Renal Toxicity of Mercuric Chloride at Different Time Intervals in Rats

W.A. Al-Madani, N. J. Siddiqi, A. Alhomida
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引用次数: 18

Abstract

This study was undertaken to study the renal toxicity of mercuric chloride in rats at different periods of time. The following groups of rats were studied: i) control, ii) placebo, iii) rats injected with a single ip dose of 100 mg/kg body weight of 2, 3 dimercapto-1-propanesulfonic acid, iv) rats injected with a single ip dose of 100 mg/kg body weight of 2, 3 dimercapto-1-propanesulfonic acid (DMPS) followed by a single dose ip of 2.0 mg HgCl2/kg body weight one hour after DMPS injection v) rats injected with a single ip dose of 2.0 mg HgCl2/kg body weight. Results indicate that mercuric chloride was more toxic after 48 hours of its administration when compared to 24 hours. Mercuric chloride administration caused an impairment of renal function which was evident from a significant decrease in urine volume, urinary excretion of urea, creatinine and glomerular filteration rate (P < 0.001) when compared to other treated groups. There was an increased excretion of protein, albumin and γ–-glutamyltransferase in the urine of mercuric chloride treated rats. Administration of 2, 3 dimercapto-1-propanesulfonic acid before mercuric chloride treatment caused the altered indices to return to near normal levels.
不同时间间隔氯化汞对大鼠肾毒性的影响
本研究旨在研究氯化汞在不同时期对大鼠的肾毒性。以下组大鼠进行了研究:1)控制,2)安慰剂,iii)大鼠注射一个ip剂量100毫克/公斤体重的2、3 dimercapto-1-propanesulfonic酸,(四)大鼠注射一个ip剂量100毫克/公斤体重的2、3 dimercapto-1-propanesulfonic酸(纯数字)其次是一剂ip HgCl2 2.0毫克/公斤体重后一小时纯注入v)大鼠注射一个ip HgCl2剂量为2.0毫克/公斤体重。结果表明,氯化汞给药48小时毒性大于24小时。与其他治疗组相比,氯化汞治疗组的尿量、尿尿素排泄量、肌酐和肾小球滤过率明显下降(P < 0.001),从而导致肾功能受损。氯化汞处理大鼠尿液中蛋白质、白蛋白和γ -谷氨酰转移酶的排泄量增加。在氯化汞处理前给予2,3二巯基-1-丙磺酸,使改变的指标恢复到接近正常水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biochemistry Insights
Biochemistry Insights BIOCHEMISTRY & MOLECULAR BIOLOGY-
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