Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677184
Title: The role of epicardial adipose tissue adipokines in the genesis of postoperative atrial fibrillation
Author: Viviano , Alessandro
ISNI:       0000 0004 5368 4303
Awarding Body: St George's, University of London
Current Institution: St George's, University of London
Date of Award: 2015
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Abstract:
Objectives: We aim to explore the Epicardial Adipose Tissue (EAT) proteome to identify its role in the genesis of postoperative atrial fibrillation (AF). Methods: EAT samples were collected in 76 patients with no history of AF undergoing CABG. 50 were incubated in culture medium. Conditioned media representing EAT secretome were harvested and proteins extracted from the remaining tissues. Samples were analysed by two-dimensional difference in-gel electrophoresis (2D-DIGE) and high-performance liquid chromatographytandem mass spectrometry (HPLC-MSIMS). Gene expression analysis was performed on 24 samples (8 AF vs. 16 controls). Findings were validated by Western blotting. Results: 20 secretome samples (10 vs. 10) and 12 EAT extracts (6 vs. 6), divided according to development of postoperative AF, were analysed by proteomics. The proteomics analysis returned 35 differentially expressed protein spots in the secretome and 16 differentially expressed protein spots in the EAT extracts (p 1.2). Gelsolin (GSN) was significantly reduced in AF (p=O.03). Dimethylarginine dimethylaminohydrolase 2 (DDAH2) was upregulated in AF (p=O.04). SBP1 was increased in AF for the secretome and reduced in the EAT extracts. Catalase (CATA) was downregulated in AF. GSN was consistently found to be downregulated in the AF group by three independent techniques. Conclusions. Systemic inflammatory response to cardiac surgery and oxidative stress are known triggers for AF. GSN exerts antinflammatory properties by severing actin filaments. DDAH2 degrades nitric oxide synthase inhibitor ADMA (asymmetric dimethylarginine), known to increase oxidative stress.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (M.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.677184  DOI: Not available
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