Dp. Thomas et al., Collagen gene expression in rat left ventricle: interactive effect of age and exercise training, J APP PHYSL, 89(4), 2000, pp. 1462-1468
Whether or not exercise training of sufficient intensity and duration to pr
oduce left ventricle (LV) hypertrophy also regulates deposition of intersti
tial collagen and cross-linking at the pretranslational level is unknown. T
herefore, the effects of exercise training on gene expression for the two p
rincipal fibrillar collagens in LV, types I and III, were assessed in young
adult (5 mo), middle-aged (15 mo), and old (26 mo) rats. We also evaluated
the potential interaction of changes in mRNA for these procollagens with a
lterations in LV extracellular matrix characteristics by simultaneously mea
suring collagen concentration (hydroxyproline) and extent of mature collage
n cross-linking hydroxylysylpyridinoline, HP). Ten weeks of treadmill runni
ng resulted in LV hypertrophy and an increased maximal oxygen uptake in all
three age groups of trained rats compared with sedentary controls. Percent
collagen in rat LV almost doubled (P < 0.0001) from 5 to 26 mo of age, an
increase unaffected by exercise training. With aging, a significant decline
in expression of mRNAs for both collagen type I (P < 0.005) and type III (
P < 0.001) was observed in LV free wall (LVF) but not septum (LVS). Trainin
g prevented this decline in LVF mRNAs for the two principal fibrillar colla
gens in middle-aged rats whereas it attenuated the decline in senescent ani
mals. KP concentration increased significantly with aging in both LVF (P <
0.005) and LVS (P < 0.01). Training modulated this effect, but again only i
n LVF, so that HP was significantly lower (P < 0.05) in this region of the
LV in old trained rats compared with sedentary counterparts. We conclude th
at exercise training modulates the effects of aging on collagen gene mRNAs
and HP cross-linking regionally within the LV.