Exercise can increase small heat shock proteins (sHSP) and pre- and post-synaptic proteins in the hippocampus

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

A novel kinase cascade triggered by stress and heat shock that stimulates MAPKAP kinase-2 and phosphorylation of the small heat shock proteins

Rouse, J. W., Cohen, P., Trigon, S., Morange, M., Alonso‐Llamazares, A., Zamanillo, D., Hunt, T., & Nebreda, Á. R. (1994) · Cell · doi:10.1016/0092-8674(94)90277-1 · Cited by 1,674 · see citing works

Effect of Physical Activity on Cognitive Function in Older Adults at Risk for Alzheimer Disease: A Randomized Trial

Lautenschlager, N. T., Cox, K. L., Flicker, L., Foster, J. K., van Bockxmeer, F. M., Xiao, J., Greenop, K. R., & Almeida, O. P. (2008) · JAMA · doi:10.1001/jama.300.9.1027 · Cited by 1,637 · see citing works

Hippocampal BDNF mediates the efficacy of exercise on synaptic plasticity and cognition

Vaynman, S., Ying, Z., & Gomez‐Pinilla, F. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03720.x · Cited by 1,460 · see citing works

Cells in Stress: Transcriptional Activation of Heat Shock Genes

Morimoto, R. I. (1993) · Science · doi:10.1126/science.8451637 · Cited by 1,429 · see citing works

Heat Shock Transcription Factors: Structure and Regulation

Wu, C. (1995) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cb.11.110195.002301 · Cited by 1,231 · cited 9× · see citing works

Physical activity and enhanced fitness to improve cognitive function in older people without known cognitive impairment

Angevaren, M., Aufdemkampe, G., Verhaar, H., Aleman, A., & Vanhees, L. (2008) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd005381.pub3 · Cited by 1,130 · see citing works

Stimulus-transcription coupling in neurons: role of cellular immediate-early genes

Morgan, J. I., & Curran, T. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90096-9 · Cited by 969 · cited 1× · see citing works

Activation of Heat Shock Gene Transcription by Heat Shock Factor 1 Involves Oligomerization, Acquisition of DNA-Binding Activity, and Nuclear Localization and Can Occur in the Absence of Stress

Sarge, K. D., Murphy, S. P., & Morimoto, R. I. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.3.1392 · Cited by 883 · see citing works

Interleukin-1 activates a novel protein kinase cascade that results in the phosphorylation of hsp27

Freshney, N. W., Rawlinson, L. M., Guesdon, F., Jones, E., Cowley, S. A., Hsuan, J. J., & Saklatvala, J. (1994) · Cell · doi:10.1016/0092-8674(94)90278-x · Cited by 865 · see citing works

Effects of voluntary exercise on synaptic plasticity and gene expression in the dentate gyrus of adult male Sprague-Dawley rats in vivo

Farmer, J., Zhao, X., van Praag, H., Wodtke, K., Gage, F. H., & Christie, B. R. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.09.029 · Cited by 836 · see citing works

Ras and Rap control AMPA receptor trafficking during synaptic plasticity

Zhu, J. J., Qin, Y., Zhao, M., Van Aelst, L., & Malinow, R. (2002) · Cell · doi:10.1016/s0092-8674(02)00897-8 · Cited by 769 · see citing works

Exercise, cognition, and the aging brain

Kramer, A. F., Erickson, K. I., & Colcombe, S. J. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00500.2006 · Cited by 719 · see citing works

Regulation of actin filament dynamics by p38 map kinase-mediated phosphorylation of heat shock protein 27

Guay, J., Lambert, H., Gingras-Breton, G., Lavoie, J. N., Huot, J., & Landry, J. (1997) · Journal of Cell Science · doi:10.1242/jcs.110.3.357 · Cited by 705 · 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

Insulin-like growth factor I interfaces with brain-derived neurotrophic factor-mediated synaptic plasticity to modulate aspects of exercise-induced cognitive function

Ding, Q., Vaynman, S., Akhavan, M., Ying, Z., & Gomez-Pinilla, F. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.02.084 · Cited by 555 · see citing works

αB-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain

Iwaki, T., Kume-Iwaki, A., Liem, R. K. H., & Goldman, J. E. (1989) · Cell · doi:10.1016/0092-8674(89)90173-6 · Cited by 549 · see citing works

Activation of Human Heat Shock Genes Is Accompanied by Oligomerization, Modification, and Rapid Translocation of Heat Shock Transcription Factor HSF1

Baler, R., Dahl, G., & Voellmy, R. W. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.4.2486 · Cited by 460 · see citing works

Differential effects of acute and chronic exercise on plasticity‐related genes in the rat hippocampus revealed by microarray

Molteni, R., Ying, Z., & Gómez‐Pinilla, F. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02158.x · Cited by 441 · see citing works

Brain endothelial cells and the glio-vascular complex

Wolburg, H., Noell, S., Mack, A., Wolburg-Buchholz, K., & Fallier-Becker, P. (2009) · Cell and Tissue Research · doi:10.1007/s00441-008-0658-9 · Cited by 438 · see citing works

Physical activity and enhanced fitness to improve cognitive function in older people without known cognitive impairment

Angevaren, M., Aufdemkampe, G., Verhaar, H. J. J., Aleman, A., & Vanhees, L. (2008) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd005381.pub2 · Cited by 436 · see citing works

The heat-shock response: regulation and function of heat-shock proteins and molecular chaperones.

Morimoto, R. I., Kline, M. P., Bimston, D. N., & Cotto, J. J. (1997) · PubMed · Cited by 435 · see citing works

Stress-induced oligomerization and chromosomal relocalization of heat-shock factor

Westwood, J. T., Clos, J., & Wu, C. (1991) · Nature · doi:10.1038/353822a0 · Cited by 370 · see citing works

BDNF Induces Transport of PSD-95 to Dendrites Through PI3K-AKT Signaling After NMDA Receptor Activation

Yoshii, A., & Constantine-Paton, M. (2007) · Nature Neuroscience · doi:10.1038/nn1903 · Cited by 345 · 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

Cellular distribution of alpha B-crystallin in non-lenticular tissues.

Iwaki, T., Kume-Iwaki, A., & Goldman, J. E. (1990) · Journal of Histochemistry & Cytochemistry · doi:10.1177/38.1.2294148 · Cited by 298 · see citing works

BDNF induction with mild exercise in the rat hippocampus

Soya, H., Nakamura, T., Deocaris, C. C., Kimpara, A., Iimura, M., Fujikawa, T., Chang, H., McEwen, B. S., & Nishijima, T. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.04.173 · Cited by 269 · see citing works

Accumulation of alpha B-crystallin in central nervous system glia and neurons in pathologic conditions.

Iwaki, T., Wısnıewskı, T., Iwaki, A., Corbin, E., Tomokane, N., Tateishi, J., & Goldman, J. E. (1992) · PubMed Central · Cited by 265 · see citing works

Exercise differentially regulates synaptic proteins associated to the function of BDNF

Vaynman, S. S., Ying, Z., Yin, D., & Gomez-Pinilla, F. (2006) · Brain Research · doi:10.1016/j.brainres.2005.11.062 · Cited by 248 · see citing works

Central Mechanisms of HPA Axis Regulation by Voluntary Exercise

Stranahan, A. M., Lee, K., & Mattson, M. P. (2008) · NeuroMolecular Medicine · doi:10.1007/s12017-008-8027-0 · Cited by 235 · see citing works

Dual MAP kinase pathways mediate opposing forms of long-term plasticity at CA3–CA1 synapses

Bolshakov, V. Y., Carboni, L., Cobb, M. H., Siegelbaum, S. A., & Belardetti, F. (2000) · Nature Neuroscience · doi:10.1038/80624 · Cited by 220 · see citing works

Small heat shock proteins inhibit amyloid-β protein aggregation and cerebrovascular amyloid-β protein toxicity

Wilhelmus, M. M. M., Boelens, W. C., Otte‐Höller, I., Kamps, B., de Waal, R. M. W., & Verbeek, M. M. (2006) · Brain Research · doi:10.1016/j.brainres.2006.03.058 · 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

Environmental enrichment results in cortical and subcortical changes in levels of synaptophysin and PSD-95 proteins

Nithianantharajah, J. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.02.002 · Cited by 191 · see citing works

Small heat shock proteins protect against α-synuclein-induced toxicity and aggregation

Outeiro, T. F., Klucken, J., Strathearn, K. E., Liu, F., Nguyen, P. T., Rochet, J., Hyman, B. T., & McLean, P. J. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.10.085 · Cited by 185 · see citing works

Converging concepts: Adaptive response, preconditioning, and the Yerkes–Dodson Law are manifestations of hormesis

Calabrese, E. J. (2008) · Ageing Research Reviews · doi:10.1016/j.arr.2007.07.001 · Cited by 180 · cited 1× · see citing works

Dementia, gliosis and expression of the small heat shock proteins hsp27 and alpha B-crystallin in Parkinson's disease.

Renkawek, K., Stege, G., & Bosman, G. C. G. M. (1999) · NeuroReport · doi:10.1097/00001756-199908020-00009 · Cited by 178 · see citing works

Exercise affects energy metabolism and neural plasticity-related proteins in the hippocampus as revealed by proteomic analysis

Ding, Q., Vaynman, S., Souda, P., Whitelegge, J. P., & Gomez‐Pinilla, F. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05026.x · Cited by 174 · see citing works

Neurons, glia, and plasticity in normal brain aging

Finch, C. E. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00051-4 · Cited by 170 · see citing works

Functional expression of p-glycoprotein and multidrug resistance-associated protein (mrp1) in primary cultures of rat astrocytes

Declèves, X., Régina, A., Laplanche, J., Roux, F. S., Boval, B., Launay, J., & Scherrmann, J. (2000) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(20000601)60:5 · Cited by 159 · see citing works

Assembly of Proteins to Postsynaptic Densities after Transient Cerebral Ischemia

Hu, B. R., Park, M., Martone, M. E., Fischer, W. H., Ellisman, M. H., & Zivin, J. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-02-00625.1998 · Cited by 158 · see citing works

The sperm outer dense fiber protein is the 10th member of the superfamily of mammalian small stress proteins

Fontaine, J., Rest, J. S., Welsh, M. J., & Benndorf, R. (2003) · Cell Stress and Chaperones · doi:10.1379/1466-1268(2003)8 · Cited by 145 · 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

Dexamethasone inhibits proliferation of adult hippocampal neurogenesis in vivo and in vitro

Kim, J. B., Ju, J. Y., Kim, J. H., Kim, T., Yang, B., Lee, Y., & Son, H. (2004) · Brain Research · doi:10.1016/j.brainres.2004.07.093 · Cited by 144 · see citing works

Increased astrocyte proliferation in rats after running exercise

Li, J., Ding, Y.-H., Rafols, J. A., Lai, Q., McAllister, J. P., & Ding, Y. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.06.009 · Cited by 143 · see citing works

Phosphorylation-dependent Cellular Localization and Thermoprotective Role of Heat Shock Protein 25 in Hippocampal Progenitor Cells

Geum, D., Son, G. H., & Kim, K. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m104396200 · Cited by 136 · see citing works

The Down Syndrome Critical Region Protein RCAN1 Regulates Long-Term Potentiation and Memory via Inhibition of Phosphatase Signaling

Hoeffer, C. A., Dey, A., Sachan, N., Wong, H., Patterson, R. J., Shelton, J. M., Richardson, J. A., Klann, E., & Rothermel, B. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3974-07.2007 · Cited by 135 · see citing works

Transduction of the stress signal and mechanisms of transcriptional regulation of heat shock/stress protein gene expression in higher eukaryotes.

Voellmy, R. W. (1994) · PubMed · Cited by 134 · see citing works

Exercise activates the phosphatidylinositol 3-kinase pathway

Chen, M. J., & Russo‐Neustadt, A. A. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.12.001 · Cited by 132 · see citing works

Heat shock proteins and the heat shock response during hyperthermia and its modulation by altered physiological conditions

Horowitz, M., & Robinson, S. D. M. (2007) · Progress in brain research · doi:10.1016/s0079-6123(06)62021-9 · Cited by 128 · see citing works

Physical activity elicits sustained activation of the cyclic AMP response element-binding protein and mitogen-activated protein kinase in the rat hippocampus

Shen, H., Tong, L., Balázs, R., & Cotman, C. W. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00315-3 · Cited by 124 · see citing works

Phosphorylated tau and the neurodegenerative foldopathies

Kosik, K. S., & Shimura, H. (2004) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2004.10.011 · Cited by 123 · see citing works

Heat-shock protein-25/27 phosphorylation by the δ isoform of protein kinase C

Maizels, E. T., Peters, C. A., Kline, M. P., Cutler, R. E., Shanmugam, M., & Hunzicker-Dunn, M. E. (1998) · Biochemical Journal · doi:10.1042/bj3320703 · Cited by 118 · see citing works

Differential effects of corticosterone and dexamethasone on hippocampal neurogenesis in vitro

Yu, I. T., Lee, S., Lee, Y.-S., & Son, H. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.03.071 · Cited by 105 · see citing works

Exercise induces the release of heat shock protein 72 from the human brain in vivo

Lancaster, G. I., Møller, K., Nielsen, B., Secher, N. H., Febbraio, M. A., & Nybo, L. (2004) · Cell Stress and Chaperones · doi:10.1379/csc-18r.1 · Cited by 103 · see citing works

The select action of hippocampal calcium calmodulin protein kinase II in mediating exercise-enhanced cognitive function

Vaynman, S., Ying, Z., & Gómez‐Pinilla, F. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.10.005 · Cited by 100 · see citing works

Upregulation of hippocampal TrkB and synaptotagmin is involved in treadmill exercise-enhanced aversive memory in mice

Liu, Y.-F., Chen, H.-I., Yu, L., Kuo, Y.-M., Wu, F.-S., Chuang, J.-I., Liao, P.-C., & Jen, C. J. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.02.005 · Cited by 98 · see citing works

Exercise pre-conditioning strengthens brain microvascular integrity in a rat stroke model

Ding, Y.-H., Ding, Y., Li, J., Bessert, D. A., & Rafols, J. A. (2006) · Neurological Research · doi:10.1179/016164106x98053 · Cited by 95 · see citing works

Presence of molecular chaperones, heat shock cognate (Hsc) 70 and heat shock proteins (Hsp) 40, in the postsynaptic structures of rat brain

Suzuki, T., Usuda, N., Murata, S., Nakazawa, A., Ohtsuka, K., & Takagi, H. (1999) · Brain Research · doi:10.1016/s0006-8993(98)01083-x · Cited by 82 · see citing works

Abnormal small heat shock protein interactions involving neuropathy‐associated HSP22 (HSPB8) mutants

Fontaine, J., Sun, X., Hoppe, A. D., Simon, S., Vicart, P., Michael J. Welsh, *., & Benndorf, R. (2006) · The FASEB Journal · doi:10.1096/fj.06-5911fje · Cited by 80 · see citing works

Changes in heat shock protein 27 phosphorylation and immunocontent in response to preconditioning to oxygen and glucose deprivation in organotypic hippocampal cultures

Valentim, L. M., Rodnight, R., Geyer, A. B., Horn, A. P., Tavares, A. C., Cimarosti, H., Netto, C. A., & Salbego, C. G. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00919-3 · Cited by 78 · see citing works

Heat shock proteins Hsp27 and Hsp32 localize to synaptic sites in the rat cerebellum following hyperthermia

Bechtold, D. A., & Brown, I. R. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00323-x · Cited by 74 · see citing works

The effect of single or repeated restraint stress on several signal molecules in paraventricular nucleus, arcuate nucleus and locus coeruleus

Kwon, M., Seo, Y., Shim, E., Choi, S.-S., Lee, J.-Y., & Suh, H. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.07.027 · Cited by 71 · see citing works

Mechanisms of Activation and Regulation of the Heat Shock-Sensitive Signaling Pathways

Nadeau, S. I., & Landry, J. (2007) · Springer eBooks · doi:10.1007/978-0-387-39975-1_10 · Cited by 62 · see citing works

Heat shock protein 27 shows a distinctive widespread spatial and temporal pattern of induction in CNS glial and neuronal cells compared to heat shock protein 70 and caspase 3 following kainate administration

Akbar, M. T., Wells, D. J., Latchman, D. S., & de Belleroche, J. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00199-1 · Cited by 62 · see citing works

Dependence of rat hippocampal c-Fos expression on intensity and duration of exercise

Lee, T.-H., Jang, M.-H., Shin, M.-C., Lim, B., Kim, Y., Kim, H. K., Choi, H.-H., Lee, K., Kim, E., & Kim, C. (2003) · Life Sciences · doi:10.1016/s0024-3205(02)02406-2 · Cited by 61 · see citing works

Depolarization of Neural Cells Induces Transcription of the Down Syndrome Critical Region 1 Isoform 4 via a Calcineurin/Nuclear Factor of Activated T Cells-dependent Pathway

Cano, E., Canellada, A. M., Minami, T., Iglesias, T., & Redondo, J. M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m506205200 · Cited by 61 · see citing works

In vivo heat-shock response in the brain: signalling pathway and transcription factor activation

Maroni, P., Bendinelli, P., Tiberio, L., Rovetta, F., Piccoletti, R., & Schiaffonati, L. (2003) · Molecular Brain Research · doi:10.1016/j.molbrainres.2003.08.018 · Cited by 58 · see citing works

Enhancement of expression of stress proteins by agents that lower the levels of glutathione in cells

Ito, H., Okamoto, K., & Kato, K. (1998) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(98)00010-4 · Cited by 56 · see citing works

Contribution of Astrocytes to Activity-Dependent Structural Plasticity in the Adult Brain

Theodosis, D. T., & Poulain, D. A. (1999) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-4685-6_14 · Cited by 55 · see citing works

Differential Expression of Small Heat Shock Proteins in Reactive Astrocytes after Focal Ischemia: Possible Role of β-Adrenergic Receptor

Imura, T., Shimohama, S., Sato, M., Nishikawa, H., Madono, K., Akaike, A., & Kimura, J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09768.1999 · Cited by 53 · see citing works

HSP70 expression in the CNS in response to exercise and heat stress in rats

Walters, J., Ryan, K. L., Tehrany, M. R., Jones, M. B., Paulus, L. A., & Mason, P. A. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.84.4.1269 · Cited by 43 · see citing works

Heat shock-mediated regulation of MKP-1

Wong, H. R., Dunsmore, K. E., Page, K., & Shanley, T. P. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00138.2005 · Cited by 42 · see citing works

Endoplasmic reticulum stress induces the phosphorylation of small heat shock protein, Hsp27

Ito, H., Iwamoto, I., Inaguma, Y., Takizawa, T., Nagata, K., Asano, T., & Kato, K. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20445 · Cited by 40 · see citing works

Heat Shock Protein 25 or Inducible Heat Shock Protein 70 Activates Heat Shock Factor 1

Seo, H. R., Chung, D.-Y., Lee, Y.-J., Lee, D.-H., Kim, J.-I., Bae, S., Chung, H.-Y., Lee, S.-J., Jeoung, D., & Lee, Y. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600062200 · Cited by 35 · see citing works

Impact of Physical Fitness on Strategy Development in Decision-Making Tasks

Suominen-Troyer, S. M., Davis, K. J., Ismail, A. H., & Salvendy, G. (1986) · Perceptual and Motor Skills · doi:10.2466/pms.1986.62.1.71 · Cited by 35 · see citing works

Nitric oxide synthase (NOS) in the brain of the cephalopod Sepia officinalis

Cosmo, A. D., Cristo, C. D., Palumbo, A., d’Ischia, M., & Messenger, J. B. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001218)428:3 · Cited by 34 · see citing works

Different Effect of High Fat Diet and Physical Exercise in the Hippocampal Signaling

Muller, A. P., Cammarota, M., Dietrich, M. O., Rotta, L. N., Portela, L. V., Souza, D. O., Izquierdo, I., Bevilaqua, L. R., & Perry, M. L. S. (2007) · Neurochemical Research · doi:10.1007/s11064-007-9530-7 · Cited by 32 · see citing works

Effect of exercise on activation of the p38 mitogen-activated protein kinase pathway, c-Jun NH2 terminal kinase, and heat shock protein 27 in equine skeletal muscle

van Ginneken, M. M. E., de Graaf‐Roelfsema, E., KEIZER, H. A., van Dam, K. G., Wijnberg, I. D., van der Kolk, J. H., & van Breda, E. (2006) · American Journal of Veterinary Research · doi:10.2460/ajvr.67.5.837 · Cited by 31 · see citing works

De-repression of heat shock transcription factor-1 in interleukin-6- treated hepatocytes is mediated by downregulation of glycogen synthase kinase 3beta and MAPK/ERK-1.

Wigmore, S. J., Sangster, K., McNally, S. J., Harrison, E. M., Ross, J. A., Fearon, K. C. H., & Garden, O. J. (2007) · PubMed · Cited by 28 · see citing works

Dramatic attenuation of hypusine formation on eukaryotic initiation factor 5A during senescence of IMR-90 human diploid fibroblasts

Chen, Z. P., & Chen, K. Y. (1997) · Journal of Cellular Physiology · doi:10.1002/(sici)1097-4652(199703)170:3 · Cited by 23 · see citing works

The MAPK pathway is required for depolarization-induced “promiscuous” immediate-early gene expression but not for depolarization-restricted immediate-early gene expression in neurons

Machado, H. B., Vician, L. J., & Herschman, H. R. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21529 · Cited by 17 · see citing works

Mitogen‐activated protein kinase phosphatase‐1 (MKP‐1) preferentially dephosphorylates p42/44MAPK but not p38MAPK in rat pinealocytes

Price, D. M., Wloka, M. T., Chik, C. L., & Ho, A. K. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04557.x · Cited by 11 · see citing works

[The influence of severe long-term exercise on the mouse hippocampus].

Sumitani, K., Miyamoto, O., Yamagami, S.-I., Okada, Y., Itano, T., Murakami, T. H., & Negi, T. (2002) · PubMed · Cited by 11 · see citing works

A Review of the Effects of Physical Activity and Exercise on Cognitive and Brain Functions in Older Adults

Bherer, L., Erickson, K. I., & Liu-Ambrose, T. (2013) · Journal of Aging Research · doi:10.1155/2013/657508 · Cited by 899 · see citing works

Hippocampal Plasticity in Response to Exercise in Schizophrenia

Pajonk, F.-G., Wobrock, T., Gruber, O., Scherk, H., Berner, D., Kaizl, I., Kierer, A., Müller, S., Oest, M., Meyer, T., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.193 · Cited by 592 · see citing works

Energy intake and exercise as determinants of brain health and vulnerability to injury and disease

Mattson, M. P. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.08.012 · Cited by 434 · see citing works

The neuropathology of sport

McKee, A. C., Daneshvar, D. H., Alvarez, V. E., & Stein, T. D. (2014) · Acta Neuropathologica · doi:10.1007/s00401-013-1230-6 · Cited by 422 · see citing works

Biological Mechanisms of Physical Activity in Preventing Cognitive Decline

Lista, I., & Sorrentino, G. (2009) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-009-9488-x · Cited by 367 · see citing works

High dose hydrocortisone immediately after trauma may alter the trajectory of PTSD: Interplay between clinical and animal studies

Zohar, J., Yahalom, H., Kozlovsky, N., Cwikel-Hamzany, S., Matar, M. A., Kaplan, Z., Yehuda, R., & Cohen, H. (2011) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2011.06.001 · Cited by 292 · see citing works

Depression and adult neurogenesis: Positive effects of the antidepressant fluoxetine and of physical exercise

Micheli, L., Ceccarelli, M., D’Andrea, G., & Tirone, F. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2018.09.002 · Cited by 288 · see citing works

Cognitive function, physical activity, and aging: Possible biological links and implications for multimodal interventions

Kraft, E. (2012) · Aging Neuropsychology and Cognition · doi:10.1080/13825585.2011.645010 · Cited by 181 · see citing works

Benefits of Physical Exercise on the Aging Brain: The Role of the Prefrontal Cortex

Berchicci, M., Lucci, G., & Russo, F. D. (2013) · The Journals of Gerontology Series A · doi:10.1093/gerona/glt094 · Cited by 155 · see citing works

Exercise Training Attenuates Neuropathic Pain and Cytokine Expression After Chronic Constriction Injury of Rat Sciatic Nerve

Chen, Y., Li, Y., Chen, Y. C., Li, Z.-Y., & Hung, C. (2012) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e31824c4ed4 · Cited by 147 · see citing works

A framework to understand the variations of PSD-95 expression in brain aging and in Alzheimer's disease

Savioz, A., Leuba, G., & Vallet, P. G. (2014) · Ageing Research Reviews · doi:10.1016/j.arr.2014.09.004 · Cited by 127 · see citing works

Physical exercise improves synaptic dysfunction and recovers the loss of survival factors in 3xTg-AD mouse brain

Revilla, S., Sunol, C. E., García‐Mesa, Y., Giménez‐Llort, L., Sanfeliu, C., & Cristòfol, R. M. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.01.037 · Cited by 127 · see citing works

Effect of treadmill exercise on the BDNF-mediated pathway in the hippocampus of stressed rats

Fang, Z., Lee, C. H., Seo, M. K., Cho, H., Lee, J. G., Lee, B. J., Park, S. W., & Kim, Y. (2013) · Neuroscience Research · doi:10.1016/j.neures.2013.04.005 · Cited by 126 · see citing works

A Randomized Controlled Trial of Exercise to Improve Mood After Traumatic Brain Injury

Hoffman, J. M., Bell, K. R., Powell, J. M., Behr, J., Dunn, E. C., DIKMEN, S. S., & Bombardier, C. H. (2010) · PM&R · doi:10.1016/j.pmrj.2010.06.008 · Cited by 122 · see citing works

Different types of exercise induce differential effects on neuronal adaptations and memory performance

Lin, T.-W., Chen, S.-J., Huang, T.-Y., Chang, C.-Y., Chuang, J., Wu, F., Kuo, Y., & Jen, C. J. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.10.006 · Cited by 122 · see citing works

Effects of Long-Term Environmental Enrichment on Anxiety, Memory, Hippocampal Plasticity and Overall Brain Gene Expression in C57BL6 Mice

Hüttenrauch, M., Salinas, G., & Wirths, O. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00062 · Cited by 120 · see citing works

The effects of hormones and physical exercise on hippocampal structural plasticity

Triviño-Paredes, J., Patten, A. R., Gil‐Mohapel, J., & Christie, B. R. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.03.001 · Cited by 83 · see citing works

Modulation of synaptic plasticity by exercise

Bettio, L. E. B., Thacker, J. S., Hutton, C. P., & Christie, B. R. (2019) · International review of neurobiology · doi:10.1016/bs.irn.2019.07.002 · Cited by 82 · see citing works

Physical Exercise Induces Excess Hsp72 Expression and Delays the Development of Hyperalgesia and Allodynia in Painful Diabetic Neuropathy Rats

Chen, Y., Hsieh, P., Chen, Y.-C., Hung, C., & Cheng, J. (2013) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e318274e4a0 · Cited by 81 · see citing works

Physical activity delays hippocampal neurodegeneration and rescues memory deficits in an Alzheimer disease mouse model

Hüttenrauch, M., Brauß, A., Kurdakova, A., Borgers, H., Klinker, F., Liebetanz, D., Salinas-Riester, G., Wiltfang, J., Klafki, H. W., & Wirths, O. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.65 · Cited by 78 · see citing works

DNA methylation in vulnerability to post-traumatic stress in rats: evidence for the role of the post-synaptic density protein Dlgap2

Chertkow-Deutsher, Y., Cohen, H., Klein, E., & Ben‐Shachar, D. (2009) · The International Journal of Neuropsychopharmacology · doi:10.1017/s146114570999071x · Cited by 73 · see citing works

What and How Can Physical Activity Prevention Function on Parkinson’s Disease?

Fan, B., Jabeen, R., Bo, B., Guo, C., Meng-jie, H., Zhang, H., Cen, J., Ji, X., & Wei, J. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/4293071 · Cited by 64 · see citing works

Treadmill exercise facilitates synaptic plasticity on dopaminergic neurons and fibers in the mouse model with Parkinson’s disease

Shin, M., Jeong, H.-Y., An, D.-I., Lee, H.-Y., & Sung, Y.-H. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.04.015 · Cited by 60 · see citing works

The dusp1 immediate early gene is regulated by natural stimuli predominantly in sensory input neurons

Horita, H., Wada, K., Rivas, M. V., Hara, E., & Jarvis, E. D. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22370 · Cited by 54 · see citing works

High-intensity physical exercise disrupts implicit memory in mice: involvement of the striatal glutathione antioxidant system and intracellular signaling

Aguiar, A. S., Boemer, G., Rial, D., de Córdova, F. M., Mancini, G., Walz, R., Bem, A. F. D., Latini, A., Leal, R. B., Pinho, R. A., et al. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.09.053 · Cited by 55 · see citing works

Late‐life physical activity relates to brain tissue synaptic integrity markers in older adults

Casaletto, K., Ramos‐Miguel, A., VandeBunte, A., Memel, M., Buchman, A., Bennett, D., & Honer, W. (2022) · Alzheimer's & Dementia · doi:10.1002/alz.12530 · Cited by 53 · see citing works

Benefit effect of REM-sleep deprivation on memory impairment induced by intensive exercise in male wistar rats: with respect to hippocampal BDNF and TrkB

Mahboubi, S., Nasehi, M., Imani, A., Sadat‐Shirazi, M., Zarrindast, M., Vousooghi, N., & Noroozıan, M. (2019) · Nature and Science of Sleep · doi:10.2147/nss.s207339 · Cited by 47 · see citing works

HSP27 immunization reinforces AII amacrine cell and synapse damage induced by S100 in an autoimmune glaucoma model

Reinehr, S., Kuehn, S., Casola, C., Koch, D. C., Stute, G., Grotegut, P., Dick, H. B., & Joachim, S. C. (2017) · Cell and Tissue Research · doi:10.1007/s00441-017-2710-0 · Cited by 38 · see citing works

Treadmill running improves motor function and alters dendritic morphology in the striatum after collagenase-induced intracerebral hemorrhage in rats

Takamatsu, Y., Ishida, A., Hamakawa, M., Tamakoshi, K., Jung, C., & Ishida, K. (2010) · Brain Research · doi:10.1016/j.brainres.2010.07.070 · Cited by 36 · see citing works

Asiaticoside ameliorates β-amyloid-induced learning and memory deficits in rats by inhibiting mitochondrial apoptosis and reducing inflammatory factors

Zhang, Z., Li, X., Li, D., Luo, M., Li, Y., Li, S., & Jiang, X. (2016) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2016.4004 · Cited by 35 · see citing works

Aerobic exercise attenuates inhibitory avoidance memory deficit induced by paradoxical sleep deprivation in rats

Fernandes, J., Baliego, L. G. Z. D. A., Peixinho-Pena, L. F., de Almeida, A. A., Venâncio, D. P., Scorza, F. A., de Mello, M. T., & Arida, R. M. (2013) · Brain Research · doi:10.1016/j.brainres.2013.07.019 · Cited by 32 · see citing works

Maternal separation enhances object location memory and prevents exercise-induced MAPK/ERK signalling in adult Sprague–Dawley rats

Makena, N., Bugarith, K., & Russell, V. A. (2012) · Metabolic Brain Disease · doi:10.1007/s11011-012-9298-6 · Cited by 31 · see citing works

Long-term running alleviates some behavioral and molecular abnormalities in Down syndrome mouse model Ts65Dn

Kida, E., Rabe, A., Walus, M., Albertini, G., & Golabek, A. A. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.11.022 · Cited by 30 · see citing works

Using causal models to distinguish between neurogenesis-dependent and -independent effects on behaviour

Lazic, S. E. (2011) · Journal of The Royal Society Interface · doi:10.1098/rsif.2011.0510 · Cited by 27 · see citing works

Learning and memory disabilities in IUGR babies: Functional and molecular analysis in a rat model

Camprubí-Camprubí, M., Balada, R., Ortega, J. A., de la Torre, M. D. L. A. O., Fernández-Feijóo, C. D., Farrés, M. G., Aloy, J. F., Krauel, X., & Alcántara, S. (2017) · Brain and Behavior · doi:10.1002/brb3.631 · Cited by 26 · see citing works

Heat shock protein 90 is a potential therapeutic target for ameliorating skeletal muscle abnormalities in Parkinson′s disease

Al-Jarrah, M. D., Erekat, N. S., & Alkhatib, A. J. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.130105 · Cited by 25 · see citing works

Aerobic exercise reduces hippocampal ERK and p38 activation and improves memory of middle‐aged rats

Cardoso, F. D. S., França, E. F., Serra, F. T., Victorino, A. B., de Almeida, A. A., Fernandes, J., Cabral, F. R., Venâncio, D. P., Arida, R. M., & da Silva, S. G. (2017) · Hippocampus · doi:10.1002/hipo.22740 · Cited by 21 · see citing works

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

Exercise and Early-Onset Alzheimer’s Disease: Theoretical Considerations

Hooghiemstra, A. M., Eggermont, L. H. P., Scheltens, P., van der Flier, W. M., & Scherder, E. (2012) · Dementia and Geriatric Cognitive Disorders Extra · doi:10.1159/000335493 · Cited by 20 · see citing works

Pathophysiology of Schizophrenia

Falkai, P., Schmitt, A., & Cannon, T. D. (2011) · doi:10.1002/9780470978672.ch2 · Cited by 11 · see citing works

Exercise prevents downregulation of hippocampal presynaptic proteins following olanzapine-elicited metabolic dysregulation in rats: distinct roles of inhibitory and excitatory terminals.

Ramos-Miguel, A., Honer, W. G., Boyda, H. N., Sawada, K., Beasley, C. L., Procyshyn, R. M., & Barr, A. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.022 · Cited by 18 · see citing works

Swimming improves the emotional memory deficit by scopolamine via mu opioid receptors

Nasehi, M., Nasehi, M., Rahmani‐Nia, F., Mirzaei, B., Nami, M., & Zarrindast, M. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.02.011 · Cited by 18 · see citing works

Aerobic exercise training improves memory function through modulation of brain-derived neurotrophic factor and synaptic proteins in the hippocampus and prefrontal cortex of type 2 diabetic rats

Sadri, I., Nikookheslat, S. D., Karimi, P., Khani, M., & Nadimi, S. (2023) · Journal of Diabetes & Metabolic Disorders · doi:10.1007/s40200-023-01360-9 · Cited by 17 · see citing works

Protecting against ischaemic stroke in rats by heat shock protein 20‐mediated exercise

Lin, C., Chang, C., Chang, C., Hsu, Y., Lin, M., & Lin, J. (2015) · European Journal of Clinical Investigation · doi:10.1111/eci.12551 · Cited by 17 · see citing works

Dissecting the Inhibitory Mechanism of the αB-Crystallin Domain against Aβ42 Aggregation and Its Effect on Aβ42 Protofibrils: A Molecular Dynamics Simulation Study

Xu, Z., Gong, Y., Zou, Y. F., Wan, J., Tang, J., Zhan, C., Wei, G., & Zhang, Q. (2022) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.2c00224 · Cited by 16 · see citing works

Effects of exercise-induced fatigue on the morphology of asymmetric synapse and synaptic protein levels in rat striatum

Wang, Z., Hou, L., & Wang, D. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104476 · Cited by 16 · see citing works

Neuropsycological gender differences in healthy individuals and in pediatric neurodevelopmental disorders. A role for SNAP-25

Ghezzo, A., Guerini, F. R., Bolognesi, E., Matteoli, M., Manca, S., Sotgiu, S., Bejor, M., Clerici, M., & Chiappedi, M. A. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2009.05.045 · Cited by 16 · see citing works

Widespread cerebellar transcriptome changes in Ts65Dn Down syndrome mouse model after lifelong running

Walus, M., Kida, E., Rabe, A., Albertini, G., & Golabek, A. A. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.08.015 · Cited by 15 · see citing works

Environmental Enrichment Improved Learning and Memory, Increased Telencephalic Cell Proliferation, and Induced Differential Gene Expression in Colossoma macropomum

Pereira, P. D. C., Henrique, E. P., Porfírio, D. M., Crispim, C. C. D. S., Campos, M. T. B., de Oliveira, R. M., Silva, I. M. S., Guerreiro, L. C. F., da Silva, T. W. P., da Silva, A. D. J. F., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00840 · Cited by 15 · see citing works

Effects of exercise on proactive interference in memory: potential neuroplasticity and neurochemical mechanisms

Li, C., Liu, T., Li, R., & Zhou, C. (2020) · Psychopharmacology · doi:10.1007/s00213-020-05554-4 · Cited by 14 · see citing works

Mediating Age-related Cognitive Decline Through Lifestyle Activities: A Brief Review Of The Effects Of Physical Exercise And Sports-playing On Older Adult Cognition

Sogaard, I., & Ni, R. (2018) · Acta Psychopathologica · doi:10.4172/2469-6676.100178 · Cited by 15 · see citing works

Exercise and cognitive function: a hypothesis for the association of type II diabetes mellitus and Alzheimer's disease from an evolutionary perspective

Brito, G. N. O. (2009) · Diabetology & Metabolic Syndrome · doi:10.1186/1758-5996-1-7 · Cited by 11 · see citing works

Mechanisms of time-restricted feeding-induced neuroprotection and neuronal plasticity in ischemic stroke as a function of circadian rhythm

Jeong, S., Davis, C. K., & Vemuganti, R. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.115045 · Cited by 9 · see citing works

Effect of 3,4-methylenedioxyamphetamine on dendritic spine dynamics in rat neocortical neurons — Involvement of heat shock protein 27

Ruscher, K., Fernandes, E. G. R., Capela, J. P., Bastos, M. D. L., Wieloch, T. W., Dirnagl, U., Meisel, A., & Carvalho, F. D. (2010) · Brain Research · doi:10.1016/j.brainres.2010.11.022 · Cited by 7 · see citing works

Efectos de un programa cognitivo-motriz sobre la función ejecutiva en una muestra de personas mayores. [Effects of a cognitive-motor programme on executive function in a sample of elderly people].

Spain, U. D. G., Reigal, R. E., & Hernández-Mendo, A. (2014) · RICYDE Revista Internacional de Ciencias del Deporte · doi:10.5232/ricyde2014.03703 · Cited by 7 · see citing works

Exercise-driven modulation of glutamatergic signaling: mechanisms and clinical implications.

Yu, C., Tyler, J. R., Elman, I., Blum, K., Lewandrowski, K., Sharafshah, A., Gold, M., Pinhasov, A., & Thanos, P. K. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.10.029 · Cited by 6 · see citing works

Exercise Modulates Exocytosis: Chemical Insights from the Intracellular Vesicle Perspective.

Liu, R., He, X., Liu, J., Sun, Z.-N., Yu, P., Hou, L.-J., & Mao, L.-Q. (2025) · Angewandte Chemie · doi:10.1002/anie.202511277 · Cited by 5 · see citing works

Environmental enrichment applied with sensory components prevents age-related decline in synaptic dynamics: Evidence from the zebrafish model organism

Karoglu-Eravsar, E. T., Tuz-Sasik, M. U., & Adams, M. M. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2021.111346 · Cited by 5 · see citing works

EXERCÍCIO FÍSICO E NEUROPLASTICIDADE HIPOCAMPAL: REVISÃO DE LITERATURA

Castro, C. D. P. N., Gil‐Mohapel, J., & Brocardo, P. S. (2017) · VITTALLE - Revista de Ciências da Saúde · doi:10.14295/vittalle.v29i2.7461 · Cited by 4 · see citing works

Effects of aerobic training on brain architecture, hippocampal volume, cardiorespiratory parameters, and health-related quality of life among patients with schizophrenia: A systematic review

Sharma, A., Sharma, N., Singh, R. K., & Chahal, A. (2024) · Indian Journal of Psychiatry · doi:10.4103/indianjpsychiatry.indianjpsychiatry_735_23 · Cited by 2 · see citing works

Effect of Exercise on Oxidative Stress in Neurological Disorders

Farooqui, A. A. (2014) · Springer eBooks · doi:10.1007/978-3-319-04111-7_10 · Cited by 2 · see citing works

Alpha‐lipoic acid does not alter stress protein response to acute exercise in diabetic brain

Lappalainen, J., Lappalainen, Z., Oksala, N., Laaksonen, D. E., Khanna, S., Sen, C. K., & Atalay, M. (2010) · Cell Biochemistry and Function · doi:10.1002/cbf.1702 · Cited by 2 · see citing works

Exercise Modulates Exocytosis: Chemical Insights from the Intracellular Vesicle Perspective

Liu, R., He, X., Liu, J., Sun, Z., Yu, P., Hou, L., & Mao, L. (2025) · Angewandte Chemie · doi:10.1002/ange.202511277 · Cited by 1 · see citing works

The Exercise-induced BDNF and synaptic proteins via PI3K/AKT on Hippocampal CA1 in aged mice.

su-ju, E., 임예현, & 김동문 (2012) · Exercise Science · doi:10.15857/ksep.2012.21.1.131 · Cited by 1 · see citing works

Environmental Enrichment and Aerobic Exercise Enhances Spatial Memory and Synaptophysin Expression in Rats

Dita, D. A. A., Paramita, N., Kodariah, R., & Kartinah, N. T. (2020) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v12i1.945 · Cited by 1 · see citing works

Ashwagandha and Its Active Ingredient, Withanolide A, Increase Phosphorylation of TrkB in Cultured Hippocampal Neurons

Chen, M., & Russo‐Neustadt, A. A. (2023) · European Journal of Medicinal Plants · doi:10.9734/ejmp/2023/v34i21120 · Cited by 1 · see citing works

Neurobiologische Grundlagen der Schizophrenie

Gruber, O., Falkai, P., & Schmitt, A. (2010) · Nervenheilkunde · doi:10.1055/s-0038-1628763

Summary, Perspective and Direction for Future Studies

Farooqui, A. A. (2014) · Springer eBooks · doi:10.1007/978-3-319-04111-7_11

Efeitos do exercicio físico sobre a expressão de receptores de glutamato no encéfalo de ratos.

Real, C. C. (2009) · doi:10.11606/d.42.2009.tde-01072009-103424

Understanding the role of cerebrovascular health in cognitive aging: a multi-modal noninvasive human neuroimaging approach

Zimmerman, B. (2016) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)

Effect of Aerobic Training on Synaptic Integrity Proteins in Hippocampus and Prefrontal Cortex of Type II Diabetic Rats

Nikookheslat, S. D., Karimi, P., & Sadri, I. (2020) · Medical Journal of Tabriz University of Medical Sciences and Health Services · doi:10.34172/mj.2020.032

Effect of aerobic training on heat shock protein 27 and brain-derived neurotrophic factor in hippocampus and prefrontal cortex of type II diabetic rats

Nikookheslat, S. D., Karimi, P., & Sadri, I. (2021) · Medical Journal of Tabriz University of Medical Sciences and Health Services · doi:10.34172/mj.2021.033

Summary, Perspective, and Direction for Future Studies

Farooqui, T., & Farooqui, A. A. (2015) · doi:10.1002/9781118840634.ch28

Association between continuous exercise and cognitive function in Chinese elderly with chronic diseases: the mediating role of positive emotions

Wang, G., Tang, H., Lü, Y., Yu, Y., Li, Y., & Tang, S. (2025) · Archives of Medical Science · doi:10.5114/aoms/202503

Stratégies non pharmacologiques et réponse aux antidépresseurs dans un modèle murin de dépression : effets comportementaux et mécanismes neurobiologiques

Coutens, B. (2022) · doi:10.70675/7ffbfd7ezefb5z4e4ez82f4z42a6ac0ff754

Exercise as a Systemic Prevention and Management for Alzheimer’s Disease: Restoring Brain–Body Homeostasis Through Metabolic, Neurovascular, Anti-Inflammatory, and Regenerative Mechanisms

Xiao, L., Green, J. M., Mochizuki, M., & Nakahara, T. (2026) · Cells · doi:10.3390/cells15151368

Aging and dementia : Clinical relevance of early markers and late interventions

Thurm, F. (2012)

Exercise-induced Hypoxia, Angiogenesis, and Behavioral Flexibility in the Adult Rat

Berggren, K. L. (2013) · UWM Digital Commons (University of Wisconsin–Milwaukee)

Untersuchung von Proteomveränderungen im Synaptosom von Patienten mit sporadischer Creutzfeldt-Jakob-Krankheit

Nowak, M. (2013) · doi:10.53846/goediss-3760

Exercise affects energy metabolism and neural plasticity-related proteins in the hippocampus as revealed by proteomic analysis

Ding, Q., Vaynman, S., Souda, P., Whitelegge, J. P., & Gomez‐Pinilla, F. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05026.x · Cited by 174 · see citing works

Resistance Exercise Enhances Cognitive Function in Mouse

Suijo, K., Inoue, S., Ohya, Y., Odagiri, Y., Takamiya, T., Ishibashi, H., Itoh, M., Fujieda, Y., & Shimomitsu, T. (2012) · International Journal of Sports Medicine · doi:10.1055/s-0032-1323747 · Cited by 54 · see citing works

hippocampus of

Hescham, S., Grace, L. K., Kellaway, L. A., Bugarith, K., & Vivienne, A. (2015)

Upregulation of hippocampal TrkB and synaptotagmin is involved in treadmill exercise-enhanced aversive memory in mice

Liu, Y.-F., Chen, H.-I., Yu, L., Kuo, Y.-M., Wu, F.-S., Chuang, J.-I., Liao, P.-C., & Jen, C. J. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.02.005 · Cited by 98 · see citing works

Modulation of the hippocampal protein machinery in voluntary and treadmill exercising rats

Chen, W., Diao, W., Viidik, A., Skalicky, M., Höger, H., & Lübec, G. (2008) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2008.01.002 · Cited by 10 · see citing works