Oxidative Stress Does Not Modulate Metabolic Rate or Skeletal Muscle Sympathetic Activity with Primary Aging in Adult Humans
Christopher Bell,
Pamela P. Jones and
Douglas R. Seals
Department of Integrative Physiology (C.B., P.P.J., D.R.S.), University of Colorado, Boulder, Colorado 80309-0354; and Department of Medicine (D.R.S.), University of Colorado Health Sciences Center, Denver, Colorado 80262
Address all correspondence and requests for reprints to: Christopher Bell, Ph.D., Department of Integrative Physiology, 354UCB, University of Colorado, Boulder, Colorado 80309-0354. E-mail: Christopher.Bell{at}Colorado.edu.
Support of resting metabolic rate (RMR) by the ß-adrenergicreceptors of the sympathetic nervous system is attenuated withage and contributes to declines in RMR. This may be mediatedby an age-associated increase in oxidative stress that can suppressß-adrenergic responsiveness and/or modulate sympatheticactivity. To address these issues, RMR was determined in 12young (23 ± 1 yr, mean ± SE) and 21 older (68± 3 yr) adults before and during systemic infusion ofascorbic acid [bolus, 0.06 g/kg fat free mass (FFM); drip, 0.02].Ascorbic acid increased plasma concentrations similarly in young(72 ± 5 to 1107 ± 114 µmol/liter) and older(70 ± 6 to 1022 ± 63 µmol/liter) adults,and reduced (P = 0.001) plasma concentrations of isoprostanes(young, -82.8 ± 47; older, -107 ± 29 pg/ml). BaselineRMRFFM was lower (5719 ± 215 vs. 6703 ± 328 kJ/d;P = 0.001) and muscle sympathetic nerve activity (MSNA) wasgreater (MSNA, 28 ± 2 vs. 23 ± 3 bursts/min; P< 0.05) in older compared with young. However, neither RMRFFM(young, +117 ± 63; older, +163 ± 48 kJ/d; P =0.14) or MSNA (young, 0 ± 2; older, -1 ± 1 bursts/min;P = 0.71) changed in either age group during ascorbic acid infusioncompared with saline control. These results indicate that increasedoxidative stress: 1) is not a mechanism contributing to decreasesin RMR with primary aging; and 2) does not modulate MSNA inhealthy adult humans.
This research was supported by NIH Grants AG06537, AG00828,1 P30 DK48520, and AHA 0225438Z.
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[Abstract][Full Text][PDF]
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556(1):
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[Abstract][Full Text][PDF]