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Harvey-Girard, E.

Publications and source records attributed to Harvey-Girard, E..

3 recordsLinked to original sources

A slow 5-HT1AR-mediated recurrent inhibitory network in raphe computes contextual value through synaptic facilitation

Serotonin (5-HT) neurons in the dorsal raphe nucleus (DRN) receive a constellation of long-range inputs, yet guiding principles of local circuit organization and underlying computations in this nucleus are largely unknown. Using inputs from the lateral habenula (LHb) to interrogate the processing features of the DRN, we uncovered 5-HT1A receptor-mediated recurrent connections between 5-HT neurons, refuting classical theories of autoinhibition. Cellular electrophysiology and imaging of a genetically encoded 5-HT sensor revealed that these recurrent inhibitory connections spanned the raphe, were slow, stochastic, strongly facilitating, and gated spike output. These features collectively conveyed highly non-linear dynamics to this network, generating excitation-driven inhibition and winner-take-all computations. In vivo optogenetic activation of LHb inputs to DRN, at frequencies where these computations are predicted to ignite, transiently disrupted expression of a reward-conditioned response in an auditory conditioning task. Together, these data identify a core computation supported by an unsuspected slow serotonergic recurrent inhibitory network.

neuroscience↗

Cellular and network mechanisms may generate sparse coding of sequential object encounters in hippocampal-like circuits

In mammals, the localization of distinct landmarks is performed by hippocampal neurons that sparsely encode an animals location relative to surrounding objects. Similarly, the dorsal lateral pallium (DL) is essential for spatial learning in teleost fish. The DL of weakly electric gymnotiform fish receives sensory inputs from the preglomerular nucleus (PG), which has been hypothesized to encode the temporal sequence of electrosensory or visual landmark/food encounters. Here, we show that DL neurons have a hyperpolarized resting membrane potential combined with a high and dynamic spike threshold that increases following each spike. Current-evoked spikes in DL cells are followed by a strong small-conductance calcium-activated potassium channel (SK) mediated after-hyperpolarizing potential (AHP). Together, these properties prevent high frequency and continuous spiking. The resulting sparseness of discharge and dynamic threshold suggest that DL neurons meet theoretical requirements for generating spatial memory engrams by decoding the landmark/food encounter sequences encoded by PG neurons.

neuroscience↗

A novel time-stamp mechanism transforms egocentric encounters into an allocentric spatial representation

Learning the spatial organization of the environment is essential for most animals survival. This often requires the animal to derive allocentric information about the environment from egocentric sensory and motor experience. The neural circuits and mechanisms underlying this transformation are currently unknown. We addressed this problem in electric fish, which can precisely navigate in complete darkness and whose requisite brain circuitry is relatively simple. We conducted the first neural recordings in the preglomerular complex, the thalamic region exclusively connecting the optic tectum with the spatial learning circuits in the dorsolateral pallium. While tectal egocentric information was eliminated in preglomerular neurons, the time-intervals between object encounters were precisely encoded. We show that this highly-reliable temporal information, combined with a speed signal, can permit accurate path-integration that then enables computing allocentric spatial relations. Our results suggest that similar mechanisms are involved in spatial learning via sequential encounters in all vertebrates.

neuroscience↗