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磷脂对庆大霉素肾毒性的改善作用。

Amelioration of gentamicin nephrotoxicity by phospholipids.

作者信息

Chan M K, Chan K W, Ng W L

机构信息

Department of Medicine, University of Hong Kong, Queen Mary Hospital.

出版信息

Nephrol Dial Transplant. 1991;6(9):608-14. doi: 10.1093/ndt/6.9.608.

Abstract

The effect of phospholipids on gentamicin-induced nephrotoxicity was studied in Sprague-Dawley rats. Group 1a (5 rats) were given daily intraperitoneal injections of 100 mg/kg of gentamicin and sacrificed on day 7. Group 1b (10 rats) were similarly treated but were sacrificed on day 14. Group 2a (5 rats) were given 30 mg/kg of phospholipids for 6 days and sacrificed on day 7, serving as phospholipid controls. Group 2b (5 rats) were similarly treated, and from day 7 onwards daily intraperitoneal injections of 100 mg/kg of gentamicin were given while oral phospholipids were continued until the rats were sacrificed 7 days after gentamicin treatment. Group 2c (10 rats) were treated in the same manner as group 2b but the animals were sacrificed on day 28 after gentamicin treatment. Group 3 (10 rats) were given 30 mg/kg of phospholipids concurrently with intraperitoneal gentamicin injections and were sacrificed on day 28. Protein concentrations, N-acetyl-beta-glucosaminidase (NAG) activities and creatinine were measured in 24-h urine samples. Serum creatinine concentrations were measured in blood samples and 24-h creatinine clearance calculated. Gentamicin concentrations were determined in kidney tissues from which sections were also taken for light- and electron-microscopy. Results showed that gentamicin induced a marked increase in NAG and protein excretion, and a marked decrease in creatinine clearance with six rats succumbing to uraemia. Phospholipid treatment, whether started before or concurrently with gentamicin injections, reduced gentamicin-induced nephrotoxicity. The rats did not lose weight. Urinary excretion of NAG and protein was significantly reduced.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在斯普拉格-道利大鼠中研究了磷脂对庆大霉素诱导的肾毒性的影响。1a组(5只大鼠)每天腹腔注射100mg/kg庆大霉素,并在第7天处死。1b组(10只大鼠)接受类似处理,但在第14天处死。2a组(5只大鼠)给予30mg/kg磷脂,持续6天,在第7天处死,作为磷脂对照组。2b组(5只大鼠)接受类似处理,从第7天起每天腹腔注射100mg/kg庆大霉素,同时继续口服磷脂,直至庆大霉素治疗7天后处死大鼠。2c组(10只大鼠)的处理方式与2b组相同,但在庆大霉素治疗后第28天处死动物。测量24小时尿液样本中的蛋白质浓度、N-乙酰-β-葡萄糖苷酶(NAG)活性和肌酐。测量血样中的血清肌酐浓度并计算24小时肌酐清除率。测定肾组织中的庆大霉素浓度,并从中取材制作光镜和电镜切片。结果显示,庆大霉素导致NAG和蛋白质排泄显著增加,肌酐清除率显著降低,6只大鼠死于尿毒症。无论在庆大霉素注射前还是同时开始的磷脂治疗,均减轻了庆大霉素诱导的肾毒性。大鼠体重未减轻。NAG和蛋白质的尿排泄显著减少。(摘要截短于250字)

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