4.6 Article

Selective inhibition of gamma aminobutyric acid release from mouse hippocampal interneurone subtypes by the volatile anaesthetic isoflurane

期刊

BRITISH JOURNAL OF ANAESTHESIA
卷 127, 期 4, 页码 587-599

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ELSEVIER SCI LTD
DOI: 10.1016/j.bja.2021.06.042

关键词

exocytosis; GABA; glutamate; interneurone; isoflurane; synaptic transmission; synaptic vesicle; voltage-gated sodium channel

资金

  1. US National Institutes of Health [R01GM058055-21]

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The study reveals that isoflurane inhibits synaptic vesicle exocytosis from hippocampal glutamatergic neurones and GABAergic interneurones in a cell-type-specific manner depending on their expression of voltage-gated sodium channel subtypes.
Background: The cellular and molecular mechanisms by which general anaesthesia occurs is poorly understood. Hippocampal interneurone subpopulations, which are critical regulators of cognitive function, have diverse neurophysiological and synaptic properties, but their responses to anaesthetics are unclear. Methods: We used live-cell imaging of fluorescent biosensors expressed in mouse hippocampal neurones to delineate interneurone subtype-specific effects of isoflurane on synaptic vesicle exocytosis. The role of voltage-gated sodium channel (Na-v) subtype expression in determining isoflurane sensitivity was probed by overexpression or knockdown of specific Na-v subtypes in identified interneurones. Results: Clinically relevant concentrations of isoflurane differentially inhibited synaptic vesicle exocytosis: to 83.1% (11.7%) of control in parvalbumin-expressing interneurones, and to 58.6% (13.3%) and 64.5% (8.5%) of control in somatostatin-expressing interneurones and glutamatergic neurones, respectively. The relative expression of Na(v)1.1 (associated with lower sensitivity) and Na(v)1.6 (associated with higher sensitivity) determined the sensitivity of exocytosis to isoflurane. Conclusions: Isoflurane inhibits synaptic vesicle exocytosis from hippocampal glutamatergic neurones and GABAergic interneurones in a cell-type-specific manner depending on their expression of voltage-gated sodium channel subtypes.

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