Effects of aging on the responsiveness of the human cardiac sympathetic nerves to stressors.

BACKGROUND Aging increases human sympathetic nervous activity at rest. Beause of the probable importance of neural stress responses in the heart as triggers for clinical end points of coronary artery disease, it is pertinent to investigate whether sympathetic nervous responses to stresses are increased by aging. METHODS AND RESULTS We applied kinetic methods for measuring the fluxes to plasma of neurochemicals relevant to sympathetic neurotransmission in younger (aged 20 to 30 years) and older (aged 60 to 75 years) healthy men during mental stress (difficult mental arithmetic), isometric exercise (sustained handgrip), and dynamic exercise (supine cycling). The increase in total norepinephrine spillover to plasma with mental stress was unaffected by age. In contrast, the increase in cardiac norepinephrine spillover was two to three times higher in the older subjects (P < .05). The probable mechanism of this higher cardiac norepinephrine spillover was reduced neuronal reuptake of the transmitter, because age had no influence on the overflow of the norepinephrine precursor, dihydroxyphenylalanine, or intraneuronal metabolite, dihydroxyphenylglycol (levels of these two substances reflect rates of cardiac norepinephrine synthesis and intraneuronal metabolism), and the transcardiac extraction of plasma radiolabeled norepinephrine was lower in the older subjects (P < .05). An almost identical pattern of neurochemical response was seen with isometric exercise. During cycling, total norepinephrine spillover was 16% lower in the older men, but cardiac norepinephrine spillover was 53% higher. CONCLUSIONS Reduced norepinephrine reuptake increases the overflow of the neurotransmitter to plasma from the aging heart during stimulation of the cardiac sympathetic outflow. Failure of transmitter inactivation at postjunctional receptors with aging would amplify the neural signal, and in the presence of myocardial disease could trigger adverse stress-induced cardiovascular events, particularly when accompanied by an age-dependent reduction in vagal tone. Reduction of postsynaptic adrenergic responsiveness with aging, however, might protect against this, as indicated by our finding that in no case was the heart rate increase during stress greater in older men, despite their having larger increases in cardiac norepinephrine spillover.

[1]  J. Taylor,et al.  Sympathoadrenal-circulatory regulation during sustained isometric exercise in young and older men. , 1991, The American journal of physiology.

[2]  D. Goldstein,et al.  In vivo measurement of neuronal uptake of norepinephrine in the human heart. , 1988, Circulation.

[3]  S. Willich,et al.  Physical exertion as a trigger of acute myocardial infarction. Triggers and Mechanisms of Myocardial Infarction Study Group. , 1993, The New England journal of medicine.

[4]  B. Kingwell,et al.  Functional and neurochemical evidence for partial cardiac sympathetic reinnervation after cardiac transplantation in humans. , 1993, Circulation.

[5]  R. Hoeldtke,et al.  Assessment of norepinephrine secretion and production. , 1983, The Journal of laboratory and clinical medicine.

[6]  M. Esler,et al.  Increased cardiac production of dihydroxyphenylalanine (DOPA) during sympathetic stimulation in anaesthetized dogs , 1992, Neurochemistry International.

[7]  Bigger Jt Why patients with congestive heart failure die: arrhythmias and sudden cardiac death. , 1987 .

[8]  J. Halter,et al.  Age differences in plasma norepinephrine kinetics in humans. , 1986, Journal of gerontology.

[9]  I. Meredith,et al.  Increased plasma dihydroxyphenylalanine during sympathetic activation in humans is related to increased norepinephrine turnover. , 1991, The Journal of laboratory and clinical medicine.

[10]  G. Jennings,et al.  Direct determination of homovanillic acid release from the human brain, an indicator of central dopaminergic activity. , 1991, Life sciences.

[11]  P. Korner,et al.  Age-dependence of noradrenaline kinetics in normal subjects. , 1981, Clinical science.

[12]  L. Nalefski,et al.  Action of atropine on the cardiovascular system in normal persons. , 1950, A.M.A. archives of internal medicine.

[13]  P. Korner,et al.  Determination of norepinephrine apparent release rate and clearance in humans. , 1979, Life sciences.

[14]  R. D. Kennedy,et al.  Cardiology in Old Age , 1976, Springer US.

[15]  S. G. Rosen,et al.  Age differences in the plasma clearance mechanisms for epinephrine and norepinephrine in humans. , 1987, The Journal of clinical endocrinology and metabolism.

[16]  J. Rowe,et al.  Enhanced plasma norepinephrine response to upright posture and oral glucose administration in elderly human subjects. , 1980, Metabolism: clinical and experimental.

[17]  E. Lakatta,et al.  Cardiovascular regulatory mechanisms in advanced age. , 1993, Physiological reviews.

[18]  O. Tochikubo,et al.  Age‐Related Changes in Muscle Sympathetic Nerve Activity in Essential Hypertension , 1989, Hypertension.

[19]  J. Port,et al.  Age‐Related Changes in β‐Adrenergic Neuroeffector Systems in the Human Heart , 1994, Circulation.

[20]  L. Kuller Sudden death--definition and epidemiologic considerations. , 1980, Progress in cardiovascular diseases.

[21]  A. Svanborg,et al.  Physiology of cardiovascular aging. , 1993, Physiological reviews.

[22]  J. Docherty Cardiovascular responses in ageing: a review. , 1990, Pharmacological reviews.

[23]  J. Fleg,et al.  Age-related augmentation of plasma catecholamines during dynamic exercise in healthy males. , 1985, Journal of applied physiology.

[24]  J. .. Abildskov,et al.  Influence of sympathetic tone on ventricular fibrillation threshold during experimental coronary occlusion. , 1975, The American journal of cardiology.

[25]  A. Ng,et al.  Age and gender influence muscle sympathetic nerve activity at rest in healthy humans. , 1993, Hypertension.

[26]  G. Jennings,et al.  Cyclosporine therapy after cardiac transplantation causes hypertension and renal vasoconstriction without sympathetic activation. , 1993, Circulation.

[27]  A Pedotti,et al.  Blood Pressure and Heart Rate Variabilities in Normotensive and Hypertensive Human Beings , 1983, Circulation research.

[28]  I. Kopin,et al.  Plasma noradrenaline increases with age , 1976, Nature.

[29]  I. Meredith,et al.  Overflow of catecholamine neurotransmitters to the circulation: source, fate, and functions. , 1990, Physiological reviews.

[30]  J. Fleg,et al.  Pathophysiology of the Aging Heart and Circulation , 1984 .

[31]  J. Cohn,et al.  Plasma norepinephrine as a guide to prognosis in patients with chronic congestive heart failure. , 1984, The New England journal of medicine.

[32]  D. Goldstein,et al.  Source and physiological significance of plasma 3,4-dihydroxyphenylglycol and 3-methoxy-4-hydroxyphenylglycol. , 1988, Journal of the autonomic nervous system.

[33]  J. Roberts,et al.  An ultrastructural study of the effects of age on sympathetic innervation and atrial tissue in the rat. , 1983, Journal of molecular and cellular cardiology.

[34]  A. Ng,et al.  Sympathetic neural reactivity to stress does not increase with age in healthy humans. , 1994, The American journal of physiology.

[35]  L. Rubenstein,et al.  Plasma norepinephrine responses to posture and isometric exercise increase with age in the absence of obesity. , 1983, Journal of gerontology.

[36]  A. S. Harris,et al.  The induction of arrhythmias by sympathetic activity before and after occlusion of a coronary artery in the canine heart. , 1971, Journal of electrocardiology.

[37]  R. Hoeldtke,et al.  Effects of aging on catecholamine metabolism. , 1985, The Journal of clinical endocrinology and metabolism.

[38]  R. Verrier,et al.  Behavioral stress and cardiac arrhythmias. , 1984, Annual review of physiology.

[39]  E. Lakatta,et al.  Contractile and biochemical correlates of beta-adrenergic stimulation of the aged heart. , 1980, The American journal of physiology.

[40]  J. Taylor,et al.  Sympathoadrenal-circulatory regulation of arterial pressure during orthostatic stress in young and older men. , 1992, The American journal of physiology.

[41]  I. Meredith,et al.  Evidence of a selective increase in cardiac sympathetic activity in patients with sustained ventricular arrhythmias. , 1991, The New England journal of medicine.

[42]  S. Willich,et al.  Increased morning incidence of myocardial infarction in the ISAM Study: absence with prior beta-adrenergic blockade. ISAM Study Group. , 1989, Circulation.

[43]  H. L. Stone,et al.  THE ROLE OF THE AUTONOMIC NERVOUS SYSTEM IN SUDDEN CORONARY DEATH * , 1982, Annals of the New York Academy of Sciences.

[44]  K. Hagbarth,et al.  Comparison of Sympathetic Nerve Activity in Normotensive and Hypertensive Subjects , 1973, Circulation research.

[45]  A. Mark,et al.  Postexercise hypotension and sympathoinhibition in borderline hypertensive men. , 1989, Hypertension.

[46]  A. Quyyumi,et al.  Sympathetic Nervous Function in Human Heart as Assessed by Cardiac Spillovers of Dihydroxyphenylglycol and Norepinephrine , 1992, Circulation.