首页> 外文期刊>Toxicology and Applied Pharmacology >The role of glucuronidation in N-(3,5-dichlorophenyl)succinimide (NDPS) nephrotoxicity: nephrotoxic potential of NDPS and NDPS metabolites in Gunn, Wistar, and Fischer 344 rats.
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The role of glucuronidation in N-(3,5-dichlorophenyl)succinimide (NDPS) nephrotoxicity: nephrotoxic potential of NDPS and NDPS metabolites in Gunn, Wistar, and Fischer 344 rats.

机译:葡萄糖醛酸化作用在N-(3,5-二氯苯基)琥珀酰亚胺(NDPS)肾毒性中的作用:NDPS和NDPS代谢产物在Gunn,Wistar和Fischer 344大鼠中的肾毒性潜力。

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The agricultural fungicide N-(3,5-dichlorophenyl)succinimide (NDPS) is an acute nephrotoxicant in rats. Although the mechanism of NDPS nephrotoxicity is not clear, our previous studies have strongly suggested that glucuronide conjugation of NDPS metabolite(s) is an important biotransformation reaction leading to the ultimate nephrotoxicant metabolite(s) mediating NDPS nephrotoxicity. In this study, the nephrotoxic potential of NDPS and its nephrotoxicant metabolites, N-(3,5-dichlorophenyl)-2-hydroxysuccinimide (NDHS) and N-(3,5-dichlorophenyl)-2-hydroxysuccinamic acid (NDHSA), was examined in Gunn rats, which contain a genetic deficiency in bilirubin uridine diphosphate-glucuronosyltransferase (UDPGT), to explore further the role of glucuronidation in NDPS nephrotoxicity. The nephrotoxic potential of NDPS, NDHS, and NDHSA was also examined in Wistar rats, the parent strain for Gunn rats and which generally have normal UDPGT activity. Comparisons were then made with the nephrotoxicity induced by these compounds in Fischer 344 (F344) rats. Age-matched male F344, homozygous (j/j) Gunn, and Wistar rats were used. Rats (four to eight rats/group) of each strain were administered NDPS (0.4 mmol/kg ip), NDHS (0.1 or 0.2 mmol/kg ip), NDHSA (0.1 mmol/kg ip), or vehicle, and renal effects were monitored functionally and morphologically for 48 h. NDPS and its nephrotoxicant metabolites, NDHS and NDHSA, were much weaker nephrotoxicants in Gunn rats than in F344 rats, while Wistar rats were susceptible to the nephrotoxicity induced by NDPS, NDHS, or NDHSA. These results suggest that the lack of NDPS nephrotoxicity observed in Gunn rats is due to the deficiency in UDPGT in this strain rather than the parent Wistar strain being inherently nonresponsive to NDPS nephrotoxicity. Therefore, it appears that glucuronide metabolite(s) of NDHS and/or NDHSA contribute(s) to NDPS nephrotoxicity, although the exact nature of the nephrotoxicant glucuronide metabolite(s) of NDPS remains to be determined. Copyright 1999 Academic Press.
机译:农业杀真菌剂N-(3,5-二氯苯基)琥珀酰亚胺(NDPS)是大鼠的急性肾毒性药物。尽管尚不清楚NDPS肾毒性的机制,但我们以前的研究强烈建议,葡萄糖醛酸化物结合NDPS代谢物是重要的生物转化反应,导致最终的肾毒性代谢物介导NDPS肾毒性。在这项研究中,NDPS及其肾毒性代谢产物N-(3,5-二氯苯基)-2-羟基丁二酰亚胺(NDHS)和N-(3,5-二氯苯基)-2-羟基丁二酸(NDHSA)的肾毒性潜力为在古恩(Gunn)大鼠中进行了检查,该基因在胆红素尿苷二磷酸-葡萄糖醛糖基转移酶(UDPGT)中存在遗传缺陷,以探索葡萄糖醛酸化在NDPS肾毒性中的作用。还对Wistar大鼠(耿氏大鼠的亲本菌株,通常具有正常的UDPGT活性)Wistar大鼠进行了NDPS,NDHS和NDHSA的肾毒性研究。然后将这些化合物在Fischer 344(F344)大鼠中引起的肾毒性进行比较。使用年龄匹配的雄性F344,纯合(j / j)Gunn和Wistar大鼠。给每个菌株的大鼠(每组四到八只大鼠)分别给予NDPS(0.4 mmol / kg ip),NDHS(0.1或0.2 mmol / kg ip),NDHSA(0.1 mmol / kg ip)或赋形剂,对肾脏的影响是在功能和形态上监测48小时。 NDPS及其肾毒性代谢产物NDHS和NDHSA在Gunn大鼠中的肾毒性比F344大鼠弱得多,而Wistar大鼠易受NDPS,NDHS或NDHSA诱导的肾毒性。这些结果表明,在耿氏大鼠中观察到的NDPS肾毒性的缺乏是由于该菌株中UDPGT的缺乏,而不是亲本Wistar菌株固有地对NDPS肾毒性无反应。因此,似乎NDHS和/或NDHSA的葡糖醛酸代谢物对NDPS的肾毒性有贡献,尽管NDPS的肾毒性葡糖醛酸代谢物的确切性质尚待确定。版权所有1999,学术出版社。

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