Effects of aging and exercise training on leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise: role of cGMP signaling

Aging is associated with slower skeletal muscle O 2 uptake (V̇o 2 ) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects of exercise training in elderly on the initial vascular and metabolic response to exercise remain to be elucidated. We measured leg hemod...

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Published inAmerican journal of physiology. Regulatory, integrative and comparative physiology Vol. 315; no. 2; pp. R274 - R283
Main Authors Piil, Peter, Jørgensen, Tue Smith, Egelund, Jon, Rytter, Nicolai, Gliemann, Lasse, Bangsbo, Jens, Hellsten, Ylva, Nyberg, Michael
Format Journal Article
LanguageEnglish
Published United States American Physiological Society 01.08.2018
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ISSN0363-6119
1522-1490
1522-1490
DOI10.1152/ajpregu.00446.2017

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Abstract Aging is associated with slower skeletal muscle O 2 uptake (V̇o 2 ) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects of exercise training in elderly on the initial vascular and metabolic response to exercise remain to be elucidated. We measured leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise engaging the knee-extensor muscles in young ( n = 15, 25 ± 1 yr) and older ( n = 15, 72 ± 1 yr) subjects before and after a period of aerobic high-intensity exercise training. To enhance cGMP signaling, pharmacological inhibition of phosphodiesterase 5 (PDE5) was performed. Before training, the older group had a slower ( P <0.05) increase in femoral arterial blood flow and leg vascular conductance in the transition from rest to steady-state exercise at low- and moderate-intensity compared with the young group. The rate of increase in leg V̇o 2 was, however, similar in the two groups as a result of higher ( P < 0.05) arteriovenous O 2 difference in the older group. Potentiation of cGMP signaling did not affect the rate of increase in blood flow or V̇o 2 in either group. Exercise training augmented ( P < 0.05) the increase in leg vascular conductance and blood flow during the onset of moderate-intensity exercise in both groups without altering V̇o 2 . These findings suggest that an age-related reduction in the initial vascular response to low- and moderate-intensity knee-extensor exercise is not limiting for V̇o 2 in older individuals. A lower blood flow response in aging does not appear to be a result of reduced cGMP signaling.
AbstractList Aging is associated with slower skeletal muscle O 2 uptake (V̇o 2 ) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects of exercise training in elderly on the initial vascular and metabolic response to exercise remain to be elucidated. We measured leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise engaging the knee-extensor muscles in young ( n = 15, 25 ± 1 yr) and older ( n = 15, 72 ± 1 yr) subjects before and after a period of aerobic high-intensity exercise training. To enhance cGMP signaling, pharmacological inhibition of phosphodiesterase 5 (PDE5) was performed. Before training, the older group had a slower ( P <0.05) increase in femoral arterial blood flow and leg vascular conductance in the transition from rest to steady-state exercise at low- and moderate-intensity compared with the young group. The rate of increase in leg V̇o 2 was, however, similar in the two groups as a result of higher ( P < 0.05) arteriovenous O 2 difference in the older group. Potentiation of cGMP signaling did not affect the rate of increase in blood flow or V̇o 2 in either group. Exercise training augmented ( P < 0.05) the increase in leg vascular conductance and blood flow during the onset of moderate-intensity exercise in both groups without altering V̇o 2 . These findings suggest that an age-related reduction in the initial vascular response to low- and moderate-intensity knee-extensor exercise is not limiting for V̇o 2 in older individuals. A lower blood flow response in aging does not appear to be a result of reduced cGMP signaling.
Aging is associated with slower skeletal muscle O2 uptake (V̇o2) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects of exercise training in elderly on the initial vascular and metabolic response to exercise remain to be elucidated. We measured leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise engaging the knee-extensor muscles in young (n = 15, 25 ± 1 yr) and older (n = 15, 72 ± 1 yr) subjects before and after a period of aerobic high-intensity exercise training. To enhance cGMP signaling, pharmacological inhibition of phosphodiesterase 5 (PDE5) was performed. Before training, the older group had a slower (P <0.05) increase in femoral arterial blood flow and leg vascular conductance in the transition from rest to steady-state exercise at low- and moderate-intensity compared with the young group. The rate of increase in leg V̇o2 was, however, similar in the two groups as a result of higher (P < 0.05) arteriovenous O2 difference in the older group. Potentiation of cGMP signaling did not affect the rate of increase in blood flow or V̇o2 in either group. Exercise training augmented (P < 0.05) the increase in leg vascular conductance and blood flow during the onset of moderate-intensity exercise in both groups without altering V̇o2. These findings suggest that an age-related reduction in the initial vascular response to low- and moderate-intensity knee-extensor exercise is not limiting for V̇o2 in older individuals. A lower blood flow response in aging does not appear to be a result of reduced cGMP signaling.
Aging is associated with slower skeletal muscle O uptake (V̇o ) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects of exercise training in elderly on the initial vascular and metabolic response to exercise remain to be elucidated. We measured leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise engaging the knee-extensor muscles in young ( n = 15, 25 ± 1 yr) and older ( n = 15, 72 ± 1 yr) subjects before and after a period of aerobic high-intensity exercise training. To enhance cGMP signaling, pharmacological inhibition of phosphodiesterase 5 (PDE5) was performed. Before training, the older group had a slower ( P <0.05) increase in femoral arterial blood flow and leg vascular conductance in the transition from rest to steady-state exercise at low- and moderate-intensity compared with the young group. The rate of increase in leg V̇o was, however, similar in the two groups as a result of higher ( P < 0.05) arteriovenous O difference in the older group. Potentiation of cGMP signaling did not affect the rate of increase in blood flow or V̇o in either group. Exercise training augmented ( P < 0.05) the increase in leg vascular conductance and blood flow during the onset of moderate-intensity exercise in both groups without altering V̇o . These findings suggest that an age-related reduction in the initial vascular response to low- and moderate-intensity knee-extensor exercise is not limiting for V̇o in older individuals. A lower blood flow response in aging does not appear to be a result of reduced cGMP signaling.
Aging is associated with slower skeletal muscle O2 uptake (V̇o2) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects of exercise training in elderly on the initial vascular and metabolic response to exercise remain to be elucidated. We measured leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise engaging the knee-extensor muscles in young ( n = 15, 25 ± 1 yr) and older ( n = 15, 72 ± 1 yr) subjects before and after a period of aerobic high-intensity exercise training. To enhance cGMP signaling, pharmacological inhibition of phosphodiesterase 5 (PDE5) was performed. Before training, the older group had a slower ( P <0.05) increase in femoral arterial blood flow and leg vascular conductance in the transition from rest to steady-state exercise at low- and moderate-intensity compared with the young group. The rate of increase in leg V̇o2 was, however, similar in the two groups as a result of higher ( P < 0.05) arteriovenous O2 difference in the older group. Potentiation of cGMP signaling did not affect the rate of increase in blood flow or V̇o2 in either group. Exercise training augmented ( P < 0.05) the increase in leg vascular conductance and blood flow during the onset of moderate-intensity exercise in both groups without altering V̇o2. These findings suggest that an age-related reduction in the initial vascular response to low- and moderate-intensity knee-extensor exercise is not limiting for V̇o2 in older individuals. A lower blood flow response in aging does not appear to be a result of reduced cGMP signaling.Aging is associated with slower skeletal muscle O2 uptake (V̇o2) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects of exercise training in elderly on the initial vascular and metabolic response to exercise remain to be elucidated. We measured leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise engaging the knee-extensor muscles in young ( n = 15, 25 ± 1 yr) and older ( n = 15, 72 ± 1 yr) subjects before and after a period of aerobic high-intensity exercise training. To enhance cGMP signaling, pharmacological inhibition of phosphodiesterase 5 (PDE5) was performed. Before training, the older group had a slower ( P <0.05) increase in femoral arterial blood flow and leg vascular conductance in the transition from rest to steady-state exercise at low- and moderate-intensity compared with the young group. The rate of increase in leg V̇o2 was, however, similar in the two groups as a result of higher ( P < 0.05) arteriovenous O2 difference in the older group. Potentiation of cGMP signaling did not affect the rate of increase in blood flow or V̇o2 in either group. Exercise training augmented ( P < 0.05) the increase in leg vascular conductance and blood flow during the onset of moderate-intensity exercise in both groups without altering V̇o2. These findings suggest that an age-related reduction in the initial vascular response to low- and moderate-intensity knee-extensor exercise is not limiting for V̇o2 in older individuals. A lower blood flow response in aging does not appear to be a result of reduced cGMP signaling.
Author Jørgensen, Tue Smith
Gliemann, Lasse
Bangsbo, Jens
Egelund, Jon
Piil, Peter
Nyberg, Michael
Hellsten, Ylva
Rytter, Nicolai
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Cites_doi 10.1111/anec.12170
10.1152/japplphysiol.00634.2017
10.1113/jphysiol.1985.sp015794
10.1161/01.RES.0000087541.15600.2B
10.1152/jappl.1998.85.4.1394
10.1152/physiol.00029.2016
10.14814/phy2.12508
10.1152/ajpheart.00806.2014
10.1164/arrd.1984.129.2P2.S68
10.1152/japplphysiol.00483.2017
10.1152/jappl.1998.85.4.1404
10.1152/japplphysiol.01237.2009
10.1152/physrev.00035.2013
10.1152/ajpregu.00730.2009
10.1161/01.CIR.101.25.2896
10.1152/japplphysiol.00787.2014
10.1152/ajpheart.00135.2003
10.1152/japplphysiol.01355.2009
10.1113/jphysiol.2012.239053
10.1002/tsm2.1
10.1124/mol.63.6.1364
10.1016/j.autneu.2012.10.013
10.1249/MSS.0b013e31815ef29b
10.1113/jphysiol.2008.166397
10.1152/japplphysiol.00179.2004
10.1113/jphysiol.2012.233064
10.1113/expphysiol.2014.081141
10.1113/JP270594
10.1152/japplphysiol.00186.2001
10.1139/H07-121
10.1152/ajpheart.00433.2015
10.1249/MSS.0000000000000936
10.1161/01.CIR.100.10.1085
10.1016/S0022-5347(01)63299-3
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Snippet Aging is associated with slower skeletal muscle O 2 uptake (V̇o 2 ) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the...
Aging is associated with slower skeletal muscle O uptake (V̇o ) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects...
Aging is associated with slower skeletal muscle O2 uptake (V̇o2) kinetics; however, the mechanisms underlying this effect of age are unclear. Also, the effects...
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SubjectTerms Age factors
Aging
Blood flow
Circulatory system
Conductance
Cyclic GMP
Exercise
Femur
Geriatrics
Hemodynamics
Knee
Leg
Metabolic response
Metabolism
Muscle function
Muscles
Older people
Oxidative metabolism
Oxygen uptake
Pharmacology
Phosphodiesterase
Physical training
Rest
Signaling
Skeletal muscle
Steady state
Training
Vascular endothelial growth factor
Title Effects of aging and exercise training on leg hemodynamics and oxidative metabolism in the transition from rest to steady-state exercise: role of cGMP signaling
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