# Exogenous estradiol does not regulate daily metabolic rhythms underlying diet-induced obesity in male mice

**Authors:** W. Brad Osborne, Oliver Vöcking, Victoria M. Alvord, Oluwabukola B. Omotola, Yuriko Katsumata, Julie S. Pendergast

PMC · DOI: 10.1371/journal.pone.0343513 · PLOS One · 2026-03-17

## TL;DR

Exogenous estradiol does not protect male mice from disrupted metabolic rhythms caused by high-fat diets, unlike in females.

## Contribution

The study reveals that estradiol does not regulate daily metabolic rhythms in male mice fed high-fat diets.

## Key findings

- Estradiol-treated males had lower blood glucose on high-fat diets compared to controls.
- Estradiol did not affect body weight, eating rhythms, or locomotor activity rhythms in males.
- Circadian rhythms in tissues like the SCN and liver were not altered by estradiol treatment.

## Abstract

Male mice fed high-fat diet become obese, but female mice are resistant to diet-induced weight gain. We previously found that circulating estradiol in females protects their daily rhythms from disruption by high-fat feeding to prevent diet-induced obesity. The goal of this study was to determine the effects of estradiol on daily metabolic rhythms in male mice. Male C57BL/6J mice were treated with estradiol and fed high-fat diet for 2 weeks. We measured the effects of high-fat diet feeding on daily rhythms of eating behavior and locomotor activity, and on the phases, or timing, of circadian rhythms in central and peripheral tissues. We found that males treated with estradiol had lower blood glucose when fed high-fat diet than males treated with vehicle even though there were no effects of estradiol treatment on body weight and adiposity. There was no effect of estradiol on the daily rhythm of eating behavior as it was low-amplitude or arrhythmic during high-fat diet feeding in both vehicle- and estradiol-treated males. Locomotor activity rhythms were also unaffected by estradiol treatment. Likewise, the phases of circadian rhythms in the suprachiasmatic nucleus (SCN), liver, muscle, and other peripheral tissues were not altered by estradiol treatment. Thus, treatment of male mice with estradiol did not protect daily rhythms from disruption by high-fat diet, as it does in females. Together these data suggest that the mechanisms underlying sex differences in daily metabolic rhythms are complex and may require both developmental and adult exposure to hormones.

## Linked entities

- **Chemicals:** estradiol (PubChem CID 450)
- **Diseases:** obesity (MONDO:0011122)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Lep (leptin) [NCBI Gene 16846] {aka ob, obese}
- **Diseases:** stroke (MESH:D020521), rhythms (MESH:D021081), death (MESH:D003643), type 2 diabetes (MESH:D003924), Obesity (MESH:D009765), hyperinsulinemia (MESH:D006946), heart disease (MESH:D006331), cardiovascular disease (MESH:D002318), diabetes (MESH:D003920), metabolic disorders (MESH:D008659), arrhythmic (OMIM:212500), weight gain (MESH:D015430), disrupted (MESH:D019958), cancer (MESH:D009369), cardiometabolic diseases (MESH:D024821), hyperglycemia (MESH:D006943), adiposity (MESH:D018205)
- **Chemicals:** Ketofen (-), Silastic (MESH:C013830), sesame oil (MESH:D012715), Meloxicam (MESH:D000077239), fat (MESH:D005223), 17beta-estradiol (MESH:D004958), isoflurane (MESH:D007530), blood glucose (MESH:D001786), glucose (MESH:D005947), water (MESH:D014867)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** D12450K
- **Cell lines:** /6J — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_W797), C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12994778/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12994778/full.md

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Source: https://tomesphere.com/paper/PMC12994778