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• W1981178049 abstract "18-Methoxycoronaridine, a novel iboga alkaloid congener, reduces drug self-administration in animal models of addiction. Previously, we proposed that these effects are mediated by the ability of 18-methoxycoronaridine to inhibit nicotinic α3β4 acetylcholine receptors. In an attempt to identify more potent 18-methoxycoronaridine analogs, we have tested a series of 18-methoxycoronaridine congeners by whole-cell patch clamp recording of HEK 293 cells expressing recombinant nicotinic α3β4 receptors or glutamate NR1/NR2B N-methyl-d-aspartate (NMDA) receptors. The congeners exhibited a range of inhibitory potencies at α3β4 receptors. Five congeners had IC50 values similar to 18-methoxycoronaridine, and all of these were ineffective at NMDA receptors. The congeners also retained their ability to reduce morphine and methamphetamine self-administration. These data are consistent with the importance of nicotinic α3β4 receptors as a therapeutic target to modulate drug seeking. These compounds may constitute a new class of synthetic agents that act via the nicotinic α3β4 mechanism to combat addiction." @default.
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• W1981178049 date "2004-05-01" @default.
• W1981178049 modified "2023-09-27" @default.
• W1981178049 title "Novel iboga alkaloid congeners block nicotinic receptors and reduce drug self-administration" @default.
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• W1981178049 doi "https://doi.org/10.1016/j.ejphar.2004.03.062" @default.
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