Kwak, Hyo Bum (2008-05). Exercise training regulation of extracellular matrix and remodeling in the aging rat heart. Doctoral Dissertation. Thesis uri icon

abstract

  • Aging is characterized by a progressive impairment of cardiac structure and function. The cardiac remodeling involves loss of cardiac myocytes, reactive hypertrophy of the remaining cells, and increased extracellular matrix (ECM) and fibrosis in the aging heart. In contrast, exercise training not only improves cardiac function, but also reduces the risk of heart disease. However, the ability of exercise training to modulate ECM and remodeling in the aging heart remains unknown. Therefore, the purpose of this study was to determine the effects of exercise training on ECM remodeling in the aging heart. We hypothesized that (1) exercise training would attenuate age-related changes in left ventricle morphology including extramyocyte space and collagen contents, and (2) exercise training would ameliorate age-induced changes in ECM-related factors including MMPs, TIMPs, TNF-?, TGF-?1, and ?-SMA in the heart. Three and 31 month old Fischer 344 x Brown Norway F1 hybrid rats were assigned to four groups: young sedentary (YS), young exercise-trained (YE), old sedentary (OS), and old exercise-trained (OE). Exercise training groups walked briskly on a treadmill for 45 min/day (12? incline) at 20m/min (young) or 10 m/min (old), 5 d/wk for 12 wk. We found that endurance exercise training might ameliorate the ageinduced increase in extramyocyte space and collagen contents of the left ventricle. Exercise training might protect against age-induced fibrosis by increasing MMP-2, MMP-14 in the soluble fraction and MMP-1, MMP-3, MMP-14 in the insoluble fraction of old rat hearts. Conversely, exercise training might reduce the fibrosis by decreasing TIMP-1 in the soluble fraction of old rat hearts. Further, exercise training reduced potential upstream pro-fibrotic mediators including TNF-? and TGF-?1 in the aging rat hearts. These results are the first to demonstrate that exercise training has a protective effect against age-induced extracellular collagen matrix remodeling in the aging heart, associated with increased MMP-1, -2, -3, -14 and decreased TIMP-1, TNF-?, and TGF- ?1.
  • Aging is characterized by a progressive impairment of cardiac structure and
    function. The cardiac remodeling involves loss of cardiac myocytes, reactive
    hypertrophy of the remaining cells, and increased extracellular matrix (ECM) and
    fibrosis in the aging heart. In contrast, exercise training not only improves cardiac
    function, but also reduces the risk of heart disease. However, the ability of exercise
    training to modulate ECM and remodeling in the aging heart remains unknown.
    Therefore, the purpose of this study was to determine the effects of exercise training on
    ECM remodeling in the aging heart. We hypothesized that (1) exercise training would
    attenuate age-related changes in left ventricle morphology including extramyocyte space
    and collagen contents, and (2) exercise training would ameliorate age-induced changes
    in ECM-related factors including MMPs, TIMPs, TNF-?, TGF-?1, and ?-SMA in the
    heart. Three and 31 month old Fischer 344 x Brown Norway F1 hybrid rats were
    assigned to four groups: young sedentary (YS), young exercise-trained (YE), old sedentary (OS), and old exercise-trained (OE). Exercise training groups walked briskly
    on a treadmill for 45 min/day (12? incline) at 20m/min (young) or 10 m/min (old), 5
    d/wk for 12 wk. We found that endurance exercise training might ameliorate the ageinduced
    increase in extramyocyte space and collagen contents of the left ventricle.
    Exercise training might protect against age-induced fibrosis by increasing MMP-2,
    MMP-14 in the soluble fraction and MMP-1, MMP-3, MMP-14 in the insoluble fraction
    of old rat hearts. Conversely, exercise training might reduce the fibrosis by decreasing
    TIMP-1 in the soluble fraction of old rat hearts. Further, exercise training reduced
    potential upstream pro-fibrotic mediators including TNF-? and TGF-?1 in the aging rat
    hearts. These results are the first to demonstrate that exercise training has a protective
    effect against age-induced extracellular collagen matrix remodeling in the aging heart,
    associated with increased MMP-1, -2, -3, -14 and decreased TIMP-1, TNF-?, and TGF-
    ?1.

publication date

  • May 2008