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细菌核糖核酸酶对离体灌注大鼠肾脏的肾毒性作用。

Nephrotoxic effects of bacterial ribonucleases in the isolated perfused rat kidney.

作者信息

Ilinskaya O N, Vamvakas S

机构信息

GENTOX Laboratory, Microbiology Department, Kazan State University, Tatarstan, Russia.

出版信息

Toxicology. 1997 Jun 6;120(1):55-63. doi: 10.1016/s0300-483x(97)03639-1.

Abstract

Alterations of the renal function in the isolated perfused rat kidney system after application of two bacterial RNases, Bacillus intermedius RNase (binase) and ribonuclease produced by Bacillus amyloliquefaciens (barnase), were investigated with two different treatment regimens in comparison with catalytically inactive derivates of the enzymes, photooxidated at the active site His101 binase and inactive mutant His102Gln barnase. For the in vitro approach the test enzymes were dissolved in the perfusion media and applied to the kidney after removal from the animal. Alternatively, the test ribonucleases were administered to rats in vivo and the renal effects were assessed in the isolated perfused rat kidney 1 and 6 h after treatment. In the in vitro regimen both active enzymes induced time- and concentration-dependent nephrotoxicity reflected in enhancement of urinary protein excretion, decline of glucose reabsorption, increase of gamma-glutamyltranspeptidase and alkaline phosphatase activities in urine. In vivo administration of active binase induced functional impairment of the isolated perfused organ in a similar way. None of the inactive RNases in both regimens and at all concentrations tested altered any renal parameter. The results suggest that RNA degradation may be involved in the nephrotoxic effects of bacillar RNases.

摘要

在分离灌注大鼠肾脏系统中,应用两种细菌核糖核酸酶(中间芽孢杆菌核糖核酸酶(binase)和解淀粉芽孢杆菌产生的核糖核酸酶(barnase))后,研究了肾脏功能的改变。将这两种酶与在活性位点His101处进行光氧化的催化无活性衍生物binase以及无活性突变体His102Gln barnase进行比较,采用两种不同的处理方案。对于体外实验方法,将测试酶溶解在灌注介质中,并在从动物体内取出肾脏后应用于肾脏。或者,将测试核糖核酸酶在体内给予大鼠,并在处理后1小时和6小时评估分离灌注大鼠肾脏中的肾脏效应。在体外实验方案中,两种活性酶均诱导了时间和浓度依赖性肾毒性,表现为尿蛋白排泄增加、葡萄糖重吸收下降、尿中γ-谷氨酰转肽酶和碱性磷酸酶活性增加。体内给予活性binase以类似方式诱导了分离灌注器官的功能损害。在两种实验方案中以及所有测试浓度下,无活性核糖核酸酶均未改变任何肾脏参数。结果表明,RNA降解可能参与了芽孢杆菌核糖核酸酶的肾毒性作用。

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