Abstract
Approach-avoidance conflict is induced when an organism encounters a stimulus that carries both positive and negative attributes. Accumulating evidence implicates the ventral hippocampus (VH) in the detection and resolution of approach-avoidance conflict, largely on the basis of maze-based tasks assaying innate and conditioned responses to situations of conflict. However, its role in discrete trial approach-avoidance decision-making has yet to be elucidated. In this study, we designed a novel cued operant conflict decision-making task in which rats were required to choose and respond for a low reward option or high reward option paired with varying shock intensities on a differential reinforcement of low rates of responding schedule. Post training, the VH was chemogenetically inhibited while animals performed the task with the usual outcomes delivered, and with the presentation of cues associated with the reward vs. conflict options only (extinction condition). We found that VH inhibition led to an avoidance of the conflict option and longer latency to choose this option when decision-making was being made on the basis of cues alone with no outcomes. Consistent with these findings, VH-inhibited animals spent more time in the central component of the elevated plus maze (EPM), indicating a potential deficit in decision-making under innate forms of approach-avoidance conflict. Taken together, these findings implicate the VH in cue-driven approach-avoidance decisions in the face of motivational conflict.
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Acknowledgements
We are grateful to Dr. Maithe Arruda Carvalho for providing the training and use of her Nikon-Ni U fluorescent microscope.
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Conceptualization, BC, RI; methodology, BC, RI; data collection, BC, SR, EY; data analysis, BC; visualization, BC, RI; writing, review, and editing, BC, ACHL, RI.
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Çavdaroğlu, B., Riaz, S., Yeung, E.H.L. et al. The ventral hippocampus is necessary for cue-elicited, but not outcome driven approach-avoidance conflict decisions: a novel operant choice decision-making task. Neuropsychopharmacol. 46, 632–642 (2021). https://doi.org/10.1038/s41386-020-00898-z
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DOI: https://doi.org/10.1038/s41386-020-00898-z
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