4.8 Article

Distinct circuits in rat central amygdala for defensive behaviors evoked by socially signaled imminent versus remote danger

Journal

CURRENT BIOLOGY
Volume 31, Issue 11, Pages 2347-+

Publisher

CELL PRESS
DOI: 10.1016/j.cub.2021.03.047

Keywords

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Funding

  1. European Research Council [H 415148]
  2. National Science Center [2013/08/W/NZ4/00691, 2012/05/D/NZ3/02085, 2013/11/B/NZ3/01560]
  3. ANIMOD project within the Team Tech Core Facility Plus program of the Foundation for Polish Science
  4. European Union under the European Regional Development Fund

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Animals exhibit various defensive responses to threats, which can also be influenced by the behavior of fearful conspecifics. Research shows that observing a partner undergoing aversive stimulation triggers passive defensive responses, while interacting with a partner that has just undergone aversive stimulation prompts active exploration in animals. The study suggests that the responses of observer animals to social triggers are caused by changes in their affective state rather than mimicry, and that different populations of neurons in the central amygdala are involved in promoting passive or active defensive responses.
Animals display a rich repertoire of defensive responses adequate to the threat proximity. In social species, these reactions can be additionally influenced by the behavior of fearful conspecifics. However, the majority of neuroscientific studies on socially triggered defensive responses focuses on one type of behavior, freezing. To study a broader range of socially triggered reactions and underlying mechanisms, we directly compared two experimental paradigms, mimicking occurrence of the imminent versus remote threat. Observation of a partner currently experiencing aversive stimulation evokes passive defensive responses in the observer rats. Similar interaction with a partner that has just undergone the aversive stimulation prompts animals to increase active exploration. Although the observers display behaviors similar to those of the aversively stimulated demonstrators, their reactions are not synchronized in time, suggesting that observers' responses are caused by the change in their affective state rather than mimicry. Using opsins targeted to behaviorally activated neurons, we tagged central amygdala (CeA) cells implicated in observers' responses to either imminent or remote threat and reactivated them during the exploration of a novel environment. The manipulation revealed that the two populations of CeA cells promote passive or active defensive responses, respectively. Further experiments confirmed that the two populations of cells at least partially differ in expression of molecular markers (protein kinase C-delta [PKC-delta] and corticotropin-releasing factor [CRF]) and connectivity patterns (receiving input from the basolateral amygdala or from the anterior insula). The results are consistent with the literature on single subjects' fear conditioning, suggesting that similar neuronal circuits control defensive responses in social and non-social contexts.

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