Simranjit K Sidhu1, Joshua C Weavil2, Tyler S Mangum2, Jacob E Jessop3, Russell S Richardson4, David E Morgan3, Markus Amann5. 1. Department of Internal Medicine, University of Utah, Salt Lake City, Utah, United States; Discipline of Physiology, Adelaide Medical School, The University of Adelaide, Australia. Electronic address: simran.sidhu@adelaide.edu.au. 2. Department of Exercise & Sport Science, University of Utah, Salt Lake City, Utah, United States. 3. Department of Anaesthesiology, University of Utah, Salt Lake City, Utah, United States. 4. Department of Internal Medicine, University of Utah, Salt Lake City, Utah, United States; Department of Exercise & Sport Science, University of Utah, Salt Lake City, Utah, United States; Geriatric Research, Education & Clinical Center, VA Medical Center, Salt Lake City, Utah, United States. 5. Department of Internal Medicine, University of Utah, Salt Lake City, Utah, United States; Department of Exercise & Sport Science, University of Utah, Salt Lake City, Utah, United States; Department of Anaesthesiology, University of Utah, Salt Lake City, Utah, United States; Geriatric Research, Education & Clinical Center, VA Medical Center, Salt Lake City, Utah, United States.
Abstract
OBJECTIVE: To investigate the influence of group III/IV muscle afferents on the development of central fatigue and corticospinal excitability during exercise. METHODS: Fourteen males performed cycling-exercise both under control-conditions (CTRL) and with lumbar intrathecal fentanyl (FENT) impairing feedback from leg muscle afferents. Transcranial magnetic- and cervicomedullary stimulation was used to monitor cortical versus spinal excitability. RESULTS: While fentanyl-blockade during non-fatiguing cycling had no effect on motor-evoked potentials (MEPs), cervicomedullary-evoked motor potentials (CMEPs) were 13±3% higher (P<0.05), resulting in a decrease in MEP/CMEP (P<0.05). Although the pre- to post-exercise reduction in resting twitch was greater in FENT vs. CTRL (-53±3% vs. -39±3%; P<0.01), the reduction in voluntary muscle activation was smaller (-2±2% vs. -10±2%; P<0.05). Compared to the start of fatiguing exercise, MEPs and CMEPs were unchanged at exhaustion in CTRL. In contrast, MEPs and MEP/CMEP increased 13±3% and 25±6% in FENT (P<0.05). CONCLUSION: During non-fatiguing exercise, group III/IV muscle afferents disfacilitate, or inhibit, spinal motoneurons and facilitate motor cortical cells. In contrast, during exhaustive exercise, group III/IV muscle afferents disfacilitate/inhibit the motor cortex and promote central fatigue. SIGNIFICANCE: Group III/IV muscle afferents influence corticospinal excitability and central fatigue during whole-body exercise in humans.
OBJECTIVE: To investigate the influence of group III/IV muscle afferents on the development of central fatigue and corticospinal excitability during exercise. METHODS: Fourteen males performed cycling-exercise both under control-conditions (CTRL) and with lumbar intrathecal fentanyl (FENT) impairing feedback from leg muscle afferents. Transcranial magnetic- and cervicomedullary stimulation was used to monitor cortical versus spinal excitability. RESULTS: While fentanyl-blockade during non-fatiguing cycling had no effect on motor-evoked potentials (MEPs), cervicomedullary-evoked motor potentials (CMEPs) were 13±3% higher (P<0.05), resulting in a decrease in MEP/CMEP (P<0.05). Although the pre- to post-exercise reduction in resting twitch was greater in FENT vs. CTRL (-53±3% vs. -39±3%; P<0.01), the reduction in voluntary muscle activation was smaller (-2±2% vs. -10±2%; P<0.05). Compared to the start of fatiguing exercise, MEPs and CMEPs were unchanged at exhaustion in CTRL. In contrast, MEPs and MEP/CMEP increased 13±3% and 25±6% in FENT (P<0.05). CONCLUSION: During non-fatiguing exercise, group III/IV muscle afferents disfacilitate, or inhibit, spinal motoneurons and facilitate motor cortical cells. In contrast, during exhaustive exercise, group III/IV muscle afferents disfacilitate/inhibit the motor cortex and promote central fatigue. SIGNIFICANCE: Group III/IV muscle afferents influence corticospinal excitability and central fatigue during whole-body exercise in humans.
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