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Hippocampal Inhibitory Synapsis Deficits Induced by α5-Containing GABA A Receptors Mediate Chronic Neuropathic Pain-Related Cognitive Impairment.
- Source :
-
Molecular neurobiology [Mol Neurobiol] 2022 Oct; Vol. 59 (10), pp. 6049-6061. Date of Electronic Publication: 2022 Jul 18. - Publication Year :
- 2022
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Abstract
- Chronic neuropathic pain often leads to cognitive impairment, but the exact mechanism remains unclear. Gamma-aminobutyric acid A receptors (GABA <subscript>A</subscript> Rs) are the major inhibitory receptors in the brain, of which the α5-containing GABA <subscript>A</subscript> Rs (GABA <subscript>A</subscript> Rs-α5) are implicated in a range of neuropsychiatric disorders with cognitive deficits. However, whether GABA <subscript>A</subscript> Rs-α5 are involved in chronic neuropathic pain-related cognitive impairment remains unknown. In this study, the rats with chronic neuropathic pain induced by right sciatic nerve ligation injury (SNI) exhibited cognitive impairment with declined spontaneous alternation in Y-maze test and discrimination index in novel object recognition test. The GABA <subscript>A</subscript> Rs-α5 expressing on parvalbumin and somatostatin interneurons increased remarkably in hippocampus, resulting in decreased mean frequency of spontaneous inhibitory postsynaptic currents in hippocampal pyramidal neurons. Significantly, antagonizing the GABA <subscript>A</subscript> Rs-α5 by L655708 rescued weakened inhibitory synaptic transmission and cognitive impairment induced by chronic neuropathic pain. Taken together, these data suggest that the GABA <subscript>A</subscript> Rs-α5 play a crucial role in chronic neuropathic pain-induced cognitive impairment by weakening inhibitory synaptic transmission, which may provide insights into the pharmacologic treatment of chronic neuropathic pain-related cognitive impairment.<br /> (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
Details
- Language :
- English
- ISSN :
- 1559-1182
- Volume :
- 59
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Molecular neurobiology
- Publication Type :
- Academic Journal
- Accession number :
- 35849280
- Full Text :
- https://doi.org/10.1007/s12035-022-02955-8