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EFFECTS OF MEDIAL SEPTAL LESION ON HIPPOCAMPAL EXTRACELLULAR GLUTAMATE AND GABA LEVELS DURING SPATIAL ALTERNATION
S Mataradze1, T Naneishvili1, M Sephashvili1
1I. Beritashvili Center of Experimental Biomedicine, Tbilisi; St. Andrew the First-Called Georgian University of Georgian Patriarchate, Tbilisi, Georgia.
Georgian Medical News
|November 16, 2016
Summary
Medial septal lesions impair spatial working memory in rats by reducing hippocampal glutamate release. This study links neurochemical changes to cognitive decline, offering insights into memory disorders.
Area of Science:
- Neuroscience
- Cognitive Neuroscience
- Neurobiology
Background:
- Spatial working memory is crucial for cognitive function.
- The medial septum (MS) plays a role in hippocampal function and memory.
- Neurotransmitter release in the hippocampus is implicated in memory processes.
Purpose of the Study:
- To investigate the impact of medial septal (MS) lesions on spatial working memory (SA task).
- To examine hippocampal glutamate and GABA release during and after SA testing in lesioned and control rats.
- To assess the effect of MS lesions on KCl-stimulated glutamate and GABA release in the hippocampus.
Main Methods:
- Electrolytic medial septal (MS) lesions in rats.
- Spontaneous alternation (SA) task for spatial working memory assessment.
- In vivo microdialysis to measure hippocampal glutamate and GABA release.
- KCl stimulation to assess neurotransmitter release capacity.
Main Results:
- MS lesions significantly impaired SA performance.
- Hippocampal glutamate efflux during SA was blunted in MS-lesioned rats compared to controls.
- MS lesions significantly reduced KCl-stimulated glutamate release in the hippocampus.
- GABA levels and release showed no significant changes during SA testing or KCl stimulation.
Conclusions:
- Decreased hippocampal glutamate release, particularly upon stimulation, may underlie the spatial working memory deficits observed in MS-lesioned rats.
- SA testing combined with in vivo microdialysis is a valuable method for studying the neurochemical basis of hippocampal-dependent memory.
- This approach can aid in understanding cognitive decline in various neurological disorders and neurodegenerative diseases.

