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      BML-190 and AM251 act as inverse agonists at the human cannabinoid CB2 receptor: signalling via cAMP and inositol phosphates.

      Febs Letters
      Cell Line, Colforsin, pharmacology, Cyclic AMP, metabolism, Dose-Response Relationship, Drug, Drug Synergism, Humans, Indomethacin, analogs & derivatives, Inositol Phosphates, Ligands, Morpholines, Piperidines, Pyrazoles, Receptors, Cannabinoid, Receptors, Drug, agonists, Second Messenger Systems

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          Abstract

          The aminoalkylindole BML-190 and diarylpyrazole AM251 ligands have previously been shown to bind to cannabinoid CB(2) and CB(1) receptors, respectively. In HEK-293 cells stably expressing the human CB(2) receptor, BML-190 and AM251 potentiated the forskolin-stimulated accumulation of cAMP. Moreover, the CB(2) receptor can interact productively with 16z44, a promiscuous G alpha(16/z) chimera. BML-190 and AM251 reduce the basal levels of inositol phosphate production in cells expressing the CB(2) receptor and 16z44. These results demonstrate that BML-190 and AM251 act as inverse agonists at the human CB(2) receptor acting via G alpha(i/o) and G alpha(q) family-coupled pathways.

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