Abstract Acetaldehyde is the main metabolite of ethanol ingested through alcoholic beverages. Traditionally considered aversive is presently being viewed as an activating agent of the mesolimbic dopamine system but underlying mechanisms are only partially known. Here we show that acetaldehyde-induced increase in firing rate, burst firing and spikes/burst of antidromically-identified ventro-tegmental area Nucleus Accumbens-projecting neurons are abolished by pretreatment with the opiate unselective antagonist naltrexone (1mg/kg/ip). Similar effects are obtained after administration of naloxone (0.1mg/kg/iv). These results indicate: 1) endogenous opiate system(s) participate in acetaldehyde-induced increments in dopaminergic neuronal activity. 2) These results may explain the reduction in acetaldehyde-induced dopamine release in the nucleus accumbens after blockade of opiate receptors. 3) These findings may offer hints for devising new therapies aimed at reducing alcohol intake and abuse. Considering the paucity of efficacious therapies in alcoholism, acetaldehyde should be considered as a biomarker potentially useful to develop new strategies in the search for effective compounds aimed at reducing excessive alcohol intake, abuse and ultimately alcoholism.
(2014). Naltrexone antagonizes acetaldehyde-induced increments in dopamine neurons activity. (Tesi di dottorato, Università degli Studi di Palermo, 2014).
Naltrexone antagonizes acetaldehyde-induced increments in dopamine neurons activity
DIANA, Marco
2014-03-17
Abstract
Abstract Acetaldehyde is the main metabolite of ethanol ingested through alcoholic beverages. Traditionally considered aversive is presently being viewed as an activating agent of the mesolimbic dopamine system but underlying mechanisms are only partially known. Here we show that acetaldehyde-induced increase in firing rate, burst firing and spikes/burst of antidromically-identified ventro-tegmental area Nucleus Accumbens-projecting neurons are abolished by pretreatment with the opiate unselective antagonist naltrexone (1mg/kg/ip). Similar effects are obtained after administration of naloxone (0.1mg/kg/iv). These results indicate: 1) endogenous opiate system(s) participate in acetaldehyde-induced increments in dopaminergic neuronal activity. 2) These results may explain the reduction in acetaldehyde-induced dopamine release in the nucleus accumbens after blockade of opiate receptors. 3) These findings may offer hints for devising new therapies aimed at reducing alcohol intake and abuse. Considering the paucity of efficacious therapies in alcoholism, acetaldehyde should be considered as a biomarker potentially useful to develop new strategies in the search for effective compounds aimed at reducing excessive alcohol intake, abuse and ultimately alcoholism.File | Dimensione | Formato | |
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