<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Erden L</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Canadian Institutes of Health Research</funding><pagination>1025-1041</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11528876</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>38(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Mechanisms underlying psychostimulant euphoria remain poorly understood. In adult rats, positive emotional states are associated with alterations in 50-kHz ultrasonic vocalizations (USVs): specifically, "trill" calls are promoted over "flat" calls. Here, we investigated the effects of acute and repeated cocaine administration, and-based on previous findings with amphetamine-their possible dependence on beta-adrenergic receptors.&lt;h4>Methods&lt;/h4>Adult male Long-Evans rats received intraperitoneal drug or saline injections before daily USV recording. Fourteen 50-kHz call subtypes were analyzed. In Experiments 1 and 2, cocaine (1-10 mg/kg) and propranolol (10 mg/kg) were tested alone. In Experiment 3, propranolol/cocaine interactions were sought within a conditioned place preference (CPP) procedure. Experiment 4 investigated acute and chronic cocaine effects (Phase 1), and propranolol/cocaine interactions either in an open field (Phase 2) or within a CPP procedure (Phase 3).&lt;h4>Results&lt;/h4>In drug-naïve animals, cocaine increased the 50-kHz call rate, with sensitization developing rapidly. After more extended exposure, cocaine now also increased the relative prevalence of trill versus flat calls; effects on other subtypes were also revealed. The beta-blocker propranolol prevented neither cocaine CPP nor cocaine effects on USV emission or locomotion but exerted significant USV-related effects when given alone. CPP magnitude and USV-related measures were uncorrelated.&lt;h4>Conclusions&lt;/h4>With long-term intraperitoneal administration, cocaine can alter the relative prevalence of several 50-kHz call subtypes; its ability to promote trill versus flat calls, in particular, is consistent with a positive affect interpretation. Cocaine's behavioral effects (i.e., USV-related, locomotor, CPP) appear independent of beta-adrenergic receptor activity.</pubmed_abstract><journal>Journal of psychopharmacology (Oxford, England)</journal><pubmed_title>Adult rat ultrasonic vocalizations and reward: Effects of propranolol and repeated cocaine administration.</pubmed_title><pmcid>PMC11528876</pmcid><funding_grant_id>155055</funding_grant_id><funding_grant_id>156045</funding_grant_id><pubmed_authors>Clarke PBS</pubmed_authors><pubmed_authors>Sundarakrishnan A</pubmed_authors><pubmed_authors>Erden L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Adult rat ultrasonic vocalizations and reward: Effects of propranolol and repeated cocaine administration.</name><description>&lt;h4>Background&lt;/h4>Mechanisms underlying psychostimulant euphoria remain poorly understood. In adult rats, positive emotional states are associated with alterations in 50-kHz ultrasonic vocalizations (USVs): specifically, "trill" calls are promoted over "flat" calls. Here, we investigated the effects of acute and repeated cocaine administration, and-based on previous findings with amphetamine-their possible dependence on beta-adrenergic receptors.&lt;h4>Methods&lt;/h4>Adult male Long-Evans rats received intraperitoneal drug or saline injections before daily USV recording. Fourteen 50-kHz call subtypes were analyzed. In Experiments 1 and 2, cocaine (1-10 mg/kg) and propranolol (10 mg/kg) were tested alone. In Experiment 3, propranolol/cocaine interactions were sought within a conditioned place preference (CPP) procedure. Experiment 4 investigated acute and chronic cocaine effects (Phase 1), and propranolol/cocaine interactions either in an open field (Phase 2) or within a CPP procedure (Phase 3).&lt;h4>Results&lt;/h4>In drug-naïve animals, cocaine increased the 50-kHz call rate, with sensitization developing rapidly. After more extended exposure, cocaine now also increased the relative prevalence of trill versus flat calls; effects on other subtypes were also revealed. The beta-blocker propranolol prevented neither cocaine CPP nor cocaine effects on USV emission or locomotion but exerted significant USV-related effects when given alone. CPP magnitude and USV-related measures were uncorrelated.&lt;h4>Conclusions&lt;/h4>With long-term intraperitoneal administration, cocaine can alter the relative prevalence of several 50-kHz call subtypes; its ability to promote trill versus flat calls, in particular, is consistent with a positive affect interpretation. Cocaine's behavioral effects (i.e., USV-related, locomotor, CPP) appear independent of beta-adrenergic receptor activity.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-02T22:14:11.829Z</modification><creation>2025-04-06T14:25:28.853Z</creation></dates><accession>S-EPMC11528876</accession><cross_references><pubmed>39129423</pubmed><doi>10.1177/02698811241268894</doi></cross_references></HashMap>