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Effect of high-intensity exercise on aged mouse brain mitochondria, neurogenesis, and inflammation
Open accessAbstract
In aged mice, we assessed how intensive exercise affects brain bioenergetics, inflammation, and neurogenesis-relevant parameters. After 8 weeks of a supra-lactate threshold treadmill exercise intervention, 21-month-old C57BL/6 mice showed increased brain peroxisome proliferator-activated receptor gamma coactivator-1α protein, mammalian target of rapamycin and phospho-mammalian target of rapamycin protein, citrate synthase messenger RNA, and mitochondrial DNA copy number. Hippocampal vascular endothelial growth factor A (VEGF-A) gene expression trended higher, and a positive correlation between VEGF-A and PRC messenger RNA levels was observed. Brain doublecortin, brain-derived neurotrophic factor, tumor necrosis factor-α, and CCL11 gene expression, as well as plasma CCL11 protein levels, were unchanged. Despite these apparent negative findings, a negative correlation between plasma CCL11 protein levels and hippocampal doublecortin gene expression was observed; further analysis indicated exercise may mitigate this relationship. Overall, our data suggest supra-lactate threshold exercise activates a partial mitochondrial biogenesis in aged mice, and a gene (VEGF-A) known to support neurogenesis. Our data are consistent with another study that found systemic inflammation in general, and CCL11 protein specifically, suppresses hippocampal neurogenesis. Our study supports the view that intense exercise above the lactate threshold may benefit the aging brain; future studies to address the extent to which exercise-generated lactate mediates the observed effects are warranted.
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“Studies conducted both in vitro and in animal models suggest that inflammation in general, and IL-1β and IFNα in particular, inhibit neurogenesis and reduce the magnitude of neurogenesis that is normally induced by exercise”
From Inflammageing: chronic inflammation in ageing, cardiovascular disease, and frailty (2018) · cites this paper as [288]
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1 retracted
Safdar, A., Bourgeois, J. M., Ogborn, D. I., Little, J. P., Hettinga, B. P., Akhtar, M., Thompson, J. E., Melov, S., Mocellin, N. J., Kujoth, G. C., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019581108 · Cited by 320
RetractedMatthews, D. R., Hosker, J. P., Rudenski, A. S., Naylor, B. A., Treacher, D. F., & Turner, R. C. (1985) · Diabetologia · doi:10.1007/bf00280883 · Cited by 31,502
Mechanism of activation of protein kinase B by insulin and IGF‐1.
Alessi, D. R., Andjelković, M., Caudwell, B., Cron, P. D., MORRICE, N. A., Cohen, P., & Hemmings, B. A. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb01045.x · Cited by 3,014
Premature ageing in mice expressing defective mitochondrial DNA polymerase
Trifunovic, A., Wredenberg, A., Falkenberg, M., Spelbrink, J. N., Rovio, A. T., Bruder, C. E., Bohlooly-Y, M., Gidlöf, S., Oldfors, A., Wibom, R., et al. (2004) · Nature · doi:10.1038/nature02517 · Cited by 2,734
Physiology of Sport and Exercise
Wilmore, J. H., COSTILL, D. L., & Gleim, G. W. (1995) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-199505000-00024 · Cited by 2,240
Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
Kujoth, G. C., Hiona, A., Pugh, T. D., Someya, S., Panzer, K., Wohlgemuth, S. E., Hofer, T., Seo, A. Y., Sullivan, R., Jobling, W. A., et al. (2005) · Science · doi:10.1126/science.1112125 · Cited by 2,165
Exercise enhances learning and hippocampal neurogenesis in aged mice
van Praag, H., Shubert, T., Zhao, C., & Gage, F. H. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1731-05.2005 · Cited by 2,078
The ageing systemic milieu negatively regulates neurogenesis and cognitive function
Villeda, S. A., Luo, J., Mosher, K. I., Zou, B., Britschgi, M., Bieri, G., Stan, T. M., Fainberg, N., Ding, Z., Eggel, A., et al. (2011) · Nature · doi:10.1038/nature10357 · Cited by 1,763
Transcriptional paradigms in mammalian mitochondrial biogenesis and function
Scarpulla, R. C. (2008) · Physiological Reviews · doi:10.1152/physrev.00025.2007 · Cited by 1,666
Inflammation is detrimental for neurogenesis in adult brain
Ekdahl, C. T., Claasen, J.-H., Bonde, S., Kokaia, Z., & Lindvall, O. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2234031100 · Cited by 1,559
Vascular endothelial growth factor (VEGF) stimulates neurogenesis in vitro and in vivo
Jin, K., Zhu, Y., Sun, Y., Mao, X. O., Xie, L., & Greenberg, D. A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182296499 · Cited by 1,507
mTOR controls mitochondrial oxidative function through a YY1–PGC-1α transcriptional complex
Cunningham, J. T., Rodgers, J. T., Arlow, D. H., Vazquez, F., Mootha, V. K., & Puigserver, P. (2007) · Nature · doi:10.1038/nature06322 · Cited by 1,488
Doublecortin Is a Microtubule-Associated Protein and Is Expressed Widely by Migrating Neurons
Gleeson, J. G., Lin, P. T., Flanagan, L. A., & Walsh, C. A. (1999) · Neuron · doi:10.1016/s0896-6273(00)80778-3 · Cited by 1,365
Metabolic control of mitochondrial biogenesis through the PGC-1 family regulatory network
Scarpulla, R. C. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.09.019 · Cited by 1,281
Effects of Aerobic Exercise on Mild Cognitive Impairment: A Controlled Trial
Baker, L. D., Frank, L. L., Foster-Schubert, K., Green, P. S., Wilkinson, C. W., McTiernan, A., Plymate, S. R., Fishel, M. A., Watson, G. S., Cholerton, B. A., et al. (2010) · Archives of Neurology · doi:10.1001/archneurol.2009.307 · Cited by 1,171
Woolley, C. S., Gould, E., & McEwen, B. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)90778-a · Cited by 1,020
Doublecortin expression levels in adult brain reflect neurogenesis
Couillard‐Després, S., Winner, B., Schaubeck, S., Aigner, R., Vroemen, M., Weidner, N., Bogdahn, U., Winkler, J., Kuhn, H. G., & Aigner, L. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03813.x · Cited by 990
NAVÉ, B. T., Ouwens, D. M., Withers, D. J., Alessi, D. R., & Shepherd, P. R. (1999) · Biochemical Journal · doi:10.1042/bj3440427 · Cited by 926
VEGF is necessary for exercise‐induced adult hippocampal neurogenesis
Fabel, K., Fabel, K., Tam, B., Kaufer, D., Baiker, A., Simmons, N., Kuo, C. J., & Palmer, T. D. (2003) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2003.03041.x · Cited by 861
Rossi, C., Angelucci, A., Costantin, L., Braschi, C., Mazzantini, M., Babbini, F., Fabbri, M. E., Tessarollo, L., Maffei, L., Berardi, N., et al. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05059.x · Cited by 619
Aerobic exercise improves hippocampal function and increases BDNF in the serum of young adult males
Griffin, É. W., Mullally, S. L., Foley, C., Warmington, S. A., O’Mara, S. M., & Kelly, A. M. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.06.005 · Cited by 581
PGC-1α regulation by exercise training and its influences on muscle function and insulin sensitivity
Lira, V. A., Benton, C. R., Yan, Z., & Bonen, A. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00755.2009 · Cited by 412
Exercise training increases mitochondrial biogenesis in the brain
Steiner, J. L., Murphy, E. A., McClellan, J. L., Carmichael, M. D., & Davis, J. M. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00343.2011 · Cited by 368
BrdU assay for neurogenesis in rodents
Wojtowicz, J. M., & Kee, N. (2006) · Nature Protocols · doi:10.1038/nprot.2006.224 · Cited by 357
FOXO3a regulates reactive oxygen metabolism by inhibiting mitochondrial gene expression
Ferber, E. C., Peck, B., Delpuech, O., Bell, G. P., East, P., & Schulze, A. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2011.179 · Cited by 320
Katoh‐Semba, R., TAKEUCHI, I. K., Semba, R., & Kato, K. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.69010034.x · Cited by 308
Mitochondrial biogenesis in exercise and in ageing☆
Viña, J., Gómez‐Cabrera, M. C., Borrás, C., Froio, T., Sanchis‐Gomar, F., Martinez-Bello, V. E., & Pallardó, F. V. (2009) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2009.06.006 · Cited by 261
Angiogenesis, Neurogenesis and Neuroplasticity in Ischemic Stroke
Font, M. À., Arboix, A., & Krupiński, J. (2010) · Current Cardiology Reviews · doi:10.2174/157340310791658802 · Cited by 222
Acute and chronic effects of exercise on tissue sensitivity to glucocorticoids
Duclos, M., Gouarne, C., & Bonnemaison, D. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00108.2002 · Cited by 193
Samavati, L., Lee, I., Mathes, I., Lottspeich, F., & Hüttemann, M. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801954200 · Cited by 186
Long-term exercise treatment reduces oxidative stress in the hippocampus of aging rats
Marosi, K., Bori, Z., Hart, N., Sárga, L., Koltai, E., Radák, Z., & Nyakas, C. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.001 · Cited by 186
Rothman, S. M., Griffioen, K. J., Wan, R., & Mattson, M. P. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06525.x · Cited by 185
DNA extraction procedures meaningfully influence qPCR-based mtDNA copy number determination
Guo, W., Jiang, L., Bhasin, S., Khan, S. M., & Swerdlow, R. H. (2009) · Mitochondrion · doi:10.1016/j.mito.2009.03.003 · Cited by 183
Self-citationInter- and intrastrain variation in mouse critical running speed
Billat, V. L., Mouisel, É., Roblot, N., & Melki, J. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00991.2004 · Cited by 176
Karadedou, C. T., Gomes, A., Chen, J., Petkovic, M., Ho, K. K. K., Zwolińska, A., Feltes, A., Wong, S. Y. S., Chan, K. Y. K., Cheung, Y., et al. (2011) · Oncogene · doi:10.1038/onc.2011.368 · Cited by 155
Systemic and mitochondrial adaptive responses to moderate exercise in rodents
Boveris, A., & Navarro, A. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.08.015 · Cited by 154
Assessing mitochondria biogenesis
Medeiros, D. M. (2008) · Methods · doi:10.1016/j.ymeth.2008.09.026 · Cited by 135
Mukhopadhyay, P., Horváth, B., Zsengellér, Z. K., Bátkai, S., Cao, Z., Kechrid, M., Holovac, E., Erdélyi, K., Tanchian, G., Liaudet, L., et al. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.05.036 · Cited by 132
Exercise training below and above the lactate threshold in the elderly
Belman, M. J., & Gaesser, G. A. (1991) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-199105000-00008 · Cited by 120
Tumor Necrosis Factor Alpha Inhibits Hepatocyte Mitochondrial Respiration
Stadler, J., Bentz, B. G., Harbrecht, B. G., Silvio, M. D., CURRAN, R. D., Billiar, T. R., HOFFMAN, R. A., & Simmons, R. L. (1992) · Annals of Surgery · doi:10.1097/00000658-199211000-00003 · Cited by 115
Lactate administration reproduces specific brain and liver exercise‐related changes
Lezi, E., Lu, J., Selfridge, J. E., Burns, J. M., & Swerdlow, R. H. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12394 · Cited by 115
Self-citationGSK3 as a Sensor Determining Cell Fate in the Brain
Cole, A. R. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00004 · Cited by 81
Effect of exercise on mouse liver and brain bioenergetic infrastructures
Lezi, E., Lu, J., Burns, J. M., & Swerdlow, R. H. (2012) · Experimental Physiology · doi:10.1113/expphysiol.2012.066688 · Cited by 49
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Ferrucci, L., & Fabbri, E. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0064-2 · Cited by 3,690
Physical Activity and Brain Health
Liegro, C. M. D., Schiera, G., Proia, P., & Liegro, I. D. (2019) · Genes · doi:10.3390/genes10090720 · Cited by 451
Raefsky, S. M., & Mattson, M. P. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.11.045 · Cited by 280
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Ma, C., Ma, X., Wang, J., Liu, H., Chen, Y., & Yang, Y. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.09.067 · Cited by 207
Ryan, S. M., & Nolan, Y. M. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.12.004 · Cited by 205
Metadata
- Authors
- E, L., Burns, J. M., & Swerdlow, R. H.
- Affiliations
- University of Kansas (US)
- University of Kansas Medical Center (US)
- Corresponding author
- Swerdlow, Russell H.
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2014-11
- Volume
- 35
- Issue
- 11
- Pages
- 2574-2583
- ISSN
- 0197-4580 (ISSN-L)
- PMC
- PMC4171347
- OpenAlex
- W2036466453
- Cited by
- 106
- References
- 43
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 10 · 2023: 6 · 2022: 8 · 2021: 18 · 2020: 14 · 2019: 8 · 2018: 6 · 2017: 10 · 2016: 6 · 2015: 4 · 2014: 1
- FWCI
- 2.43
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Neurobiology of Aging (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- University of Kansas Alzheimer's Disease Center (P30 AG035982)
- Mabel Woodyard Fellowship Award
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Physiology (medical) › Exercise and Physiological Responses
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- high-intensity exercise, brain aging, mitochondrial biogenesis, neurogenesis, systemic inflammation, eotaxin, VEGF-A, PGC-1α, mTOR, mitochondrial DNA copy number, citrate synthase, hippocampus, doublecortin, brain-derived neurotrophic factor, TNF-α, lactate threshold, treadmill exercise, aged mice
- MeSH terms
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Doublecortin Domain Proteins, Aging, Animals, Organelle Biogenesis, Brain, Citrate (si)-Synthase, DNA, Mitochondrial, Hippocampus, Humans, Inflammation, Lactates, Male, Mice, Inbred C57BL, Microtubule-Associated Proteins, Mitochondria, Neuropeptides, Physical Conditioning, Animal, RNA, Messenger, Transcription Factors, Gene Dosage, Vascular Endothelial Growth Factor A, Chemokine CCL11, Neurogenesis, TOR Serine-Threonine Kinases
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