Table 1.
Description of the training protocol.
Fig 1.
Effects of aerobic exercise on LV dilation and LV systolic function after TAC.
(a) Representative M-mode echocardiographic images were taken at the level of the papillary muscle, where left ventricular diameters can be measured. Quantification of the left ventricular end diastolic diameter (LVEDd) (b), left ventricular end systolic diameter (LVESd) (c), left ventricular ejection fraction (EF) (d) and fractional shortening (FS) (e) 10 weeks after TAC. (b) (c) (d) (e) (n = 12 per group. *P<0.05 vs. SHAM. #P<0.05 vs. SHAM and TAC).
Fig 2.
Effects of aerobic exercise on cardiomyocyte cross sectional area and fibrosis induced by TAC.
(a) Representative Masson’s trichrome staining revealed left ventricular fibrosis 9 weeks after exercise training. Red indicates viable myocardium; blue indicates fibrosis. Scale bar represents 20 μm. (b) Representative WGA staining revealed cardiomyocyte cross sectional area. Green fluorescence delineate cardiomyocyte membranes (c) Quantitative analysis of cardiomyocyte cross sectional area (n = 100 per group. *P<0.05 vs. SHAM and TAC+E. †P<0.05 vs. SHAM). (d) Quantitative analysis of the fibrotic area (n = 20 per group.*P<0.05 vs. SHAM and TAC+E. †P<0.05 vs. SHAM).
Fig 3.
Effect of aerobic exercise on cardiac hypertrophy after TAC.
(a) Representative heart weight to body weight ratio 10 weeks after TAC. (n = 12 per group. *P<0.05 vs. SHAM and TAC+E. †P<0.05 vs. SHAM). Quantification of calculated left ventricular mass (LVM) (b), left ventricular end systolic posterior wall (LVPWS) (c), and interventricular septum end systolic thickness (IVSS) (d) 10 weeks after TAC. (b) (c) (d) (n = 12 per group. *P<0.05 vs. SHAM. #P<0.05 vs. TAC and SHAM).
Fig 4.
Effect of aerobic exercise on catecholamine levels after TAC.
The plasma catecholamine levels determined by enzyme-linked immunosorbent assay (ELISA). (a) Quantitative of the plasma catecholamine levels at basal. (n = 5 per group. *P<0.05 vs. SHAM. †P <0.05 vs. TAC) (b) Quantification analysis of the plasma catecholamine levels right after exercise. (n = 5 per group. *P<0.05 vs. basal).
Fig 5.
Effects of aerobic exercise on the expression of β-AR subtypes after TAC.
(a) Representative immunoblots of β1-AR, β2-AR and β3-AR in the SHAM, SHAM+E, TAC and TAC+E groups. (b) Semiquantitative analysis of β1-AR, β2-AR and β3-AR expression (n = 6 per group. *P<0.05 vs. SHAM and TAC+E. †P<0.05 vs. SHAM).
Fig 6.
Aerobic exercise increases cardiac NO production and decreases oxidative stress after TAC.
(a) Representative images of heart sections fluorescently stained for ROS from the SHAM, SHAM+E, TAC and TAC+E groups. Green fluorescence indicates ROS production. Scale bar represents 50 μm. (b) Quantitative analysis of the ROS levels (n = 10 per group. *P<0.05 vs. SHAM and TAC+E. †P<0.05 vs. SHAM). (c) Quantitative analysis of NO production assessed using the nitrate reductase method 10 weeks after TAC. (d) Quantitative analysis of MDA levels assessed using the TBA method. (e) Quantitative analysis of SOD levels assessed using the hydroxylamine method. (c) (d) (e) (n = 8 per group. *P<0.05 vs. SHAM and TAC+E. †P<0.05 vs. SHAM).
Fig 7.
Effects of aerobic exercise on the expression and phosphorylation status of eNOS and nNOS after TAC.
(a) Representative immunoblots of p-eNOS (Ser1177/Ser114), total eNOS, p-nNOS (Ser1412/Ser847) and total nNOS in the SHAM, SHAM+E, TAC and TAC+E groups. Semiquantitative analysis of eNOS and nNOS expression (b) (n = 6 per group. *P<0.05 vs. SHAM. †P<0.05 vs. TAC). Semiquantitative analysis of p-eNOS Ser114 (c), p-eNOS Ser1177 (d), p-nNOS Ser1412 (e), and p-nNOS Ser847 expression (f) (n = 6 per group. *P<0.05 vs. SHAM and TAC+E. †P<0.05 vs. SHAM).
Fig 8.
Cardioprotective effects of aerobic exercise was abolished by β3-AR antagonism.
(a) Representative M-mode echocardiographic images were taken at the level of the papillary muscle, where left ventricular diameters can be measured. (b) Representative heart weight to body weight ratio. (n = 12 per group. *P<0.05 vs. TAC+E). (c) Quantification of calculated left ventricular mass (LVM). Quantification of calculated left ventricular end systolic posterior wall (LVPWS) (d), interventricular septum end systolic thickness (IVSS) (e). (c) (d) (e) (n = 12 per group. *P<0.05 vs. TAC and TAC+E+SR). Quantification of the left ventricular end systolic diameter (LVESd) (f), left ventricular end diastolic diameter (LVEDd) (g), left ventricular ejection fraction (EF) (h) and fractional shortening (FS) (i). (f) (g) (h) (i) (n = 12 per group. *P<0.05 vs. TAC and TAC+E+SR).
Fig 9.
Effects of β3-AR antagonism on myocyte hypertrophy, fibrosis and catecholamine levels.
(a) Representative Masson’s trichrome staining revealed left ventricular fibrosis 9 weeks after exercise training. Red indicates viable myocardium; blue indicates fibrosis. Scale bar represents 20 μm. (b) Representative WGA staining revealed cardiomyocyte cross sectional area. Green fluorescence delineate cardiomyocyte membranes. Scale bar represents 20 μm. (c) Quantitative analysis of the fibrotic area (n = 20 per group. *P<0.05 vs. TAC+E). (d) Quantitative analysis of cardiomyocyte cross sectional area (n = 100 per group. *P<0.05 TAC+E). (e) Quantitative of the plasma catecholamine levels at basal. (n = 5 per group. *P<0.05 vs. TAC) (f) Quantification analysis of the plasma catecholamine levels right after exercise. (n = 5 per group. *P<0.05 vs. basal).
Fig 10.
Effects of SR59230A on cardiac NO production and oxidative stress after aerobic exercise.
(a) Representative images of heart sections fluorescently stained for ROS from the TAC, TAC+E and TAC+E+SR groups. Green fluorescence indicates ROS production. Scale bar represents 50 μm. (b) Quantitative analysis of the ROS levels (n = 10 per group. *P<0.05 vs. TAC+E). (c) Quantitative analysis of NO production assessed using the nitrate reductase method (n = 8 per group. *P<0.05 vs. TAC+E). (d) Quantitative analysis of MDA levels assessed using the TBA method (n = 8 per group. *P<0.05 vs. TAC+E). (e) Quantitative analysis of SOD levels assessed using the hydroxylamine method (n = 8 per group. *P<0.05 vs. TAC+E).
Fig 11.
Aerobic exercise induced β3-AR signaling activation was abolished by SR59230A.
(a) Representative immunoblots of β1-AR, β2-AR and β3-AR in the TAC, TAC+E+SR and TAC+E groups. (b) Representative immunoblots of p-eNOS (Ser1177 /Ser114), total eNOS, p-nNOS (Ser1412/Ser847) and total nNOS levels in the TAC, TAC+E+SR and TAC+E groups. (c) Semiquantitative analysis of β1-AR, β2-AR and β3-AR expression (n = 6 per group. *P<0.05 vs. TAC+E. †P<0.05 vs. TAC+E+SR). (d)Semiquantitative analysis of eNOS and nNOS expression (n = 6 per group. *P<0.05 vs. TAC+E. †P<0.05 vs. TAC). Semiquantitative analysis of p-eNOS Ser114(e), p-eNOS Ser1177 (f), p-nNOS Ser1412 (g) and p-nNOS Ser847 (h) (n = 6 per group. *P<0.05 vs. TAC+E).