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头孢菌素I对大鼠肾脏溶酶体稳定性的体内效应的进一步研究。

Further studies on the in vivo effect of cephaloridine on the stability of rat kidney lysosomes.

作者信息

Ngaha E O

出版信息

Biochem Pharmacol. 1982 May 15;31(10):1843-7. doi: 10.1016/0006-2952(82)90486-5.

Abstract

The stabilizing effect of cephaloridine, an antibiotic, on rat kidney lysosomal membranes was tested by a single subcutaneous injection. The release of two lyososomal enzymes, acid phosphatase and muramidase, was used as an index of lysosome membrane integrity. The levels of these enzymes in the kidney extracts as well as in the isolated kidney lysosome fractions were found to be raised considerably, compared to the controls. In rats treated with cephaloridine, the supernatant fraction obtained from the kidney homogenates, after centrifugation at 15,000 gav, contained lower enzyme activities than were found in the control animals. It is suggested that cephaloridine may inhibit the release of acid phosphatase and muramidase from rat kidney lysosomes and, therefore, may exert a stabilizing effect on the lysosomal membrane system. The possible mechanism of interaction of this antibiotic with rat kidney lysosomal membranes is proposed.

摘要

通过单次皮下注射测试了抗生素头孢菌素对大鼠肾溶酶体膜的稳定作用。使用两种溶酶体酶(酸性磷酸酶和溶菌酶)的释放作为溶酶体膜完整性的指标。与对照组相比,发现肾提取物以及分离的肾溶酶体组分中这些酶的水平显著升高。在用头孢菌素治疗的大鼠中,在15,000 gav离心后从肾匀浆获得的上清液组分中所含的酶活性低于对照动物。提示头孢菌素可能抑制大鼠肾溶酶体中酸性磷酸酶和溶菌酶的释放,因此可能对溶酶体膜系统发挥稳定作用。提出了这种抗生素与大鼠肾溶酶体膜相互作用的可能机制。

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Cephaloridine and the rat kidney lysosomes stability in vitro.
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