<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Barry J</submitter><pubmed_abstract>Opioids are the most common medications for moderate to severe pain. Unfortunately, they also have addictive properties that have precipitated opioid misuse and the opioid epidemic. In the present study, we examined the effects of acute administration of oxycodone, a μ-opioid receptor (MOR) agonist, on Ca&lt;sup>2+&lt;/sup> transient activity of medium-sized spiny neurons (MSNs) in freely moving animals. Ca&lt;sup>2+&lt;/sup> imaging of MSNs in dopamine D1-Cre mice (expressing Cre predominantly in the direct pathway) or adenosine A2A-Cre mice (expressing Cre predominantly in the indirect pathway) was obtained with the aid of miniaturized microscopes (Miniscopes) and a genetically encoded Cre-dependent Ca&lt;sup>2+&lt;/sup> indicator (GCaMP6f). Systemic injections of oxycodone (3 mg/kg) increased locomotor a</pubmed_abstract><journal>Frontiers in neural circuits</journal><pagination>983323</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9643681</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Dissociable effects of oxycodone on behavior, calcium transient activity, and excitability of dorsolateral striatal neurons.</pubmed_title><pmcid>PMC9643681</pmcid><pubmed_authors>Oikonomou KD</pubmed_authors><pubmed_authors>Levine MS</pubmed_authors><pubmed_authors>Cepeda C</pubmed_authors><pubmed_authors>Barry J</pubmed_authors><pubmed_authors>Peng A</pubmed_authors><pubmed_authors>Yu D</pubmed_authors><pubmed_authors>Golshani P</pubmed_authors><pubmed_authors>Evans CJ</pubmed_authors><pubmed_authors>Yang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dissociable effects of oxycodone on behavior, calcium transient activity, and excitability of dorsolateral striatal neurons.</name><description>Opioids are the most common medications for moderate to severe pain. Unfortunately, they also have addictive properties that have precipitated opioid misuse and the opioid epidemic. In the present study, we examined the effects of acute administration of oxycodone, a μ-opioid receptor (MOR) agonist, on Ca&lt;sup>2+&lt;/sup> transient activity of medium-sized spiny neurons (MSNs) in freely moving animals. Ca&lt;sup>2+&lt;/sup> imaging of MSNs in dopamine D1-Cre mice (expressing Cre predominantly in the direct pathway) or adenosine A2A-Cre mice (expressing Cre predominantly in the indirect pathway) was obtained with the aid of miniaturized microscopes (Miniscopes) and a genetically encoded Cre-dependent Ca&lt;sup>2+&lt;/sup> indicator (GCaMP6f). Systemic injections of oxycodone (3 mg/kg) increased locomotor a</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-25T19:27:09.448Z</modification><creation>2025-04-06T08:01:18.141Z</creation></dates><accession>S-EPMC9643681</accession><cross_references><pubmed>36389179</pubmed><doi>10.3389/fncir.2022.983323</doi></cross_references></HashMap>