<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Owens MY</submitter><funding>NCRR NIH HHS</funding><pagination>447-53</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3970845</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(4)</volume><pubmed_abstract>To evaluate neurological effects of terbutaline, rats were injected with saline, terbutaline (Sigma or American Pharmaceutical Partners (APP™)) at 0.5 mg/kg-d or 10 mg/kg-d between postnatal days (PND) 2-5 or 11-14. Brains collected 24 h after last injection were used to determine corpus-callosum thickness, Purkinje cell and neuronal number in the cerebellum. Ambulation, distance traveled, resting time and time on rotarod were analyzed. Terbutaline (both doses/grades at PND 11-14) decreased corpus-callosum thickness. Ambulation time was significantly decreased in the 10 mg/kg-d (Sigma) and 0.5 mg/kg-d of terbutaline (APP™) (PND 2-5) juvenile-rats and 10 mg/kg-d-Sigma adult-rats, 0.5 mg/kg-d APP™ (PND 11-14) adult-rats. Resting time was increased in both doses of APP™ (PND 2-5) in juvenile-rats, 10 mg/kg-d Sigma adult-rats. 10 mg/kg-d-Sigma (PND 2-5) decreased distance traveled in adult-rats. 0.5 mg/kg-d-Sigma (PND 2-5 and PND 11-14) decreased the time spent on rotarod (30 RPM) in adult-rats. Sigma terbutaline Sigma had 2× as much free base compared to APP™. In conclusion, APP™ terbutaline did not have a deleterious effect on the developing rat brain.</pubmed_abstract><journal>Reproductive toxicology (Elmsford, N.Y.)</journal><pubmed_title>Absence of neurotoxicity with medicinal grade terbutaline in the rat model.</pubmed_title><pmcid>PMC3970845</pmcid><funding_grant_id>P20 RR017701</funding_grant_id><funding_grant_id>RR17701</funding_grant_id><pubmed_authors>Wallace KL</pubmed_authors><pubmed_authors>Owens MY</pubmed_authors><pubmed_authors>Mamoon N</pubmed_authors><pubmed_authors>Bennett WA</pubmed_authors><pubmed_authors>Wyatt-Ashmead J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Absence of neurotoxicity with medicinal grade terbutaline in the rat model.</name><description>To evaluate neurological effects of terbutaline, rats were injected with saline, terbutaline (Sigma or American Pharmaceutical Partners (APP™)) at 0.5 mg/kg-d or 10 mg/kg-d between postnatal days (PND) 2-5 or 11-14. Brains collected 24 h after last injection were used to determine corpus-callosum thickness, Purkinje cell and neuronal number in the cerebellum. Ambulation, distance traveled, resting time and time on rotarod were analyzed. Terbutaline (both doses/grades at PND 11-14) decreased corpus-callosum thickness. Ambulation time was significantly decreased in the 10 mg/kg-d (Sigma) and 0.5 mg/kg-d of terbutaline (APP™) (PND 2-5) juvenile-rats and 10 mg/kg-d-Sigma adult-rats, 0.5 mg/kg-d APP™ (PND 11-14) adult-rats. Resting time was increased in both doses of APP™ (PND 2-5) in juvenile-rats, 10 mg/kg-d Sigma adult-rats. 10 mg/kg-d-Sigma (PND 2-5) decreased distance traveled in adult-rats. 0.5 mg/kg-d-Sigma (PND 2-5 and PND 11-14) decreased the time spent on rotarod (30 RPM) in adult-rats. Sigma terbutaline Sigma had 2× as much free base compared to APP™. In conclusion, APP™ terbutaline did not have a deleterious effect on the developing rat brain.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 May</publication><modification>2025-04-04T01:27:05.676Z</modification><creation>2019-03-27T01:24:13Z</creation></dates><accession>S-EPMC3970845</accession><cross_references><pubmed>21262341</pubmed><doi>10.1016/j.reprotox.2011.01.001</doi></cross_references></HashMap>