<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schall TA</submitter><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute on Drug Abuse (NIDA)</funding><funding>NIDA NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute on Drug Abuse</funding><funding>NINDS NIH HHS</funding><pagination>9285</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11519475</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>The nucleus accumbens (NAc) regulates reward-motivated behavior, but the temporal dynamics of NAc neurons that enable "free-willed" animals to obtain rewards remain elusive. Here, we recorded Ca&lt;sup>2+&lt;/sup> activity from individual NAc neurons when mice performed self-paced lever-presses for sucrose. NAc neurons exhibited three temporally-sequenced clusters, defined by times at which they exhibited increased Ca&lt;sup>2+&lt;/sup> activity: approximately 0, -2.5 or -5 sec relative to the lever-pressing. Dopamine D1 receptor (D1)-expressing neurons and D2-neurons formed the majority of the -5-sec versus -2.5-sec clusters, respectively, while both neuronal subtypes were represented in the 0-sec cluster. We found that pre-press activity patterns of D1- or D2-neurons could predict subsequent lever-p</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Temporal dynamics of nucleus accumbens neurons in male mice during reward seeking.</pubmed_title><pmcid>PMC11519475</pmcid><funding_grant_id>DA60868</funding_grant_id><funding_grant_id>DA51010</funding_grant_id><funding_grant_id>DA46491</funding_grant_id><funding_grant_id>T32 NS007433</funding_grant_id><funding_grant_id>R01 DA046491</funding_grant_id><funding_grant_id>DA53388</funding_grant_id><funding_grant_id>DA23206</funding_grant_id><funding_grant_id>R21 DA051010</funding_grant_id><funding_grant_id>R01 DA040620</funding_grant_id><funding_grant_id>R01 DA060868</funding_grant_id><funding_grant_id>K99 DA053388</funding_grant_id><funding_grant_id>R01 DA023206</funding_grant_id><funding_grant_id>R00 DA053388</funding_grant_id><funding_grant_id>DA40620</funding_grant_id><funding_grant_id>R37 DA023206</funding_grant_id><pubmed_authors>Alpaugh EE</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Dong Y</pubmed_authors><pubmed_authors>Wright WJ</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Lee BT</pubmed_authors><pubmed_authors>Nestler EJ</pubmed_authors><pubmed_authors>Zhao RJ</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Zeng B</pubmed_authors><pubmed_authors>Schall TA</pubmed_authors><pubmed_authors>Huang YH</pubmed_authors><pubmed_authors>Nieh EH</pubmed_authors><pubmed_authors>Qi X</pubmed_authors><pubmed_authors>Schluter OM</pubmed_authors><pubmed_authors>Li KL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Temporal dynamics of nucleus accumbens neurons in male mice during reward seeking.</name><description>The nucleus accumbens (NAc) regulates reward-motivated behavior, but the temporal dynamics of NAc neurons that enable "free-willed" animals to obtain rewards remain elusive. Here, we recorded Ca&lt;sup>2+&lt;/sup> activity from individual NAc neurons when mice performed self-paced lever-presses for sucrose. NAc neurons exhibited three temporally-sequenced clusters, defined by times at which they exhibited increased Ca&lt;sup>2+&lt;/sup> activity: approximately 0, -2.5 or -5 sec relative to the lever-pressing. Dopamine D1 receptor (D1)-expressing neurons and D2-neurons formed the majority of the -5-sec versus -2.5-sec clusters, respectively, while both neuronal subtypes were represented in the 0-sec cluster. We found that pre-press activity patterns of D1- or D2-neurons could predict subsequent lever-p</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-07-15T17:45:54.775Z</modification><creation>2025-04-04T03:01:33.698Z</creation></dates><accession>S-EPMC11519475</accession><cross_references><pubmed>39468146</pubmed><doi>10.1038/s41467-024-53690-8</doi></cross_references></HashMap>