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"Second Hit" Models of Alcoholic Liver Disease
被引:120
作者:
Tsukamoto, Hidekazu
[1
,2
,4
]
Machida, Keigo
[1
,3
]
Dynnyk, Alla
[1
,2
]
Mkrtchyan, Hasmik
[1
,2
]
机构:
[1] Univ So Calif, Keck Sch Med, So Calif Res Ctr ALPD & Cirrhosis, Los Angeles, CA 90033 USA
[2] Univ So Calif, Keck Sch Med, Dept Pathol, Los Angeles, CA 90033 USA
[3] Univ So Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
[4] Dept Vet Affairs, Los Angeles, CA USA
关键词:
Gene-environment interactions;
alcoholic liver disease;
alcoholic steatohepatitis;
nonalcoholic steatohepatitis;
nonalcoholic fatty liver disease;
animal models;
HEPATITIS-C VIRUS;
ENDOPLASMIC-RETICULUM STRESS;
NF-KAPPA-B;
INSULIN-RECEPTOR SUBSTRATE-1;
INDUCED FATTY LIVER;
ETHANOL-FED RATS;
OXIDATIVE STRESS;
METHIONINE METABOLISM;
ACETALDEHYDE ADDUCTS;
CORE PROTEIN;
D O I:
10.1055/s-0029-1214373
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
100201 [内科学];
摘要:
Alcoholic liver disease (ALD) is a lifestyle disease with its pathogenesis and individual predisposition governed by gene-environment interactions. Based on the "second hit" or "multiple hits" hypothesis, patients are predisposed to progressive ALD when a magic combination of gene and environmental interactions exists. Reproduction of second or multiple hits in animal models serves to test a combination and to gain mechanistic insights into synergism achieved by such combination. Numerous environmental factors have been incorporated into animal models, largely classified into nutritional, xenobiotic/pharmacologic, hemodynamic, and viral groups. A loss or gain of function genetic model has become a popular experimental approach to test the role of a gene as a second hit. Future research will need to test more subtle or natural hits combined with excessive alcohol intake to test multiple hits in the genesis of ALD. Additionally, animal models of comorbidities are urgently needed particularly for synergistic liver disease and oncogenesis caused by alcohol, obesity, and hepatitis virus.
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页码:178 / 187
页数:10
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