The activation of CB1 and CB2 inhibits the formation of intracellular cAMP, that's why resulting in a huge reduction of the excitatory influence within the neurons [88,89]. Moreover, the activation of CB2 can further more prevent the mast mobile degranulation and the release of pro-inflammatory mediators, generating the reduction https://manuelgdwmd.jts-blog.com/26508342/the-ultimate-guide-to-block-pain-receptors-with-proleviate