Key result
Cardiac chronotropic sensitivity to isoprenaline was reduced in elderly compared with young subjects before autonomic blockade but was similar after blockade.
Why the study?
Does autonomic blockade alter cardiac beta-adrenergic chronotropic responsiveness to isoprenaline differently in healthy young, healthy elderly, and endurance-trained elderly subjects?
Cross-Sectional (n=27)
Does autonomic blockade alter cardiac beta-adrenergic chronotropic responsiveness to isoprenaline differently in healthy young, healthy elderly, and endurance-trained elderly subjects?
The age-associated reduction in cardiac chronotropic responses to beta-agonists is primarily due to reflex cardiovascular responses rather than a true reduction in cardiac beta-adrenergic sensitivity.
Answers are grounded in this paper and cite their sources.
Reflex mechanisms predominate in age-related chronotropic decline; leaves open relevance to β-agonist use in patients.
Cardiac chronotropic responses to isoprenaline are reduced with ageing in man. It is unclear whether this is due to reduced cardiac β-adrenergic sensitivity or to age-associated differences in reflex cardiovascular responses to the vasodilatory effects of isoprenaline. Age-associated changes in physical activity are also reported to influence β-adrenergic sensitivity. 2. The aim of the present study was to determine the contribution of alterations in reflex changes in parasympathetic and sympathetic influences and physical fitness to the age-associated reduction in cardiac chronotropic responses to β-adrenergic agonists. 3. The effect of ‘autonomic blockade’ with atropine (40 μg/kg intravenously) and clonidine (4 μg/kg intravenously) on blood pressure, heart rate and chronotropic responses to intravenous bolus isoprenaline doses was determined in eight healthy young (mean age 21 years), nine healthy elderly (72 years) and 10 endurance-trained elderly (69 years) subjects. 4. Elderly subjects had a reduced increase in heart rate after atropine (young, 49 ± 9 beats/min; elderly, 36 ± 5 beats/min; endurance-trained elderly, 34 ± 12 beats/min; P < 0.01) and did not demonstrate the transient increase in systolic blood pressure after clonidine observed in young subjects (young, 11 ± 10 mmHg; elderly, −12 ± 16 mmHg; endurance-trained elderly, −18 ± 11 mmHg; P < 0.01). 5. Cardiac chronotropic sensitivity to isoprenaline after ‘autonomic blockade’ increased in the young but decreased in the elderly subjects. The isoprenaline dose that increased heart rate by 25 beats/min before and after autonomic blockade' was: young, before 1.6 μg, after 2.8 μg, P < 0.01 (geometric mean, paired test); elderly, before 6.9 μg, after 3.6 μg, P < 0.05; endurance-trained elderly, before 5.9 μg, after 4.0 μg, P < 0.05. Cardiac chronotropic sensitivity to isoprenaline was significantly reduced in elderly compared with young subjects before (P < 0.01) but was similar after (P = 0.09) ‘autonomic blockade’. Chronotropic sensitivity did not differ between healthy and endurance-trained elderly subjects before or after ‘autonomic blockade’. 6. The age-associated reduction in cardiac chronotropic responses to bolus isoprenaline is primarily due to an age-related reduction in the influence of reflex cardiovascular responses on heart rate and not to an age-related reduction in cardiac β-adrenergic sensitivity. Endurance training is not associated with altered β-adrenergic chronotropic sensitivity in the elderly. The transient pressor response to intravenously administered clonidine may be lost in ageing man.
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Ford et al. (1994) conducted a cross-sectional in Healthy (n=27). Autonomic blockade (atropine and clonidine) vs. Baseline (before autonomic blockade) and between age groups was evaluated on Isoprenaline dose required to increase heart rate by 25 beats/min (p=<0.01). Cardiac chronotropic sensitivity to isoprenaline was reduced in elderly compared with young subjects before autonomic blockade but was similar after blockade.
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