Regular treadmill running improves spatial learning and memory performance in young mice through increased hippocampal neurogenesis and decreased stress

Running increases cell proliferation and neurogenesis in the adult mouse dentate gyrus

van Praag, H., Kempermann, G., & Gage, F. H. (1999) · Nature Neuroscience · doi:10.1038/6368 · Cited by 3,880 · see citing works

Running enhances neurogenesis, learning, and long-term potentiation in mice

van Praag, H., Christie, B. R., Sejnowski, T. J., & Gage, F. H. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13427 · Cited by 2,904 · see citing works

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 · see citing works

A Functional Role for Adult Hippocampal Neurogenesis in Spatial Pattern Separation

Clelland, C. D., Choi, M., Romberg, C., Clemenson, G. D., Fragniere, A., Tyers, P., Jessberger, S., Saksida, L. M., Barker, R. A., Gage, F. H., et al. (2009) · Science · doi:10.1126/science.1173215 · Cited by 1,642 · see citing works

Milestones of neuronal development in the adult hippocampus

Kempermann, G., Jessberger, S., Steiner, B., & Kronenberg, G. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.05.013 · Cited by 1,411 · see citing works

Effects of physical exercise on anxiety, depression, and sensitivity to stress

Salmon, P. (2001) · Clinical Psychology Review · doi:10.1016/s0272-7358(99)00032-x · Cited by 1,363 · see citing works

Neurogenesis and Exercise: Past and Future Directions

van Praag, H. (2008) · NeuroMolecular Medicine · doi:10.1007/s12017-008-8028-z · Cited by 645 · see citing works

Subpopulations of proliferating cells of the adult hippocampus respond differently to physiologic neurogenic stimuli

Kronenberg, G., Reuter, K., Steiner, B., Brandt, M. D., Jessberger, S., Yamaguchi, M., & Kempermann, G. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10945 · Cited by 640 · see citing works

Transient calretinin expression defines early postmitotic step of neuronal differentiation in adult hippocampal neurogenesis of mice

Brandt, M., Jessberger, S., Steiner, B., Kronenberg, G., Reuter, K., Bick‐Sander, A., von der Behrens, W., & Kempermann, G. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00207-0 · Cited by 498 · see citing works

The effect of exercise on depression, anxiety and other mood states: A review

Byrne, A., & Byrne, D. G. (1993) · Journal of Psychosomatic Research · doi:10.1016/0022-3999(93)90050-p · Cited by 497 · see citing works

Additive effects of physical exercise and environmental enrichment on adult hippocampal neurogenesis in mice

Fabel, K. (2009) · Frontiers in Neuroscience · doi:10.3389/neuro.22.002.2009 · Cited by 429 · see citing works

Exposure to fox odor inhibits cell proliferation in the hippocampus of adult rats via an adrenal hormone‐dependent mechanism

Tanapat, P., Hastings, N. B., Rydel, T. A., Galea, L. A. M., & Gould, E. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1297 · Cited by 376 · see citing works

BrdU assay for neurogenesis in rodents

Wojtowicz, J. M., & Kee, N. (2006) · Nature Protocols · doi:10.1038/nprot.2006.224 · Cited by 349 · see citing works

Effects of long-term voluntary exercise on the mouse hypothalamic–pituitary–adrenocortical axis

Droste, S. K., Gesing, A., Ulbricht, S., Müller, M. B., Linthorst, A. C. E., & Reul, J. M. H. M. (2003) · Endocrinology · doi:10.1210/en.2003-0097 · Cited by 324 · see citing works

Cognitive and Physical Activity Differently Modulate Disease Progression in the Amyloid Precursor Protein (APP)-23 Model of Alzheimer’s Disease

Wolf, S. A., Kronenberg, G., Lehmann, K., Blankenship, A., Overall, R., Staufenbiel, M., & Kempermann, G. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.04.004 · Cited by 288 · see citing works

Oxygen consumption in adult and aged C57BL/6J mice during acute treadmill exercise of different intensity

Schefer, V., & Talan, M. I. (1996) · Experimental Gerontology · doi:10.1016/0531-5565(95)02032-2 · Cited by 278 · see citing works

Voluntary exercise induces anxiety‐like behavior in adult C57BL/6J mice correlating with hippocampal neurogenesis

Fuss, J., Ben Abdallah, N. M. ‐., Vogt, M. A., Touma, C., Pacifici, P. G., Palme, R., Witzemann, V., Hellweg, R., & Gass, P. (2010) · Hippocampus · doi:10.1002/hipo.20634 · Cited by 240 · see citing works

Acute stress enhances adult rat hippocampal neurogenesis and activation of newborn neurons via secreted astrocytic FGF2

Kirby, E. D., Muroy, S. E., Sun, W. G., Covarrubias, D., Leong, M. J., Barchas, L. A., & Kaufer, D. (2013) · eLife · doi:10.7554/elife.00362 · Cited by 238 · see citing works

Adult hippocampal neurogenesis and voluntary running activity: Circadian and dose‐dependent effects

Holmes, M. M., Galea, L. A. M., Mistlberger, R. E., & Kempermann, G. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20039 · Cited by 233 · see citing works

Exercise influences spatial learning in the radial arm maze

Anderson, B. J., Rapp, D. N., Baek, D. H., McCloskey, D. P., Coburn-Litvak, P. S., & Robinson, J. K. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(00)00282-1 · Cited by 213 · see citing works

The effects of exercise training on mood and perceived coping ability in anxious adults from the general population

Steptoe, A., Edwards, S., Moses, J. L., & Mathews, A. (1989) · Journal of Psychosomatic Research · doi:10.1016/0022-3999(89)90061-5 · Cited by 206 · see citing works

Effects of chronic treadmill running on neurogenesis in the dentate gyrus of the hippocampus of adult rat

Uda, M., Ishido, M., Kami, K., & Masuhara, M. (2006) · Brain Research · doi:10.1016/j.brainres.2006.05.066 · Cited by 193 · see citing works

Recruitment of adult-generated neurons into functional hippocampal networks contributes to updating and strengthening of spatial memory

Trouche, S. G., Bontempi, B., Roullet, P., & Rampon, C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811054106 · Cited by 192 · see citing works

The effects of exercise and stress on the survival and maturation of adult‐generated granule cells

Snyder, J. S., Glover, L. R., Sanzone, K. M., Kamhi, J. F., & Cameron, H. A. (2009) · Hippocampus · doi:10.1002/hipo.20552 · Cited by 181 · see citing works

Treadmill exercise counteracts the suppressive effects of peripheral lipopolysaccharide on hippocampal neurogenesis and learning and memory

Wu, C., Chen, Y., Yu, L., Chen, H., Jen, C. J., Huang, A., Tsai, H., Chang, Y., & Kuo, Y. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04987.x · Cited by 175 · see citing works

Brain norepinephrine and metabolites after treadmill training and wheel running in rats

DUNN, A. L., REIGLE, T. G., YOUNGSTEDT, S. D., ARMSTRONG, R. B., & DISHMAN, R. K. (1996) · Medicine &amp Science in Sports &amp Exercise · doi:10.1097/00005768-199602000-00008 · Cited by 165 · see citing works

Ataxia telangiectasia mutated is essential during adult neurogenesisPreprint

Allen, D. M., van Praag, H., Ray, J., Ohler, Z. W., Winrow, C. J., Carter, T. A., Braquet, R., Harrington, E. A., Ried, T., Brown, K. D., et al. (2001) · Genes & Development · doi:10.1101/gad.869001 · Cited by 159 · see citing works

Time-dependent corticosteroid modulation of prefrontal working memory processing

Henckens, M. J. A. G., van Wingen, G. A., Joëls, M., & Fernández, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019128108 · Cited by 155 · see citing works

Alterations in spatial learning and memory after forced exercise

Ang, E.-T., Dawe, G. S., Wong, P. T. H., Moochhala, S., & Ng, Y.-K. (2006) · Brain Research · doi:10.1016/j.brainres.2006.07.023 · Cited by 144 · see citing works

Enhancement of spatial learning in F344 rats by physical activity and related learning-associated alterations in hippocampal and cortical cholinergic functioning

Fordyce, D. E., & Farrar, R. P. (1991) · Behavioural Brain Research · doi:10.1016/s0166-4328(05)80105-6 · Cited by 144 · see citing works

A systematic forward genetic analysis identified components of the Chlamydomonas circadian systemPreprint

Matsuo, T., Okamoto, K., Onai, K., Niwa, Y., Shimogawara, K., & Ishiura, M. (2008) · Genes & Development · doi:10.1101/gad.1650408 · Cited by 126 · see citing works

Learning-Induced Survival of New Neurons Depends on the Cognitive Status of Aged Rats

Drapeau, E., Montaron, M., Aguerre, S., & Abrous, D. N. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1031-07.2007 · Cited by 119 · see citing works

Deletion of Running-Induced Hippocampal Neurogenesis by Irradiation Prevents Development of an Anxious Phenotype in Mice

Fuss, J., Ben Abdallah, N. M. B., Hensley, F. W., Weber, K.-J., Hellweg, R., & Gass, P. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012769 · Cited by 110 · see citing works

Hippocampal cell proliferation across the day: Increase by running wheel activity, but no effect of sleep and wakefulness

van der Borght, K., Ferrari, F., Klauke, K., Román, V., Havekes, R., Sgoifo, A., van der Zee, E. A., & Meerlo, P. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.08.012 · Cited by 101 · see citing works

Magnitude- and Time-Dependence of the Effect of Treadmill Exercise on Cell Proliferation in the Dentate Gyrus of Rats

Kim, Y.-P., Kim, H.-B., Jang, M.-H., Lim, B., Kim, Y.-J., Kim, H., Kim, S.-S., Kim, E.-H., & Kim, C. (2003) · International Journal of Sports Medicine · doi:10.1055/s-2003-38202 · Cited by 96 · see citing works

Treadmill running and swimming increase cell proliferation in the hippocampal dentate gyrus of rats

Ra, S.-M., Kim, H. K., Jang, M.-H., Shin, M.-C., Lee, T.-H., Lim, B., Kim, C., Kim, E., Kim, K.-M., & Kim, S. (2002) · Neuroscience Letters · doi:10.1016/s0304-3940(02)01031-5 · Cited by 83 · see citing works

Adrenal steroids suppress granule cell death in the developing dentate gyrus through an NMDA receptor-dependent mechanism

Gould, E., Tanapat, P., & Cameron, H. A. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00079-5 · Cited by 75 · see citing works

Chronic unpredictable mild stress alters an anxiety-related defensive response, Fos immunoreactivity and hippocampal adult neurogenesis

de Andrade, J. S., Céspedes, I. C., Abrão, R. O., Santos, T. B., Diniz, L., Britto, L. R. G., Spadari-Bratfisch, R. C., Ortolani, D., Melo-Thomas, L., da Silva, R. C. B., et al. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.031 · Cited by 69 · see citing works

Time-of-Day-Dependent Enhancement of Adult Neurogenesis in the Hippocampus

Tamai, S.-I., Sanada, K., & Fukada, Y. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003835 · Cited by 62 · see citing works

Voluntary wheel running initially increases adrenal sensitivity to adrenocorticotrophic hormone, which is attenuated with long-term training

Campbell, J. E., Rakhshani, N., Fediuc, S., Bruni, S. G., & Riddell, M. C. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.91128.2008 · Cited by 60 · see citing works

Effect of the exercise-induced increase in glucocorticoids on endurance in the rat

Sellers, T. L., Jaussi, A. W., Yang, H., Heninger, R. W., & Winder, W. W. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.65.1.173 · Cited by 56 · see citing works

Cognitive Reserve and Alzheimer’s Disease

Xu, W., Yu, J., Tan, M., & Tan, L. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8720-y · Cited by 240 · see citing works

The exercise-glucocorticoid paradox: How exercise is beneficial to cognition, mood, and the brain while increasing glucocorticoid levels

Chen, C., Nakagawa, S., An, Y., Ito, K., Kitaichi, Y., & Kusumi, I. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.12.001 · Cited by 191 · see citing works

Human umbilical cord mesenchymal stem cells transplantation improves cognitive function in Alzheimer’s disease mice by decreasing oxidative stress and promoting hippocampal neurogenesis

Cui, Y., Ma, S., Zhang, C., Cao, W., Liu, M., Li, D., Lv, P., Xing, Q., Qu, R., Yao, N., et al. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.12.021 · Cited by 147 · see citing works

Moderate treadmill exercise ameliorates amyloid-β-induced learning and memory impairment, possibly via increasing AMPK activity and up-regulation of the PGC-1α/FNDC5/BDNF pathway

Azimi, M., Gharakhanlou, R., Naghdi, N., Khodadadi, D., & Heysieattalab, S. (2018) · Peptides · doi:10.1016/j.peptides.2017.12.027 · Cited by 109 · see citing works

Healthy Body, Healthy Mind?

Halperin, J. M., Berwid, O. G., & O’Neill, S. (2014) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2014.05.005 · Cited by 75 · see citing works

A Runner’s High for New Neurons? Potential Role for Endorphins in Exercise Effects on Adult Neurogenesis

Schoenfeld, T. J., & Swanson, C. (2021) · Biomolecules · doi:10.3390/biom11081077 · Cited by 78 · see citing works

Food and water restriction lead to differential learning behaviors in a head-fixed two-choice visual discrimination task for mice

Goltstein, P. M., Reinert, S., Glas, A., Bonhoeffer, T., & Hübener, M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0204066 · Cited by 68 · see citing works

Leisure‐time physical activity sustained since midlife and preservation of cognitive function: The Atherosclerosis Risk in Communities Study

Palta, P., Sharrett, A. R., Deal, J. A., Evenson, K. R., Gabriel, K. P., Folsom, A. R., Gross, A. L., Windham, B. G., Knopman, D. S., Mosley, T. H., et al. (2018) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2018.08.008 · Cited by 67 · see citing works

The benefits of exercise on structural and functional plasticity in the rodent hippocampus of different disease models.

Patten, A. R., Yau, S. Y., Fontaine, C. J., Meconi, A., Wortman, R. C., & Christie, B. R. (2015) · Brain Plasticity · doi:10.3233/bpl-150016 · Cited by 64 · see citing works

Long-term effects of early adolescent stress: dysregulation of hypothalamic–pituitary–adrenal axis and central corticotropin releasing factor receptor 1 expression in adult male rats

Li, C., Liu, Y., Yin, S., Cui-yan, L., Liu, D., Jiang, H., & Pan, F. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.04.007 · Cited by 62 · see citing works

Exercise effects on brain and behavior in healthy mice, Alzheimer’s disease and Parkinson’s disease model—A systematic review and meta-analysis

da Costa Daniele, T. M., de Bruin, P. F. C., de Matos, R. S., de Bruin, G. S., Maia Chaves, C., & de Bruin, V. M. S. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112488 · Cited by 59 · see citing works

Lifestyle Shapes the Dialogue between Environment, Microglia, and Adult Neurogenesis

Valero, J., Paris, I., & Sierra, A. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00009 · Cited by 60 · see citing works

Glucocorticoid‐mediated mechanisms of hippocampal damage: Contribution of subgranular neurogenesis

Podgorny, O. V., & Gulyaeva, N. V. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15265 · Cited by 59 · see citing works

Exercise improves learning and memory impairments in sleep deprived female rats

Saadati, H., Esmaeili‐Mahani, S., Esmaeilpour, K., Nazeri, M., Mazhari, S., & Sheibani, V. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.10.006 · Cited by 57 · see citing works

Exercise and cerebrovascular plasticity

Nishijima, T., Torres‐Alemán, I., & Soya, H. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.03.010 · Cited by 53 · see citing works

Effects of Different Exercise Strategies and Intensities on Memory Performance and Neurogenesis

Diederich, K., Bastl, A., Wersching, H., Teuber, A., Strecker, J., Schmidt, A., Minnerup, J., & Schäbitz, W. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00047 · Cited by 53 · see citing works

Effects of treadmill exercise intensity on spatial working memory and long-term memory in rats

Wang, X., & Wang, G.-W. (2016) · Life Sciences · doi:10.1016/j.lfs.2016.02.070 · Cited by 49 · see citing works

Mouse genetic differences in voluntary wheel running, adult hippocampal neurogenesis and learning on the multi-strain-adapted plus water maze

Merritt, J. R., & Rhodes, J. S. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.11.030 · Cited by 46 · see citing works

Therapeutic Effects of High-Intensity Interval Training Exercise Alone and Its Combination with Ecdysterone Against Amyloid Beta-Induced Rat Model of Alzheimer’s Disease: A Behavioral, Biochemical, and Histological Study

Gholipour, P., Komaki‬, A., Parsa, H., & Ramezani, M. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03603-2 · Cited by 43 · see citing works

Walking, Running, Swimming: An Analysis of the Effects of Land and Water Aerobic Exercises on Cognitive Functions and Neural Substrates

Serra, L., Petrosini, L., Mandolesi, L., Bonarota, S., Balsamo, F., Bozzali, M., Caltagirone, C., & Gelfo, F. (2022) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph192316310 · Cited by 43 · see citing works

Effects of the combination of high-intensity interval training and Ecdysterone on learning and memory abilities, antioxidant enzyme activities, and neuronal population in an Amyloid-beta-induced rat model of Alzheimer’s disease

Gholipour, P., Komaki, A., Ramezani, M., & Parsa, H. (2022) · Physiology & Behavior · doi:10.1016/j.physbeh.2022.113817 · Cited by 37 · see citing works

Can Exercise Make You Smarter, Happier, and Have More Neurons? A Hormetic Perspective

Gradari, S., Pallé, A., McGreevy, K. R., Fontán‐Lozano, Á., & Trejo, J. L. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00093 · Cited by 37 · see citing works

High-Intensity Exercise Training Protects the Brain Against Autoimmune Neuroinflammation: Regulation of Microglial Redox and Pro-inflammatory Functions

Zaychik, Y., Fainstein, N., Touloumi, O., Goldberg, Y., Hamdi, L., Segal, S., Nabat, H., Zoidou, S., Grigoriadis, N., Katz, A., et al. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.640724 · Cited by 38 · see citing works

Exercise Modalities Improve Aversive Memory and Survival Rate in Aged Rats: Role of Hippocampal Epigenetic Modifications

de Meireles, L. C. F., Galvão, F., Walker, D. M., Cechinel, L. R., Grefenhagen, Á. I. D. S., de Andrade, G. G., Palazzo, R. P., Lovatel, G. A., Basso, C. G., Nestler, E. J., et al. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-01675-w · Cited by 35 · see citing works

Does leaving water make fish smarter? Terrestrial exposure and exercise improve spatial learning in an amphibious fish

Rossi, G. S., & Wright, P. A. (2021) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2021.0603 · Cited by 29 · see citing works

Ceasing exercise induces depression-like, anxiety-like, and impaired cognitive-like behaviours and altered hippocampal gene expression

Morgan, J., Singhal, G., Corrigan, F., Jaehne, E. J., Jawahar, M. C., Breen, J., Pederson, S., & Baune, B. T. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.02.014 · Cited by 29 · see citing works

Potential Involvement of Adiponectin Signaling in Regulating Physical Exercise-Elicited Hippocampal Neurogenesis and Dendritic Morphology in Stressed Mice

Wang, P., Liang, Y., Chen, K., Yau, S., Sun, X., Cheng, K. K. Y., Xu, A., So, K., & Li, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00189 · Cited by 29 · see citing works

Three-Week Treadmill Exercise Enhances Persistent Inward Currents, Facilitates Dendritic Plasticity, and Upregulates the Excitability of Dorsal Raphe Serotonin Neurons in ePet-EYFP Mice

Ge, R., & Dai, Y. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.575626 · Cited by 29 · see citing works

Sequential treadmill exercise and cognitive training synergistically increase adult hippocampal neurogenesis in mice

Ávila‐Gámiz, F., Pérez-Cano, A. M., Pérez-Berlanga, J. M., Mullor-Vigo, R. M., Zambrana-Infantes, E. N., Santín, L. J., & de Guevara‐Miranda, D. L. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114184 · Cited by 25 · see citing works

Is hippocampal neurogenesis modulated by the sensation of self-motion encoded by the vestibular system?

Smith, P. F. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.09.013 · Cited by 23 · see citing works

Central monoaminergic systems are a site of convergence of signals conveying the experience of exercise to brain circuits involved in cognition and emotional behavior

Nicastro, T. M., & Greenwood, B. N. (2016) · Current Zoology · doi:10.1093/cz/zow027 · Cited by 21 · see citing works

An integrated model of acute exercise on memory function

Loprinzi, P. D. (2019) · Medical Hypotheses · doi:10.1016/j.mehy.2019.03.010 · Cited by 20 · see citing works

Effects of different exercise modes and intensities on cognitive performance, adult hippocampal neurogenesis, and synaptic plasticity in mice

Jiang, H., Kimura, Y., Inoue, S., Li, C., Hatakeyama, J., Wakayama, M., Takamura, D., & Moriyama, H. (2024) · Experimental Brain Research · doi:10.1007/s00221-024-06854-3 · Cited by 19 · see citing works

Evaluating Exercise as a Therapeutic Intervention for Methamphetamine Addiction-Like Behavior

Somkuwar, S. S., Staples, M. C., Fannon, M. J., Ghofranian, A., & Mandyam, C. D. (2015) · Brain Plasticity · doi:10.3233/bpl-150007 · Cited by 19 · see citing works

Mechanical Regulation Underlies Effects of Exercise on Serotonin-Induced Signaling in the Prefrontal Cortex Neurons

Ryu, Y., Maekawa, T., Yoshino, D., Sakitani, N., Takashima, A., Inoue, T., Suzurikawa, J., Toyohara, J., Tago, T., Makuuchi, M., et al. (2020) · iScience · doi:10.1016/j.isci.2020.100874 · Cited by 17 · see citing works

Effects of Hippocampal Microinjection of Irisin, an Exercise-Induced Myokine, on Spatial and Passive Avoidance Learning and Memory in Male Rats

Mohammadi, S., Oryan, S., Komaki‬, A., Eidi, A., & Zarei, M. (2019) · International Journal of Peptide Research and Therapeutics · doi:10.1007/s10989-019-09842-2 · Cited by 16 · see citing works

The endocannabinoid system regulates the moderate exercise-induced enhancement of learning and memory in mice

Wang, H., & Han, J. (2020) · The Journal of Sports Medicine and Physical Fitness · doi:10.23736/s0022-4707.19.10235-6 · Cited by 16 · see citing works

Long-term voluntary running improves cognitive ability in developing mice by modulating the cholinergic system, antioxidant ability, and BDNF/PI3K/Akt/CREB pathway

Wan, C., Shi, L., Lai, Y.-Y., Wu, Z., Zou, M., Liu, Z., Meng, W., & Wang, S. (2024) · Neuroscience Letters · doi:10.1016/j.neulet.2024.137872 · Cited by 15 · see citing works

Potential Biomarkers for Physical Exercise-Induced Brain Health

Yau, S. Y., Li, A., Sun, X., Fontaine, C. J., Christie, B. R., & So, K. (2016) · InTech eBooks · doi:10.5772/62458 · Cited by 16 · see citing works

Role of Biomarkers in Medicine

Wang, M., & Witzmann, F. A. (2016) · InTech eBooks · doi:10.5772/61449 · Cited by 15 · see citing works

Microglial modulation as a mechanism behind the promotion of central nervous system well‐being by physical exercise

Jensen, S. K., & Yong, V. W. (2014) · Clinical and Experimental Neuroimmunology · doi:10.1111/cen3.12093 · Cited by 12 · see citing works

Exercise before pregnancy attenuates the effects of prenatal stress in adult mice in a sex‐dependent manner

Luft, C., Levices, I. P., da Costa, M. S., Haute, G. V., Grassi‐Oliveira, R., de Oliveira, J. R., & Donadio, M. V. F. (2020) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10001 · Cited by 11 · see citing works

Active transportation, physical activity, and health

Woodward, A. J., & Wild, K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819136-1.00005-x · Cited by 11 · see citing works

Ecdysterone and High-Intensity Interval Training Mitigate Alzheimer’s Pathology in Rats: Impacts on Depression, Synaptic Plasticity, and Neuroinflammation

Gholipour, P., Komaki‬, A., Parsa, H., & Ramezani, M. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05168-x · Cited by 10 · see citing works

Stress

Sun, M., & Alkon, D. L. (2014) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000045 · Cited by 10 · see citing works

Developmental effects of wheel running on hippocampal glutamate receptor expression in young and mature adult rats

Staples, M. C., Somkuwar, S. S., & Mandyam, C. D. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.07.058 · Cited by 9 · see citing works

Running wheel training does not change neurogenesis levels or alter working memory tasks in adult rats

Acevedo-Triana, C. A., Rojas, M. J., & Cárdenas, F. P. (2017) · PeerJ · doi:10.7717/peerj.2976 · Cited by 8 · see citing works

Running to remember: The effects of exercise on perineuronal nets, microglia, and hippocampal angiogenesis in female and male mice

Maheu, M. G., James, N., Clark, Z., Yang, A. J. T., Patel, R., Beaudette, S. M., MacPherson, R. E. K., & Duarte‐Guterman, P. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115478 · Cited by 7 · see citing works

Maternal gastrointestinal nematode infection enhances spatial memory of uninfected juvenile mouse pups

Noel, S. C., Fortin-Hamel, L., Haque, M., & Scott, M. E. (2022) · Scientific Reports · doi:10.1038/s41598-022-13971-y · Cited by 7 · see citing works

Sex-dependent metabolic effects of pregestational exercise on prenatally stressed mice

Luft, C., Levices, I. P., Pedrazza, L., de Oliveira, J. R., & Donadio, M. V. F. (2020) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174420000343 · Cited by 6 · see citing works

Animal Models of Exercise–Brain Interactions

Hamilton, G. F., & Rhodes, J. S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800778-5.00003-7 · Cited by 5 · see citing works

The Exercise–Cognition Interaction and ADHD

O’Neill, S. C., Berwid, O. G., & Bedard, A. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800778-5.00018-9 · Cited by 5 · see citing works

High-intensity interval and moderate-intensity continuous training ameliorate the deteriorating acute effect of noise stress on corticosterone and testosterone in rats

Sharifabadi, A., Safari, M., Hofmeister, M., Rezaei, R., Farahbakht, E., & Jahromi, M. K. (2022) · Steroids · doi:10.1016/j.steroids.2022.109134 · Cited by 5 · see citing works

Pomegranate Extract Administration Reverses Loss of Motor Coordination and Prevents Oxidative Stress in Cerebellum of Aging Mice

Verdú, D., Valls, A., Díaz, A., Carretero, A., Dromant, M., Kuligowski, J., Serna, E., & Viña, J. (2023) · Antioxidants · doi:10.3390/antiox12111991 · Cited by 4 · see citing works

Interplay between Learning and Voluntary Wheel Running in Male C57BL/6NCrl Mice

Niiranen, L., Stenbäck, V., Tulppo, M. P., Herzig, K., & Mäkelä, K. A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054259 · Cited by 3 · see citing works

Non-Pharmacological Interventions for Enhancing Brain Plasticity and Promoting Brain Recovery: A Review

Farzana, F., Ahuja, Y. R., & Vemula, S. (2013) · Research in neuroscience · Cited by 3 · see citing works

Other Approaches: From Neurofeedback to Cognitive-Enhancing Drugs

Jaušovec, N., & Pahor, A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809407-5.00005-1 · Cited by 2 · see citing works

Application of Passive Head Motion to Generate Defined Accelerations at the Heads of Rodents

Maekawa, T., Sakitani, N., Ryu, Y., Takashima, A., Murase, S., Fink, J. E., Nagao, M., Ogata, T., Shinohara, M., & Sawada, Y. (2022) · Journal of Visualized Experiments · doi:10.3791/63100 · Cited by 2 · see citing works

Concomitant administration of resveratrol and resistance training ameliorates acrylamide-induced spatial learning impairment in rats.

Jouy, S. H., Shahraki, J., Rezaee, R., Ghorani, V., & Gholami, M. (2024) · PubMed Central · doi:10.22038/ajp.2023.22937 · Cited by 1 · see citing works

Hippocampal Neurogenesis via Light-Intensity Running and Its Mechanism

Inoue, K., & Soya, H. (2025) · Advances in neurobiology · doi:10.1007/978-981-95-0066-6_3 · Cited by 1 · see citing works

Avaliação comportamental de ratos treinados em natação forçada

Peretti, A. L., Rosa, C. T., Errero, T. K., Baretta, V., Schneider, S. C. S., & Bertolini, G. R. F. (2015) · Scientia Medica · doi:10.15448/1980-6108.2015.1.20113 · Cited by 1 · see citing works

Neuronal Survival of the Fittest: The Importance of Aerobic Capacity in Exercise-Induced Neurogenesis and Cognition

Tognoni, C. M. (2014) · DukeSpace (Duke University) · Cited by 1 · see citing works

Physical Exercise

Yau, S., Patten, A. R., Sharp, Z., & Christie, B. R. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801977-1.00005-2

Mechanisms of Neurogenesis-Mediated Forgetting in the Hippocampus

Evans, A. (2020) · doi:10.11575/prism/38507

The Impact of Age and Exercise on Stressed Mice

Oakley, K. (2021)

WALKING AND RUNNING IN THE CONTEXT OF THEIR IMPACT ON BRAIN HEALTH AND COGNITIVE FUNCTION

Tretyakova, V. D. (2023) · PERSONALITY IN A CHANGING WORLD HEALTH ADAPTATION DEVELOPMENT · doi:10.23888/humj2023113277-296

Evaluating the molecular drivers of physical inactivity and muscle atrophy as initiating factors in cognitive impairment

Kerr, N. R. (2023) · doi:10.32469/10355/97056

Exercise training enhances learning and memory abilities and hippocampal neurogenesis

Liang, A.-M., Li, H., & Yang, B. (2012) · Chinese Journal of Neuromedicine · doi:10.3760/cma.j.issn.1671-8925.2012.04.007

Influence of Wheel Running and Restraint Stress on Hippocampal Neurogenesis and Spatial Learning-Memory in Adult Mice

Ze-jun, W. (2013) · Beijing Tiyu Daxue xuebao

Treadmill Exercise Improves Memory Function Depending on Circadian Rhythm Changes in Mice

Hwang, D. S., Kwak, H. B., Ko, I. G., Kim, S. E., Jin, J. J., Ji, E. S., Choi, H. H., & Kwon, O. Y. (2016) · International Neurourology Journal · doi:10.5213/inj.1632738.369 · Cited by 20 · see citing works

THE EFFECT OF RUNNING ON TREADMILL IN LEARNING, MEMORY AND MOTOR ACTIVITY OF MALE RAT

Seghatoleslami, A., Shaikh, M., Naghdi, N., Ameri, E. A., & Namvarasl, N. A. (2013) · DOAJ (DOAJ: Directory of Open Access Journals) · doi:10.22059/jmlm.2013.35007

Voluntary Running Exercise-Mediated Enhanced Neurogenesis Does Not Obliterate Retrograde Spatial Memory

Kodali, M., Megahed, T., Mishra, V., Shuai, B., Hattiangady, B., & Shetty, A. K. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0766-16.2016 · Cited by 50 · see citing works