<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Leyrer-Jackson JM</submitter><funding>NIAAA NIH HHS</funding><funding>National Institutes of Health</funding><pagination>108674</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8475285</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>195</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Alcohol abuse is a worldwide public health concern and leads to an estimated 90,000 alcohol-related deaths in the United States annually. Alcohol may promote its euphoric and motivational effects, in part, by activating the endogenous opioid system. Pro-opiomelanocortin (POMC) producing neurons located within the arcuate nucleus (ArcN) of the hypothalamus make up one circuit of the endogenous opioid system, and heavily projects to reward-related brain areas such as the amygdala, nucleus accumbens (NAc) and ventral tegmental area (VTA). POMC producing neurons release β-endorphin and other peptides that target opioid receptors within reward areas to elicit their associated rewarding effects. Here we explore ArcN POMC neuronal activation, as assessed via FosB expression, fo</pubmed_abstract><journal>Neuropharmacology</journal><pubmed_title>Alcohol consumption preferentially activates a subset of pro-opiomelanocortin (POMC) producing neurons targeting the amygdala.</pubmed_title><pmcid>PMC8475285</pmcid><funding_grant_id>F32 AA027962</funding_grant_id><funding_grant_id>F32AA027962-01</funding_grant_id><funding_grant_id>R01 AA025590</funding_grant_id><funding_grant_id>R01AA025590</funding_grant_id><pubmed_authors>Leyrer-Jackson JM</pubmed_authors><pubmed_authors>Hood LE</pubmed_authors><pubmed_authors>Olive MF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Alcohol consumption preferentially activates a subset of pro-opiomelanocortin (POMC) producing neurons targeting the amygdala.</name><description>&lt;h4>Background&lt;/h4>Alcohol abuse is a worldwide public health concern and leads to an estimated 90,000 alcohol-related deaths in the United States annually. Alcohol may promote its euphoric and motivational effects, in part, by activating the endogenous opioid system. Pro-opiomelanocortin (POMC) producing neurons located within the arcuate nucleus (ArcN) of the hypothalamus make up one circuit of the endogenous opioid system, and heavily projects to reward-related brain areas such as the amygdala, nucleus accumbens (NAc) and ventral tegmental area (VTA). POMC producing neurons release β-endorphin and other peptides that target opioid receptors within reward areas to elicit their associated rewarding effects. Here we explore ArcN POMC neuronal activation, as assessed via FosB expression, fo</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-04-19T05:57:07.805Z</modification><creation>2025-04-19T05:57:07.805Z</creation></dates><accession>S-EPMC8475285</accession><cross_references><pubmed>34153315</pubmed><doi>10.1016/j.neuropharm.2021.108674</doi></cross_references></HashMap>