ePoster

DEEP BRAIN STIMULATION OF THE ENTORINAL CORTEX IMPROVES COGNITIVE IMPAIRMENT IN AN ANIMAL MODEL OF AGING

Maia Burjanadzeand 3 co-authors

Ivane Beritashvili Center of Experimental Biomedicine

FENS Forum 2026 (2026)
Barcelona, Spain
Board PS03-08AM-321

Presentation

Date TBA

Board: PS03-08AM-321

Poster preview

DEEP BRAIN STIMULATION OF THE ENTORINAL CORTEX IMPROVES COGNITIVE IMPAIRMENT IN AN ANIMAL MODEL OF AGING poster preview

Event Information

Poster Board

PS03-08AM-321

Abstract

With an increase in the aging population and the prevalence of various cognitive disorders, there is an increasing need to find therapeutic measures. Therefore, several non-pharmaceutical approaches are currently being tested, including deep brain stimulation (DBS). Given that the entorinal cortex (EC) is a critical modulator of the hippocampal neural network the aims of this study were to investigate the effects of chronic administration of D-galactose (D-gal) and the EC-DBS on cognitive functions and the brain-derived neurotrophic factor (BDNF) expression level in the sub-fields of the hippocampus in behaviorally characterized rats. Male outbred albino rats – aged 3 months served as subjects at the start of experimentation. Rats were randomly assigned to prepare four experimental groups: control; D-gal - with chronic administration (for 8 weeks) of D-gal; D-gal/I - with electrode implantation; D-gal/S - with electrical stimulation. The results showed a statistically significant reduction in BDNF expression levels in the hippocampal CA1, CA3 and DG subfields in rats administrated D-gal (groups: D-gal and D-gal/I). Rats in these groups showed impaired long-term spatial memory, novel object recognition memory. Present study showed that stimulation of the LEC causes an increase the expression level of BDNF in the DG (70%) and in the CA3 (18%): rats of these group exhibited enhanced cognitive functions. Overall, these results suggest that chronic EC-DBS may serve as an effective therapeutic target for aging-related memory disorders.
Supported by the funding from the SRNSFG: Grant #-FR-23-18847

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