# Circadian Timing, Rather than Hydration Status, Determines Metabolic Adaptation to Ramadan-like Fasting in Diet-Induced Obese Rats

**Authors:** Noof M. Alshahrani, Maha H. Alhussain, Mohammed F. Alahmed, Ahmad T. Almnaizel, Ahmed S. BaHammam

PMC · DOI: 10.3390/nu18040663 · Nutrients · 2026-02-18

## TL;DR

This study finds that fasting during the inactive phase of the day has a stronger effect on improving metabolism in obese rats than hydration levels.

## Contribution

The study identifies circadian timing as a key factor in metabolic adaptation during fasting in diet-induced obese rats.

## Key findings

- Morning fasting significantly reduced body-weight gain and improved insulin sensitivity in obese rats.
- Fasting during the inactive phase was associated with better metabolic outcomes than hydration status.
- Hydration primarily affected fluid and electrolyte levels but not core metabolic parameters.

## Abstract

Background: Ramadan fasting involves daily abstinence from food and water between dawn and sunset, but human studies cannot readily disentangle the effects of fasting timing, circadian alignment, and hydration status on metabolic regulation. Objective: To determine whether fasting timing or hydration status exerts a stronger influence on metabolic outcomes in diet-induced obese rats under controlled Ramadan-like conditions. Methods: Forty diet-induced obese rats were assigned to four Ramadan-like fasting groups differing by timing and hydration: dry morning (DM), wet morning (WM), dry night (DN), or wet night (WN) fasting, in addition to healthy control (HC) and obese control (OC) groups (n = 8 each). Because rats are nocturnal, morning fasting restricted food during the inactive (light) phase, whereas night fasting restricted food during the active (dark) phase. Body weight, glucose, insulin, HOMA-IR, lipid profile, adipokines, and electrolytes were assessed after four weeks. Results: Morning fasting significantly reduced body-weight gain (F(5,42) = 10.72, p < 0.0001; η2 = 0.56) and improved insulin sensitivity, reflected by lower insulin (F(5,30) = 2.98, p = 0.027; η2 = 0.33) and HOMA-IR (F(5,30) = 3.76, p = 0.0092; η2 = 0.39), independent of hydration status. Serum glucose differed across groups (F(5,42) = 5.82, p = 0.00036). After body-weight adjustment, total cholesterol and triglycerides were reduced in fasting groups, whereas hydration primarily influenced fluid and electrolyte parameters without materially altering core metabolic outcomes. Conclusions: Under controlled conditions, fasting timing exerted a stronger influence on metabolic regulation than hydration status. Fasting aligned with the inactive circadian phase was associated with more favorable metabolic outcomes, highlighting circadian alignment as a key determinant of fasting-related metabolic adaptation in obesity.

## Linked entities

- **Diseases:** obesity (MONDO:0011122)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Adipoq (adiponectin, C1Q and collagen domain containing) [NCBI Gene 246253] {aka Acdc, Acrp30, Adid}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Lep (leptin) [NCBI Gene 25608] {aka OB, obese}, Sirt3 (sirtuin 3) [NCBI Gene 293615], Sirt1 (sirtuin 1) [NCBI Gene 309757] {aka Sir2}
- **Diseases:** WM (MESH:D057135), cervical dislocation (MESH:D002575), metabolic dysregulation (MESH:D021081), impaired glucose tolerance (MESH:D018149), metabolic dysfunction (MESH:D008659), body-weight gain (MESH:D015430), OC (MESH:D009765), adiposity (MESH:D018205), DN (MESH:D015352), weight loss (MESH:D015431), Insulin resistance (MESH:D007333), HC (MESH:D000067329), atherogenic (MESH:D050197), injury (MESH:D014947), inflammatory (MESH:D007249), DM (MESH:D048968)
- **Chemicals:** Glucose (MESH:D005947), cholesterol (MESH:D002784), blood glucose (MESH:D001786), Lipid (MESH:D008055), Water (MESH:D014867), TG (MESH:D014280), fatty acid (MESH:D005227), xylazine (MESH:D014991), cortisol (MESH:D006854), K+ (MESH:D011188), Na+ (MESH:D012964), fat (MESH:D005223), AIN-93G (-)
- **Species:** gut metagenome (species) [taxon 749906], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942902/full.md

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Source: https://tomesphere.com/paper/PMC12942902