Effect of Voluntary Exercise on Endogenous Pain Control Systems and Post-traumatic Headache in Mice

被引:10
作者
Bharadwaj, Vimala N. [1 ]
Sahbaie, Peyman [1 ,2 ]
Shi, Xiaoyou [1 ,2 ]
Irvine, Karen-Amanda [1 ,2 ]
Yeomans, David C. [1 ]
Clark, J. David [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Anesthesia Perioperat & Pain Med, Stanford, CA 94305 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Anesthesiol Serv, Palo Alto, CA USA
关键词
Exercise; traumatic brain injury; pain; post-traumatic headache; diffuse noxious inhibitory control; TRAUMATIC BRAIN-INJURY; C-TERMINAL HYDROLASE-L1; NEUROPATHIC PAIN; NERVE INJURY; PHYSICAL-EXERCISE; MEMORY DEFICITS; UP-REGULATION; MODULATION; MODEL; ANALGESIA;
D O I
10.1016/j.jpain.2023.05.015
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Traumatic brain injury (TBI) can cause acute and chronic pain along with motor, cognitive, and emotional problems. Although the mechanisms are poorly understood, previous studies suggest disruptions in endogenous pain modulation may be involved. Voluntary exercise after a TBI has been shown to reduce some consequences of injury including cognitive impairment. We hypothesized, therefore, that voluntary exercise could augment endogenous pain control systems in a rodent model of TBI. For these studies, we used a closed-head impact procedure in male mice modeling mild TBI. We investigated the effect of voluntary exercise on TBI-induced hindpaw nociceptive sensitization, diffuse noxious inhibitory control failure, and periorbital sensitization after bright light stress, a model of post-traumatic headache. Furthermore, we investigated the effects of exercise on memory, circulating markers of brain injury, neuroinflammation, and spinal cord gene expression. We observed that exercise significantly reduced TBI-induced hindpaw allodynia and periorbital allodynia in the first week following TBI. We also showed that exercise improved the deficits associated with diffuse noxious inhibitory control and reduced bright light stress-induced allodynia up to 2 months after TBI. In addition, exercise preserved memory and reduced TBI-induced increases in spinal BDNF, CXCL1, CXCL2, and prodynorphin expression, all genes previously linked to TBI-induced nociceptive sensitization. Taken together, our observations suggest that voluntary exercise may reduce pain after TBI by reducing TBI-induced changes in nociceptive signaling and preserving endogenous pain control systems.Perspective: This article evaluates the effects of exercise on pain-related behaviors in a preclinical model of traumatic brain injury (T8I). The findings show that exercise reduces nociceptive sensitization, loss of diffuse noxious inhibitory control, memory deficits, and spinal nociception-related gene expression after T8I. Exercise may reduce or prevent pain after T8I.(R) 2023 Published by Elsevier Inc. on behalf of United States Association for the Study of Pain, Inc All rights reserved.
引用
收藏
页码:1859 / 1874
页数:16
相关论文
共 92 条
[1]   The association between migraine and physical exercise [J].
Amin, Faisal Mohammad ;
Aristeidou, Stavroula ;
Baraldi, Carlo ;
Czapinska-Ciepiela, Ewa K. ;
Ariadni, Daponte D. ;
Di Lenola, Davide ;
Fenech, Cherilyn ;
Kampouris, Konstantinos ;
Karagiorgis, Giorgos ;
Braschinsky, Mark ;
Linde, Mattias .
JOURNAL OF HEADACHE AND PAIN, 2018, 19 :83
[2]   The benefits of voluntary physical exercise after traumatic brain injury on rat's object recognition memory: A comparison of different temporal schedules [J].
Amoros-Aguilar, Laura ;
Portell-Cortes, Isabel ;
Costa-Miserachs, David ;
Torras-Garcia, Meritxell ;
Riubugent-Camps, Elia ;
Almolda, Beatriz ;
Coll-Andreu, Margalida .
EXPERIMENTAL NEUROLOGY, 2020, 326
[3]   Post-traumatic headache attributed to traumatic brain injury: classification, clinical characteristics, and treatment [J].
Ashina, Hakan ;
Eigenbrodt, Anna K. ;
Seifert, Tad ;
Sinclair, Alexandra J. ;
Scher, Ann, I ;
Schytz, Henrik W. ;
Lee, Mi Ji ;
De Icco, Roberto ;
Finkel, Alan G. ;
Ashina, Messoud .
LANCET NEUROLOGY, 2021, 20 (06) :460-469
[4]   Post-traumatic headache: epidemiology and pathophysiological insights [J].
Ashina, Hetkan ;
Porreca, Frank ;
Anderson, Trent ;
Amin, Faisal Mohammad ;
Ashina, Messoud ;
Schytz, Henrik Winther ;
Dodick, David W. .
NATURE REVIEWS NEUROLOGY, 2019, 15 (10) :607-617
[5]  
Basbaum AI, 2009, NEUROMODULATION, VOLS 1 AND 2, P303, DOI 10.1016/B978-0-12-374248-3.00023-9
[6]   Role of brainstem serotonin in analgesia produced by low-intensity exercise on neuropathic pain after sciatic nerve injury in mice [J].
Bobinski, Franciane ;
Ferreira, Tamara A. A. ;
Cordova, Marina M. ;
Dombrowski, Patricia A. ;
da Cunha, Claudio ;
do Espirito Santo, Caroline C. ;
Poli, Anicleto ;
Pires, Rita G. W. ;
Martins-Silva, Cristina ;
Sluka, Kathleen A. ;
Santos, Adair R. S. .
PAIN, 2015, 156 (12) :2595-2606
[7]   Enhanced post-traumatic headache-like behaviors and diminished contribution of peripheral CGRP in female rats following a mild closed head injury [J].
Bree, Dara ;
Mackenzie, Kimberly ;
Stratton, Jennifer ;
Levy, Dan .
CEPHALALGIA, 2020, 40 (07) :748-760
[8]   Measuring Pain in TBI: Development of the TBI-QOL Pain Interference Item Bank and Short Form [J].
Carlozzi, Noelle E. ;
Kisala, Pamela A. ;
Boulton, Aaron J. ;
Roth, Elliot ;
Kratz, Anna L. ;
Sherer, Mark ;
Sander, Angelle M. ;
Heinemann, Allen W. ;
Chiaravalloti, Nancy D. ;
Bushnik, Tamara ;
Tulsky, David S. .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 2020, 101 (01) :11-19
[9]  
Centers for Disease Control and Prevention, Moderate and severe TBI
[10]   QUANTITATIVE ASSESSMENT OF TACTILE ALLODYNIA IN THE RAT PAW [J].
CHAPLAN, SR ;
BACH, FW ;
POGREL, JW ;
CHUNG, JM ;
YAKSH, TL .
JOURNAL OF NEUROSCIENCE METHODS, 1994, 53 (01) :55-63