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. 2014 Jul 21;20(27):9038–9049. doi: 10.3748/wjg.v20.i27.9038

Table 1.

Summary of the major findings obtained among the most widespread in vivo models

Model Genetic manipulation Diet modifications Obesity Metabolic syndrome (IR) Hepatosteatosis Steatohepatitis Fibrosis
ob/ob Leptin Deficient No Yes Yes Yes Yes (in males) No (protected)
mice Yes Variable Yes Yes Yes Yes
MCD (loss weight in some)
db/db Mutation on leptin receptor No Yes Yes Yes No No
mice Yes Variable No Yes Yes Yes
MCD (age-related weight gain)
AOX Nullizygous for acycil - CoA oxidase No No No Yes Yes No
null mice [before 6-8 mo (before 6-8 mo)
Resistant Resistant
(after 8 mo)] (after 8 mo)
MATO Nullizygous for (MAT)-1A No No No Yes Yes Yes
null mice
pten Liver specific pten deletion No No No Yes Yes Yes
null mice
(SREBP)-1c SREBP-1c overexpressed in adipose tissue No No Yes Yes Yes Yes
transgenic mice
KK-Ay Heterozygous mutation on agouti gene (KK-Ay/a) No Yes Yes Yes No No
mice Yes Yes Yes Yes Yes No
MCD
LIRKO Liver-specific Leptin receptor KO No No Hepatic IR No - -
mice
C57Bl/6J No Yes Yes Yes Yes Yes Yes
HFHC (mild)
HF
Cholesterol-Cholate No Yes No No Yes Yes Yes
(Atherogenic diet) Cholesterol (only hepatic IR) (over 1-6 mo) (over 1-6 mo) (over 1-6 mo)
Cholate

MCD: Methionine choline deficient diet; HFHC: High fat-high carbohydrate diet; HF: High fructose diet; KO: Knock-out; IR: Insulin resistance.