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Perception of effort during exercise is independent of afferent feedback from skeletal muscles, heart, and lungs
Abstract
VIEWPOINTPerception of effort during exercise is independent of afferent feedback from skeletal muscles, heart, and lungsSamuele MarcoraSamuele MarcoraPublished Online:01 Jun 2009https://doi.org/10.1152/japplphysiol.90378.2008This is the final version - click for previous versionMoreSectionsPDF (55 KB)Download PDF ToolsExport citationAdd to favoritesGet permissionsTrack citations perception of effort, also known as perceived exertion or sense of effort, is a major feature of fatigue (7), and it is widely used to monitor and prescribe exercise intensity (18). However, despite its importance, the neurophysiological bases of this atypical sensation are poorly understood. A model popular among physiologists investigating central regulation of exercise performance is that perceived exertion results from the complex integration of different inputs to the central nervous system (CNS). These inputs include afferent feedback from the peripheral organs most active during aerobic exercise (i.e., skeletal muscles, heart, and lungs) and other interoceptors, with or without additional inputs from the CNS itself, such as knowledge of the exercise task endpoint (3, 6, 28).The purpose of this article is to challenge this view by reviewing evidence that perception of effort during dynamic whole body exercise is independent of afferent feedback from small-diameter muscle afferents, heart, and lungs. For isolated and/or isometric exercise, the reader is referred to other reviews demonstrating that the sense of effort is independent of sensory inputs from muscle spindles and Golgi tendon organs (15, 24).Definitions.The common assumption that afferent feedback contributes significantly to perception of effort may derive from a too broad operational definition. Indeed, if subjects are instructed that rating of perceived exertion (RPE) refers to the discomfort experienced during exercise, then muscle pain, thermal discomfort, and thirst can be appropriately included in the perceptual rating because hedonicity is one of the four dimensions of any sensation (quality, intensity, duration, and hedonicity) (3). However, these and other unpleasant sensations experienced during exercise have their own specific neurophysiological mechanisms and verbal descriptors (i.e., quality) and can be differentiated from perception of effort (e.g., Ref. 19). Therefore, we believe that a narrower definition of exertion as “the effort expended in performing a physical activity” (Oxford Dictionary of Sports Science and Medicine) is physiologically more appropriate. Furthermore, this definition is in line with the verbal descriptors chosen by Borg for his RPE scale (“heavy/hard” and “light/easy”) (18) rather than ratings of hedonicity (“pleasant/unpleasant,” “feeling good/feeling bad,” “comfortable/uncomfortable”) (3).Perceived exertion and afferent feedback from skeletal muscles.Skeletal muscles are richly innervated by group III and IV fibers that provide afferent feedback related to metabolic, ionic, thermal, and mechanical stress (12). These small-diameter afferent fibers project, through lamina I neurons, to various spinal and supraspinal sites including the sensory cortex (5). Given the existence of such sensory system and the well-known increases in muscle metabolic by-products, potassium, temperature, and mechanical stress during intense exercise (12), it seems logical to assume that perception of effort is based on these afferent stimuli (Fig. 1A). Furthermore, there are high correlations between markers of metabolic stress (e.g., blood lactate concentration and %V̇o2max) with RPE during incremental exercise (18). However, the presence of the sensory machinery and a high correlation between the proposed metabolic stimuli and perceived exertion does not necessarily mean that the two are causally related. Indeed, several experimental studies in which perception of effort and metabolic stress have been dissociated argue against such common assumption.Fig. 1.Simplified afferent feedback (A) and corollary discharge (B) models of perceived exertion.Download figureDownload PowerPointFor example, when skeletal muscle weakness is induced by a small dose of curare (a drug that blocks transmission at the neuromuscular junction without affecting afferent pathways) there is a significant increase in RPE during cycling exercise (9). In theory, recruitment of glycolytic fibers due to the selective effect of curare on oxidative fibers may increase metabolic stimuli and perception of effort. However, the small increase in blood lactate concentration (0.36 mM) compared with the disproportionate increase in perceived exertion (4.8 points on Borg's 15-point RPE scale) argue against this hypothesis. Similarly, changes in afferent feedback from prefatigued locomotor muscles cannot explain the significant increase in perceived exertion we measured during a high-intensity cycling test (14). Indeed, we induced a significant reduction in locomotor muscle force using an e
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Cites
How do you feel? Interoception: The sense of the physiological condition of the body
Craig, A. D. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn894 · Cited by 6,006
Piña, I. L., Apstein, C. S., Balady, G. J., Belardinelli, R., Chaitman, B. R., Duscha, B. D., Fletcher, B. J., Fleg, J. L., Myers, J. N., & Sullivan, M. J. (2003) · Circulation · doi:10.1161/01.cir.0000055013.92097.40 · Cited by 1,030
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Buchheit, M., & Laursen, P. B. (2013) · Sports Medicine · doi:10.1007/s40279-013-0029-x · Cited by 1,490
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Shenhav, A., Musslick, S., Lieder, F., Kool, W., Griffiths, T. L., Cohen, J. D., & Botvinick, M. M. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031526 · Cited by 1,077
The Effects of Mental Fatigue on Physical Performance: A Systematic Review
Van Cutsem, J., Marcora, S., De Pauw, K., Bailey, S., Meeusen, R., & Roelands, B. (2017) · Sports Medicine · doi:10.1007/s40279-016-0672-0 · Cited by 924
Self-citationThe Importance of Respiratory Rate Monitoring: From Healthcare to Sport and Exercise
Nicolò, A., Massaroni, C., Schena, E., & Sacchetti, M. (2020) · Sensors · doi:10.3390/s20216396 · Cited by 440
On the origin of interoception
Ceunen, E., Vlaeyen, J. W. S., & Van Diest, I. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.00743 · Cited by 329
Metadata
- Authors
- Marcora, S.
- Venue
- Journal of Applied Physiology
- Publisher
- American Physiological Society
- Published
- 2009-06
- Volume
- 106
- Issue
- 6
- Pages
- 2060-2062
- ISSN
- 0161-7567 (ISSN-L)
- 8750-7587
- 1522-1601
- OpenAlex
- W2126718722
- Cited by
- 532
- References
- 2
- FWCI
- 38.67
- Type
- journal article
- Language
- en
- Open access
- closed
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