TY - JOUR
T1 - A microbiome-dependent gut–brain pathway regulates motivation for exercise
AU - Dohnalová, Lenka
AU - Lundgren, Patrick
AU - Carty, Jamie R.E.
AU - Goldstein, Nitsan
AU - Wenski, Sebastian L.
AU - Nanudorn, Pakjira
AU - Thiengmag, Sirinthra
AU - Huang, Kuei Pin
AU - Litichevskiy, Lev
AU - Descamps, Hélène C.
AU - Chellappa, Karthikeyani
AU - Glassman, Ana
AU - Kessler, Susanne
AU - Kim, Jihee
AU - Cox, Timothy O.
AU - Dmitrieva-Posocco, Oxana
AU - Wong, Andrea C.
AU - Allman, Erik L.
AU - Ghosh, Soumita
AU - Sharma, Nitika
AU - Sengupta, Kasturi
AU - Cornes, Belinda
AU - Dean, Nitai
AU - Churchill, Gary A.
AU - Khurana, Tejvir S.
AU - Sellmyer, Mark A.
AU - FitzGerald, Garret A.
AU - Patterson, Andrew D.
AU - Baur, Joseph A.
AU - Alhadeff, Amber L.
AU - Helfrich, Eric J.N.
AU - Levy, Maayan
AU - Betley, J. Nicholas
AU - Thaiss, Christoph A.
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2022/12/22
Y1 - 2022/12/22
N2 - Exercise exerts a wide range of beneficial effects for healthy physiology1. However, the mechanisms regulating an individual’s motivation to engage in physical activity remain incompletely understood. An important factor stimulating the engagement in both competitive and recreational exercise is the motivating pleasure derived from prolonged physical activity, which is triggered by exercise-induced neurochemical changes in the brain. Here, we report on the discovery of a gut–brain connection in mice that enhances exercise performance by augmenting dopamine signalling during physical activity. We find that microbiome-dependent production of endocannabinoid metabolites in the gut stimulates the activity of TRPV1-expressing sensory neurons and thereby elevates dopamine levels in the ventral striatum during exercise. Stimulation of this pathway improves running performance, whereas microbiome depletion, peripheral endocannabinoid receptor inhibition, ablation of spinal afferent neurons or dopamine blockade abrogate exercise capacity. These findings indicate that the rewarding properties of exercise are influenced by gut-derived interoceptive circuits and provide a microbiome-dependent explanation for interindividual variability in exercise performance. Our study also suggests that interoceptomimetic molecules that stimulate the transmission of gut-derived signals to the brain may enhance the motivation for exercise.
AB - Exercise exerts a wide range of beneficial effects for healthy physiology1. However, the mechanisms regulating an individual’s motivation to engage in physical activity remain incompletely understood. An important factor stimulating the engagement in both competitive and recreational exercise is the motivating pleasure derived from prolonged physical activity, which is triggered by exercise-induced neurochemical changes in the brain. Here, we report on the discovery of a gut–brain connection in mice that enhances exercise performance by augmenting dopamine signalling during physical activity. We find that microbiome-dependent production of endocannabinoid metabolites in the gut stimulates the activity of TRPV1-expressing sensory neurons and thereby elevates dopamine levels in the ventral striatum during exercise. Stimulation of this pathway improves running performance, whereas microbiome depletion, peripheral endocannabinoid receptor inhibition, ablation of spinal afferent neurons or dopamine blockade abrogate exercise capacity. These findings indicate that the rewarding properties of exercise are influenced by gut-derived interoceptive circuits and provide a microbiome-dependent explanation for interindividual variability in exercise performance. Our study also suggests that interoceptomimetic molecules that stimulate the transmission of gut-derived signals to the brain may enhance the motivation for exercise.
UR - http://www.scopus.com/inward/record.url?scp=85143760144&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85143760144&partnerID=8YFLogxK
U2 - 10.1038/s41586-022-05525-z
DO - 10.1038/s41586-022-05525-z
M3 - Article
C2 - 36517598
AN - SCOPUS:85143760144
SN - 0028-0836
VL - 612
SP - 739
EP - 747
JO - Nature
JF - Nature
IS - 7941
ER -