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Effect of propargylglycine on synthesis of glutathione in mice

机译:炔丙基甘氨酸对小鼠谷胱甘肽合成的影响

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Effects of propargylglycine (PPG) treatment on the hepatic glutathione (GSH) synthesis were examined in adult male ICR mice. Administration of PPG (200 mu mole/kg, ip) to mice resulted in a complete inhibition of the hepatic cystathionine gamma -lyase (C gammaL) activity measured in cytosol fraction for 40 hr after the treatment. A single injection of PPG rapidly reduced the hepatic GSH levels, which appeared to be sustained at least for 40 hr. The GSH concentration in plasma was significantly decreased for 20 hr, but recovered to the control level in 40 hr. Renal GSH levels did not appear to be changed by PPG treatment. The cysteine concentrations in liver, kidney and plasma were also decreased by PPG. The effect of PPG pretreatment was examined in mice challenged with methionine (1 mmole/kg, po), the sulfur donor in the transsulfuration pathway. Methionine administration elevated S-adenosylmethionine (SAM) and GSH concentrations in liver significantly when measured 3 hr following the treatment. In PPG pretreated mice the hepatic SAM level was increased, however, elevation of GSH by methionine was inhibited completely suggesting that the supply of cysteine from the methionine cycle for GSH synthesis in liver was blocked by PPG. The results show that generation of cysteine in the transsulfuration pathway has a critical role in the hepatic synthesis of GSH, and PPG can be used as an effective tool for study of sulfur-containing amino acid metabolism in liver.
机译:在成年雄性ICR小鼠中检查了炔丙基甘氨酸(PPG)处理对肝谷胱甘肽(GSH)合成的影响。对小鼠施用PPG(200μmol/ kg,ip)后,在治疗40小时后,完全抑制了在细胞溶质中测得的肝胱硫醚γ-裂解酶(C gammaL)活性。单次注射PPG可以迅速降低肝脏GSH水平,这似乎可以持续至少40小时。血浆中的GSH浓度在20小时内显着降低,但在40小时内恢复到对照水平。 PPG治疗似乎未改变肾脏GSH水平。 PPG还可以降低肝脏,肾脏和血浆中半胱氨酸的浓度。在转硫途径中的硫供体甲硫氨酸(1 mmole / kg,口服)攻击的小鼠中检查了PPG预处理的效果。当在治疗后3小时进行测量时,甲硫氨酸的给药显着提高了肝脏中S-腺苷甲硫氨酸(SAM)和GSH的浓度。在PPG预处理的小鼠中,肝SAM水平升高,但是,蛋氨酸对GSH的升高被完全抑制,这表明PPG阻断了蛋氨酸循环中半胱氨酸对肝脏GSH合成的供应。结果表明,转硫途径中半胱氨酸的生成在肝脏GSH的合成中起着关键作用,而PPG可作为研究肝脏中含硫氨基酸代谢的有效工具。

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