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Behavioral and dopaminergic signatures of resilience

View ORCID ProfileLindsay Willmore, Courtney Cameron, John Yang, View ORCID ProfileIlana Witten, View ORCID ProfileAnnegret Falkner
doi: https://doi.org/10.1101/2022.03.18.484885
Lindsay Willmore
1Princeton Neuroscience Institute, Princeton University, Princeton NJ 08544
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Courtney Cameron
1Princeton Neuroscience Institute, Princeton University, Princeton NJ 08544
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John Yang
1Princeton Neuroscience Institute, Princeton University, Princeton NJ 08544
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Ilana Witten
1Princeton Neuroscience Institute, Princeton University, Princeton NJ 08544
2Department of Psychology, Princeton University, Princeton NJ 08544
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  • For correspondence: iwitten@princeton.edu afalkner@princeton.edu
Annegret Falkner
1Princeton Neuroscience Institute, Princeton University, Princeton NJ 08544
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  • For correspondence: iwitten@princeton.edu afalkner@princeton.edu
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Abstract

Chronic stress can have lasting adverse consequences in some individuals, yet others are resilient to the same stressor1,2. While previous work found differences in the intrinsic properties of mesolimbic dopamine (DA) neurons in susceptible and resilient individuals after stress was over;3–10 the causal links between DA activity during stress, dynamic stress-evoked behavior, and individual differences in susceptibility and resilience are not known. Here, we record behavior and neural activity in DA projections to the nucleus accumbens (NAc, signals reward11–14) and to the tail striatum (TS, signals threat15–18) during a multiday chronic social defeat paradigm and discover behavioral and neural signatures of resilience. Using supervised and unsupervised behavioral quantification, we find that resilient and susceptible individuals employ different behavioral strategies during stress. In addition, NAc-DA (but not TS-DA) activity is higher in the proximity of the aggressor in resilient mice, consistent with a greater subjective value of the aggressor. Moreover, NAc-DA tends to be elevated at the onset of fighting back in resilient mice and at the offset of attacks in susceptible mice. To test whether DA activation during defeat can generate resilience, and if its timing with respect to behavior is critical, we performed optogenetic stimulation of NAc-DA in open-loop (randomly timed) during defeat or timed to specific behaviors using real-time pose-tracking and behavioral classification. We find that both open-loop DA activation and fighting-back-timed activation promote resilience, in both cases reorganizing behavior during defeat toward resilience-associated patterns. Attack offset-timed activation promotes avoidance during defeat but does not promote susceptibility afterwards. Together, these data suggest a model whereby, during stress, DA in the NAc can increase resilience primarily by elevating the subjective value of the stressor rather than by reinforcing particular stress-responsive behaviors.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • https://github.com/lwillmore/QuantifyingDefeat/

Copyright 
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 March 19, 2022.
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Behavioral and dopaminergic signatures of resilience
Lindsay Willmore, Courtney Cameron, John Yang, Ilana Witten, Annegret Falkner
bioRxiv 2022.03.18.484885; doi: https://doi.org/10.1101/2022.03.18.484885
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Behavioral and dopaminergic signatures of resilience
Lindsay Willmore, Courtney Cameron, John Yang, Ilana Witten, Annegret Falkner
bioRxiv 2022.03.18.484885; doi: https://doi.org/10.1101/2022.03.18.484885

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