Key result
Aging reduced peak early filling rates at rest and during isoproterenol administration, but the increase in diastolic filling responses to isoproterenol was not reduced with aging.
Why the study?
Does aging or endurance training alter diastolic filling responses to beta-adrenergic stimulation with isoproterenol in healthy men?
Does aging or endurance training alter diastolic filling responses to beta-adrenergic stimulation with isoproterenol in healthy men?
Unlike heart rate and ejection fraction, diastolic filling responses to beta-adrenergic stimulation with isoproterenol are preserved and do not decline with normal cardiac aging.
Answers are grounded in this paper and cite their sources.
Preserved beta-agonist effects on diastolic filling despite age-related resting impairment; leaves open whether training modulates filling dynamics in older adults.
Reduced heart rate and contractile responses to beta-agonist stimulation characterize normal cardiac aging, but whether diastolic responses also decline with aging has not been determined in humans. Diastolic filling responses to isoproterenol were determined in 13 older (60-82 yr) and 11 young (24-32 yr) healthy men before and after endurance training. Filling rates were expressed in three ways: 1) normalized to end-diastolic volume per second, 2) normalized to stroke volume per second, and 3) as absolute milliliters of blood (ml.s-1.m-2). Peak early filling rates by all methods were reduced at rest and all isoproterenol doses with aging (all P < 0.0001 for old vs. young), whereas peak atrial filling rates were increased with aging. During isoproterenol, both peak early and peak atrial filling rates increased significantly (all P < 0.01); the increase in filling rates with isoproterenol was not different with aging (all NS for old vs. young x dose). Endurance training did not augment diastolic filling responses to isoproterenol. Although diastolic filling rates at rest are markedly altered by aging, diastolic filling responses to isoproterenol are not reduced with aging. Thus the age-associated declines in heart rate, ejection fraction, and cardiac output responses to beta-adrenergic stimulation with isoproterenol do not extend to diastolic filling responses.
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Stratton et al. (1994) studied Healthy (n=24). Aging vs. Young healthy men was evaluated on Peak early filling rates at rest and during isoproterenol administration (p=<0.0001). Aging reduced peak early filling rates at rest and during isoproterenol administration, but the increase in diastolic filling responses to isoproterenol was not reduced with aging.
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