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Fructooligosaccharide ameliorates estrogen-gut-microbiome-brain axis dysfunction in estrogen-deficient rats
Rishabh Chaudhary1, Nitin Bansal2, Roshan Lal3,4
1Department of Pharmacology, M. M. College of Pharmacy, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala, 133207, Haryana, India. 2006.seema@gmail.com.
Food & Function
|February 19, 2026
Summary
Fructooligosaccharide (FOS) supplementation improved estrogen deficiency-induced gut and brain deficits in ovariectomized rats. This prebiotic fiber shows potential for managing postmenopausal complications by restoring the estrogen-gut-microbiome-brain axis (EGMBA).
Area of Science:
- Neuroscience
- Microbiology
- Endocrinology
Background:
- Post-menopausal estrogen decline negatively impacts brain and gut function.
- Dysfunction of the estrogen-gut-microbiome-brain axis (EGMBA) is a significant concern.
- Novel non-hormonal strategies are needed to mitigate EGMBA dysfunction.
Purpose of the Study:
- To investigate the effects of fructooligosaccharide (FOS) on EGMBA alterations in an estrogen-deficient rat model.
- To assess FOS's impact on behavioral, biochemical, molecular, and histopathological changes induced by estrogen deficiency.
Main Methods:
- Ovariectomized (OVX) rats were used to model estrogen deficiency.
- Rats were administered FOS (50 mg/kg) orally for 28 days.
- Assessments included behavioral tests, oxidative stress markers, inflammatory markers, gene expression (HPA axis, neurotransmission, apoptosis, gut microbiota, barrier integrity), and histopathology.
Main Results:
- FOS administration significantly improved anxiety, depression, and memory in OVX rats.
- FOS attenuated oxidative stress and inflammation, regulated apoptosis, and normalized HPA axis and monoamine neurotransmission.
- FOS restored gut microbial balance, enhanced gut barrier integrity, and preserved colon microstructure.
Conclusions:
- Fructooligosaccharide (FOS) exerts multifaceted protective effects on the estrogen-gut-microbiome-brain axis (EGMBA).
- FOS demonstrates potential as a non-hormonal therapeutic agent for managing postmenopausal complications.
- These findings highlight FOS's role in modulating both gut and brain functions.

