Key result
Exercise training and metoprolol, alone or combined, significantly improved LV inotropic responses to beta-AR stimulation and restored cardiac beta-AR density in aged rats.
Why the study?
Does exercise training and/or metoprolol improve beta-adrenergic receptor signaling and LV inotropic reserve in aged rats?
RCT (n=50)
randomized
Does exercise training and/or metoprolol improve beta-adrenergic receptor signaling and LV inotropic reserve in aged rats?
Exercise and beta-blockade with metoprolol similarly ameliorate age-dependent impairment of beta-adrenergic receptor signaling and enhance cardiac responsiveness in aged rats.
May support exercise and metoprolol for age-related beta-AR impairment in rodents; leaves open human translation.
Cardiac beta-adrenergic receptor (beta-AR) signaling and left ventricular (LV) responses to beta-AR stimulation are impaired with aging. It is shown that exercise and beta-AR blockade have a favorable effect on cardiac and vascular beta-AR signaling in several cardiovascular diseases. In the present study, we examined the effects of these two different strategies on beta-AR dysregulation and LV inotropic reserve in the aging heart. Forty male Wistar-Kyoto aged rats were randomized to sedentary, exercise (12 wk treadmill training), metoprolol (250 mg.kg(-1).day(-1) for 4 wk), and exercise plus metoprolol treatment protocols. Ten male Wistar-Kyoto sedentary young rats were also used as a control group. Old trained, old metoprolol-treated, and old trained plus metoprolol-treated rats showed significantly improved LV maximal and minimal first derivative of the pressure rise responses to beta-AR stimulation (isoproterenol) compared with old untrained animals. We found a significant reduction in cardiac sarcolemmal membrane beta-AR density and adenylyl cyclase activity in old untrained animals compared with young controls. Exercise training and metoprolol, alone or combined, restored cardiac beta-AR density and G-protein-dependent adenylyl cyclase activation in old rats. Although cardiac membrane G-protein-receptor kinase 2 levels were not upregulated in untrained old compared with young control rats, both exercise and metoprolol treatment resulted in a dramatic reduction of G-protein-receptor kinase 2 protein levels, which is a further indication of beta-AR signaling amelioration in the aged heart induced by these treatment modalities. In conclusion, we demonstrate for the first time that exercise and beta-AR blockade can similarly ameliorate beta-AR signaling in the aged heart, leading to improved beta-AR responsiveness and corresponding LV inotropic reserve.
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Leosco et al. (2007) conducted an RCT in Age-dependent impairment of beta-adrenergic receptor signaling (n=50). Exercise training and metoprolol vs. Sedentary old rats was evaluated on LV maximal and minimal first derivative of the pressure rise responses to beta-AR stimulation. Exercise training and metoprolol, alone or combined, significantly improved LV inotropic responses to beta-AR stimulation and restored cardiac beta-AR density in aged rats.
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