Literature DB >> 20817828

Low-intensity aerobic interval training attenuates pathological left ventricular remodeling and mitochondrial dysfunction in aortic-banded miniature swine.

Craig A Emter1, Christopher P Baines.   

Abstract

Cardiac hypertrophy in response to hypertension or myocardial infarction is a pathological indicator associated with heart failure (HF). A central component of the remodeling process is the loss of cardiomyocytes via cell death pathways regulated by the mitochondrion. Recent evidence has indicated that exercise training can attenuate or reverse pathological remodeling, creating a physiological phenotype. The purpose of this study was to examine left ventricular (LV) function, remodeling, and cardiomyocyte mitochondrial function in aortic-banded (AB) sedentary (HFSED; n = 6), AB exercise-trained (HFTR, n = 5), and control sedentary (n = 5) male Yucatan miniature swine. LV hypertrophy was present in both AB groups before the start of training, as indicated by increases in LV end-diastolic volume, LV end-systolic volume (LVESV), and LV end-systolic dimension (LVESD). Exercise training (15 wk) prevented further increases in LVESV and LVESD (P < 0.05). The heart weight-to-body weight ratio, LV + septum-to-body weight ratio, LV + septum-to-right ventricle ratio, and cardiomyocyte cross-sectional area were increased in both AB groups postmortem regardless of training status. Preservation of LV function after exercise training, as indicated by the maintenance of fractional shortening, ejection fraction, and mean wall shortening and increased stroke volume, was associated with an attenuation of the increased LV fibrosis (23%) and collagen (36%) observed in HFSED animals. LV mitochondrial dysfunction, as measured by Ca(2+)-induced mitochondrial permeability transition, was increased in HFSED (P < 0.05) but not HFTR animals. In conclusion, low-intensity interval exercise training preserved LV function as exemplified by an attenuation of fibrosis, maintenance of a positive inotropic state, and inhibition of mitochondrial dysfunction, providing further evidence of the therapeutic potential of exercise in a clinical setting.

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Year:  2010        PMID: 20817828      PMCID: PMC2993221          DOI: 10.1152/ajpheart.00578.2010

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  52 in total

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2.  Opening of the mitochondrial permeability transition pore causes depletion of mitochondrial and cytosolic NAD+ and is a causative event in the death of myocytes in postischemic reperfusion of the heart.

Authors:  F Di Lisa; R Menabò; M Canton; M Barile; P Bernardi
Journal:  J Biol Chem       Date:  2000-11-09       Impact factor: 5.157

3.  Effects of exercise training on cardiac function, gene expression, and apoptosis in rats.

Authors:  H Jin; R Yang; W Li; H Lu; A M Ryan; A K Ogasawara; J Van Peborgh; N F Paoni
Journal:  Am J Physiol Heart Circ Physiol       Date:  2000-12       Impact factor: 4.733

4.  Improvement in midwall myocardial shortening with regression of left ventricular hypertrophy.

Authors:  J Mayet; B Ariff; B Wasan; N Chapman; M Shahi; N R Poulter; P S Sever; R A Foale; S A Thom
Journal:  Hypertension       Date:  2000-11       Impact factor: 10.190

5.  Progression from compensated hypertrophy to failure in the pressure-overloaded human heart: structural deterioration and compensatory mechanisms.

Authors:  Stefan Hein; Eyal Arnon; Sawa Kostin; Markus Schönburg; Albrecht Elsässer; Victoria Polyakova; Erwin P Bauer; Wolf-Peter Klövekorn; Jutta Schaper
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6.  Inhibiting mitochondrial permeability transition pore opening at reperfusion protects against ischaemia-reperfusion injury.

Authors:  Derek J Hausenloy; Michael R Duchen; Derek M Yellon
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7.  Antiremodeling effect of long-term exercise training in patients with stable chronic heart failure: results of the Exercise in Left Ventricular Dysfunction and Chronic Heart Failure (ELVD-CHF) Trial.

Authors:  Pantaleo Giannuzzi; Pier Luigi Temporelli; Ugo Corrà; Luigi Tavazzi
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8.  Sanglifehrin A acts as a potent inhibitor of the mitochondrial permeability transition and reperfusion injury of the heart by binding to cyclophilin-D at a different site from cyclosporin A.

Authors:  Samantha J Clarke; Gavin P McStay; Andrew P Halestrap
Journal:  J Biol Chem       Date:  2002-07-02       Impact factor: 5.157

9.  A mechanistic role for cardiac myocyte apoptosis in heart failure.

Authors:  Detlef Wencker; Madhulika Chandra; Khanh Nguyen; Wenfeng Miao; Stavros Garantziotis; Stephen M Factor; Jamshid Shirani; Robert C Armstrong; Richard N Kitsis
Journal:  J Clin Invest       Date:  2003-05       Impact factor: 14.808

Review 10.  Mitochondrial permeability transition pore opening during myocardial reperfusion--a target for cardioprotection.

Authors:  Andrew P Halestrap; Samantha J Clarke; Sabzali A Javadov
Journal:  Cardiovasc Res       Date:  2004-02-15       Impact factor: 10.787

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  28 in total

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Journal:  Age (Dordr)       Date:  2016-01-23

Review 2.  The still uncertain identity of the channel-forming unit(s) of the mitochondrial permeability transition pore.

Authors:  Christopher P Baines; Manuel Gutiérrez-Aguilar
Journal:  Cell Calcium       Date:  2018-05-16       Impact factor: 6.817

3.  Aerobic exercise training in the treatment of non-alcoholic fatty liver disease related fibrosis.

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Journal:  J Physiol       Date:  2016-05-27       Impact factor: 5.182

4.  Chronic exercise training prevents coronary artery stiffening in aortic-banded miniswine: role of perivascular adipose-derived advanced glycation end products.

Authors:  An Ouyang; T Dylan Olver; Craig A Emter; Bradley S Fleenor
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5.  Chronic interval exercise training prevents BKCa channel-mediated coronary vascular dysfunction in aortic-banded miniswine.

Authors:  T Dylan Olver; Jenna C Edwards; Brian S Ferguson; Jessica A Hiemstra; Pamela K Thorne; Michael A Hill; M Harold Laughlin; Craig A Emter
Journal:  J Appl Physiol (1985)       Date:  2018-03-29

6.  Hypercholesterolemia increases mitochondrial oxidative stress and enhances the MPT response in the porcine myocardium: beneficial effects of chronic exercise.

Authors:  Kyle S McCommis; Allison M McGee; M Harold Laughlin; Douglas K Bowles; Christopher P Baines
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-08-24       Impact factor: 3.619

7.  Sex- and age-based differences in the effect of central serotonin on arterial blood pressure regulation.

Authors:  Jennifer L Magnusson; Craig A Emter; Kevin J Cummings
Journal:  J Appl Physiol (1985)       Date:  2020-09-10

8.  Exercise reestablishes autophagic flux and mitochondrial quality control in heart failure.

Authors:  Juliane C Campos; Bruno B Queliconi; Luiz H M Bozi; Luiz R G Bechara; Paulo M M Dourado; Allen M Andres; Paulo R Jannig; Kátia M S Gomes; Vanessa O Zambelli; Cibele Rocha-Resende; Silvia Guatimosim; Patricia C Brum; Daria Mochly-Rosen; Roberta A Gottlieb; Alicia J Kowaltowski; Julio C B Ferreira
Journal:  Autophagy       Date:  2017-08-03       Impact factor: 16.016

9.  Chronic low-intensity exercise attenuates cardiomyocyte contractile dysfunction and impaired adrenergic responsiveness in aortic-banded mini-swine.

Authors:  Jessica A Hiemstra; Adam B Veteto; Michelle D Lambert; T Dylan Olver; Brian S Ferguson; Kerry S McDonald; Craig A Emter; Timothy L Domeier
Journal:  J Appl Physiol (1985)       Date:  2018-01-04

10.  Heart failure with preserved ejection fraction: chronic low-intensity interval exercise training preserves myocardial O2 balance and diastolic function.

Authors:  Kurt D Marshall; Brittany N Muller; Maike Krenz; Laurin M Hanft; Kerry S McDonald; Kevin C Dellsperger; Craig A Emter
Journal:  J Appl Physiol (1985)       Date:  2012-10-25
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