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氨基糖苷类抗生素在体外可抑制大鼠肝脏的溶酶体磷脂酶A和磷脂酶C。

Aminoglycoside antibiotics inhibit lysosomal phospholipase A and C from rat liver in vitro.

作者信息

Hostetler K Y, Hall L B

出版信息

Biochim Biophys Acta. 1982 Mar 12;710(3):506-9. doi: 10.1016/0005-2760(82)90136-9.

Abstract

Accumulation of aminoglycoside antibiotics and phospholipids in lysosomes is a prominent feature of aminoglycoside nephrotoxicity, suggesting the possibility that these agents may inhibit the activity of lysosomal phospholipases. We examined the effect of four aminoglycoside antibiotics, amikacin, dibekacin gentamicin and tobramycin, on the hydrolysis of [3H]dioleoylphosphatidylcholine by a lysosomal protein fraction obtained from rat liver which contains phospholipase A and C. Phospholipase A was inhibited strongly by these agents. Phospholipase C was also inhibited, especially by amikacin and tobramycin. These results suggest that the accumulation of phospholipids in the kidney cortex in aminoglycoside nephrotoxicity may be due to inhibition of lysosomal phospholipase action.

摘要

氨基糖苷类抗生素和磷脂在溶酶体中的蓄积是氨基糖苷类肾毒性的一个显著特征,这提示这些药物可能抑制溶酶体磷脂酶活性。我们检测了四种氨基糖苷类抗生素(阿米卡星、地贝卡星、庆大霉素和妥布霉素)对从大鼠肝脏获得的含有磷脂酶A和C的溶酶体蛋白组分水解[3H]二油酰磷脂酰胆碱的影响。这些药物强烈抑制磷脂酶A。磷脂酶C也受到抑制,尤其是阿米卡星和妥布霉素。这些结果表明,氨基糖苷类肾毒性时肾皮质中磷脂的蓄积可能是由于溶酶体磷脂酶作用受到抑制。

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