TY - JOUR
T1 - Exercise training normalizes sympathetic outflow by central antioxidant mechanisms in rabbits with pacing-induced chronic heart failure
AU - Gao, Lie
AU - Wang, Wei
AU - Liu, Dongmei
AU - Zucker, Irving H.
PY - 2007/6
Y1 - 2007/6
N2 - BACKGROUND - In a recent study, we demonstrated that an increase in oxidative stress in the rostral ventrolateral medulla plays a critical role in the sympathoexcitation observed in chronic heart failure (CHF). Growing evidence indicates that exercise training evokes an antioxidative effect in CHF. In the present study, we therefore hypothesized that long-term exercise exerts its beneficial effect on autonomic activity in CHF via central antioxidative mechanisms. METHODS AND RESULTS - Experiments were performed on New Zealand White rabbits. All rabbits were instrumented to measure mean arterial pressure, heart rate, and renal sympathetic nerve activity and to test baroreflex sensitivity. Exercise training significantly decreased baseline renal sympathetic nerve activity (65.8±5.2% to 41.3±3.9% of Max [where "Max" is the maximum renal sympathetic nerve activity induced by a 50-mL puff of smoke directed to the external nares of the rabbit], P<0.05) and increased the maximal gain of the baroreflex curves for heart rate (2.2±0.2 to 4.6±0.7 bpm per mm Hg, P<0.01) and renal sympathetic nerve activity (1.9±0.2% to 4.5±0.4% of Max per mm Hg, P<0.01) in CHF rabbits. Exercise training increased expression of CuZn superoxide dismutase (0.3±0.1 to 1.5±0.3 [ratio of CuZn superoxide dismutase to tubulin], P<0.01) and decreased NAD(P)H oxidase subunit gp91 protein expression (1.9±0.2 to 1.2±0.1 [ratio of gp91 to tubulin], P<0.05) in the rostral ventrolateral medulla of CHF rabbits. Central overexpression of CuZn superoxide dismutase dose-dependently decreased baseline renal sympathetic nerve activity (control, 68.5±7.1% of Max; 10 particles of adenovirus, 53.2±4.4% of Max; and 10 particles of adenovirus, 33.7±3.5% of Max; P<0.05) in CHF rabbits. CONCLUSIONS - These results suggest that an upregulation in central antioxidative mechanisms and suppressed central prooxidant mechanisms may contribute to the exercise training-induced beneficial effects on autonomic activity in CHF.
AB - BACKGROUND - In a recent study, we demonstrated that an increase in oxidative stress in the rostral ventrolateral medulla plays a critical role in the sympathoexcitation observed in chronic heart failure (CHF). Growing evidence indicates that exercise training evokes an antioxidative effect in CHF. In the present study, we therefore hypothesized that long-term exercise exerts its beneficial effect on autonomic activity in CHF via central antioxidative mechanisms. METHODS AND RESULTS - Experiments were performed on New Zealand White rabbits. All rabbits were instrumented to measure mean arterial pressure, heart rate, and renal sympathetic nerve activity and to test baroreflex sensitivity. Exercise training significantly decreased baseline renal sympathetic nerve activity (65.8±5.2% to 41.3±3.9% of Max [where "Max" is the maximum renal sympathetic nerve activity induced by a 50-mL puff of smoke directed to the external nares of the rabbit], P<0.05) and increased the maximal gain of the baroreflex curves for heart rate (2.2±0.2 to 4.6±0.7 bpm per mm Hg, P<0.01) and renal sympathetic nerve activity (1.9±0.2% to 4.5±0.4% of Max per mm Hg, P<0.01) in CHF rabbits. Exercise training increased expression of CuZn superoxide dismutase (0.3±0.1 to 1.5±0.3 [ratio of CuZn superoxide dismutase to tubulin], P<0.01) and decreased NAD(P)H oxidase subunit gp91 protein expression (1.9±0.2 to 1.2±0.1 [ratio of gp91 to tubulin], P<0.05) in the rostral ventrolateral medulla of CHF rabbits. Central overexpression of CuZn superoxide dismutase dose-dependently decreased baseline renal sympathetic nerve activity (control, 68.5±7.1% of Max; 10 particles of adenovirus, 53.2±4.4% of Max; and 10 particles of adenovirus, 33.7±3.5% of Max; P<0.05) in CHF rabbits. CONCLUSIONS - These results suggest that an upregulation in central antioxidative mechanisms and suppressed central prooxidant mechanisms may contribute to the exercise training-induced beneficial effects on autonomic activity in CHF.
KW - Exercise
KW - Free radicals
KW - Heart failure
KW - Nervous system, sympathetic
KW - Oxidative stress
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U2 - 10.1161/CIRCULATIONAHA.106.677989
DO - 10.1161/CIRCULATIONAHA.106.677989
M3 - Article
C2 - 17548725
AN - SCOPUS:34250772396
SN - 0009-7322
VL - 115
SP - 3095
EP - 3102
JO - Circulation
JF - Circulation
IS - 24
ER -