4.6 Article

The modulation of striatonigral and nigrotectal pathways by CB1 signalling in the substantia nigra pars reticulata regulates panic elicited in mice by urutu-cruzeiro lancehead pit vipers

Journal

BEHAVIOURAL BRAIN RESEARCH
Volume 401, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bbr.2020.112996

Keywords

Substantia nigra pars reticulata (SNpr); Deep layers of the superior colliculus (dlSC); Nigrotectal pathway; Anandamide; Prey vs urutu-cruzeiro lancehead pit viper paradigm; Innate fear

Funding

  1. Conselho Nacional de Pesquisa e Desenvolvimento Tecnologico (CNPq) [470119/2004-7, 427397/2018-9]
  2. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2007/01174-1, 2012/03798-0, 2017/11855-8]
  3. University of Sao Paulo (USP) Research Grant (NAP-USP-NuPNE) [IaPq2012-156-USP12.1.25440.01.6]
  4. German-Israeli Foundation for Scientific Research and Development (GIF) [I-1442421.13/2017]

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This study investigated the role of the cannabinoid receptor type 1 (CB1R) in the substantia nigra pars reticulata (SNpr) in modulating fear responses in mice facing pit vipers. The results indicate that CB1R in the SNpr may regulate the defensive behaviors of mice in threatening situations by modulating the activity of GABAergic neurons from the striatum in this region.
Cannabinoid receptor type 1 (CB1R) is widely distributed in the substantia nigra pars reticulata (SNpr). However, the role of CB1R at the SNpr level in threatening situations is poorly understood. We investigated the role of CB1R in the SNpr on the expression of fear responses in mice confronted with urutu-cruzeiro pit vipers. First, a bidirectional neumtracer was injected into the SNpr; then, immunostaining of the vesicular GABA transporter was conducted at the levels of the striatum (CPu) and deep layers of the superior colliculus (d1SC). In addition, CB1R immunostaining and GABA labelling were performed in the SNpr. Using a prey-versus-snake paradigm, mice were pretreated with the CB1R antagonist AM251 (100 pmol) and treated with the endocannabinoid anandamide (AEA, 5 pmol) in the SNpr, followed by bicuculline (40 ng) in the dlSC, and were then confronted with a snake. Bidirectional neural tract tracers associated with immunofluorescence showed the GABAergic striatonigral disinhibitory and nigrotectal inhibitory pathways. Furthermore, we showed that CB1R labelling was restricted to axonal fibres surrounding SNpr GABAergic cells. We also demonstrated a decrease in the defensive behaviours of mice treated with AEA in the SNpr, but this effect was blocked by pre-treatment with AM251 in this structure. Taken together, our results show that the panicolytic consequences of the AEA enhancement in the SNpr are signalled by CB1R, suggesting that CB1R localised in axon terminals of CPu GABAergic neurons in the SNpr modulates the activity of the nigrotectal GABAergic pathway during the expression of defensive behaviours in threatening situations.

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