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- W3004961655 endingPage "19.2020" @default.
- W3004961655 startingPage "ENEURO.0422" @default.
- W3004961655 abstract "Propofol is the most common general anesthetic used for surgery in humans, yet its complete mechanism of action remains elusive. In addition to potentiating inhibitory synapses in the brain, propofol also impairs excitatory neurotransmission. We use electrophysiological recordings from individual glutamatergic boutons in male and female larval Drosophila melanogaster motor nerve terminals to characterize this effect. We recorded from two bouton types, which have distinct presynaptic physiology and different average numbers of release sites or active zones. We show that a clinically relevant dose of propofol (3 μ m ) impairs neurotransmitter release similarly at both bouton types by decreasing the number of active release sites by half, without affecting release probability. In contrast, an analog of propofol has no effect on glutamate release. Coexpressing a truncated syntaxin1A protein in presynaptic boutons completely blocked this effect of propofol. Overexpressing wild-type syntaxin1A in boutons also conferred a level of resistance by increasing the number of active release sites to a physiological ceiling set by the number of active zones or T-bars, and in this way counteracting the effect of propofol. These results point to the presynaptic release machinery as a target for the general anesthetic. Proportionally equivalent effects of propofol on the number of active release sites across the different bouton types suggests that glutamatergic circuits that involve smaller boutons with fewer release sites may be more vulnerable to the presynaptic effects of the drug." @default.
- W3004961655 created "2020-02-14" @default.
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- W3004961655 date "2020-01-01" @default.
- W3004961655 modified "2023-10-11" @default.
- W3004961655 title "Proportional Downscaling of Glutamatergic Release Sites by the General Anesthetic Propofol at<i>Drosophila</i>Motor Nerve Terminals" @default.
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- W3004961655 doi "https://doi.org/10.1523/eneuro.0422-19.2020" @default.
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