Abstract
Vertical transmission of obesity is a critical contributor to the unabated obesity pandemic and the associated surge in metabolic diseases. Existing experimental models insufficiently recapitulate “human-like” obesity phenotypes, limiting the discovery of how severe obesity in pregnancy instructs vertical transmission of obesity. Here, via utility of thermoneutral housing and obesogenic diet feeding coupled to syngeneic mating of WT obese female and lean male mice on a C57BL/6 background, we present a tractable, more “human-like” approach to specifically investigate how maternal obesity contributes to offspring health. Using this model, we found that maternal obesity decreased neonatal survival, increased offspring adiposity, and accelerated offspring predisposition to obesity and metabolic disease. We also show that severe maternal obesity was sufficient to skew offspring microbiome and create a proinflammatory gestational environment that correlated with inflammatory changes in the offspring in utero and adulthood. Analysis of a human birth cohort study of mothers with and without obesity and their infants was consistent with mouse study findings of maternal inflammation and offspring weight gain propensity. Together, our results show that dietary induction of obesity in female mice coupled to thermoneutral housing can be used for future mechanistic interrogations of obesity and metabolic disease in pregnancy and vertical transmission of pathogenic traits.
| Original language | English |
|---|---|
| Article number | 4958 |
| Journal | Nutrients |
| Volume | 15 |
| Issue number | 23 |
| DOIs | |
| State | Published - Dec 2023 |
Bibliographical note
Publisher Copyright:© 2023 by the authors.
Funding
This research was funded in part by: Cincinnati Children’s Hospital Medical Center (Arnold W. Strauss Fellow Award to J.R.D.; Research Innovation and Pilot Award to S.D.); National Institute of Diabetes and Digestive and Kidney Diseases (R01DK099222 to S.D.; R01DK099222-02S1 to M.E.M.-F.; R01DK099222-08S1 to J.R.O.; P30 DK078392 associated with S.D.); National Institute of Allergy and Infectious Diseases (R21AI139829 to S.D.); March of Dimes Prematurity Research Center Ohio Collaborative (Innovation Catalyst Grant 22-FY16-125 to S.D.); Burroughs Wellcome Fund (Preterm Birth Research Grant 1015032 to S.D.); United States Department of Defense (W81XWH2010392 to S.D.).
| Funders | Funder number |
|---|---|
| U.S. Department of Defense | W81XWH2010392 |
| National Institute of Allergy and Infectious Diseases | R21AI139829 |
| National Institute of Diabetes and Digestive and Kidney Diseases | R01DK099222, P30 DK078392 |
| Burroughs Wellcome Fund | 1015032 |
| Cincinnati Children's Hospital Medical Center | |
| March of Dimes Prematurity Research Center Ohio Collaborative | 22-FY16-125 |
Keywords
- amniotic fluid
- developmental origin of health and disease (DOHaD)
- high-fat diet
- inflammation
- intrauterine programming
- metabolic dysfunction-associated steatotic liver disease (MASLD)
- pregnancy
- stillbirth
- type 2 diabetes
ASJC Scopus subject areas
- Food Science
- Nutrition and Dietetics