150mg PMG/kg时,吡啶核苷酸还原没有明显受到抑制,但当剂量提高到240mg PMG/kg时,抑制程度增加。当分别以外加ATP和高能中间体作为能量来源时,在240mg PMG/kg剂量下分别获得了34.5%和45.4%的最大抑制率。这些发现表明,PMG的抑制作用可能是由于其对氧化磷酸化的解偶联作用。

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