<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kandadi MR</submitter><funding>NCRR NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>134</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3520786</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Lethal and edema toxins secreted by Bacillus anthracis during anthrax infection were found to incite serious cardiovascular complications. However, the underlying mechanisms in anthrax lethal toxin-induced cardiac anomalies remain unknown. This study was designed to evaluate the impact of antioxidant enzyme catalase in anthrax lethal toxin-induced cardiomyocyte contractile dysfunction.&lt;h4>Methods&lt;/h4>Wild type (WT) and cardiac-specific catalase overexpression mice were challenged with lethal toxin (2 μg/g, intraperotineally (i.p.)). Cardiomyocyte contractile and intracellular Ca(2+) properties were assessed 18 h later using an IonOptix edge-detection system. Proteasome function was assessed using chymotrypsin-like and caspase-like activities. GFP-LC3 puncta and Western b</pubmed_abstract><journal>BMC medicine</journal><pubmed_title>Cardiac-specific catalase overexpression rescues anthrax lethal toxin-induced cardiac contractile dysfunction: role of oxidative stress and autophagy.</pubmed_title><pmcid>PMC3520786</pmcid><funding_grant_id>5P20 RR016474</funding_grant_id><funding_grant_id>8P20 GM103432-12</funding_grant_id><pubmed_authors>Kandadi MR</pubmed_authors><pubmed_authors>Ren J</pubmed_authors><pubmed_authors>Yu X</pubmed_authors><pubmed_authors>Frankel AE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cardiac-specific catalase overexpression rescues anthrax lethal toxin-induced cardiac contractile dysfunction: role of oxidative stress and autophagy.</name><description>&lt;h4>Background&lt;/h4>Lethal and edema toxins secreted by Bacillus anthracis during anthrax infection were found to incite serious cardiovascular complications. However, the underlying mechanisms in anthrax lethal toxin-induced cardiac anomalies remain unknown. This study was designed to evaluate the impact of antioxidant enzyme catalase in anthrax lethal toxin-induced cardiomyocyte contractile dysfunction.&lt;h4>Methods&lt;/h4>Wild type (WT) and cardiac-specific catalase overexpression mice were challenged with lethal toxin (2 μg/g, intraperotineally (i.p.)). Cardiomyocyte contractile and intracellular Ca(2+) properties were assessed 18 h later using an IonOptix edge-detection system. Proteasome function was assessed using chymotrypsin-like and caspase-like activities. GFP-LC3 puncta and Western b</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Nov</publication><modification>2025-04-26T10:47:16.128Z</modification><creation>2019-03-27T01:01:44Z</creation></dates><accession>S-EPMC3520786</accession><cross_references><pubmed>23134810</pubmed><doi>10.1186/1741-7015-10-134</doi></cross_references></HashMap>