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Functional dissection of basal ganglia inhibitory input onto SNc dopaminergic neurons

View ORCID ProfileRC Evans, EL Twedell, M Zhu, J Ascencio, R Zhang, View ORCID ProfileZM Khaliq
doi: https://doi.org/10.1101/856617
RC Evans
Cellular Neurophysiology Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892 USA
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  • ORCID record for RC Evans
EL Twedell
Cellular Neurophysiology Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892 USA
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M Zhu
Cellular Neurophysiology Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892 USA
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J Ascencio
Cellular Neurophysiology Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892 USA
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R Zhang
Cellular Neurophysiology Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892 USA
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ZM Khaliq
Cellular Neurophysiology Unit, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892 USA
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  • For correspondence: Zayd.Khaliq@nih.gov
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Abstract

Substania nigra (SNc) dopaminergic neurons show a pause-rebound firing pattern in response to aversive events. Because these neurons integrate information from predominately inhibitory brain areas, it is important to determine which inputs functionally inhibit the dopamine neurons and whether this pause-rebound firing pattern can be produced by a solely inhibitory input. Here, we functionally map genetically-defined inhibitory projections from the dorsal striatum (striosome and matrix) and globus pallidus (GPe; parvalbumin and Lhx6) onto SNc neurons. We find that GPe and striosomal inputs both pause firing in SNc neurons, but rebound firing only occurs after inhibition from striosomes. Indeed, we find that striosomes are synaptically optimized to produce rebound and preferentially inhibit a subpopulation of ventral, intrinsically rebound-ready SNc dopaminergic neurons on their reticulata dendrites. Therefore, we describe a self-contained dendrite-specific striatonigral circuit that can produce pause-rebound firing in the absence of excitatory input.

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  • Competing Interests – The authors report no conflict of interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted December 03, 2019.
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Functional dissection of basal ganglia inhibitory input onto SNc dopaminergic neurons
RC Evans, EL Twedell, M Zhu, J Ascencio, R Zhang, ZM Khaliq
bioRxiv 856617; doi: https://doi.org/10.1101/856617
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Functional dissection of basal ganglia inhibitory input onto SNc dopaminergic neurons
RC Evans, EL Twedell, M Zhu, J Ascencio, R Zhang, ZM Khaliq
bioRxiv 856617; doi: https://doi.org/10.1101/856617

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