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BackgroundCannabinoid receptors and T-type calcium channels are potential targets for treating pain. Here we report on the design… Expand Mu-opioid and CB1-cannabinoid agonists produce analgesia; however, adverse effects limit use of drugs in both classes. Additive… Expand Both natural and synthetic cannabinoid receptor (e.g., CB1) agonists such as Δ9‐THC, WIN 55,212‐2 (WIN‐2), and HU‐210 disrupt… Expand Activation of the sympathetic nervous system is fundamental to the coordinated response to stress or danger. The midbrain… Expand The acute effects of cannabinoid drugs on the synthesis of noradrenaline, dopamine, and serotonin (5-HT) were assessed… Expand The study was undertaken to explore the effect of CP55,940 ((-)-cis-3-[2-Hydroxy4-(1,1-dimethylheptyl) phenyl]-trans-4-(3… Expand The study was undertaken to explore the effect of CP55,940 ((-)-cis-3-[2-hydroxy-4-(1,1-dimethylheptyl)phenyl]-trans-4-(3… Expand The effect of CP55,940, a presumed CB1/CB2 cannabinoid receptor agonist, on intracellular free Ca2+ levels ([Ca2+]i) in Madin… Expand