Dopamine enhances signal-to-noise ratio in cortical-brainstem encoding of aversive stimuli

Dopamine modulates medial prefrontal cortex (mPFC) activity to mediate diverse behavioural functions 1 , 2 ; however, the precise circuit computations remain unknown. One potentially unifying model by which dopamine may underlie a diversity of functions is by modulating the signal-to-noise ratio in...

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Published in:Nature (London) Vol. 563; no. 7731; pp. 397 - 401
Main Authors: Vander Weele, Caitlin M., Siciliano, Cody A., Matthews, Gillian A., Namburi, Praneeth, Izadmehr, Ehsan M., Espinel, Isabella C., Nieh, Edward H., Schut, Evelien H. S., Padilla-Coreano, Nancy, Burgos-Robles, Anthony, Chang, Chia-Jung, Kimchi, Eyal Y., Beyeler, Anna, Wichmann, Romy, Wildes, Craig P., Tye, Kay M.
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 01-11-2018
Nature Publishing Group
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Summary:Dopamine modulates medial prefrontal cortex (mPFC) activity to mediate diverse behavioural functions 1 , 2 ; however, the precise circuit computations remain unknown. One potentially unifying model by which dopamine may underlie a diversity of functions is by modulating the signal-to-noise ratio in subpopulations of mPFC neurons 3 – 6 , where neural activity conveying sensory information (signal) is amplified relative to spontaneous firing (noise). Here we demonstrate that dopamine increases the signal-to-noise ratio of responses to aversive stimuli in mPFC neurons projecting to the dorsal periaqueductal grey (dPAG). Using an electrochemical approach, we reveal the precise time course of pinch-evoked dopamine release in the mPFC, and show that mPFC dopamine biases behavioural responses to aversive stimuli. Activation of mPFC–dPAG neurons is sufficient to drive place avoidance and defensive behaviours. mPFC–dPAG neurons display robust shock-induced excitations, as visualized by single-cell, projection-defined microendoscopic calcium imaging. Finally, photostimulation of dopamine terminals in the mPFC reveals an increase in the signal-to-noise ratio in mPFC–dPAG responses to aversive stimuli. Together, these data highlight how dopamine in the mPFC can selectively route sensory information to specific downstream circuits, representing a potential circuit mechanism for valence processing. Dopamine in the medial prefrontal cortex modulates behavioural responses to aversive stimuli by increasing the signal-to-noise ratio of neurons projecting to the dorsal periaqueductal grey.
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K.M.T. is a New York Stem Cell Foundation - Robertson Investigator, a McKnight Scholar and this work was supported by funding from the JPB Foundation, PIIF, PNDRF, JFDP, Klingenstein Foundation, NARSAD Young Investigator Award, New York Stem Cell Foundation, NIH R01-MH102441-01 (NIMH), NIH Director’s New Innovator Award DP2-DK-102256-01 (NIDDK), and Pioneer Award DP1-AT009925 (NCCIH). C.M.V.W. and E.H.N were supported by the NSF Graduate Research Fellowship and Integrative Neuronal Systems Training Fellowship (T32 GM007484). C.A.S. is supported by NIH grants F32 MH111216 (NIMH) and K99 DA045103 (NIDA). G.A.M. was supported by the Charles A. King Trust Postdoctoral Research Fellowship Program, Bank of America, N.A., Co-Trustees. R.W. acknowledged funding from the Simons Center and the Netherlands Organization for Scientific Research (NWO) RUBICON. C.A.S., A.B., and R.W. recognize support from the NARSAD Young Investigator Award. Authors declare no competing interests.
AUTHOR CONTRIBUTIONS
C.M.V.W. and K.M.T. conceived the project. C.M.V.W., E.H.N., G.A.M., C.A.S., I.C.E., C.-J.C., P.N. & K.M.T. analyzed data. E.H.N., P.N., C.-J.C., & E.Y.K. provided MATLAB scripts and advice for data analysis. R.W., A.B., C.P.W., & A.B.R. provided technical training. C.M.V.W., C.A.S., G.A.M., E.H.N., & K.M.T. contributed to experimental design. C.M.V.W. and K.M.T. wrote the paper. All authors collected data and contributed to the editing of the manuscript.
ISSN:0028-0836
1476-4687
DOI:10.1038/s41586-018-0682-1