Gartland K P, Eason C T, Bonner F W, Nicholson J K
Department of Chemistry, Birkbeck College, University of London, UK.
Arch Toxicol. 1990;64(1):14-25. doi: 10.1007/BF01973371.
The effects of a glutathione depletor, buthionine sulphoximine (BSO) and biliary cannulation on the nephrotoxicity of p-aminophenol (PAP) have been investigated in the F344 rat. Pretreatment with BSO completely protected against the nephrotoxicity of a 50 mg/kg dose of PAP, assessed by clinical chemistry, renal histopathology, and 1H-NMR urinalysis. Biliary cannulation partially protects against nephrotoxicity induced by 100 mg/kg PAP. These data suggest that the nephrotoxicity of PAP may be due in part to the formation of a proximate toxic metabolite in the liver which is excreted in the bile, subsequently reabsorbed and transported via the systemic circulation to the kidney where the toxic effects occur.
在F344大鼠中研究了谷胱甘肽耗竭剂丁硫氨酸亚砜胺(BSO)和胆管插管对对氨基酚(PAP)肾毒性的影响。通过临床化学、肾脏组织病理学和1H-NMR尿液分析评估,用BSO预处理可完全预防50mg/kg剂量PAP的肾毒性。胆管插管可部分预防100mg/kg PAP诱导的肾毒性。这些数据表明,PAP的肾毒性可能部分归因于在肝脏中形成一种近端毒性代谢物,该代谢物经胆汁排泄,随后被重吸收并通过体循环转运至肾脏,在肾脏产生毒性作用。