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Estradiol Protects Female ApoE KO Mice against Western-Diet-Induced Non-Alcoholic Steatohepatitis.

International journal of molecular sciences
June 7, 2023
Layanne C C Araujo et al. (10 authors)
Journal ArticleAnimal Study
Study Details

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

Extracted Claims (22)
InterventionDirectionEndpointPopulationDosageImpactClaim #
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
Abstract

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.

Medical Subject Headings (MeSH)
AnimalsFemaleMiceApolipoproteins EDietEstradiolGlucoseGlucose IntoleranceInflammationInsulinsLiverLiver CirrhosisMice, Inbred C57BLNon-alcoholic Fatty Liver DiseaseTriglycerides
Study Links
Quality Scores
Safety20
Efficacy85/10
Quality75/10
Citation Metrics
Total Citations6
Citations/Year3.0
Relative Citation Ratio1.10
NIH Percentile53.8%
Research Impact Scores
APT Score0.05
Weight Score1.96
Normalized Score0.57
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