TY - JOUR
T1 - Multitissue responses to exercise
T2 - a MoTrPAC feasibility study
AU - Chambers, Toby L.
AU - Stroh, Andrew M.
AU - Chavez, Clarisa
AU - Brandt, Anna R.
AU - Claiborne, Alex
AU - Fountain, William A.
AU - Gries, Kevin J.
AU - Jones, Andrew M.
AU - Kuszmaul, Dillon J.
AU - Lee, Gary A.
AU - Lester, Bridget E.
AU - Lynch, Colleen E.
AU - Minchev, Kiril
AU - Montenegro, Cristhian F.
AU - Naruse, Masatoshi
AU - Raue, Ulrika
AU - Trappe, Todd A.
AU - Trappe, Scott
N1 - Publisher Copyright:
© 2023 American Physiological Society. All rights reserved.
PY - 2023
Y1 - 2023
N2 - We assessed the feasibility of the Molecular Transducers of Physical Activity Consortium (MoTrPAC) human adult clinical exercise protocols, while also documenting select cardiovascular, metabolic, and molecular responses to these protocols. After phenotyping and familiarization sessions, 20 subjects (25 ± 2 yr, 12 M, 8 W) completed an endurance exercise bout (n = 8, 40 min cycling at 70% V_ O2max), a resistance exercise bout (n = 6, 45 min, 3 sets of 10 repetition maximum, 8 exercises), or a resting control period (n = 6, 40 min rest). Blood samples were taken before, during, and after (10 min, 2 h, and 3.5 h) exercise or rest for levels of catecholamines, cortisol, glucagon, insulin, glucose, free fatty acids, and lactate. Heart rate was recorded throughout exercise (or rest). Skeletal muscle (vastus lateralis) and adipose (periumbilical) biopsies were taken before and 4 h following exercise or rest for mRNA levels of genes related to energy metabolism, growth, angiogenesis, and circadian processes. Coordination of the timing of procedural components (e.g., local anesthetic delivery, biopsy incisions, tumescent delivery, intravenous line flushes, sample collection and processing, exercise transitions, and team dynamics) was reasonable to orchestrate while considering subject burden and scientific objectives. The cardiovascular and metabolic alterations reflected a dynamic and unique response to endurance and resistance exercise, whereas skeletal muscle was transcriptionally more responsive than adipose 4 h postexercise. In summary, the current report provides the first evidence of protocol execution and feasibility of key components of the MoTrPAC human adult clinical exercise protocols. Scientists should consider designing exercise studies in various populations to interface with the MoTrPAC protocols and DataHub.
AB - We assessed the feasibility of the Molecular Transducers of Physical Activity Consortium (MoTrPAC) human adult clinical exercise protocols, while also documenting select cardiovascular, metabolic, and molecular responses to these protocols. After phenotyping and familiarization sessions, 20 subjects (25 ± 2 yr, 12 M, 8 W) completed an endurance exercise bout (n = 8, 40 min cycling at 70% V_ O2max), a resistance exercise bout (n = 6, 45 min, 3 sets of 10 repetition maximum, 8 exercises), or a resting control period (n = 6, 40 min rest). Blood samples were taken before, during, and after (10 min, 2 h, and 3.5 h) exercise or rest for levels of catecholamines, cortisol, glucagon, insulin, glucose, free fatty acids, and lactate. Heart rate was recorded throughout exercise (or rest). Skeletal muscle (vastus lateralis) and adipose (periumbilical) biopsies were taken before and 4 h following exercise or rest for mRNA levels of genes related to energy metabolism, growth, angiogenesis, and circadian processes. Coordination of the timing of procedural components (e.g., local anesthetic delivery, biopsy incisions, tumescent delivery, intravenous line flushes, sample collection and processing, exercise transitions, and team dynamics) was reasonable to orchestrate while considering subject burden and scientific objectives. The cardiovascular and metabolic alterations reflected a dynamic and unique response to endurance and resistance exercise, whereas skeletal muscle was transcriptionally more responsive than adipose 4 h postexercise. In summary, the current report provides the first evidence of protocol execution and feasibility of key components of the MoTrPAC human adult clinical exercise protocols. Scientists should consider designing exercise studies in various populations to interface with the MoTrPAC protocols and DataHub.
KW - adipose
KW - gene expression
KW - metabolism
KW - MoTrPAC
KW - skeletal muscle
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U2 - 10.1152/japplphysiol.00210.2023
DO - 10.1152/japplphysiol.00210.2023
M3 - Article
C2 - 37318985
AN - SCOPUS:85165519482
SN - 8750-7587
VL - 135
SP - 302
EP - 315
JO - Journal of applied physiology
JF - Journal of applied physiology
IS - 2
ER -