Carbamazepine-induced liver injury using type 2 diabetes Spontaneously Diabetic Torii-Leprfa (SDT fatty) rats as a model for human type 2 diabetes
Author:
Affiliation:
1. Toxicology Research Lab., Central Pharmaceutical Research Institute, JAPAN TOBACCO INC.
2. Graduate School of Integrated Pharmaceutical and Nutritional Sciences, Graduate Program in Environmental Health Sciences, University of Shizuoka
Publisher
Japanese Society of Toxicology
Link
https://www.jstage.jst.go.jp/article/fts/6/8/6_287/_pdf
Reference28 articles.
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2. Bernus, I., Dickinson, R.G., Hooper, W.D. and Eadie, M.J. (1996): Dose-dependent metabolism of carbamazepine in humans. Epilepsy Res., 24, 163-172.
3. Benedetti, M.S., Ruty, B. and Baltes, E. (2005): Induction of endogenous pathways by antiepileptics and clinical implications. Fundam. Clin. Pharmacol., 19, 511-529.
4. Chen, Y., Dong, H., Thompson, D.C., Shertzer, H.G., Nebert, D.W. and Vasiliou, V. (2013): Glutathione defense mechanism in liver injury: insights from animal models. Food Chem. Toxicol., 60, 38-44.
5. Driefus, F.E. and Langer, D.H. (1987): Hepatic considerations in the use of antiepileptic drugs. Epilepsia, 28, S23-S29.
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2. Comparison of the liver findings after simvastatin-treatment between Spontaneously Diabetic Torii-Leprfa (SDT fatty) rats and Sprague-Dawley rats;Fundamental Toxicological Sciences;2020
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