# Effects of Swimming at Different Water Temperatures on Muscle and Adipose Tissue Adaptation in Diet-Induced Obese Mice

**Authors:** Tzu-Jung Chou, Chia-Wen Lu, Yi-Ju Hsu, Chi-Chang Huang, Kuo-Chin Huang

PMC · DOI: 10.7150/ijms.121250 · 2026-02-11

## TL;DR

Swimming in different water temperatures affects obesity-related metabolic and muscle adaptations in mice, with moderate and warm water reducing obesity and cold water improving endurance.

## Contribution

The study reveals distinct temperature-dependent effects of swimming on metabolic and muscular adaptations in diet-induced obese mice.

## Key findings

- Swimming at 25°C and 32°C reduced body weight and improved metabolic profiles in obese mice.
- Cold-water swimming (15°C) enhanced endurance performance through increased oxidative muscle fibers.
- Elevated Pgc-1α in fat and FNDC5 in muscle varied with water temperature.

## Abstract

Obesity is a major global health concern, leading to increased risk of metabolic diseases and mortality. Swimming, as a low-impact exercise, may provide metabolic benefits. However, the influence of water temperature on the metabolic and physiological responses remains underexplored. This study investigated the effects of water temperatures on muscle and adipose tissue adaptations in high-fat diet-induced obese mice.

Obese mice were subjected to swimming at different water temperatures: 15°C, 25°C, or 32°C. Changes in body and tissue weight, grip strength, exhaustive swimming performance, and key metabolic parameters were assessed. Epididymal fat pads (EFP) and gastrocnemius muscles were collected for histological analyses (muscle fiber composition and adipose tissue remodeling), gene expression (Ucp1, Pgc-1α, Prdm16, Cidea), and western blot analyses (SIRT1-PGC-1α-FNDC5 pathway).

Swimming at 25°C and 32°C significantly reduced body weight and EFP weight, improved metabolic profiles and grip strength, whereas cold-water swimming (15°C) enhanced endurance performance. Histological analysis revealed reduced adipocyte size in the 25°C group, accompanied by increased oxidative (Type I) fibers across all swimming groups. Elevated Pgc-1α expression in EFP was particularly prominent at 25°C, and FNDC5 in muscle was most pronounced at 15°C. These findings highlight distinct temperature-dependent metabolic and muscular adaptations during swimming in obese mice.

Moderate (25°C) and warm (32°C) water temperatures are optimal for reducing obesity-related metabolic dysfunctions and enhancing muscle strength, while cold water (15°C) improves endurance through oxidative muscle adaptation.

## Linked entities

- **Genes:** UCP1 (uncoupling protein 1) [NCBI Gene 7350], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891], PRDM16 (PR/SET domain 16) [NCBI Gene 63976], CIDEA (cell death inducing DFFA like effector a) [NCBI Gene 1149], SIRT1 (sirtuin 1) [NCBI Gene 23411], FNDC5 (fibronectin type III domain containing 5) [NCBI Gene 252995]
- **Diseases:** obesity (MONDO:0011122)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Mtor (mechanistic target of rapamycin kinase) [NCBI Gene 56717] {aka 2610315D21Rik, FRAP, FRAP2, Frap1, RAFT1, RAPT1}, Trim25 (tripartite motif-containing 25) [NCBI Gene 217069] {aka EFP, Zfp147}, Ppargc1a (PPARG coactivator 1 alpha) [NCBI Gene 83516] {aka LRPGC1, PGC-1v, PGCvf, PGCvf-1, PGCvf1, Ppargc1}, Sirt1 (sirtuin 1) [NCBI Gene 93759] {aka SIR2L1, Sir2, Sir2a, Sir2alpha}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, Fndc5 (fibronectin type III domain containing 5) [NCBI Gene 384061] {aka 1500001L03Rik, PeP, Pxp}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Cidea (cell death-inducing DNA fragmentation factor, alpha subunit-like effector A) [NCBI Gene 12683], Prdm16 (PR/SET domain 16) [NCBI Gene 100366024], Ucp1 (uncoupling protein 1) [NCBI Gene 24860] {aka Ucp, Ucpa, Uncp}, Irf4 (interferon regulatory factor 4) [NCBI Gene 291100], Ucp1 (uncoupling protein 1 (mitochondrial, proton carrier)) [NCBI Gene 22227] {aka Slc25a7, Ucp}, Prdm16 (PR domain containing 16) [NCBI Gene 70673] {aka 5730557K01Rik, csp1, mel1}, Mstn (myostatin) [NCBI Gene 29152] {aka Gdf8}, Mb (myoglobin) [NCBI Gene 17189], Cidea (cell death-inducing DFFA-like effector a) [NCBI Gene 291541], Nucleolin (nucleolin multifunctional protein) [NCBI Gene 17975] {aka B530004O11Rik, C23, D0Nds28, D1Nds28, Ncl, Nucl}, Hspd1 (heat shock protein 1 (chaperonin)) [NCBI Gene 15510] {aka 60kDa, CPN60, HSP-60, HSP-65, Hsp60}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}
- **Diseases:** atrophic (MESH:D020966), dyslipidemia (MESH:D050171), pain (MESH:D010146), inflammation (MESH:D007249), cervical (MESH:D002575), metabolic diseases (MESH:D008659), HFD (MESH:D004620), reduction in body weight (MESH:D001835), fatigue (MESH:D005221), Obese (MESH:D009765), weight gain (MESH:D015430), Insulin resistance (MESH:D007333), weight loss (MESH:D015431), hypertrophy (MESH:D006984), cardiovascular diseases (MESH:D002318), hypothermia (MESH:D007035), uncoordinated movements (MESH:D009069), dislocation (MESH:D004204), muscle soreness (MESH:D063806), type 2 diabetes (MESH:D003924)
- **Chemicals:** Polymer (MESH:D011108), TG (MESH:D014280), nitrogen (MESH:D009584), cortisol (MESH:D006854), lactate (MESH:D019344), paraffin (MESH:D010232), fat (MESH:D005223), Cholesterol (MESH:D002784), SDS (MESH:D012967), isoflurane (MESH:D007530), Water (MESH:D014867), fatty acid (MESH:D005227), Hematoxylin (MESH:D006416), H&amp;E (MESH:D006371), Protease and Phosphatase Inhibitor Cocktail (-), calcium (MESH:D002118), formalin (MESH:D005557), Glucose (MESH:D005947), DAB (MESH:C000469), Eosin (MESH:D004801), lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12964579/full.md

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Source: https://tomesphere.com/paper/PMC12964579