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Pavon Arocas, O.

Publications and source records attributed to Pavon Arocas, O..

2 recordsLinked to original sources

Tonically active GABAergic neurons in the dorsal periaqueductal gray control the initiation and execution of instinctive escape

To avoid predation, animals perform defensive actions that are both instinctive and adaptable to the environment. In mice, the decision to escape from imminent threats is implemented by a feed-forward circuit in the midbrain, where excitatory VGluT2+ neurons in the dorsal periaqueductal gray (dPAG) compute escape initiation and escape vigour from threat evidence. Here we show that GABAergic VGAT+ neurons in the dPAG dynamically control this process by modulating the excitability of excitatory escape neurons. Using in vitro patchclamp and in vivo neural activity recordings in freely behaving mice we found that VGAT+ dPAG neurons fire action potentials tonically in the absence of synaptic inputs and are a major source of synaptic inhibition to VGluT2+ dPAG neurons. Activity in these spontaneously firing VGAT+ cells transiently decreases at escape onset and increases during escape, peaking at escape termination. Optogenetically increasing or decreasing VGAT+ dPAG activity bidirectionally changes the probability of escape when the stimulation is delivered at the time of threat onset, and the duration of escape when delivered after escape initiation. We conclude that the activity of tonically firing VGAT+ dPAG neurons sets a threshold for escape initiation and controls the execution of the flight locomotor action.

neuroscience↗

Neuronal activity drives homeostatic sleep through engagement of the hypothalamic neuropeptide galanin

Sleep pressure homeostatically increases during wake and dissipates during sleep, but the molecular signals and neuronal substrates that measure homeostatic sleep pressure remain poorly understood. A pharmacological assay that generates acute, short-term increases in wakefulness in larval zebrafish, revealed that subsequent rebound sleep is dependent on the intensity of global neuronal activity. Whole brain activity mapping identified preoptic Galanin expressing neurons as selectively active during rebound sleep, and the induction of galanin transcripts was predictive of total rebound sleep time. Galanin is required for sleep homeostasis, as galanin mutants almost completely lack rebound sleep following both pharmacologically induced neuronal activity and physical sleep deprivation. These results suggest that Galanin expressing neurons play a key role in integrating sleep pressure signals derived from global neuronal activity and act as an output arm for the vertebrate sleep homeostat. (word count: 129).

neuroscience↗