التفاصيل البيبلوغرافية
| العنوان: |
Synapse-Specific Trapping of SNARE Machinery Proteins in the Anesthetized Drosophila Brain. |
| المؤلفون: |
Hines, Adam D.1, Kewin, Amber B.1, Van De Poll, Matthew N.1, Anggono, Victor1,2, Bademosi, Adekunle T.1,2, van Swinderen, Bruno1 b.vanswinderen@uq.edu.au |
| المصدر: |
Journal of Neuroscience. 6/12/2024, Vol. 44 Issue 24, p1-18. 18p. |
| مصطلحات موضوعية: |
*SNARE proteins, *SYNAPSES, *DROSOPHILA, *LARGE-scale brain networks, *ION channels, *GENERAL anesthesia |
| مستخلص: |
General anesthetics disrupt brain network dynamics through multiple pathways, in part through postsynaptic potentiation of inhibitory ion channels as well as presynaptic inhibition of neuroexocytosis. Common clinical general anesthetic drugs, such as propofol and isoflurane, have been shown to interact and interfere with core components of the exocytic release machinery to cause impaired neurotransmitter release. Recent studies however suggest that these drugs do not affect all synapse subtypes equally. We investigated the role of the presynaptic release machinery in multiple neurotransmitter systems under isoflurane general anesthesia in the adult female Drosophila brain using live-cell super–resolution microscopy and optogenetic readouts of exocytosis and neural excitability. We activated neurotransmitter-specific mushroom body output neurons and imaged presynaptic function under isoflurane anesthesia. We found that isoflurane impaired synaptic release and presynaptic protein dynamics in excitatory cholinergic synapses. In contrast, isoflurane had little to no effect on inhibitory GABAergic or glutamatergic synapses. These results present a distinct inhibitory mechanism for general anesthesia, whereby neuroexocytosis is selectively impaired at excitatory synapses, while inhibitory synapses remain functional. This suggests a presynaptic inhibitory mechanism that complements the other inhibitory effects of these drugs. [ABSTRACT FROM AUTHOR] |
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