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Neurosci."],"published-print":{"date-parts":[[2021,2,3]]},"abstract":"<jats:p>\n                    Substance use disorder (SUD) is associated with disruptions in circadian rhythms. The circadian transcription factor neuronal PAS domain protein 2 (NPAS2) is enriched in reward-related brain regions and regulates reward, but its role in SU is unclear. To examine the role of NPAS2 in drug taking, we measured intravenous cocaine self-administration (acquisition, dose\u2013response, progressive ratio, extinction, cue-induced reinstatement) in wild-type (WT) and\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutant mice at different times of day. In the light (inactive) phase, cocaine self-administration, reinforcement, motivation and extinction responding were increased in all\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutants. Sex differences emerged during the dark (active) phase with\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutation increasing self-administration, extinction responding, and reinstatement only in females as well as reinforcement and motivation in males and females. To determine whether circulating hormones are driving these sex differences, we ovariectomized WT and\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutant females and confirmed that unlike sham controls, ovariectomized mutant mice showed no increase in self-administration. To identify whether striatal brain regions are activated in\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutant females, we measured cocaine-induced \u0394FosB expression. Relative to WT, \u0394FosB expression was increased in D1+ neurons in the nucleus accumbens (NAc) core and dorsolateral (DLS) striatum in\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutant females after dark phase self-administration. We also identified potential target genes that may underlie the behavioral responses to cocaine in\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutant females. These results suggest NPAS2 regulates reward and activity in specific striatal regions in a sex and time of day (TOD)-specific manner. Striatal activation could be augmented by circulating sex hormones, leading to an increased effect of\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutation in females.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>SIGNIFICANCE STATEMENT<\/jats:bold>\n                    Circadian disruptions are a common symptom of substance use disorders (SUDs) and chronic exposure to drugs of abuse alters circadian rhythms, which may contribute to subsequent SU. Diurnal rhythms are commonly found in behavioral responses to drugs of abuse with drug sensitivity and motivation peaking during the dark (active) phase in nocturnal rodents. Emerging evidence links disrupted circadian genes to SU vulnerability and drug-induced alterations to these genes may augment drug-seeking. The circadian transcription factor neuronal PAS domain protein 2 (NPAS2) is enriched in reward-related brain regions and regulates reward, but its role in SU is unclear. To examine the role of NPAS2 in drug taking, we measured intravenous cocaine self-administration in wild-type (WT) and\n                    <jats:italic>Npas2<\/jats:italic>\n                    mutant mice at different times of day.\n                  <\/jats:p>","DOI":"10.1523\/jneurosci.1830-20.2020","type":"journal-article","created":{"date-parts":[[2020,12,2]],"date-time":"2020-12-02T17:51:36Z","timestamp":1606931496000},"page":"1046-1058","source":"Crossref","is-referenced-by-count":30,"title":["Circadian-Dependent and Sex-Dependent Increases in Intravenous Cocaine Self-Administration in\n                    <i>Npas2<\/i>\n                    Mutant Mice"],"prefix":"10.1523","volume":"41","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8909-2017","authenticated-orcid":false,"given":"Lauren M.","family":"DePoy","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1751-0598","authenticated-orcid":false,"given":"Darius D.","family":"Becker-Krail","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wei","family":"Zong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kaitlyn","family":"Petersen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Neha M.","family":"Shah","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica H.","family":"Brandon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alyssa M.","family":"Miguelino","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"George C.","family":"Tseng","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8579-015X","authenticated-orcid":false,"given":"Ryan W.","family":"Logan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4719-6197","authenticated-orcid":false,"given":"Colleen 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