Animal models with minimal intervention for the translational study of metabolic syndrome-associated liver diseases
Author:
Affiliation:
1. Department of Pathology and Laboratory Medicine, Tokushima University Graduate School
Publisher
Japan Society of Hepatology
Subject
Hepatology
Link
https://www.jstage.jst.go.jp/article/kanzo/59/2/59_92/_pdf
Reference37 articles.
1. 2) Kishina M, Koda M, Kato J, et al. Therapeutic effects of the direct renin inhibitor, aliskiren, on non-alcoholic steatohepatitis in fatty liver Shionogi ob/ob male mice. Hepatol Res 2014; 44 (8): 888-896
2. 3) Sahai A, Malladi P, Pan X, et al. Obese and diabetic db/db mice develop marked liver fibrosis in a model of nonalcoholic steatohepatitis: role of short-form leptin receptors and osteopontin. Am J Physiol Gastrointest Liver Physiol 2004; 287 (5): G1035-1043
3. 4) Watanabe S, Horie Y, Suzuki A. Hepatocyte-specific Pten-deficient mice as a novel model for nonalcoholic steatohepatitis and hepatocellular carcinoma. Hepatol Res 2005; 33 (2): 161-166
4. 5) Shiota G. Loss of function of retinoic acid in liver leads to steatohepatitis and liver tumor: A NASH animal model. Hepatol Res 2005; 33 (2): 155-160
5. 6) Nagasawa T, Inada Y, Nakano S, et al. Effects of bezafibrate, PPAR pan-agonist, and GW501516, PPARdelta agonist, on development of steatohepatitis in mice fed a methionine- and choline-deficient diet. Eur J Pharmacol 2006; 536 (1-2): 182-191
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