PT  - JOURNAL ARTICLE
AU  - Lindsay Willmore
AU  - Courtney Cameron
AU  - John Yang
AU  - Ilana Witten
AU  - Annegret Falkner
TI  - Behavioral and dopaminergic signatures of resilience
AID  - 10.1101/2022.03.18.484885
DP  - 2022 Jan 01
TA  - bioRxiv
PG  - 2022.03.18.484885
4099  - http://biorxiv.org/content/early/2022/03/19/2022.03.18.484885.short
4100  - http://biorxiv.org/content/early/2022/03/19/2022.03.18.484885.full
AB  - 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 StatementThe authors have declared no competing interest.