Diabetes and hypertriglyceridemia modify the mode of acetaminophen-induced hepatotoxicity and nephrotoxicity in rats and mice

被引:9
|
作者
Doi, Kunio [1 ,2 ]
Ishida, Katsuhiko [3 ]
机构
[1] Nippon Inst Biol Sci, Tokyo 1980024, Japan
[2] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Vet Pathol, Bunkyo Ku, Tokyo 1138657, Japan
[3] Biogen Idec Inc, Cambridge Ctr 14, Cambridge, MA 02142 USA
关键词
Acetaminophen; Diabetes; Hepatorenal toxicity; Hypertriglyceridemia; Mouse; Rat; FRUCTOSE-INDUCED HYPERTRIGLYCERIDEMIA; INDUCED HEPATIC NECROSIS; SPRAGUE-DAWLEY RATS; ACUTE LIVER-INJURY; CARBON-TETRACHLORIDE HEPATOTOXICITY; ADENOSINE-TRIPHOSPHATE DEPLETION; TISSUE-REPAIR UNDERLIES; UDP-GLUCURONIC ACID; FISCHER; 344; RATS; COVALENT BINDING;
D O I
10.2131/jts.34.1
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Certain disease conditions can modify drug-induced toxicities, which, in turn, may cause a medication-related health crisis. Therefore, preclinical investigations into the alterations in drug-induced toxicities using appropriate disease animal models are very important. This paper reviews the reported data related to the effects of diabetes and hypertriglyceridemia, common lifestyle-related diseases in a modern society, oil acetaminophen (APAP)-induced hepatotoxicity and nephrotoxicity in rats and mice. It has generally been reported that diabetes protects rats and mice from APAP-induced hepatotoxicity and there are several reports that help to speculate on the effects of diabetes on APAP-induced nephrotoxicity. In fructose-induced hypertriglyceridemic rats, hepatotoxicity of APAP becomes apparently less severe, whereas nephrotoxicity of APAP becomes significantly more severe. The mechanisms of alteration of APAP-induced hepatorenal toxicity under diabetic and hypertriglyceridemic conditions are also discussed in this paper.
引用
收藏
页码:1 / 11
页数:11
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