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Pericardial adipose and aromatase: A new translational target for aging, obesity and arrhythmogenesis?
Bernasochi, Gabriel B; Boon, Wah Chin; Curl, Claire L; Varma, Upasna; Pepe, Salvatore; Tare, Marianne; Parry, Laura J; Dimitriadis, Evdokia; Harrap, Stephen B; Nalliah, Chrishan J; Kalman, Jonathan M; Delbridge, Lea M D; Bell, James R.
Afiliación
  • Bernasochi GB; Department of Physiology, School of Biomedical Sciences, University of Melbourne, Australia.
  • Boon WC; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
  • Curl CL; Department of Physiology, School of Biomedical Sciences, University of Melbourne, Australia.
  • Varma U; Department of Physiology, School of Biomedical Sciences, University of Melbourne, Australia.
  • Pepe S; Murdoch Children's Research Institute, Department of Cardiology, Royal Children's Hospital, Department of Paediatrics, University of Melbourne, Australia; Department of Surgery, Monash University, Australia.
  • Tare M; Monash Rural Health, Department of Physiology, Monash University, Victoria, Australia.
  • Parry LJ; School of BioSciences, University of Melbourne, Victoria, Australia.
  • Dimitriadis E; Hudson Institute, Clayton, Victoria, Australia.
  • Harrap SB; Department of Physiology, School of Biomedical Sciences, University of Melbourne, Australia.
  • Nalliah CJ; Department of Cardiology, Royal Melbourne Hospital, Department of Medicine, University of Melbourne, Victoria, Australia.
  • Kalman JM; Department of Cardiology, Royal Melbourne Hospital, Department of Medicine, University of Melbourne, Victoria, Australia.
  • Delbridge LMD; Department of Physiology, School of Biomedical Sciences, University of Melbourne, Australia. Electronic address: lmd@unimelb.edu.au.
  • Bell JR; Department of Physiology, School of Biomedical Sciences, University of Melbourne, Australia. Electronic address: belljr@unimelb.edu.au.
J Mol Cell Cardiol ; 111: 96-101, 2017 10.
Article en En | MEDLINE | ID: mdl-28822806
ABSTRACT
A correlation exists between the extent of pericardial adipose and atrial fibrillation (AF) risk, though the underlying mechanisms remain unclear. Selected adipose depots express high levels of aromatase, capable of converting androgens to estrogens - no studies have investigated aromatase occurrence/expression regulation in pericardial adipose. The Women's Health Initiative reported that estrogen-only therapy in women elevated AF incidence, indicating augmented estrogenic influence may exacerbate cardiac vulnerability. The aim of this study was to identify the occurrence of pericardial adipose aromatase, evaluate the age- and sex-dependency of local cardiac steroid synthesis capacity and seek preliminary experimental evidence of a link between pericardial adipose aromatase capacity and arrhythmogenic vulnerability. Both human atrial appendage and epicardial adipose exhibited immunoblot aromatase expression. In rodents, myocardium and pericardial adipose aromatase expression increased >20-fold relative to young controls. Comparing young, aged and aged-high fat diet animals, a significant positive correlation was determined between the total aromatase content of pericardial adipose and the occurrence/duration of triggered atrial arrhythmias. Incidence and duration of arrhythmias were increased in hearts perfused with 17ß-estradiol. This study provides novel report of pericardial adipose aromatase expression. We show that aromatase expression is remarkably upregulated with aging, and aromatase estrogen conversion capacity significantly elevated with obesity-related cardiac adiposity. Our studies suggest an association between adiposity, aromatase estrogenic capacity and atrial arrhythmogenicity - additional investigation is required to establish causality. The potential impact of these findings may be considerable, and suggests that focus on local cardiac steroid conversion (rather than systemic levels) may yield translational outcomes.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pericardio / Arritmias Cardíacas / Envejecimiento / Aromatasa / Tejido Adiposo / Investigación Biomédica Traslacional / Obesidad Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: J Mol Cell Cardiol Año: 2017 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pericardio / Arritmias Cardíacas / Envejecimiento / Aromatasa / Tejido Adiposo / Investigación Biomédica Traslacional / Obesidad Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: J Mol Cell Cardiol Año: 2017 Tipo del documento: Article País de afiliación: Australia