| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
INTEGRATIVE |
1 Department of Integrative Physiology, University of Colorado, Boulder, CO 80309-0354, USA
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsDiscussionReferences |
|---|
EE%; indirect calorimetry, ventilated hood method) above resting EE in response to non-specific ß-AR stimulation (intravenous isoproterenol (isoprenaline): 6, 12 and 24 ng (kg fat-free mass)–1 min–1) in 25 sedentary (11 males; 51 ± 4 years; body mass index 25.0 ± 0.8 kg m–2, maximal oxygen uptake 29 ± 1 ml kg–1 min–1 (mean ±S.E.M.)) and 14 habitually aerobic exercising (9 males, 46 ± 6 years, 23.1 ± 0.7 kg m–2, 44 ± 3 ml kg–1 min–1) healthy adults under normal (control) conditions and during acute intravenous administration of a potent antioxidant, ascorbic acid (vitamin C; 0.04 g (kg fat-free mass)–1). EE% was greater (P= 0.02) in the habitually exercising (8.6 ± 1.2, 12.9 ± 1.2, 20.0 ± 1.4) versus sedentary (6.3 ± 0.7, 10.4 ± 0.8, 16.0 ± 1.0) adults. Ascorbic acid increased (P= 0.01) EE% only in the sedentary adults (to 9.5 ± 0.9, 12.4 ± 0.7, 18.5 ± 0.8), abolishing baseline group differences. EE% was not related to the amount of body fat, sex, or any other baseline characteristic. Thermogenic responsiveness to ß-AR stimulation is augmented in habitually exercising adults. The mechanism is ascorbic acid dependent, suggesting that it may be linked to decreased ROS bioactivity. Our findings advance a novel mechanism by which habitual physical activity may modulate EE in humans, with potential implications for energy balance and body weight control.
(Received 14 September 2005;
accepted after revision 17 November 2005;
first published online 24 November 2005)
Corresponding author C. Bell: Department of Health and Exercise Science, 205E Moby-B Complex/1582 Campus Delivery, Colorado State University, Fort Collins, CO 80521-1582, USA. Email: cbell{at}cahs.colostate.edu
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Adult humans who regularly perform aerobic endurance exercise often demonstrate lower body fat and greater body composition-normalized RMR and thermic effect of feeding compared with their sedentary peers (Van Pelt et al. 1997, 1998; Bell et al. 2001; Jones et al. 2004). However, sympathoadrenal system activity at rest and in response to acute energy intake is not augmented in exercise-trained compared with sedentary adults (Bell et al. 2001; Jones et al. 2004). This suggests that thermogenic responsiveness to ß-AR stimulation is increased in regularly exercising humans, but at present no data are available on this issue.
One mechanism that could contribute to habitual exercise-associated differences in thermogenic responsiveness to ß-AR stimulation is the bioactivity of reactive oxygen species (ROS). ROS or free radicals are any atom, molecule or compound that has one or more unpaired electrons (Knight, 2000). ROS, the most important of which biologically is the superoxide anion, are important signalling molecules and can modulate ß-AR responsiveness (Kaneko et al. 1991; Vatner et al. 1993; Persad et al. 1997, 1998a,b, 1999; Nishizawa et al. 2004). In patients with normal left ventricular function, dobutamine (a ß1-AR agonist)-stimulated increases in left ventricular contractility at rest are augmented in the presence of ascorbic acid (vitamin C) (Mak & Newton, 2001, 2004), a potent non-enzymatic antioxidant that scavenges superoxide anions when administered at supraphysiological concentrations (Frei et al. 1989; Jackson et al. 1998). There is some evidence that habitual aerobic endurance exercise may be associated with reduced ROS bioavailability or ‘oxidative stress’, defined as a state in which ROS formation exceeds antioxidant defences (Adams et al. 2005; Kojda & Hambrecht, 2005). However, indirect systemic plasma markers of oxidative stress are relatively insensitive and do not always reflect differences in ROS bioactivity between groups of healthy humans, including exercising and sedentary adults (Eskurza et al. 2004b). As such, inhibition of ROS bioavailability via antioxidant administration provides more direct insight into the modulatory effects of ROS on physiological function.
Accordingly, in the present investigation we hypothesized that: (1) adult humans performing regular aerobic endurance exercise would demonstrate greater increases in metabolic rate in response to ß-AR stimulation than their sedentary peers; and (2) these differences would be explained, at least in part, by corresponding differences in ROS modulation of ß-AR responsiveness. To determine this, EE was established at rest and in response to ß-AR stimulation with isoproterenol, a non-selective ß-AR agonist, during infusion of ascorbic acid or saline (placebo) in groups of healthy habitually exercising and sedentary adults. We predicted that habitually exercising adults would demonstrate greater increases in metabolic rate in response to ß-AR stimulation during placebo, but not ascorbic acid infusion, compared with sedentary adults.
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
We studied 39 healthy adult male and females (18–74 years): 25 sedentary and 14 habitual exercisers. Sedentary subjects had performed no regular, formalized physical exercise during the previous 2 years and were in the lower 50th percentile for maximal oxygen uptake 
(Franklin et al. 2000). Habitually exercising subjects had regularly performed a minimum of 40 min of vigorous physical exercise 
4 days per week for the previous 2 years, and were in the upper 10th percentile for 
. All subjects were healthy as assessed by medical history, and fasting plasma glucose and insulin concentrations. In addition, older subjects ( 35 years) underwent a physical examination with resting electrocardiogram (ECG) as well as ECG and blood pressure assessments during graded treadmill exercise to exhaustion. Subjects were non-smokers and were not regularly taking any medication or vitamin/antioxidant supplements. The nature, purpose and risks of the study were explained to each subject before written consent was obtained. The experimental protocol conformed to the standards set by the Declaration of Helsinki and was approved by the Human Research Committee at the University of Colorado at Boulder.
Experimental procedures
All measurements were made at the University of Colorado at Boulder General Clinical Research Center (GCRC) during two mornings, each after a 12 h fast, 2 h abstention from water, and 24 h abstention from vigorous physical exercise. Subjects were studied under quiet resting conditions in a semi-recumbent position. Measurements were performed between 07.00 and 09.00 h in a dimly lit room at a comfortable temperature (
23°C). The increase in energy expenditure above RMR in response to intravenous administration of the non-selective ß-AR agonist isoproterenol (6, 12 and 24 ng (kg fat-free mass (FFM))–1 min–1) was measured during: (1) continuous intravenous ascorbic acid administration (American Regent Laboratories Inc., NY, USA; 0.04 g (kg FFM)–1 dissolved in 100 ml of saline); and (2) continuous saline infusion (Fig. 1). The order of co-infusions (saline versus ascorbic acid) was randomized and administered in a single blind fashion. The rationale for the doses and method of ascorbic acid administration has been previously described (Bell et al. 2003, 2005; Eskurza et al. 2004a, b), and we have established previously that this dose acutely decreases oxidative stress in adult humans (Bell et al. 2003, 2005). Subjects were instrumented for measurement of heart rate (ECG) and blood pressure. A catheter was placed in an antecubital vein and was kept patent with heparin. After a 30 min rest period following instrumentation baseline RMR was measured, as previously described (Bell et al. 2001; Monroe et al. 2001). The first 15 min were considered an habituation period after which oxygen consumption and carbon dioxide production were averaged each minute for 30 min using a ventilated hood indirect calorimetry system (DeltaTrac II Metabolic Monitor, SensorMedics Corp., Yorba Linda, CA, USA). This measurement was then repeated over three consecutive 30 min periods during incremental infusion of isoproterenol. Energy expenditure was calculated from the average of the final 25 min of each 30 min collection using the Weir formula (Weir, 1949). Steady state was confirmed during each of these 25 min periods by comparing oxygen consumption and carbon dioxide production during the 1st and last minute.
|
Fat mass and FFM were measured using dual-energy X-ray absorptiometry (DXA-IQ; Lunar Radiation corp., Madison, WI, USA, software version 4.1). Maximal oxygen uptake was determined via incremental treadmill exercise as previously described (Bell et al. 2005).
Statistical analysis
RMR was adjusted for differences in FFM (relation between RMR and FFM: r= 0.84, P < 0.001). Two-way (saline versus ascorbic acid) analysis of variance (ANOVA) with repeated measures on one factor (relative change in energy expenditure above RMR across three doses of isoproterenol) was used to examine differences among sedentary adults and habitual exercisers. Thermogenic responsiveness to ß-AR stimulation was not adjusted for differences in FFM because the doses of isoproterenol were normalized for individual FFM. Multiple comparisons of factor means were performed using the Neuman-Keuls test. Relations between variables of interest were determined by simple correlation analysis. The level of statistical significance was set at P < 0.05. Data are expressed as mean ±S.E.M.
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
|
EE increased above RMR in response to incremental ß-AR stimulation in both sedentary and exercising adults. However, the magnitude of increase was greater (P= 0.02) in the exercising adults indicating augmented ß-AR-stimulated thermogenesis (Fig. 2A).
|
Administration of ascorbic acid did not affect baseline FFM-adjusted RMR in either sedentary (from 5503 ± 206 to 5430 ± 193 kJ day–1) or exercising adults (from 5870 ± 253 to 5665 ± 234 kJ day–1) (P= 0.72). ß-AR-stimulated thermogenesis was increased (P= 0.01) in sedentary adults during administration of ascorbic acid (Fig. 2B). In contrast, ascorbic acid had no effect on ß-AR-stimulated thermogenesis in the exercising adults (P= 0.93; Fig. 2C).
Ascorbic acid abrogates habitual exercise-associated differences in ß-AR thermogenesis
During ascorbic acid administration the baseline (saline control) difference in ß-AR thermogenesis between sedentary adults and habitual exercisers was abolished (P= 0.86; Fig. 2D).
Correlates of ß-AR thermogenesis
There were no main effects of sex or sex–exercise–ascorbic acid interactions on ß-AR thermogenesis (P > 0.05). Thus, correcting the groups for sex composition did not alter the significant main effect of habitual exercise status. Augmentation of ß-AR thermogenesis with ascorbic acid was inversely related to baseline ß-AR-stimulated thermogenesis (r=–0.66, P < 0.001), but not with any other baseline function or any subject characteristic including fasting insulin and glucose concentrations, or body-composition-related descriptor (Table 1).
Other responses
Respiratory exchange ratio was 0.82–0.84 at baseline and was not significantly affected by isoproterenol dose, habitual exercise status or ascorbic acid administration (interaction P > 0.05). Heart rate increased above baseline resting levels by up to 30 beats min–1 in both groups in response to isoproterenol, whereas arterial blood pressure was not consistently affected in either group. There were no significant interactions between isoproterenol dose, habitual exercise status and ascorbic acid administration for heart rate or blood pressure (all P > 0.05).
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Greater thermogenic responsiveness to ß-AR stimulation in adults who exercise
The mechanisms underlying our novel observation of greater thermogenic responsiveness to ß-AR stimulation in habitually exercising compared with sedentary healthy adults are unknown, but could involve differences in ß-AR density, agonist affinity, and/or post-receptor signalling. To our knowledge no information is available on the effects of habitual exercise status on the increase in energy expenditure during ß-AR stimulation. The present findings are, however, directionally consistent with reports of improved ß-AR-mediated lipolytic responses in adipose tissue (tissue biopsies and microdialysis) following aerobic exercise training (De Glisezinski et al. 1998; Stich et al. 1999). Thus, information is needed on the cellular and molecular mechanisms responsible for the augmented thermogenic responsiveness to ß-AR stimulation in habitually exercising adults.
Aside from potential differences in ß-AR signalling, another key determinant of the augmented thermogenic responsiveness to ß-AR stimulation in habitually exercising adults is mitochondrial function. It is well established that relative to sedentary adults habitual exercisers have greater mitochrondrial density, oxidative enzyme activities, and capacity for ATP production (Hawley, 2002). Accordingly, it is feasible that the augmented thermogenic responsiveness to ß-AR stimulation in habitually exercising adults is independent of ß-AR properties per se. Rather it is the superior ‘metabolic machinery’ of habitual exercisers that distinguishes their thermogenic response to ß-AR stimulation from sedentary adults.
In contrast to metabolic responsiveness, in the present study the increases in heart rate to isoproterenol were similar in the sedentary and exercising subjects. However, this cannot be interpreted as indicating a selective influence of habitual exercise status on metabolic responsiveness to ß-AR activation. Cardiovascular responsiveness to ß-AR stimulation cannot be assessed under the conditions of the present study because the haemodynamic effects of systemic isoproterenol administration activate baroreflexes that, in turn, actively buffer heart rate via cardiac autonomic adjustments (Christou et al. 2003). This effect can mask group differences in cardiovascular responsiveness to isoproterenol that are apparent under conditions of ganglionic blockade, that blocks baroreflex signalling (White & Leenen, 1994).
Modulation of the thermogenic response to ß-AR stimulation by ascorbic acid
We have established (Bell et al. 2003; Eskurza et al. 2004a,b) that the dose of ascorbic acid infused in the present study results in supraphysiological plasma concentrations known to scavenge superoxide anions (Frei et al. 1989; Jackson et al. 1998), and acutely reduces systemic markers of oxidative stress including plasma concentrations of oxidized low-density lipoprotein and isoprostanes (Bell et al. 2003, 2005). We have also demonstrated that this ascorbic acid infusion reverses vascular endothelial dysfunction associated with the sedentary state in older adults, while not affecting the preserved endothelial function observed in older exercising adults (Eskurza et al. 2004b). Considered along with the fact that ROS bioactivity/oxidative stress modulates cardiac responsiveness to ß-AR stimulation (Mak & Newton, 2001, 2004), the restoration of thermogenic responsiveness to isoproterenol by ascorbic acid in the sedentary subjects in the present study is consistent with the concept that increased ROS bioavailability or action contributes to the lower baseline ß-AR responsiveness seen in sedentary adults. These observations also suggest, in turn, that the lack of augmentation of ß-AR-stimulated thermogenesis by ascorbic acid in the habitually exercising subjects may reflect tonically decreased ROS-related effects, as has been postulated previously (Adams et al. 2005; Kojda & Hambrecht, 2005).
Although we are unaware of any non-antioxidant properties that could explain our results, we recognize that it is possible that ascorbic acid influenced ß-AR thermogenic responsiveness by another mechanism such as enhanced clearance/uptake of isoproterenol in sedentary but not habitually exercising subjects. We also cannot exclude a ‘ceiling effect’ whereby the higher baseline thermogenic responsiveness to ß-AR stimulation in the exercising subjects prohibited further augmentation by ascorbic acid (or any other potential modulating factor). Finally, it is possible that the group differences in the effect of ascorbic acid infusion on ß-AR stimulation of metabolic rate may have been influenced by differences in the plasma concentrations of ascorbic acid achieved. However, this is unlikely given that we have shown previously that sedentary and habitually exercising adults attain identical plasma concentrations of ascorbic acid during the same infusion as used in the present study (Eskurza et al. 2004b). Despite these caveats, however, taken together we believe that these observations reasonably support the idea that the smaller isoproterenol-mediated increase in EE in the sedentary state may be linked to oxidative stress in some or all tissues responsive to ß-AR stimulation. The mechanisms by which acute ascorbic acid administration could exert an antioxidant effect and restore thermogenic responsiveness in sedentary adults remain to be discerned. Translocation of ß-ARs to the cell membrane, increased agonist affinity for the receptor, enhanced G-protein activation of adenylyl cyclase, increased cyclic AMP production, and activation of downstream signalling are all possible redox-sensitive steps in the ß-AR signalling cascade that could have been influenced by ascorbic acid (Kaneko et al. 1991; Vatner et al. 1993; Persad et al. 1997, 1998a,b, 1999; Nishizawa et al. 2004). Ascorbic acid may also act in mitochondria to reduce superoxide production and this, in turn, may improve electron transport chain activity, oxidative phosphorylation, and the ability of mitochondria to increase substrate metabolism in response to ß-AR stimulation (Sharma & Mongan, 2001).
Physiological and clinical implications
The results of the present study have implications for EE under conditions of sympathoadrenal system ß-AR activation. For example, acute energy intake is associated with significant postprandial sympathetic nervous system activation and release of adrenaline (epinephrine) from the adrenal medulla (Jones et al. 2004). Indeed, up to 30–40% of the thermic effect of food is thought to be mediated by sympathoadrenal activation and stimulation of ß-AR thermogenesis (Tappy et al. 1986). Recently we have shown that the thermic effect of food is greater in habitually exercising compared with sedentary adults despite similar postprandial sympathetic activation and increases in circulating adrenaline (Jones et al. 2004). Thus, it is possible that greater thermogenic responsiveness to ß-AR stimulation could contribute to the greater thermic effect of food observed in regularly exercising adults. It is unknown if the increased metabolic responsiveness to ß-AR stimulation in habitually exercising adults modulates physical activity-related EE, particularly during types and intensities of exercise associated with marked, sustained sympathoadrenal system activation.
Summary and conclusions
In summary, our results demonstrate that thermogenic responsiveness to ß-AR stimulation is augmented in adults who perform regular aerobic exercise compared with their sedentary peers. The mechanism is ascorbic acid dependent, suggesting that it may be linked to low tonic ROS bioactivity (oxidative stress) in the habitually exercising state. These findings advance a novel mechanism by which habitual aerobic endurance exercise may modulate EE in humans, with potential implications for energy balance and the regulation of body weight.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Bachman ES, Dhillon H, Zhang CY, Cinti S, Bianco AC, Kobilka BK & Lowell BB (2002). ßAR signaling required for diet-induced thermogenesis and obesity resistance. Science 297, 843–845.
Bell C, Carson JM, Motte NW & Seals DR (2005). Ascorbic acid does not affect the age-associated reduction in maximal cardiac output and oxygen consumption in healthy adults. J Appl Physiol 98, 845–849.
Bell C, Day DS, Jones PP, Christou DD, Petitt DS, Osterberg K, Melby CL & Seals DR (2004). High energy flux mediates the tonically augmented ß-adrenergic support of resting metabolic rate in habitually exercising older adults. J Clin Endocrinol Metab 89, 3573–3578.
Bell C, Jones PP & Seals DR (2003). Oxidative stress does not modulate metabolic rate or skeletal muscle sympathetic activity with primary aging in adult humans. J Clin Endocrinol Metab 88, 4950–4954.
Bell C, Seals DR, Monroe MB, Day DS, Shapiro LF, Johnson DG & Jones (2001). Tonic sympathetic support of metabolic rate is attenuated with age, sedentary lifestyle, and female sex in healthy adults. J Clin Endocrinol Metab 86, 4440–4444.
Christou DD, Jones PP & Seals DR (2003). Baroreflex buffering in sedentary and endurance exercise-trained healthy men. Hypertension 41, 1219–1222.
De Glisezinski I, Crampes F, Harant I, Berlan M, Hejnova J, Langin D, Riviere D & Stich V (1998). Endurance training changes in lipolytic responsiveness of obese adipose tissue. Am J Physiol 275, E951–E956.[Medline]
Eskurza I, Monahan KD, Robinson JA & Seals DR (2004a). Ascorbic acid does not affect large elastic artery compliance or central blood pressure in young and older men. Am J Physiol Heart Circ Physiol 286, H1528–H1534.
Eskurza I, Monahan KD, Robinson JA & Seals DR (2004b). Effect of acute and chronic ascorbic acid on flow-mediated dilatation with sedentary and physically active human ageing. J Physiol 556, 315–324.
Franklin BH, Whaley MH & Howley ET (2000). ACSM's Guidelines for Exercise Testing and Prescription. Lippincott Williams & Wilkins, Philadelphia.
Frei B, England L & Ames BN (1989). Ascorbate is an outstanding antioxidant in human blood plasma. Proc Natl Acad Sci U S A 86, 6377–6381.
Hawley JA (2002). Adaptations of skeletal muscle to prolonged, intense endurance training. Clin Exp Pharmacol Physiol 29, 218–222.[CrossRef][Medline]
Jackson TS, Xu A, Vita JA & Keaney JF Jr (1998). Ascorbate prevents the interaction of superoxide and nitric oxide only at very high physiological concentrations. Circ Res 83, 916–922.
Jones PP, Van Pelt RE, Johnson DG & Seals DR (2004). Role of sympathetic neural activation in age- and habitual exercise-related differences in the thermic effect of food. J Clin Endocrinol Metab 89, 5138–5144.
Kaneko M, Chapman DC, Ganguly PK, Beamish RE & Dhalla NS (1991). Modification of cardiac adrenergic receptors by oxygen free radicals. Am J Physiol 260, H821–H826.[Medline]
Knight JA (2000). The biochemistry of aging. Adv Clin Chem 35, 1–62.[Medline]
Kojda G & Hambrecht R (2005). Molecular mechanisms of vascular adaptations to exercise. Physical activity as an effective antioxidant therapy?Cardiovasc Res 67, 187–197.
Lamont LS, Patel DG & Kalhan SC (1989). Beta-adrenergic blockade alters whole-body leucine metabolism in humans. J Appl Physiol 67, 221–225.
Mak S & Newton GE (2001). Vitamin C augments the inotropic response to dobutamine in humans with normal left ventricular function. Circulation 103, 826–830.
Mak S & Newton GE (2004). Redox modulation of the inotropic response to dobutamine is impaired in patients with heart failure. Am J Physiol Heart Circ Physiol 286, H789–H795.
Monroe MB, Seals DR, Shapiro LF, Bell C, Johnson D & Jones (2001). Direct evidence for tonic sympathetic support of resting metabolic rate in healthy adult humans. Am J Physiol Endocrinol Metab 280, E740–E744.
Nishizawa T, Iwase M, Kanazawa H, Ichihara S, Ichihara G, Nagata K, Obata K, Kitaichi K, Yokoi T, Watanabe M, Tsunematsu T, Ishikawa Y, Murohara T & Yokota M (2004). Serial alterations of beta-adrenergic signaling in dilated cardiomyopathic hamsters: possible role of myocardial oxidative stress. Circ J 68, 1051–1060.[CrossRef][Medline]
Persad S, Elimban V, Siddiqui F & Dhalla NS (1999). Alterations in cardiac membrane beta-adrenoceptors and adenylyl cyclase due to hypochlorous acid. J Mol Cell Cardiol 31, 101–111.[CrossRef][Medline]
Persad S, Panagia V & Dhalla NS (1998a). Role of H2O2 in changing beta-adrenoceptor and adenylyl cyclase in ischemia-reperfused hearts. Mol Cell Biochem 186, 99–106.[CrossRef][Medline]
Persad S, Rupp H, Jindal R, Arneja J & Dhalla NS (1998b). Modification of cardiac beta-adrenoceptor mechanisms by H2O2. Am J Physiol 274, H416–H423.[Medline]
Persad S, Takeda S, Panagia V & Dhalla NS (1997). Beta-adrenoceptor-linked signal transduction in ischemic-reperfused heart and scavenging of oxyradicals. J Mol Cell Cardiol 29, 545–558.[CrossRef][Medline]
Schwartz RS, Jaeger LF & Veith RC (1988). Effect of clonidine on the thermic effect of feeding in humans. Am J Physiol 254, R90–R94.[Medline]
Sharma P & Mongan PD (2001). Ascorbate reduces superoxide production and improves mitochondrial respiratory chain function in human fibroblasts with electron transport chain deficiencies. Mitochondrion 1, 191–198.[CrossRef][Medline]
Stich V, de Glisezinski I, Galitzky J, Hejnova J, Crampes F, Riviere D & Berlan M (1999). Endurance training increases the beta-adrenergic lipolytic response in subcutaneous adipose tissue in obese subjects. Int J Obes Relat Metab Disord 23, 374–381.[CrossRef][Medline]
Tappy L, Randin JP, Felber JP, Chiolero R, Simonson DC, Jequier E & DeFronzo RA (1986). Comparison of thermogenic effect of fructose and glucose in normal humans. Am J Physiol 250, E718–E724.[Medline]
Van Pelt RE, Davy KP, Stevenson ET, Wilson TM, Jones PP, Desouza CA & Seals DR (1998). Smaller differences in total and regional adiposity with age in women who regularly perform endurance exercise. Am J Physiol 275, E626–E634.[Medline]
Van Pelt RE, Jones PP, Davy KP, Desouza CA, Tanaka H, Davy BM & Seals DR (1997). Regular exercise and the age-related decline in resting metabolic rate in women. J Clin Endocrinol Metab 82, 3208–3212.
Vatner DE, Kiuchi K, Manders WT & Vatner SF (1993). Effects of coronary arterial reperfusion on beta-adrenergic receptor adenylyl cyclase coupling. Am J Physiol 264, H196–H204.[Medline]
Weir J (1949). New methods for calculating metabolic rate with special reference to protein metabolism. J Physiol 109, 1–9.
Welle S, Schwartz RG & Statt M (1991). Reduced metabolic rate during beta-adrenergic blockade in humans. Metabolism 40, 619–622.[CrossRef][Medline]
White M & Leenen FH (1994). Aging and cardiovascular responsiveness to beta-agonist in humans: role of changes in beta-receptor responses versus baroreflex activity. Clin Pharmacol Ther 56, 543–553.[Medline]
|
Acknowledgements |
|---|
This article has been cited by other articles:
|
|
 |
|
  N. R. Stob, D. R. Seals, J. Jensen, M. A. van Baak, A. J. Steig, R. C. Lindstrom, B. T. Bikman, and C. Bell Autonomic Neuroscience: Increased thermogenic responsiveness to intravenous {beta}-adrenergic stimulation in habitually exercising humans is not related to skeletal muscle {beta}2-adrenergic receptor density Exp Physiol, September 1, 2007; 92(5): 823 - 830. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 N. R. Stob, C. Bell, M. A. van Baak, and D. R. Seals Thermic effect of food and beta-adrenergic thermogenic responsiveness in habitually exercising and sedentary healthy adult humans J Appl Physiol, August 1, 2007; 103(2): 616 - 622. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A. J. Donato, I. Eskurza, A. E. Silver, A. S. Levy, G. L. Pierce, P. E. Gates, and D. R. Seals Direct Evidence of Endothelial Oxidative Stress With Aging in Humans: Relation to Impaired Endothelium-Dependent Dilation and Upregulation of Nuclear Factor-{kappa}B Circ. Res., June 8, 2007; 100(11): 1659 - 1666. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
K. L. Moreau, A. R. DePaulis, K. M. Gavin, and D. R. Seals Oxidative stress contributes to chronic leg vasoconstriction in estrogen-deficient postmenopausal women J Appl Physiol, March 1, 2007; 102(3): 890 - 895. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
