Key Considerations for Studying the Effects of High-Fat Diet on the Nulligravid Mouse Endometrium

Author:

Skalski Hilary J1ORCID,Arendt Amelia R1,Harkins Shannon K1ORCID,MacLachlan Madison1,Corbett Cody J M2,Goy Robinson W2,Kapoor Amita2ORCID,Hostetter Galen3ORCID,Chandler Ronald L14ORCID

Affiliation:

1. Department of Obstetrics, Gynecology and Reproductive Biology, College of Human Medicine, Michigan State University , Grand Rapids, MI 49503 , USA

2. Wisconsin National Primate Research Center, Assay Services, University of Wisconsin-Madison , Madison, WI 53715 , USA

3. Pathology and Biorepository Core, Van Andel Research Institute , Grand Rapids, MI 49503 , USA

4. Department for Epigenetics, Van Andel Research Institute , Grand Rapids, MI 49503 , USA

Abstract

Abstract The obesity epidemic continues to increase, with half of US women predicted to be obese by 2030. Women with obesity are at increased risk for not only cardiovascular and liver disease, but also reproductive disorders. Although mouse models are useful in studying the effects of obesity, there is inconsistency in obesity-induction methods, diet composition, and mouse strains, and studies using female mice are limited. In this study, we sought to compare the effects of a 45% high-fat diet (HFD) versus a 60% HFD on the uterine estrous cycle of nulligravid C57BL/6J mice. For 22 weeks, we placed a total of 20 mice on either a 60% HFD, 45% HFD, or each HFD-matched control diet (CD). Both HFDs produced significant weight gain, with 60% HFD and 45% HFD gaining significant weight after 2 weeks and 15 weeks, respectively. Additionally, both HFDs led to glucose intolerance, fatty liver, and adipocyte hypertrophy. Mice fed 60% HFD displayed hyperphagia in the first 12 weeks of HFD treatment. Moreover, 60% HFD-treated mice had a longer estrous cycle length and an increased percentage of estrus stage samplings compared to CD-treated mice. Estrous cycle stage-controlled 60% HFD-treated mice displayed an increased estrogen-to-progesterone ratio and decreased ovarian corpora lutea compared to CD-treated mice, which may underlie the observed estrous cycle differences. There was no significant difference between diets regarding endometrial morphology or the percent of endometrial CD45+ immune cells. Our results indicate that consideration is needed when selecting a HFD-induced obesity mouse model for research involving female reproductive health.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Child Health & Human Development

National Institutes of Health

Publisher

The Endocrine Society

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