Estradiol Protects Female ApoE KO Mice against Western-Diet-Induced Non-Alcoholic Steatohepatitis.
Study Goal
The researchers aimed to determine if female ApoE KO mice were protected against Western Diet-induced NASH and whether estradiol replacement could mitigate these effects.
Results Summary
The study found that Western Diet increased body fat, plasma glucose, insulin, hepatic triglycerides, and liver enzymes in ovariectomized mice, leading to hepatic fibrosis and inflammation. Estradiol replacement reversed these effects, reducing metabolic and hepatic damage.
Population
Female ovariectomized ApoE KO mice and sham-operated controls.
Effective Dosage
Not specified for Western Diet; estradiol dosage not detailed.
Duration
7 weeks
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
Western-diet (WD) | increase | whole-body fat | female ovariectomized (OVX) ApoE KO mice | - | increased | #1 |
Western-diet (WD) | increase | plasma glucose | female ovariectomized (OVX) ApoE KO mice | - | increased | #2 |
Western-diet (WD) | increase | plasma insulin | female ovariectomized (OVX) ApoE KO mice | - | increased | #3 |
Western-diet (WD) | increase | glucose intolerance | female ovariectomized (OVX) ApoE KO mice | - | increased | #4 |
Western-diet (WD) | increase | plasma triglycerides | female ovariectomized (OVX) ApoE KO mice | - | increased | #5 |
Western-diet (WD) | increase | hepatic triglycerides | female ovariectomized (OVX) ApoE KO mice | - | increased | #6 |
Western-diet (WD) | increase | alanine aminotransferase (ALT) | female ovariectomized (OVX) ApoE KO mice | - | increased | #7 |
Western-diet (WD) | increase | aspartate aminotransferase (AST) | female ovariectomized (OVX) ApoE KO mice | - | increased | #8 |
Western-diet (WD) | increase | hepatic fibrosis | female ovariectomized (OVX) ApoE KO mice | - | associated with | #9 |
Western-diet (WD) | increase | hepatic inflammation | female ovariectomized (OVX) ApoE KO mice | - | associated with | #10 |
estradiol replacement | decrease | body weight | OVX mice | - | reduced | #11 |
estradiol replacement | decrease | body fat | OVX mice | - | reduced | #12 |
estradiol replacement | decrease | glycemia | OVX mice | - | reduced | #13 |
estradiol replacement | decrease | plasma insulin | OVX mice | - | reduced | #14 |
estradiol replacement | decrease | glucose intolerance | OVX mice | - | reduced | #15 |
estradiol replacement | decrease | hepatic triglycerides | OVX mice | - | reduced | #16 |
estradiol replacement | decrease | alanine aminotransferase (ALT) | OVX mice | - | reduced | #17 |
estradiol replacement | decrease | aspartate aminotransferase (AST) | OVX mice | - | reduced | #18 |
estradiol replacement | decrease | hepatic fibrosis | OVX mice | - | reduced | #19 |
estradiol replacement | decrease | hepatic inflammation | OVX mice | - | reduced | #20 |
estradiol | decrease | OVX ApoE KO mice from NASH | OVX ApoE KO mice | - | protects | #21 |
estradiol | decrease | OVX ApoE KO mice from glucose intolerance | OVX ApoE KO mice | - | protects | #22 |
UNLABELLED: The prevalence of non-alcoholic fatty liver disease (NAFLD) and its severe form, non-alcoholic steatohepatitis (NASH), is higher in men than in women of reproductive age, and postmenopausal women are especially susceptible to developing the disease. AIM: we evaluated if female apolipoprotein E (ApoE) KO mice were protected against Western-diet (WD)-induced NASH. METHODS: Female ovariectomized (OVX) ApoE KO mice or sham-operated (SHAM) mice were fed either a WD or a regular chow (RC) for 7 weeks. Additionally, OVX mice fed a WD were treated with either estradiol (OVX + E2) or vehicle (OVX). RESULTS: Whole-body fat, plasma glucose, and plasma insulin were increased and associated with increased glucose intolerance in OVX mice fed a WD (OVX + WD). Plasma and hepatic triglycerides, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) hepatic enzymes were also increased in the plasma of OVX + WD group, which was associated with hepatic fibrosis and inflammation. Estradiol replacement in OVX mice reduced body weight, body fat, glycemia, and plasma insulin associated with reduced glucose intolerance. Treatment also reduced hepatic triglycerides, ALT, AST, hepatic fibrosis, and inflammation in OVX mice. CONCLUSIONS: These data support the hypothesis that estradiol protects OVX ApoE KO mice from NASH and glucose intolerance.