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Beneficial allosteric modulation from the cannabinoid type-1 receptor (CB1R) throughout periaqueductal grey (PAG) antagonizes anti-nociceptive and mobile results of a mu-opioid receptor agonist inside morphine-withdrawn rodents.
Beneficial allosteric modulation from the cannabinoid type-1 receptor (CB1R) throughout periaqueductal grey (PAG) antagonizes anti-nociceptive and mobile results of a mu-opioid receptor agonist inside morphine-withdrawn rodents.