Price R G
Chem Biol Interact. 1979 Feb;24(2):241-55. doi: 10.1016/0009-2797(79)90012-7.
Histological studies showed that the administration of p-nitrophenylarsonic acid to rats resulted in renal tubular necrosis. The nephrotoxin was administered intraperitoneally and doses greater than 30 mg/kg were found to be fatal. The severity of the renal lesion depended on the amount of the nephrotoxin used. Elevated serum urea levels, urinary protein and volume were recorded over an 8-day period following the injection of the nephrotoxin. These changes were paralleled by an increase in the activity of lactate dehydrogenase, acid and alkaline phosphatase, N-acetyl-beta-glucosaminidase and beta-glucosidase in the urine. beta-Glycosidase activities increased in kidney homogenates, immediately after the injection of the nephrotoxin, but this eventually fell to well below the normal range. Subcellular fractions were prepared from sucrose homogenates by differential centrifugation and beta-glycosidases and cytochrome oxidase were used as enzyme markers. Only minor changes in the activity of cytochrome oxidase activity resulted from the administration of p-nitrophenylarsonic acid. One of the earliest indications of renal damage was a decrease in lysosomal latency. The activities of the lysosomal and soluble enzymes were elevated above normal during the first two days after the injection of p-nitrophenylarsonic acid, but they fell to values, significantly lower than normal, on the third day. The isoenzymic forms of beta-galactosidase, beta-glucosidase and N-acetyl-beta-glucosaminidase in normal and damaged kidneys were studied, using starch gel electrophoresis. The activities of both the lysosomal and the soluble forms of these enzymes decreased following the injection of the nephrotoxin, confirming the results obtained with whole homogenates. The relationship between the changes in renal enzyme activity and urinary enzyme excretion during the nephrotoxic process is discussed.
组织学研究表明,给大鼠施用对硝基苯胂酸会导致肾小管坏死。该肾毒素通过腹腔注射给药,发现剂量大于30 mg/kg是致命的。肾脏病变的严重程度取决于所使用的肾毒素量。在注射肾毒素后的8天内,血清尿素水平、尿蛋白和尿量均有所升高。这些变化伴随着尿液中乳酸脱氢酶、酸性和碱性磷酸酶、N-乙酰-β-葡萄糖胺酶和β-葡萄糖苷酶活性的增加。注射肾毒素后,肾脏匀浆中的β-糖苷酶活性立即增加,但最终降至远低于正常范围。通过差速离心从蔗糖匀浆中制备亚细胞组分,并使用β-糖苷酶和细胞色素氧化酶作为酶标志物。施用对硝基苯胂酸后,细胞色素氧化酶活性仅发生轻微变化。肾脏损伤的最早迹象之一是溶酶体潜伏期缩短。注射对硝基苯胂酸后的前两天,溶酶体酶和可溶性酶的活性高于正常水平,但在第三天降至明显低于正常的值。使用淀粉凝胶电泳研究了正常和受损肾脏中β-半乳糖苷酶、β-葡萄糖苷酶和N-乙酰-β-葡萄糖胺酶的同工酶形式。注射肾毒素后,这些酶的溶酶体形式和可溶性形式的活性均降低,证实了从全匀浆中获得的结果。本文讨论了肾毒性过程中肾脏酶活性变化与尿酶排泄之间的关系。