Lipoxin A4 Preconditioning and Postconditioning Protect Myocardial Ischemia/Reperfusion Injury in Rats. (17th July 2013)

• Record Type: Journal Article
• Authors: Zhao, Qifeng; Shao, Lan; Hu, Xingti; Wu, Guowei; Du, Jie; Xia, Jie; Qiu, Huixian
• Other Names: D'Acquisto Fulvio Academic Editor.
• Is Part Of: Mediators of inflammation. Volume 2013(2013)
• Publication Date: 2013-07-17
• Subjects: Inflammation -- Mediators -- Periodicals; Biological response modifiers -- Periodicals; Inflammation (Pathologie) -- Médiateurs; Immunomodulateurs; Biological response modifiers; Inflammation -- Mediators; Immunology; Autacoids; Immunologic Factors; Cell Adhesion Molecules; Cell Communication; Cytokines; Inflammation; Periodicals; Electronic journals; 616.0473
• DOI: 10.1155/2013/231351
• Languages: English
• ISSNs: 0962-9351

Abstract

Abstract : This study aims to investigate the pre- and postconditioning effects of lipoxin A4 (LXA4 ) on myocardial damage caused by ischemia/reperfusion (I/R) injury. Seventy-two rats were divided into 6 groups: sham groups (C1 and C2 ), I/R groups (I/R1 and I/R2 ), and I/R plus LXA4 preconditioning and postconditioning groups (LX1 and LX2 ). The serum levels of IL-1 β, IL-6, IL-8, IL-10, TNF- α, and cardiac troponin I (cTnI) were measured. The content and the activity of Na + -K + -ATPase as well as the superoxide dismutase (SOD), and malondialdehyde (MDA) levels were determined. Along with the examination of myocardium ultrastructure and ventricular arrhythmia scores (VAS), connexin 43 (Cx43) expression were also detected. Lower levels of IL-1 β, IL-6, IL-8, TNF- α, cTnI, MDA content, and VAS and higher levels of IL-10, SOD activity, Na + -K + -ATPase content and activity, and Cx43 expression appeared in LX groups than I/R groups. Besides, H&E staining, TEM examination as well as analysis of gene, and protein confirmed that LXA4 preconditioning was more effective than postconditioning in preventing arrhythmogenesis via the upregulation of Cx43. That is, LXA4 postconditioning had better protective effect on Na + -K + -ATPase and myocardial ultrastructure.