{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,7]],"date-time":"2026-07-07T15:00:13Z","timestamp":1783436413753,"version":"3.54.6"},"reference-count":49,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["Circulation"],"published-print":{"date-parts":[[1995,1,15]]},"abstract":"<jats:p><jats:italic>Background<\/jats:italic>Aging increases human sympathetic nervous activity at rest. Because 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.<\/jats:p><jats:p><jats:italic>Methods and Results<\/jats:italic>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 (<jats:italic>P<\/jats:italic>&lt;.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 (<jats:italic>P<\/jats:italic>&lt;.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.<\/jats:p><jats:p><jats:italic>Conclusions<\/jats:italic>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.<\/jats:p>","DOI":"10.1161\/01.cir.91.2.351","type":"journal-article","created":{"date-parts":[[2012,6,12]],"date-time":"2012-06-12T00:34:42Z","timestamp":1339461282000},"page":"351-358","update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":146,"title":["Effects of Aging on the Responsiveness of the Human Cardiac Sympathetic Nerves to Stressors"],"prefix":"10.1161","volume":"91","author":[{"given":"Murray D.","family":"Esler","sequence":"first","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jane M.","family":"Thompson","sequence":"additional","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David M.","family":"Kaye","sequence":"additional","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrea G.","family":"Turner","sequence":"additional","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Garry L.","family":"Jennings","sequence":"additional","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Helen S.","family":"Cox","sequence":"additional","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gavin W.","family":"Lambert","sequence":"additional","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Douglas R.","family":"Seals","sequence":"additional","affiliation":[{"name":"From the Baker Medical Research Institute, Melbourne, Australia (M.D.E., J.M.T., D.M.K., A.G.T., G.L.J., H.S.C., G.W.L.), and the Department of Kinesiology, University of Colorado, Boulder (D.R.S.)."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"e_1_3_2_1_2","doi-asserted-by":"publisher","DOI":"10.1042\/cs0600217"},{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-60-3-479"},{"key":"e_1_3_2_3_2","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-65-3-508"},{"key":"e_1_3_2_4_2","doi-asserted-by":"publisher","DOI":"10.1093\/geronj\/41.3.319"},{"key":"e_1_3_2_5_2","doi-asserted-by":"publisher","DOI":"10.1161\/circ.80.4.2571430"},{"key":"e_1_3_2_6_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM199312023292302"},{"key":"e_1_3_2_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/0033-0620(80)90002-X"},{"key":"e_1_3_2_8_2","unstructured":"Bigger JT Jr. Why patients with congestive heart failure die: arrhythmias and sudden cardiac death. 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