Hall R L, Wilke W L, Fettman M J
Vet Hum Toxicol. 1986 Aug;28(4):305-7.
An attempt was made to develop a model of chronic renal disease in the rat through repeated administration of a nephrotoxin specific for proximal tubular epithelium. Mercuric chloride was administered by subcutaneous injection in gradually increasing amounts over a period of 21 weeks. The dose ranged from 1.125 mg/kg once a week to 2.0 mg/kg twice a week. Measured parameters of renal function include plasma urea nitrogen, plasma creatinine, 24-hour urine output volume, and 24-hour urinary protein excretion. When compared to their own pretreatment values and those of the age/weight-matched control animals, the mercuric chloride-treated rats exhibited no significant abnormalities in these parameters of kidney function with the exception of a mild proteinuria at 21 weeks. Light microscopic examination of the kidneys of the mercury-treated rats revealed mild tubular, interstitial, and glomerular lesions which were significantly worse than those in the kidneys of the controls. This study demonstrates the ability of the kidney to sustain a considerable degree of resistance to inorganic mercury toxicity when exposure is continuous over a prolonged period of time. It also demonstrates the inability of commonly measured clinical laboratory parameters of kidney function to identify the effects of chronic mercuric chloride toxicity in the rat.
研究人员试图通过反复给予一种对近端肾小管上皮细胞具有特异性的肾毒素,来建立大鼠慢性肾病模型。在21周的时间里,通过皮下注射逐渐增加剂量的氯化汞。剂量范围从每周一次1.125毫克/千克到每周两次2.0毫克/千克。测定的肾功能参数包括血浆尿素氮、血浆肌酐、24小时尿量和24小时尿蛋白排泄量。与自身治疗前的值以及年龄/体重匹配的对照动物的值相比,除了在21周时出现轻度蛋白尿外,氯化汞处理的大鼠在这些肾功能参数上没有显著异常。对氯化汞处理大鼠的肾脏进行光镜检查发现,肾小管、间质和肾小球有轻度病变,明显比对照组肾脏的病变严重。这项研究表明,当长时间持续接触无机汞毒性时,肾脏有能力维持相当程度的抵抗能力。它还表明,常用的临床实验室肾功能参数无法识别大鼠慢性氯化汞毒性的影响。