https://doi.org/10.4081/ejtm.2026.14718
Does GABA supplementation modulate muscle cytokine expression and inflammatory status in aged rats?
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Published: 10 February 2026
Aging is a multifactorial process affecting all organs and systems in the body. Specific to aging is the establishment of a chronic subacute inflammatory state in tissues underlying age-related pathologies. GABA (Gamma-Aminobutyric Acid) is an inhibitory neurotransmitter in the central nervous system. Pharmaceutical properties of Gaba on non-neuronal peripheral tissues and organs were reported from anti-hypertension, anti-diabetes, anti-cancer, antioxidant, anti-inflammation, anti-microbial, anti-allergy, hepato-protection, reno-protection, and intestinal protection. GABA was indicated as an inflamation inhibitor via decreasing pro-inflammatory mediator production and ameliorating inflammatory symptoms. This study aimed to evaluate the effect of GABA supplementation on inflammatory status in the muscle tissue of aged rats. Male Wistar rats (n=24) were put in 3 groups: CY (3 month-old controls); CO (24 month-old controls); G (24 month-old rats supplemented with GABA at dosage of 10ml/kg for 3 months). At the experiment's end, skeletal muscle, small intestine and heart material was collected for immunohistochemical analysis. Comparative analysis of the intensity of IL-10, IL-4 and IL-1β immunoreaction in different muscle tissues showed that inflammatory responses varied with age and tissue. Aged animals showed higher IL-1β levels than young animals, and these effects amplified in IL-10- and IL-4-deficient rat muscles of same group. In group of GABA-supplemented animals, the intensity of IL-1β in skeletal muscle, heart and small intestine was reduced compared to adult controls. In conclusion, GABA supplementation can influence the inflammatory status of muscle tissue in old animals by modulating pro- and anti-inflammatory cytokine levels. GABA can be used to prevent the effects of ageing.
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CRediT authorship contribution
The authors contributed equally to the present paper.
Supporting Agencies
This work was funded by project KP-06-N71/46 of the Bulgarian National Science Fund.How to Cite

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