4.6 Article

Cannabinoid CB1 Receptor Involvement in the Actions of CBD on Anxiety and Coping Behaviors in Mice

Journal

PHARMACEUTICALS
Volume 15, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/ph15040473

Keywords

cannabidiol; anxiety; depression; cannabinoid receptor 1; cannabinoid receptor 2; G-protein-coupled receptor 55; GABA(A) receptor

Funding

  1. Instituto de Salud Carlos III (Spanish Ministerio de Ciencia e Inovacion) [RD. PI18/00576]
  2. Red de Investigacion en Atencion Primaria de Adicciones [RD21/0009/0008]

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The anxiolytic and antidepressant properties of cannabidiol (CBD) have been evaluated in several studies, but the molecular mechanisms are still unclear. This study found that CBD can modulate emotional disturbances and shows the highest effectiveness at a dose of 20mg/kg in mice. The cannabinoid receptor CB1 plays a significant role in the anxiolytic actions of CBD. CBD also modifies the gene expression of GABA(A) subunits alpha 2 and gamma 2 and CB1r, CB2r and GPR55, supporting a multimodal mechanism of action for CBD.
The anxiolytic and antidepressant properties of cannabidiol (CBD) have been evaluated in several studies. However, the molecular mechanisms involved in these actions remain unclear. A total of 130 male mice were used. CBD's ability to modulate emotional disturbances (anxiety and depressive-like behaviors) was evaluated at different doses in wild-type (CD1; 10, 20 and 30 mg/kg; i.p.) and knockout (CB1KO, CB2KO; GPR55KO; 20 mg/kg) mice. Moreover, CBD effects (20 mg/kg; i.p.) were evaluated in mice previously treated with the CB1r-antagonist SR141716A (2mg/kg; i.p.). Relative gene expression analyses of Cnr1 and Cnr2, Gpr55 and GABA(A)alpha 2 and gamma 2 receptor subunits were performed in the amygdala (AMY) and hippocampus (HIPP) of CD1 mice. CBD (10 and 20 mg/kg) showed anxiolytic and antidepressant actions in CD1 mice, being more effective at 20 mg/kg. Its administration did not induce anxiolytic actions in CB1KO mice, contrary to CB2KO and GPR55KO. In all of them, the lack of cannabinoid receptors did not modify the antidepressant activity of CBD. Interestingly, the administration of the CB1r antagonist SR141716A blocked the anxiolytic-like activity of CBD. Real-time PCR studies revealed a significant reduction in Cnr1 and GABA(A)alpha 2 and gamma 2 gene expression in the HIPP and AMY of CD1 mice treated with CBD. Opposite changes were observed in the Cnr2. Indeed, Gpr55 was increased in the AMY and reduced in the HIPP. CB1r appears to play a relevant role in modulating the anxiolytic actions of CBD. Moreover, this study revealed that CBD also modified the gene expression of GABA(A) subunits alpha 2 and gamma 2 and CB1r, CB2r and GPR55, in a dose- and brain-region-dependent manner, supporting a multimodal mechanism of action for CBD.

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