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关于D-葡萄糖酸-1,5-内酯降低氨基糖苷类药物所致肾毒性的动物研究。

Animal studies on the reduction of aminoglycoside-induced nephrotoxicity by D-glucaro-1,5-lactam.

作者信息

Marre R, Müller W, Sack K

出版信息

Infection. 1983 May-Jun;11(3):155-60. doi: 10.1007/BF01641295.

Abstract

We studied the effect of D-glucaro-1,5-lactam on aminoglycoside-induced nephrotoxicity in rats. Parameters of nephrotoxicity were urinary excretion of tubule cells and malate dehydrogenase. When given in appropriate doses, either i. m. or via an oral tube, D-glucaro-1,5-lactam significantly reduced the excretion of cells and enzymes during the administration of gentamicin, tobramycin, dibekacin, netilmicin and ribostamycin. It did not impair the therapeutic efficacy of ribostamycin in the experimental treatment of acute pyelonephritis in rats. The protective effect of D-glucaro-1,5-lactam could be ascribed to its inhibition of beta-glucuronidase, an enzyme which is located in renal lysosomes and which is activated by aminoglycosides.

摘要

我们研究了D -葡糖二酸-1,5 -内酯对大鼠氨基糖苷类药物诱导的肾毒性的影响。肾毒性参数为肾小管细胞和苹果酸脱氢酶的尿排泄量。当以适当剂量通过肌肉注射或经口插管给药时,D -葡糖二酸-1,5 -内酯在给予庆大霉素、妥布霉素、地贝卡星、奈替米星和核糖霉素期间显著减少了细胞和酶的排泄。它并未损害核糖霉素对大鼠急性肾盂肾炎实验性治疗的疗效。D -葡糖二酸-1,5 -内酯的保护作用可归因于其对β -葡萄糖醛酸酶的抑制,该酶位于肾溶酶体中且可被氨基糖苷类药物激活。

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