<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fujita A</submitter><funding>HHS | NIH | National Institute of Mental Health</funding><funding>HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIDDK NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NIH HHS</funding><pagination>9539-9560</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8612477</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(46)</volume><pubmed_abstract>The lateral hypothalamic area (LHA) is a highly conserved brain region critical for maintaining physiological homeostasis and goal-directed behavior. LHA neurons that express melanin-concentrating hormone (MCH) are key regulators of arousal, energy balance, and motivated behavior. However, cellular and functional diversity among LHA&lt;sup>MCH&lt;/sup> neurons is not well understood. Previous anatomic and molecular data suggest that LHA&lt;sup>MCH&lt;/sup> neurons may be parsed into at least two distinct subpopulations, one of which is enriched in neurokinin-3 receptor (NK3R), the receptor for neurokinin B (NKB), encoded by the &lt;i>Tac2&lt;/i> gene. This tachykininergic ligand-receptor system has been implicated in reproduction, fear memory, and stress in other brain regions, but NKB interactions with LHA</pubmed_abstract><journal>The Journal of neuroscience : the official journal of the Society for Neuroscience</journal><pubmed_title>Neurokinin B-Expressing Neurons of the Central Extended Amygdala Mediate Inhibitory Synaptic Input onto Melanin-Concentrating Hormone Neuron Subpopulations.</pubmed_title><pmcid>PMC8612477</pmcid><funding_grant_id>R01 DK118402</funding_grant_id><funding_grant_id>R01 MH112739</funding_grant_id><funding_grant_id>R01DK118402</funding_grant_id><funding_grant_id>R01MH112739</funding_grant_id><funding_grant_id>S10 OD016435</funding_grant_id><pubmed_authors>Antony MS</pubmed_authors><pubmed_authors>Kanoski SE</pubmed_authors><pubmed_authors>Flynn WF</pubmed_authors><pubmed_authors>Fujita A</pubmed_authors><pubmed_authors>Mickelsen LE</pubmed_authors><pubmed_authors>Jackson AC</pubmed_authors><pubmed_authors>Zhong L</pubmed_authors><pubmed_authors>Chamiec-Case E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neurokinin B-Expressing Neurons of the Central Extended Amygdala Mediate Inhibitory Synaptic Input onto Melanin-Concentrating Hormone Neuron Subpopulations.</name><description>The lateral hypothalamic area (LHA) is a highly conserved brain region critical for maintaining physiological homeostasis and goal-directed behavior. LHA neurons that express melanin-concentrating hormone (MCH) are key regulators of arousal, energy balance, and motivated behavior. However, cellular and functional diversity among LHA&lt;sup>MCH&lt;/sup> neurons is not well understood. Previous anatomic and molecular data suggest that LHA&lt;sup>MCH&lt;/sup> neurons may be parsed into at least two distinct subpopulations, one of which is enriched in neurokinin-3 receptor (NK3R), the receptor for neurokinin B (NKB), encoded by the &lt;i>Tac2&lt;/i> gene. This tachykininergic ligand-receptor system has been implicated in reproduction, fear memory, and stress in other brain regions, but NKB interactions with LHA</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-04T19:31:51.072Z</modification><creation>2025-02-19T02:58:13.483Z</creation></dates><accession>S-EPMC8612477</accession><cross_references><pubmed>34642212</pubmed><doi>10.1523/jneurosci.2600-20.2021</doi><doi>10.1523/JNEUROSCI.2600-20.2021</doi></cross_references></HashMap>