Anti-addictive actions of an iboga alkaloid congener: a novel mechanism for a novel treatment
@article{Maisonneuve2003AntiaddictiveAO, title={Anti-addictive actions of an iboga alkaloid congener: a novel mechanism for a novel treatment}, author={Isabelle M. Maisonneuve and Stanley D. Glick}, journal={Pharmacology Biochemistry and Behavior}, year={2003}, volume={75}, pages={607-618} }
104 Citations
Novel iboga alkaloid congeners block nicotinic receptors and reduce drug self-administration.
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Effect of Iboga Alkaloids on µ-Opioid Receptor-Coupled G Protein Activation
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Evidence regarding the activation of μ-opioid receptor (MOR)-related G proteins by iboga alkaloids is replicated and extended to suggest a novel mechanism of action, and further justify the search for alternative targets of ibogamine skeleton compounds.
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Brain regions mediating α3β4 nicotinic antagonist effects of 18- MC on methamphetamine and sucrose self-administration
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Results are consistent with the hypothesis that 18-MC decreases methamphetamine self-administration by indirectly modulating the dopaminergic mesolimbic pathway via blockade of α3β4 nicotinic receptors in the habenulo-interpeduncular pathway and the basolateral amygdala.
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- Biology, PsychologyPharmacology Biochemistry and Behavior
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Brain regions mediating α3β4 nicotinic antagonist effects of 18-MC on nicotine self-administration.
- Biology, PsychologyEuropean journal of pharmacology
- 2011
Brain regions mediating alpha3beta4 nicotinic antagonist effects of 18-MC on methamphetamine and sucrose self-administration.
- Biology, PsychologyEuropean journal of pharmacology
- 2008
Behavioural Pharmacology of Novel Kappa Opioid Compounds
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This study provides evidence to suggest the involvement of the serotonin system in Sal A and DS1 induced depression and a difference in modulation of serotonin transporter function by novel and traditional KOPr agonists was observed.
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The most recent human clinical trials of potential medications for treatment of cocaine dependence are discussed as well as pre-clinical studies for another promising agent, levo tetrahydropalmatine, whose mechanism remains to be determined.
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