Pähler A, Birner G, Ott M M, Dekant W
Institut für Toxikologie, Universität Würzburg, Federal Republic of Germany.
Toxicol Appl Pharmacol. 1997 Dec;147(2):372-80. doi: 10.1006/taap.1997.8293.
Hexachlorobutadiene (HCBD) is nephrotoxic in rats causing damage to the proximal tubules. Renal toxicity is presumed to be due to bioactivation by glutathione S-conjugate formation and further processing by the enzymes of the mercapturic acid pathway to reactive intermediates. Recent studies revealed major sex-dependent differences in the pattern of urinary metabolites and gave evidence for the excretion of unmetabolized HCBD in the urine of male, but not female, rats. The objective of this study was to investigate the basis for the excretion of unchanged HCBD in the urine. We administered [14C]-HCBD (200 mg/kg bw, po) to male and female Sprague-Dawley (SD) and NCI Black-Reiter rats (NBR), an alpha 2u-globulin-deficient strain. No major differences in the disposition and in the rates of excretion of [14C]-derived radioactivity were observed between animals of both strains. Previously observed sex-specific differences in the formation of urinary metabolites in Wistar rats were now confirmed in SD rats and were also found in NBR rats. In contrast to male SD rats, however, NBR rats did not excrete unmetabolized HCBD with urine. [14C]-HCBD (10% of total urinary metabolites) was only present in the urine of male SD rats. Anion-exchange HPLC showed radioactivity associated with the alpha 2u-globulin fraction in urine and renal cytosol of male SD rats; the radioactive compound was identified as HCBD bound to the protein. The results indicate that the male-specific urinary excretion of HCBD is associated with its binding to alpha 2u-globulin. Light microscopic examination revealed the formation of hyaline droplets indicative of the accumulation of alpha 2u-globulin in the kidney of male SD rats after staining with Lee's methylene blue basic fuchsin. H&E staining additionally confirmed the finding of more pronounced necrotic changes in renal tubules of male SD rats than in females as previously described for Wistar rats. Binding of HCBD to alpha 2u-globulin may contribute to the pronounced nephrotoxicity in male rats.
六氯丁二烯(HCBD)对大鼠具有肾毒性,可导致近端肾小管受损。肾脏毒性被认为是由于通过谷胱甘肽S-结合物形成进行生物活化,并通过巯基尿酸途径的酶进一步加工成反应性中间体所致。最近的研究揭示了尿代谢物模式中主要的性别依赖性差异,并证明雄性而非雌性大鼠尿液中存在未代谢的HCBD。本研究的目的是调查尿液中未变化的HCBD排泄的基础。我们给雄性和雌性Sprague-Dawley(SD)大鼠以及NCI Black-Reiter大鼠(NBR,一种α2u球蛋白缺陷品系)经口给予[14C]-HCBD(200 mg/kg体重)。在两个品系的动物之间,未观察到[14C]衍生放射性的处置和排泄速率有重大差异。先前在Wistar大鼠中观察到的尿代谢物形成的性别特异性差异现在在SD大鼠中得到证实,并且在NBR大鼠中也发现了。然而,与雄性SD大鼠不同,NBR大鼠尿液中未排泄未代谢的HCBD。[14C]-HCBD(占总尿代谢物的10%)仅存在于雄性SD大鼠的尿液中。阴离子交换高效液相色谱显示,雄性SD大鼠尿液和肾细胞溶质中与α2u球蛋白部分相关的放射性;放射性化合物被鉴定为与蛋白质结合的HCBD。结果表明,HCBD的雄性特异性尿排泄与其与α2u球蛋白的结合有关。光学显微镜检查显示,在用李氏亚甲蓝碱性品红染色后,雄性SD大鼠肾脏中形成了透明滴,表明α2u球蛋白积累。苏木精-伊红染色进一步证实了先前对Wistar大鼠所描述的雄性SD大鼠肾小管坏死变化比雌性更明显的发现。HCBD与α2u球蛋白的结合可能导致雄性大鼠明显的肾毒性。