The function of previously unappreciated exerkines secreted by muscle in regulation of neurodegenerative diseases
Open accessAbstract
The initiation and progression of neurodegenerative diseases (NDs), distinguished by compromised nervous system integrity, profoundly disrupt the quality of life of patients, concurrently exerting a considerable strain on both the economy and the social healthcare infrastructure. Exercise has demonstrated its potential as both an effective preventive intervention and a rehabilitation approach among the emerging therapeutics targeting NDs. As the largest secretory organ, skeletal muscle possesses the capacity to secrete myokines, and these myokines can partially improve the prognosis of NDs by mediating the muscle-brain axis. Besides the well-studied exerkines, which are secreted by skeletal muscle during exercise that pivotally exert their beneficial function, the physiological function of novel exerkines, e.g., apelin, kynurenic acid (KYNA), and lactate have been underappreciated previously. Herein, this review discusses the roles of these novel exerkines and their mechanisms in regulating the progression and improvement of NDs, especially the significance of their functions in improving NDs’ prognoses through exercise. Furthermore, several myokines with potential implications in ameliorating ND progression are proposed as the future direction for investigation. Elucidation of the function of exerkines secreted by skeletal muscle in the regulation of NDs advances the understanding of its pathogenesis and facilitates the development of therapeutics that intervene in these processes to cure NDs.
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Both GLP-1RAs and physical exercise converge on common neural pathways, influencing brain regions involved in appetite regulation, energy balance, and cognitive function.
“Emerging evidence suggests that both GLP-1RAs and physical exercise converge on common neural pathways, influencing brain regions involved in appetite regulation, energy balance, and cognitive function.”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [43]
Section 2.2 (Lactate; page unavailable) describes exercise-related signaling and neurogenesis in brain regions including the hippocampus. But the paper does not establish that exercise and GLP-1 receptor agonists converge on common neural pathways, or link that proposed convergence to appetite regulation, energy balance, and cognition. Searches for GLP-1RA, GLP-1, and glucagon-like peptide-1 found no passage addressing that comparison. (LLM, conf=0.84)
Experimental — accuracy not yet measuredExercise induces the release of myokines, such as apelin and irisin, alongside increased levels of BDNF.
“Exercise induces the release of myokines, such as apelin and irisin, alongside increased levels of BDNF (43, 44).”
From GLP-1 agonists and exercise: the future of lifestyle prioritization (2025) · cites this paper as [43]
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- Abati E. Manini A. Comi G. P. Corti S. (2022). Inhibition of myostatin and related signaling pathways for the treatment of muscle atrophy in motor neuron diseases. Cell Mol. Life Sci. 79: 374. 10.1007/s00018-022-04408-w 35727341 PMC9213329 · DOI
- Abdelhamid R. F. Nagano S. (2023). Crosstalk between oxidative stress and aging in neurodegeneration disorders. Cells 12: 753. PMC10001353 36899889
- Agudelo L. Z. Femenia T. Orhan F. Porsmyr-Palmertz M. Goiny M. Martinez-Redondo V. (2014). Skeletal muscle PGC-1alpha1 modulates kynurenine metabolism and mediates resilience to stress-induced depression. Cell 159 33– 45. 10.1016/j.cell.2014.07.051 25259918 · DOI · Paper page
- Agudelo L. Z. Ferreira D. M. S. Dadvar S. Cervenka I. Ketscher L. Izadi M. (2019). Skeletal muscle PGC-1alpha1 reroutes kynurenine metabolism to increase energy efficiency and fatigue-resistance. Nat. Commun. 10: 2767. 10.1038/s41467-019-10712-0 31235694 PMC6591322 · DOI
- Albanese M. Zagaglia S. Landi D. Boffa L. Nicoletti C. G. Marciani M. G. (2016). Cerebrospinal fluid lactate is associated with multiple sclerosis disease progression. J. Neuroinflammation 13: 36. PMC4750170 26863878
- Allison D. J. Nederveen J. P. Snijders T. Bell K. E. Kumbhare D. Phillips S. M. (2019). Exercise training impacts skeletal muscle gene expression related to the kynurenine pathway. Am. J. Physiol. Cell Physiol. 316 C444– C448. 10.1152/ajpcell.00448.2018 30649918 PMC6457098 · DOI
- Alonso Canovas A. Luquin Piudo R. Garcia Ruiz-Espiga P. Burguera J. A. Campos Arillo V. Castro A. (2014). Dopaminergic agonists in Parkinson’s disease. Neurologia 29 230– 241. 21724302
- Aminyavari S. Zahmatkesh M. Farahmandfar M. Khodagholi F. Dargahi L. Zarrindast M. R. (2019a). Protective role of Apelin-13 on amyloid beta25-35-induced memory deficit; Involvement of autophagy and apoptosis process. Prog. Neuropsychopharmacol. Biol. Psychiatry 89 322– 334. 10.1016/j.pnpbp.2018.10.005 30296470 · DOI
- Aminyavari S. Zahmatkesh M. Khodagholi F. Sanati M. (2019b). Anxiolytic impact of Apelin-13 in a rat model of Alzheimer’s disease: Involvement of glucocorticoid receptor and FKBP5. Peptides 118: 170102. 10.1016/j.peptides.2019.170102 31199948 · DOI
- Arnaiz-Cot J. J. Gonzalez J. C. Sobrado M. Baldelli P. Carbone E. Gandia L. (2008). Allosteric modulation of alpha 7 nicotinic receptors selectively depolarizes hippocampal interneurons, enhancing spontaneous GABAergic transmission. Eur. J. Neurosci. 27 1097– 1110. 10.1111/j.1460-9568.2008.06077.x 18312591 · DOI
- Arvidsson D. Johannesson E. Andersen L. B. Karlsson M. Wollmer P. Thorsson O. (2018). Longitudinal analysis of the relationships of physical activity and body fat with nerve growth factor and brain-derived neural factor in children. J. Phys. Act Health 15 620– 625. 10.1123/jpah.2017-0483 29589508 · DOI
- Arya D. Khan T. Margolius A. J. Fernandez H. H. (2019). Tardive Dyskinesia: Treatment update. Curr. Neurol. Neurosci. Rep. 19: 69. 31420757
- Ashraf J. Roshan V. D. (2012). Is short-term exercise a therapeutic tool for improvement of cardioprotection against DOX-induced cardiotoxicity? An experimental controlled protocol in rats. Asian Pac. J. Cancer Prev. 13 4025– 4030. 23098511
- Author. (1993). A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s Disease Collaborative Research Group. Cell 72 971– 983. 10.1016/0092-8674(93)90585-e 8458085 · DOI · Paper page
- Author. (1995). An alternative medicine treatment for Parkinson’s disease: results of a multicenter clinical trial. HP-200 in Parkinson’s Disease Study Group. J. Altern. Complement. Med. 1 249– 255. 10.1089/acm.1995.1.249 9395621 · DOI
- Azam S. Haque M. E. Balakrishnan R. Kim I. S. Choi D. K. (2021). The ageing brain: Molecular and cellular basis of neurodegeneration. Front. Cell Dev. Biol. 9: 683459. 10.3389/fcell.2021.683459 34485280 PMC8414981 · DOI
- Bergersen L. H. (2015). Lactate transport and signaling in the brain: potential therapeutic targets and roles in body-brain interaction. J. Cereb. Blood Flow Metab. 35 176– 185. 10.1038/jcbfm.2014.206 25425080 PMC4426752 · DOI
- Bi Y. Lin X. Liang H. Yang D. Zhang X. Ke J. (2020). Human adipose tissue-derived mesenchymal stem cells in Parkinson’s disease: Inhibition of t helper 17 cell differentiation and regulation of immune balance towards a regulatory T cell phenotype. Clin. Interv. Aging 15 1383– 1391. 10.2147/CIA.S259762 32884248 PMC7434526 · DOI
- Bickler P. E. Fahlman C. S. Gray J. McKleroy W. (2009). Inositol 1,4,5-triphosphate receptors and NAD(P)H mediate Ca2+ signaling required for hypoxic preconditioning of hippocampal neurons. Neuroscience 160 51– 60. 10.1016/j.neuroscience.2009.02.013 19217932 PMC2684521 · DOI
- Bilski J. Jaworek J. Pokorski J. Nitecki J. Nitecka E. Pokorska J. (2016). Effects of time of day and the wingate test on appetite perceptions, food intake and plasma levels of adipokines. J. Physiol. Pharmacol. 67 667– 676. 28011947
- Bloom D. E. Chatterji S. Kowal P. Lloyd-Sherlock P. McKee M. Rechel B. (2015). Macroeconomic implications of population ageing and selected policy responses. Lancet 385 649– 657. 10.1016/S0140-6736(14)61464-1 25468167 PMC4469267 · DOI · Paper page
- Bondulich M. K. Jolinon N. Osborne G. F. Smith E. J. Rattray I. Neueder A. (2017). Myostatin inhibition prevents skeletal muscle pathophysiology in Huntington’s disease mice. Sci. Rep. 7: 14275. 10.1038/s41598-017-14290-3 29079832 PMC5660167 · DOI
- Bonomi C. G. De Lucia V. Mascolo A. P. Assogna M. Motta C. Scaricamazza E. (2021). Brain energy metabolism and neurodegeneration: hints from CSF lactate levels in dementias. Neurobiol. Aging 105 333– 339. 10.1016/j.neurobiolaging.2021.05.011 34171631 · DOI
- Brooks G. A. (1986). The lactate shuttle during exercise and recovery. Med. Sci. Sports Exerc. 18 360– 368. 3523107
- Brooks G. A. (2020). Lactate as a fulcrum of metabolism. Redox Biol. 35 101454. PMC7284908 32113910
- Carbone F. Djamshidian A. Seppi K. Poewe W. (2019). Apomorphine for Parkinson’s Disease: Efficacy and Safety of Current and New Formulations. CNS Drugs 33 905– 918. 31473980 PMC6776563
- Carrard J. Rigort A. C. Appenzeller-Herzog C. Colledge F. Konigstein K. Hinrichs T. (2022). Diagnosing overtraining syndrome: A scoping review. Sports Health 14 665– 673. 34496702 PMC9460078
- Cervenka I. Agudelo L. Z. Ruas J. L. (2017). Kynurenines: Tryptophan’s metabolites in exercise, inflammation, and mental health. Science 357 eaaf9794. 28751584
- Chahine L. M. Stern M. B. (2011). Diagnostic markers for Parkinson’s disease. Curr. Opin. Neurol. 24 309– 317. 21464716
- Chapman F. A. Nyimanu D. Maguire J. J. Davenport A. P. Newby D. E. Dhaun N. (2021). The therapeutic potential of apelin in kidney disease. Nat. Rev. Nephrol. 17 840– 853. 34389827 PMC8361827
- Chen B. Wu J. Hu S. Liu Q. Yang H. You Y. (2023). Apelin-13 improves cognitive impairment and repairs hippocampal neuronal damage by activating PGC-1alpha/PPARgamma signaling. Neurochem. Res. 48 1504– 1515. 36512295
- Chen F. Swartzlander D. B. Ghosh A. Fryer J. D. Wang B. Zheng H. (2021). Clusterin secreted from astrocyte promotes excitatory synaptic transmission and ameliorates Alzheimer’s disease neuropathology. Mol. Neurodegener. 16: 5. 10.1186/s13024-021-00426-7 33517893 PMC7849119 · DOI
- Chen P. Wang Y. Chen L. Song N. Xie J. (2020). Apelin-13 Protects Dopaminergic Neurons against Rotenone-Induced Neurotoxicity through the AMPK/mTOR/ULK-1 Mediated Autophagy Activation. Int. J. Mol. Sci. 21: 8376. 10.3390/ijms21218376 33171641 PMC7664695 · DOI
- Chen S. Chen S. T. Sun Y. Xu Z. Wang Y. Yao S. Y. (2019). Fibroblast growth factor 21 ameliorates neurodegeneration in rat and cellular models of Alzheimer’s disease. Redox Biol. 22: 101133. PMC6383137 30785085
- Comai S. Bertazzo A. Brughera M. Crotti S. (2020). Tryptophan in health and disease. Adv. Clin. Chem. 95 165– 218. 32122523
- Dawid M. Mlyczynska E. Jurek M. Respekta N. Pich K. Kurowska P. (2021). Apelin, APJ, and ELABELA: Role in placental function, pregnancy, and foetal development-an overview. Cells 11: 99. 10.3390/cells11010099 35011661 PMC8750556 · DOI
- De la Rosa A. Olaso-Gonzalez G. Arc-Chagnaud C. Millan F. Salvador-Pascual A. Garcia-Lucerga C. (2020). Physical exercise in the prevention and treatment of Alzheimer’s disease. J. Sport Health Sci. 9 394– 404. 32780691 PMC7498620
- de Oliveira A. A. Vergara A. Wang X. Vederas J. C. Oudit G. Y. (2022). Apelin pathway in cardiovascular, kidney, and metabolic diseases: Therapeutic role of apelin analogs and apelin receptor agonists. Peptides 147: 170697. 10.1016/j.peptides.2021.170697 34801627 · DOI
- de Retana S. F. Marazuela P. Sole M. Colell G. Bonaterra A. Sanchez-Quesada J. L. (2019). Peripheral administration of human recombinant ApoJ/clusterin modulates brain beta-amyloid levels in APP23 mice. Alzheimers Res. Ther. 11: 42. 10.1186/s13195-019-0498-8 31077261 PMC6511153 · DOI
- de Silva H. V. Harmony J. A. Stuart W. D. Gil C. M. Robbins J. (1990). Apolipoprotein J: structure and tissue distribution. Biochemistry 29 5380– 5389. 1974459
- Delavar R. Heidarianpour A. (2016). The effect of aerobic exercise training on plasma apelin levels and pain threshold in T1DM rats. Iran Red. Crescent. Med. J. 18 e31737. 10.5812/ircmj.31737 28144460 PMC5253213 · DOI
- Deng N. Hu J. Hong Y. Ding Y. Xiong Y. Wu Z. (2021). Indoleamine-2,3-Dioxygenase 1 deficiency suppresses seizures in epilepsy. Front. Cell Neurosci. 15: 638854. 10.3389/fncel.2021.638854 33679331 PMC7935521 · DOI
- Dezsi L. Vecsei L. (2017). Monoamine oxidase B Inhibitors in Parkinson’s Disease. CNS Neurol. Disord. Drug Targets 16 425– 439. 28124620
- Dodevska M. S. Sobajic S. S. Dragicevic V. D. Stankovic I. Ivanovic N. D. Djordjevic B. I. (2021). The impact of diet and fibre fractions on plasma adipocytokine levels in prediabetic adults. Nutrients 13: 487. 10.3390/nu13020487 33540682 PMC7913095 · DOI
- Dundar A. Kocahan S. Sahin L. (2021). Associations of apelin, leptin, irisin, ghrelin, insulin, glucose levels, and lipid parameters with physical activity during eight weeks of regular exercise training. Arch. Physiol. Biochem. 127 291– 295. 10.1080/13813455.2019.1635622 31290696 · DOI
- Eyjolfsdottir H. Eriksdotter M. Linderoth B. Lind G. Juliusson B. Kusk P. (2016). Targeted delivery of nerve growth factor to the cholinergic basal forebrain of Alzheimer’s disease patients: application of a second-generation encapsulated cell biodelivery device. Alzheimers Res. Ther. 8: 30. 10.1186/s13195-016-0195-9 27389402 PMC4936020 · DOI
- Fang X. Ma J. Mu D. Li B. Lian B. Sun C. (2020). FGF21 Protects Dopaminergic Neurons in Parkinson’s Disease Models Via Repression of Neuroinflammation. Neurotox Res. 37 616– 627. 10.1007/s12640-019-00151-6 31997152 · DOI
- Febbraio M. A. Hiscock N. Sacchetti M. Fischer C. P. Pedersen B. K. (2004). Interleukin-6 is a novel factor mediating glucose homeostasis during skeletal muscle contraction. Diabetes 53 1643– 1648. 10.2337/diabetes.53.7.1643 15220185 · DOI · Paper page
- Fedotova E. I. Dolgacheva L. P. Abramov A. Y. Berezhnov A. V. (2022). Lactate and pyruvate activate autophagy and mitophagy that protect cells in toxic model of Parkinson’s disease. Mol. Neurobiol. 59 177– 190. 10.1007/s12035-021-02583-8 34642892 · DOI
- Feldman M. Margolesky J. (2023). Opicapone for the treatment of Parkinson’s disease: a review. Int. J. Neurosci. 133 532– 543. 33980110
- Ferguson B. S. Rogatzki M. J. Goodwin M. L. Kane D. A. Rightmire Z. Gladden L. B. (2018). Lactate metabolism: historical context, prior misinterpretations, and current understanding. Eur. J. Appl. Physiol. 118 691– 728. 10.1007/s00421-017-3795-6 29322250 · DOI
- Filippini A. Mutti V. Faustini G. Longhena F. Ramazzina I. Rizzi F. (2021). Extracellular clusterin limits the uptake of alpha-synuclein fibrils by murine and human astrocytes. Glia 69 681– 696. 10.1002/glia.23920 33045109 PMC7821254 · DOI
- Fontecha-Barriuso M. Martin-Sanchez D. Martinez-Moreno J. M. Monsalve M. Ramos A. M. Sanchez-Nino M. D. (2020). The Role of PGC-1alpha and mitochondrial biogenesis in kidney diseases. Biomolecules 10: 347. PMC7072614 32102312
- Fortunato A. K. Pontes W. M. De Souza D. M. S. Prazeres J. S. F. Marcucci-Barbosa L. S. Santos J. M. M. (2018). Strength training session induces important changes on physiological, immunological, and inflammatory biomarkers. J. Immunol. Res. 2018: 9675216. 10.1155/2018/9675216 30046617 PMC6038656 · DOI
- Fukui S. Schwarcz R. Rapoport S. I. Takada Y. Smith Q. R. (1991). Blood-brain barrier transport of kynurenines: implications for brain synthesis and metabolism. J. Neurochem. 56 2007– 2017. 1827495
- Gellert L. Varga D. Ruszka M. Toldi J. Farkas T. Szatmari I. (2012). Behavioural studies with a newly developed neuroprotective KYNA-amide. J. Neural Transm. 119 165– 172. 10.1007/s00702-011-0692-8 21818601 · DOI
- Ghanbari-Niaki A. Saeidi A. Gharahcholo L. Moradi-Dehbaghi K. Zare-Kookandeh N. Ahmadian M. (2020). Influence of resistance training and herbal supplementation on plasma apelin and metabolic syndrome risk factors in postmenopausal women. Sci. Sports 35 e1– e109. 10.1016/j.scispo.2019.04.010 37034129 PMC10079133 · DOI
- Gidlund E. K. von Walden F. Venojarvi M. Riserus U. Heinonen O. J. Norrbom J. (2016). Humanin skeletal muscle protein levels increase after resistance training in men with impaired glucose metabolism. Physiol. Rep. 4 e13063. 10.14814/phy2.13063 27923980 PMC5357820 · DOI
- Gong G. Wan W. Liu X. Yin J. (2023). Apelin-13, a regulator of autophagy, apoptosis and inflammation in multifaceted bone protection. Int. Immunopharmacol. 117: 109991. 10.1016/j.intimp.2023.109991 37012875 · DOI
- Gonzalez-Sanchez M. Jimenez J. Narvaez A. Antequera D. Llamas-Velasco S. Martin A. H. (2020). Kynurenic acid levels are increased in the CSF of Alzheimer’s disease patients. Biomolecules 10: 571. PMC7226436 32276479
- Grinstead C. Yoon S. (2022). Apelin, a circulating biomarker in cancer evaluation: A systematic review. Cancers 14: 4656. 10.3390/cancers14194656 36230579 PMC9564299 · DOI
- Guillemin G. J. Kerr S. J. Smythe G. A. Smith D. G. Kapoor V. Armati P. J. (2001). Kynurenine pathway metabolism in human astrocytes: a paradox for neuronal protection. J. Neurochem. 78 842– 853. 10.1046/j.1471-4159.2001.00498.x 11520905 · DOI
- Guillemin G. J. Smith D. G. Kerr S. J. Smythe G. A. Kapoor V. Armati P. J. (2000). Characterisation of kynurenine pathway metabolism in human astrocytes and implications in neuropathogenesis. Redox Rep. 5 108– 111. 10939285
- Guillemin G. J. Smythe G. A. Veas L. A. Takikawa O. Brew B. J. (2003). A beta 1-42 induces production of quinolinic acid by human macrophages and microglia. Neuroreport 14 2311– 2315. 14663182
- Haghparast E. Sheibani V. Abbasnejad M. Esmaeili-Mahani S. (2019). Apelin-13 attenuates motor impairments and prevents the changes in synaptic plasticity-related molecules in the striatum of Parkinsonism rats. Peptides 117: 170091. 10.1016/j.peptides.2019.05.003 31121196 · DOI
- Harper S. (2014). Economic and social implications of aging societies. Science 346 587– 591. 25359967
- Hashida R. Matsuse H. Kawaguchi T. Yoshio S. Bekki M. Iwanaga S. (2021). Effects of a low-intensity resistance exercise program on serum miR-630, miR-5703, and Fractalkine/CX3CL1 expressions in subjects with No exercise habits: A preliminary study. Hepatol. Res. 51 823– 833. 10.1111/hepr.13670 34014020 · DOI
- Hayashi K. Ozaki N. Kawakita K. Itoh K. Mizumura K. Furukawa K. (2011). Involvement of NGF in the rat model of persistent muscle pain associated with taut band. J. Pain 12 1059– 1068. 10.1016/j.jpain.2011.04.010 21719352 · DOI
- Hilmas C. Pereira E. F. Alkondon M. Rassoulpour A. Schwarcz R. Albuquerque E. X. (2001). The brain metabolite kynurenic acid inhibits alpha7 nicotinic receptor activity and increases non-alpha7 nicotinic receptor expression: physiopathological implications. J. Neurosci. 21 7463– 7473. 10.1523/JNEUROSCI.21-19-07463.2001 11567036 PMC6762893 · DOI
- Hinkley J. M. Yu G. X. Standley R. A. Distefano G. Tolstikov V. Narain N. R. (2023). Exercise and ageing impact the kynurenine/tryptophan pathway and acylcarnitine metabolite pools in skeletal muscle of older adults. J. Physiol. 601 2165– 2188. 10.1113/JP284142 36814134 PMC10278663 · DOI
- Homer-Bouthiette C. Xiao L. Hurley M. M. (2021). Gait disturbances and muscle dysfunction in fibroblast growth factor 2 knockout mice. Sci. Rep. 11: 11005. 10.1038/s41598-021-90565-0 34040128 PMC8154953 · DOI
- Hou Y. Dan X. Babbar M. Wei Y. Hasselbalch S. G. Croteau D. L. (2019). Ageing as a risk factor for neurodegenerative disease. Nat. Rev. Neurol. 15 565– 581. 31501588
- Hu S. Shen P. Chen B. Tian S. W. You Y. (2022). Apelin-13 reduces lipopolysaccharide-induced neuroinflammation and cognitive impairment via promoting glucocorticoid receptor expression and nuclear translocation. Neurosci. Lett. 788: 136850. 10.1016/j.neulet.2022.136850 36038029 · DOI
- Huang Y. S. Ogbechi J. Clanchy F. I. Williams R. O. Stone T. W. (2020). IDO and Kynurenine Metabolites in Peripheral and CNS Disorders. Front. Immunol. 11: 388. 10.3389/fimmu.2020.00388 32194572 PMC7066259 · DOI · Paper page
- Ieraci A. Beggiato S. Ferraro L. Barbieri S. S. Popoli M. (2020). Kynurenine pathway is altered in BDNF Val66Met knock-in mice: Effect of physical exercise. Brain Behav. Immun. 89 440– 450. 10.1016/j.bbi.2020.07.031 32726686 · DOI
- Igeta H. Suzuki Y. Motegi T. Sasaki A. Yokoyama Y. Someya T. (2013). Deterioration in donepezil-induced PR prolongation after a coadministration of memantine in a patient with Alzheimer’s disease. Gen. Hosp. Psychiatry 35 e9– e10. 10.1016/j.genhosppsych.2013.04.007 23731891 · DOI
- Iwanaga T. Kishimoto A. (2015). Cellular distributions of monocarboxylate transporters: a review. Biomed. Res. 36 279– 301. 26522146
- Iwaoka K. Otsuka C. Maeda T. Yamahara K. Kato K. Takahashi K. (2020). Impaired metabolism of kynurenine and its metabolites in CSF of parkinson’s disease. Neurosci. Lett. 714: 134576. 10.1016/j.neulet.2019.134576 31654722 · DOI
- Jabbari B. Scherokman B. Gunderson C. H. Rosenberg M. L. Miller J. (1989). Treatment of movement disorders with trihexyphenidyl. Mov. Disord. 4 202– 212. 2779591
- Jacobs K. R. Lim C. K. Blennow K. Zetterberg H. Chatterjee P. Martins R. N. (2019). Correlation between plasma and CSF concentrations of kynurenine pathway metabolites in Alzheimer’s disease and relationship to amyloid-beta and tau. Neurobiol. Aging 80 11– 20. 31055163
- Jaiswal M. K. (2019). Riluzole and edaravone: A tale of two amyotrophic lateral sclerosis drugs. Med. Res. Rev. 39 733– 748. 10.1002/med.21528 30101496 · DOI
- Javelle F. Bloch W. Knoop A. Guillemin G. J. Zimmer P. (2021). Toward a neuroprotective shift: Eight weeks of high intensity interval training reduces the neurotoxic kynurenine activity concurrently to impulsivity in emotionally impulsive humans - A randomized controlled trial. Brain Behav. Immun. 96 7– 17. 10.1016/j.bbi.2021.04.020 33932526 · DOI
- Jelinek M. Jurajda M. Duris K. (2021). Oxidative stress in the brain: Basic concepts and treatment strategies in stroke. Antioxidants 10: 1886. PMC8698986 34942989
- Jeon Y. K. Kim S. S. Kim J. H. Kim H. J. Kim H. J. Park J. J. (2020). Combined aerobic and resistance exercise training reduces circulating apolipoprotein J levels and improves insulin resistance in postmenopausal diabetic women. Diabetes Metab. J. 44 103– 112. 10.4093/dmj.2018.0160 32097999 PMC7043986 · DOI · Paper page
- Ji W. Gong L. Wang J. He H. Zhang Y. (2017). Hypoxic exercise training promotes apelin/APJ expression in skeletal muscles of high fat diet-induced obese mice. Protein Pept. Lett. 24 64– 70. 10.2174/0929866524666161111111726 27834140 · DOI
- Jiang Y. Liu H. Ji B. Wang Z. Wang C. Yang C. (2018). Apelin-13 attenuates ER stress-associated apoptosis induced by MPP+ in SH-SY5Y cells. Int. J. Mol. Med. 42 1732– 1740. 10.3892/ijmm.2018.3719 29901077 · DOI
- Joisten N. Rademacher A. Warnke C. Proschinger S. Schenk A. Walzik D. (2021). Exercise diminishes plasma neurofilament light chain and reroutes the kynurenine pathway in multiple sclerosis. Neurol. Neuroimmunol. Neuroinflamm. 8 e982. 10.1212/NXI.0000000000000982 33782190 PMC8054957 · DOI
- Jonsson W. O. Ponette J. Horwath O. Rydenstam T. Soderlund K. Ekblom B. (2022). Changes in plasma concentration of kynurenine following intake of branched-chain amino acids are not caused by alterations in muscle kynurenine metabolism. Am. J. Physiol. Cell Physiol. 322 C49– C62. 10.1152/ajpcell.00285.2021 34817270 · DOI
- Jourdain P. Rothenfusser K. Ben-Adiba C. Allaman I. Marquet P. Magistretti P. J. (2018). Dual action of L-Lactate on the activity of NR2B-containing NMDA receptors: from potentiation to neuroprotection. Sci. Rep. 8: 13472. 10.1038/s41598-018-31534-y 30194439 PMC6128851 · DOI
- Jung T. W. Park H. S. Choi G. H. Kim D. Lee T. (2018). beta-aminoisobutyric acid attenuates LPS-induced inflammation and insulin resistance in adipocytes through AMPK-mediated pathway. J. Biomed. Sci. 25: 27. 10.1186/s12929-018-0431-7 29592806 PMC5875012 · DOI · Paper page
- Kaiser H. Yu K. Pandya C. Mendhe B. Isales C. M. McGee-Lawrence M. E. (2019). Kynurenine, a tryptophan metabolite that increases with age, induces muscle atrophy and lipid peroxidation. Oxid. Med. Cell Longev. 2019: 9894238. 10.1155/2019/9894238 31737181 PMC6815546 · DOI
- Kalia L. V. (2019). Diagnostic biomarkers for Parkinson’s disease: focus on alpha-synuclein in cerebrospinal fluid. Parkinsonism Relat. Disord. 59 21– 25. 30466800
- Kalman J. Palotas A. Bodi N. Kincses T. Z. Benedek G. Janka Z. (2005a). Lactate infusion fails to improve semantic categorization in Alzheimer’s disease. Brain Res. Bull. 65 533– 539. 10.1016/j.brainresbull.2005.03.009 15862926 · DOI
- Kalman J. Palotas A. Kis G. Boda K. Turi P. Bari F. (2005b). Regional cortical blood flow changes following sodium lactate infusion in Alzheimer’s disease. Eur. J. Neurosci. 21 1671– 1678. 10.1111/j.1460-9568.2005.03924.x 15845094 · DOI
- Kapilevich L. V. Zakharova A. N. Kabachkova A. V. Kironenko T. A. Orlov S. N. (2017). Dynamic and static exercises differentially affect plasma cytokine content in elite endurance- and strength-trained athletes and untrained volunteers. Front. Physiol. 8: 35. 10.3389/fphys.2017.00035 28194116 PMC5276859 · DOI
- Kasai A. Kinjo T. Ishihara R. Sakai I. Ishimaru Y. Yoshioka Y. (2011). Apelin deficiency accelerates the progression of amyotrophic lateral sclerosis. PLoS One 6 e23968. 10.1371/journal.pone.0023968 21887354 PMC3161091 · DOI
- Kazemi F. Zahediasl S. (2018). Effects of exercise training on adipose tissue apelin expression in streptozotocin-nicotinamide induced diabetic rats. Gene 662 97– 102. 10.1016/j.gene.2018.04.003 29626513 · DOI
- Klatt S. Doecke J. D. Roberts A. Boughton B. A. Masters C. L. Horne M. (2021). A six-metabolite panel as potential blood-based biomarkers for Parkinson’s disease. NPJ Parkinsons Dis. 7: 94. 10.1038/s41531-021-00239-x 34650080 PMC8516864 · DOI
- Klein C. Patte-Mensah C. Taleb O. Bourguignon J. J. Schmitt M. Bihel F. (2013). The neuroprotector kynurenic acid increases neuronal cell survival through neprilysin induction. Neuropharmacology 70 254– 260. 10.1016/j.neuropharm.2013.02.006 23422298 · DOI
- Kon M. Ebi Y. Nakagaki K. (2021). Effects of acute sprint interval exercise on follistatin-like 1 and apelin secretions. Arch. Physiol. Biochem. 127 223– 227. 10.1080/13813455.2019.1628067 31232102 · DOI
- Kon M. Suzuki Y. (2022). Effect of a single bout of resistance exercise on zinc-alpha2-glycoprotein. Arch. Physiol. Biochem. 128 248– 252. 10.1080/13813455.2019.1673433 31686532 · DOI
- Kon M. Tanimura Y. Yoshizato H. (2022). Effects of acute endurance exercise on follistatin-like 1 and apelin in the circulation and metabolic organs in rats. Arch. Physiol. Biochem. 128 1254– 1258. 10.1080/13813455.2020.1764050 32412800 · DOI
- Kreher J. B. Schwartz J. B. (2012). Overtraining syndrome: a practical guide. Sports Health 4 128– 138. 23016079 PMC3435910
- Kropackova T. Vernerova L. Storkanova H. Horvathova V. Vokurkova M. Klein M. (2021). Clusterin is upregulated in serum and muscle tissue in idiopathic inflammatory myopathies and associates with clinical disease activity and cytokine profile. Clin. Exp. Rheumatol. 39 1021– 1032. 10.55563/clinexprheumatol/k3vtg5 33124569 · DOI
- Kumar R. Donakonda S. Muller S. A. Botzel K. Hoglinger G. U. Koeglsperger T. (2020). FGF2 Affects Parkinson’s Disease-Associated Molecular Networks Through Exosomal Rab8b/Rab31. Front. Genet. 11: 572058. 10.3389/fgene.2020.572058 33101391 PMC7545478 · DOI
- Kwon H. S. Koh S. H. (2020). Neuroinflammation in neurodegenerative disorders: the roles of microglia and astrocytes. Transl. Neurodegener. 9: 42. PMC7689983 33239064
- Lajko N. Kata D. Szabo M. Matyas A. Dulka K. Foldesi I. (2020). Sensitivity of rodent microglia to kynurenines in models of epilepsy and inflammation in vivo and in vitro: Microglia activation is inhibited by kynurenic acid and the synthetic analogue SZR104. Int. J. Mol. Sci. 21: 9333. 10.3390/ijms21239333 33297593 PMC7731372 · DOI
- Lambertus M. Overberg L. T. Andersson K. A. Hjelden M. S. Hadzic A. Haugen O. P. (2021). L-lactate induces neurogenesis in the mouse ventricular-subventricular zone via the lactate receptor HCA1. Acta Physiol. 231 e13587. 10.1111/apha.13587 33244894 · DOI
- Lauritzen K. H. Morland C. Puchades M. Holm-Hansen S. Hagelin E. M. Lauritzen F. (2014). Lactate receptor sites link neurotransmission, neurovascular coupling, and brain energy metabolism. Cereb. Cortex 24 2784– 2795. 10.1093/cercor/bht136 23696276 · DOI
- Lee B. Shin M. Park Y. Won S. Y. Cho K. S. (2021). Physical exercise-induced myokines in neurodegenerative diseases. Int. J. Mol. Sci. 22: 5795. PMC8198301 34071457
- Lee J. M. Tan V. Lovejoy D. Braidy N. Rowe D. B. Brew B. J. (2017). Involvement of quinolinic acid in the neuropathogenesis of amyotrophic lateral sclerosis. Neuropharmacology 112 346– 364. 27265569
- Lee K. J. Jung K. H. Cho J. Y. Lee S. T. Kim H. S. Shim J. H. (2017). High-fat diet and voluntary chronic aerobic exercise recover altered levels of aging-related tryptophan metabolites along the kynurenine pathway. Exp. Neurobiol. 26 132– 140. 10.5607/en.2017.26.3.132 28680298 PMC5491581 · DOI
- Lee U. Stuelsatz P. Karaz S. McKellar D. W. Russeil J. Deak M. (2022). A Tead1-Apelin axis directs paracrine communication from myogenic to endothelial cells in skeletal muscle. iScience 25: 104589. 10.1016/j.isci.2022.104589 35789856 PMC9250016 · DOI
- Leegwater-Kim J. Waters C. (2006). Tolcapone in the management of Parkinson’s disease. Expert Opin. Pharmacother. 7 2263– 2270. 17059382
- Levinsky A. J. McEdwards G. Sethna N. Currie M. A. (2022). Targets of histone H3 lysine 9 methyltransferases. Front. Cell Dev. Biol. 10: 1026406. 10.3389/fcell.2022.1026406 36568972 PMC9768651 · DOI
- Lev-Vachnish Y. Cadury S. Rotter-Maskowitz A. Feldman N. Roichman A. Illouz T. (2019). L-Lactate promotes adult hippocampal neurogenesis. Front. Neurosci. 13: 403. 10.3389/fnins.2019.00403 31178678 PMC6542996 · DOI
- Lew M. F. Somogyi M. McCague K. Welsh M. Lce Qo L. S. G. (2011). Immediate versus delayed switch from levodopa/carbidopa to levodopa/carbidopa/entacapone: effects on motor function and quality of life in patients with Parkinson’s disease with end-of-dose wearing off. Int. J. Neurosci. 121 605– 613. 10.3109/00207454.2011.598982 21843110 · DOI
- Li C. Cheng H. Adhikari B. K. Wang S. Yang N. Liu W. (2022). The Role of Apelin-APJ System in Diabetes and Obesity. Front. Endocrinol. 13: 820002. 10.3389/fendo.2022.820002 35355561 PMC8959308 · DOI
- Li M. Inoue K. Branigan D. Kratzer E. Hansen J. C. Chen J. W. (2010). Acid-sensing ion channels in acidosis-induced injury of human brain neurons. J. Cereb Blood Flow Metab. 30 1247– 1260. 20216553 PMC2916164
- Ligetvari R. Szokodi I. Far G. Csondor E. Mora A. Komka Z. (2023). Apelin as a Potential Regulator of Peak Athletic Performance. Int. J. Mol. Sci. 24: 8195. 10.3390/ijms24098195 37175901 PMC10179506 · DOI
- Liguori C. Stefani A. Sancesario G. Sancesario G. M. Marciani M. G. Pierantozzi M. (2015). CSF lactate levels, tau proteins, cognitive decline: a dynamic relationship in Alzheimer’s disease. J. Neurol Neurosurg. Psychiatry 86 655– 659. 10.1136/jnnp-2014-308577 25121572 · DOI
- Liu C. Kang N. W. Wang Y. Xue Y. Chen X. Y. Chen L. (2022). Neuropeptide apelin presented in the dopaminergic neurons modulates the neuronal excitability in the substantia nigra pars compacta. Neuropharmacology 219: 109235. 10.1016/j.neuropharm.2022.109235 36041497 · DOI
- Liu K. Zheng J. Wang Y. Li Y. Xiong Y. Wang Y. (2023). Effect of TEA domain transcription factor 1 (TEAD1) on the differentiation of intramuscular preadipocytes in goats. Anim. Biotechnol. [Epub ahead of print]. 10.1080/10495398.2023.2178932 36866843 PMC13353501 · DOI
- Liu W. Yan J. Pan W. Tang M. (2020). Apelin/Elabela-APJ: a novel therapeutic target in the cardiovascular system. Ann. Transl. Med. 8: 243. 10.21037/atm.2020.02.07 32309390 PMC7154429 · DOI
- Luo H. Xiang Y. Qu X. Liu H. Liu C. Li G. (2019). Apelin-13 Suppresses neuroinflammation against cognitive deficit in a streptozotocin-induced rat model of Alzheimer’s disease through activation of BDNF-TrkB signaling pathway. Front. Pharmacol. 10: 395. 10.3389/fphar.2019.00395 31040784 PMC6477031 · DOI
- Majerova P. Olesova D. Golisova G. Buralova M. Michalicova A. Vegh J. (2022). Analog of kynurenic acid decreases tau pathology by modulating astrogliosis in rat model for tauopathy. Biomed. Pharmacother. 152: 113257. 10.1016/j.biopha.2022.113257 35714514 · DOI
- Mandi Y. Vecsei L. (2012). The kynurenine system and immunoregulation. J. Neural Transm. 119 197– 209. 21744051
- Martos D. Tuka B. Tanaka M. Vecsei L. Telegdy G. (2022). Memory enhancement with kynurenic acid and its mechanisms in neurotransmission. Biomedicines 10: 849. 10.3390/biomedicines10040849 35453599 PMC9027307 · DOI
- Mathes S. Fahrner A. Ghoshdastider U. Rudiger H. A. Leunig M. Wolfrum C. (2021). FGF-2-dependent signaling activated in aged human skeletal muscle promotes intramuscular adipogenesis. Proc. Natl. Acad. Sci. U. S. A. 118 e2021013118. 10.1073/pnas.2021013118 34493647 PMC8449320 · DOI
- Matsuoka M. Hashimoto Y. (2010). Humanin and the receptors for humanin. Mol. Neurobiol. 41 22– 28. 19997871
- Matthews L. G. Puryear C. B. Correia S. S. Srinivasan S. Belfort G. M. Pan M. K. (2023). T-type calcium channels as therapeutic targets in essential tremor and Parkinson’s disease. Ann. Clin. Transl. Neurol. 10 462– 483. 36738196 PMC10109288
- May L. T. Hill S. J. (2008). ERK phosphorylation: spatial and temporal regulation by G protein-coupled receptors. Int. J. Biochem. Cell Biol. 40 2013– 2017. 18502166
- McEwen B. S. (2020). Hormones and behavior and the integration of brain-body science. Horm. Behav. 119: 104619. 10.1016/j.yhbeh.2019.104619 31790663 · DOI
- Mee-Inta O. Zhao Z. W. Kuo Y. M. (2019). Physical Exercise Inhibits Inflammation and Microglial Activation. Cells 8: 691. PMC6678635 31324021
- Mehan S. Parveen S. Kalra S. (2017). Adenyl cyclase activator forskolin protects against Huntington’s disease-like neurodegenerative disorders. Neural Regen. Res. 12 290– 300. 10.4103/1673-5374.200812 28400813 PMC5361515 · DOI
- Millischer V. Erhardt S. Ekblom O. Forsell Y. Lavebratt C. (2017). Twelve-week physical exercise does not have a long-lasting effect on kynurenines in plasma of depressed patients. Neuropsychiatr. Dis. Treat 13 967– 972. 28408830 PMC5384718
- Minato T. Nakamura N. Saiki T. Miyabe M. Ito M. Matsubara T. (2022). beta-Aminoisobutyric acid, L-BAIBA, protects PC12 cells from hydrogen peroxide-induced oxidative stress and apoptosis via activation of the AMPK and PI3K/Akt pathway. IBRO Neurosci. Rep. 12 65– 72. 10.1016/j.ibneur.2021.12.001 35024688 PMC8724974 · DOI
- Mok M. H. Fricker A. C. Weil A. Kew J. N. (2009). Electrophysiological characterisation of the actions of kynurenic acid at ligand-gated ion channels. Neuropharmacology 57 242– 249. 19523966
- Mollenhauer B. von Arnim C. A. F. (2022). Toward preventing Parkinson’s disease. Science 377 818– 819. 35981039
- Moon H. Y. Becke A. Berron D. Becker B. Sah N. Benoni G. (2016). Running-induced systemic cathepsin B secretion is associated with memory function. Cell Metab. 24 332– 340. 10.1016/j.cmet.2016.05.025 27345423 PMC6029441 · DOI · Paper page
- Moretti D. V. Binetti G. Zanetti O. Frisoni G. B. (2014). Behavioral and neurophysiological effects of transdermal rotigotine in atypical parkinsonism. Front. Neurol. 5: 85. 10.3389/fneur.2014.00085 24926284 PMC4046164 · DOI
- Morland C. Andersson K. A. Haugen O. P. Hadzic A. Kleppa L. Gille A. (2017). Exercise induces cerebral VEGF and angiogenesis via the lactate receptor HCAR1. Nat. Commun. 8: 15557. 10.1038/ncomms15557 28534495 PMC5457513 · DOI · Paper page
- Mosienko V. Teschemacher A. G. Kasparov S. (2015). Is L-lactate a novel signaling molecule in the brain? J. Cereb. Blood Flow Metab. 35 1069– 1075. 10.1038/jcbfm.2015.77 25920953 PMC4640281 · DOI
- Mughal A. O’Rourke S. T. (2018). Vascular effects of apelin: Mechanisms and therapeutic potential. Pharmacol. Ther. 190 139– 147. 29807055 PMC6165679
- Nigam M. Leu-Semenescu S. Arnulf I. (2021). Successful treatment of drug-resistant cataplexy with the anticholinergic drug tropatepine. J. Clin. Sleep Med. 17 849– 851. 10.5664/jcsm.9030 33231168 PMC8020693 · DOI
- Njerve I. U. Byrkjeland R. Arnesen H. Akra S. Solheim S. Seljeflot I. (2016). Effects of long-term exercise training on adipose tissue expression of fractalkine and MCP-1 in patients with type 2 diabetes and stable coronary artery disease: a substudy of a randomized controlled trial. Diabetes Metab. Syndr. Obes. 9 55– 62. 10.2147/DMSO.S96299 27042130 PMC4798200 · DOI
- O’Connor J. C. Lawson M. A. Andre C. Moreau M. Lestage J. Castanon N. (2009). Lipopolysaccharide-induced depressive-like behavior is mediated by indoleamine 2,3-dioxygenase activation in mice. Mol. Psychiatry 14 511– 522. 18195714 PMC2683474
- O’Dowd B. F. Heiber M. Chan A. Heng H. H. Tsui L. C. Kennedy J. L. (1993). A human gene that shows identity with the gene encoding the angiotensin receptor is located on chromosome 11. Gene 136 355– 360. 8294032
- Oh S. B. Kim M. S. Park S. Son H. Kim S. Y. Kim M. S. (2019). Clusterin contributes to early stage of Alzheimer’s disease pathogenesis. Brain Pathol. 29 217– 231. 30295351 PMC8028273
- Opie L. H. (1978). Myocardial metabolism and heart disease. Jpn. Circ. J. 42 1223– 1247. 34741
- Otaka N. Shibata R. Ohashi K. Uemura Y. Kambara T. Enomoto T. (2018). Myonectin is an exercise-induced myokine that protects the heart from ischemia-reperfusion injury. Circ. Res. 123 1326– 1338. 10.1161/CIRCRESAHA.118.313777 30566056 · DOI
- Park J. S. Saeed K. Jo M. H. Kim M. W. Lee H. J. Park C. B. (2022). LDHB deficiency promotes mitochondrial dysfunction mediated oxidative stress and neurodegeneration in adult mouse brain. Antioxidants 11: 261. 10.3390/antiox11020261 35204143 PMC8868245 · DOI
- Pathak S. J. Zhou Z. Steffen D. Tran T. Ad Y. Ramsey J. J. (2022). 2-month ketogenic diet preferentially alters skeletal muscle and augments cognitive function in middle aged female mice. Aging Cell 21 e13706. 10.1111/acel.13706 36148631 PMC9577944 · DOI
- Pierozan P. Biasibetti-Brendler H. Schmitz F. Ferreira F. Pessoa-Pureur R. Wyse A. T. S. (2018). Kynurenic acid prevents cytoskeletal disorganization induced by quinolinic acid in mixed cultures of rat striatum. Mol. Neurobiol. 55 5111– 5124. 10.1007/s12035-017-0749-2 28840509 · DOI
- Pitkin S. L. Maguire J. J. Bonner T. I. Davenport A. P. (2010). International Union of Basic and Clinical Pharmacology. LXXIV. Apelin receptor nomenclature, distribution, pharmacology, and function. Pharmacol. Rev. 62 331– 342. 10.1124/pr.110.002949 20605969 · DOI
- Pouresmaeili-Babaki E. Esmaeili-Mahani S. Abbasnejad M. Ravan H. (2018). Protective effect of neuropeptide apelin-13 on 6-hydroxydopamine-induced neurotoxicity in SH-SY5Y dopaminergic cells: involvement of its antioxidant and antiapoptotic properties. Rejuvenation Res. 21 162– 167. 10.1089/rej.2017.1951 28782414 · DOI
- Quan H. Koltai E. Suzuki K. Aguiar A. S. Jr. Pinho R. Boldogh I. (2020). Exercise, redox system and neurodegenerative diseases. Biochim. Biophys. Acta Mol. Basis Dis. 1866: 165778. 32222542
- Rabinowitz J. D. Enerback S. (2020). Lactate: the ugly duckling of energy metabolism. Nat. Metab. 2 566– 571. 32694798 PMC7983055
- Rajendran R. Bottiger G. Stadelmann C. Karnati S. Berghoff M. (2021). FGF/FGFR pathways in multiple sclerosis and in its disease models. Cells 10: 884. PMC8068804 33924474
- Ramirez-Ortega D. Ramiro-Salazar A. Gonzalez-Esquivel D. Rios C. Pineda B. (2017). Perez de la Cruz, V. 3-Hydroxykynurenine and 3-Hydroxyanthranilic Acid Enhance the Toxicity Induced by Copper in Rat Astrocyte Culture. Oxid. Med. Cell Longev. 2017: 2371895. 10.1155/2017/2371895 28831293 PMC5555010 · DOI
- Redmann M. Darley-Usmar V. Zhang J. (2016). The role of autophagy, mitophagy and lysosomal functions in modulating bioenergetics and survival in the context of redox and proteotoxic damage: Implications for neurodegenerative diseases. Aging Dis. 7 150– 162. 10.14336/AD.2015.0820 27114848 PMC4809607 · DOI
- Rius-Perez S. Torres-Cuevas I. Millan I. Ortega A. L. Perez S. (2020). PGC-1alpha, Inflammation, and Oxidative Stress: An Integrative View in Metabolism. Oxid. Med. Cell Longev. 2020: 1452696. 10.1155/2020/1452696 32215168 PMC7085407 · DOI
- Rohe M. Synowitz M. Glass R. Paul S. M. Nykjaer A. Willnow T. E. (2009). Brain-derived neurotrophic factor reduces amyloidogenic processing through control of SORLA gene expression. J. Neurosci. 29 15472– 15478. 10.1523/JNEUROSCI.3960-09.2009 20007471 PMC6666105 · DOI
- Roszkowicz-Ostrowska K. Mlotkowska P. Kowalczyk P. Marciniak E. Barszcz M. Misztal T. (2022). Central Stimulatory Effect of Kynurenic Acid on BDNF-TrkB Signaling and BER Enzymatic Activity in the Hippocampal CA1 Field in Sheep. Int. J. Mol. Sci. 24: 136. 10.3390/ijms24010136 36613581 PMC9820639 · DOI
- Saran T. Turska M. Kocki T. Zawadka M. Zielinski G. Turski W. A. (2021). Effect of 4-week physical exercises on tryptophan, kynurenine and kynurenic acid content in human sweat. Sci. Rep. 11: 11092. 10.1038/s41598-021-90616-6 34045580 PMC8160349 · DOI
- Sas K. Szabo E. Vecsei L. (2018). Mitochondria, Oxidative Stress and the Kynurenine System, with a Focus on Ageing and Neuroprotection. Molecules 23: 191. 10.3390/molecules23010191 29342113 PMC6017505 · DOI
- Schirinzi T. Di Lazzaro G. Sancesario G. M. Summa S. Petrucci S. Colona V. L. (2020). Young-onset and late-onset Parkinson’s disease exhibit a different profile of fluid biomarkers and clinical features. Neurobiol. Aging 90 119– 124. 10.1016/j.neurobiolaging.2020.02.012 32169356 · DOI
- Schlittler M. Goiny M. Agudelo L. Z. Venckunas T. Brazaitis M. Skurvydas A. (2016). Endurance exercise increases skeletal muscle kynurenine aminotransferases and plasma kynurenic acid in humans. Am. J. Physiol. Cell Physiol. 310 C836– C840. 27030575
- Seo J. A. Kang M. C. Yang W. M. Hwang W. M. Kim S. S. Hong S. H. (2020). Apolipoprotein J is a hepatokine regulating muscle glucose metabolism and insulin sensitivity. Nat. Commun. 11 2024. PMC7181874 32332780
- Sheibani S. Hanachi P. Refahiat M. A. (2012). Effect of aerobic exercise on serum concentration of apelin, TNFalpha and insulin in obese women. Iran J. Basic Med. Sci. 15 1196– 1201. 23653851 PMC3646232
- Shi T. Shi Y. Gao H. Ma Y. Wang Q. Shen S. (2022). Exercised accelerated the production of muscle-derived kynurenic acid in skeletal muscle and alleviated the postmenopausal osteoporosis through the Gpr35/NFkappaB p65 pathway. J. Orthop. Translat. 35 1– 12. 10.1016/j.jot.2022.03.003 35846727 PMC9260440 · DOI
- Shima T. Matsui T. Jesmin S. Okamoto M. Soya M. Inoue K. (2017). Moderate exercise ameliorates dysregulated hippocampal glycometabolism and memory function in a rat model of type 2 diabetes. Diabetologia 60 597– 606. 10.1007/s00125-016-4164-4 27928614 · DOI
- Siddiqui T. Bhattarai P. Popova S. Cosacak M. I. Sariya S. Zhang Y. (2021). KYNA/Ahr Signaling Suppresses Neural Stem Cell Plasticity and Neurogenesis in Adult Zebrafish Model of Alzheimer’s Disease. Cells 10: 2748. 10.3390/cells10102748 34685728 PMC8534484 · DOI
- Siess M. (1980). Some aspects on the regulation of carbohydrate and lipid metabolism in cardiac tissue. Basic Res. Cardiol. 75 47– 56. 6992768
- Snowden S. G. Ebshiana A. A. Hye A. Pletnikova O. O’Brien R. Yang A. (2019). Neurotransmitter imbalance in the brain and Alzheimer’s disease pathology. J. Alzheimers Dis. 72 35– 43. 31561368 PMC12961646
- Soderberg L. Johannesson M. Nygren P. Laudon H. Eriksson F. Osswald G. (2023). Lecanemab, Aducanumab, and Gantenerumab - Binding Profiles to Different Forms of Amyloid-Beta Might Explain Efficacy and Side Effects in Clinical Trials for Alzheimer’s Disease. Neurotherapeutics 20 195– 206. 10.1007/s13311-022-01308-6 36253511 PMC10119362 · DOI
- Son J. S. Chae S. A. Park B. I. Du M. Song W. (2019). Plasma apelin levels in overweight/obese adults following a single bout of exhaustive exercise: A preliminary cross-sectional study. Endocrinol. Diabetes Nutr. 66 278– 290. 10.1016/j.endinu.2018.12.005 30827910 · DOI · Paper page
- Son J. S. Chae S. A. Zhao L. Wang H. de Avila J. M. Zhu M. J. (2022). Maternal exercise intergenerationally drives muscle-based thermogenesis via activation of apelin-AMPK signaling. EBioMedicine 76: 103842. 10.1016/j.ebiom.2022.103842 35081489 PMC8790600 · DOI
- Son J. S. Kim H. J. Son Y. Lee H. Chae S. A. Seong J. K. (2017). Effects of exercise-induced apelin levels on skeletal muscle and their capillarization in type 2 diabetic rats. Muscle Nerve 56 1155– 1163. 10.1002/mus.25596 28164323 · DOI
- Sorgdrager F. J. H. Vermeiren Y. Van Faassen M. van der Ley C. Nollen E. A. A. Kema I. P. (2019). Age- and disease-specific changes of the kynurenine pathway in Parkinson’s and Alzheimer’s disease. J. Neurochem. 151 656– 668. 10.1111/jnc.14843 31376341 PMC6899862 · DOI
- Souza L. C. Jesse C. R. Antunes M. S. Ruff J. R. de Oliveira Espinosa D. Gomes N. S. (2016). Indoleamine-2,3-dioxygenase mediates neurobehavioral alterations induced by an intracerebroventricular injection of amyloid-beta1-42 peptide in mice. Brain Behav. Immun. 56 363– 377. 10.1016/j.bbi.2016.03.002 26965653 · DOI
- Speranza L. di Porzio U. Viggiano D. de Donato A. Volpicelli F. (2021). Dopamine: The neuromodulator of long-term synaptic plasticity, reward and movement control. Cells 10: 735. PMC8066851 33810328
- Steiner L. Gold M. Mengel D. Dodel R. Bach J. P. (2014). The endogenous alpha7 nicotinic acetylcholine receptor antagonist kynurenic acid modulates amyloid-beta-induced inflammation in BV-2 microglial cells. J. Neurol. Sci. 344 94– 99. 10.1016/j.jns.2014.06.032 25064444 · DOI
- Stone T. W. (2007). Kynurenic acid blocks nicotinic synaptic transmission to hippocampal interneurons in young rats. Eur. J. Neurosci. 25 2656– 2665. 10.1111/j.1460-9568.2007.05540.x 17459105 · DOI
- Stromberg A. Olsson K. Dijksterhuis J. P. Rullman E. Schulte G. Gustafsson T. (2016). CX3CL1–a macrophage chemoattractant induced by a single bout of exercise in human skeletal muscle. Am. J. Physiol. Regul. Integr. Comp. Physiol. 310 R297– R304. 10.1152/ajpregu.00236.2015 26632602 · DOI · Paper page
- Su C. H. Chuang H. C. Hong C. J. (2020). Physical exercise prevents mice from L-Kynurenine-induced depression-like behavior. Asian J. Psychiatr. 48: 101894. 10.1016/j.ajp.2019.101894 31918308 · DOI
- Su K. H. Dai C. (2016). Metabolic control of the proteotoxic stress response: implications in diabetes mellitus and neurodegenerative disorders. Cell Mol. Life Sci. 73 4231– 4248. 10.1007/s00018-016-2291-1 27289378 PMC5599143 · DOI
- Subbarayan M. S. Joly-Amado A. Bickford P. C. Nash K. R. (2022). CX3CL1/CX3CR1 signaling targets for the treatment of neurodegenerative diseases. Pharmacol. Ther. 231: 107989. 34492237
- Sujkowski A. Hong L. Wessells R. J. Todi S. V. (2022). The protective role of exercise against age-related neurodegeneration. Ageing Res. Rev. 74: 101543. PMC8761166 34923167
- Suma T. Koshinaga M. Fukushima M. Kano T. Katayama Y. (2008). Effects of in situ administration of excitatory amino acid antagonists on rapid microglial and astroglial reactions in rat hippocampus following traumatic brain injury. Neurol. Res. 30 420– 429. 10.1179/016164107X251745 18248696 · DOI
- Sun Y. Li X. Bedlack R. (2023). An evaluation of the combination of sodium phenylbutyrate and taurursodiol for the treatment of amyotrophic lateral sclerosis. Expert Rev. Neurother. 23 1– 7. 36705941
- Swaih A. M. Breda C. Sathyasaikumar K. V. Allcock N. Collier M. E. W. Mason R. P. (2022). Kynurenine 3-Monooxygenase Interacts with Huntingtin at the Outer Mitochondrial Membrane. Biomedicines 10: 2294. 10.3390/biomedicines10092294 36140394 PMC9496550 · DOI
- Szabo M. Lajko N. Dulka K. Barczanfalvi G. Lorinczi B. Szatmari I. (2023). The kynurenic acid analog SZR104 induces cytomorphological changes associated with the anti-inflammatory phenotype in cultured microglia. Sci. Rep. 13: 11328. 10.1038/s41598-023-38107-8 37443330 PMC10344911 · DOI
- Szabo M. Lajko N. Dulka K. Szatmari I. Fulop F. Mihaly A. (2022). Kynurenic Acid and Its Analog SZR104 Exhibit Strong Antiinflammatory Effects and Alter the Intracellular Distribution and Methylation Patterns of H3 Histones in Immunochallenged Microglia-Enriched Cultures of Newborn Rat Brains. Int. J. Mol. Sci. 23: 1079. 10.3390/ijms23031079 35163002 PMC8835130 · DOI
- Takimoto M. Hamada T. (1985). Acute exercise increases brain region-specific expression of MCT1, MCT2, MCT4, GLUT1, and COX IV proteins. J. Appl. Physiol. 2014 1238– 1250. 10.1152/japplphysiol.01288.2013 24610532 · DOI
- Tanaka M. Bohar Z. Martos D. Telegdy G. Vecsei L. (2020). Antidepressant-like effects of kynurenic acid in a modified forced swim test. Pharmacol. Rep. 72 449– 455. 10.1007/s43440-020-00067-5 32162182 · DOI
- Tatemoto K. Hosoya M. Habata Y. Fujii R. Kakegawa T. Zou M. X. (1998). Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor. Biochem. Biophys. Res. Commun. 251 471– 476. 10.1006/bbrc.1998.9489 9792798 · DOI
- Tee C. C. L. Parr E. B. Cooke M. B. Chong M. C. Rahmat N. Md Razali M. R. (2023). Combined effects of exercise and different levels of acute hypoxic severity: A randomized crossover study on glucose regulation in adults with overweight. Front. Physiol. 14: 1174926. 10.3389/fphys.2023.1174926 37123278 PMC10133678 · DOI
- Thevandavakkam M. A. Schwarcz R. Muchowski P. J. Giorgini F. (2010). Targeting kynurenine 3-monooxygenase (KMO): implications for therapy in Huntington’s disease. CNS Neurol. Disord. Drug Targets 9 791– 800. 20942784
- van der Velpen V. Teav T. Gallart-Ayala H. Mehl F. Konz I. Clark C. (2019). Systemic and central nervous system metabolic alterations in Alzheimer’s disease. Alzheimers Res. Ther. 11: 93. PMC6883620 31779690
200 of 231 shown
- Authors
- Bian, X., Wang, Q., Wang, Y., & Lou, S.
- Affiliations
- Shanghai University of Sport (CN)
- Victoria University (AU)
- Corresponding author
- Wang, Yibing
- Lou, Shujie
- Venue
- Frontiers in Molecular Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2024-01-05
- Volume
- 16
- Pages
- 1305208-1305208
- ISSN
- 1662-5099 (ISSN-L)
- PMC
- PMC10796786
- OpenAlex
- W4390611757
- Cited by
- 15
- References
- 259
- Citations by year
- 2026: 1 · 2025: 10 · 2024: 4
- FWCI
- 0.65
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Molecular Neuroscience (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (11DZ2261100, 31971098)
- Shanghai University of Sport (31971098, 11DZ2261100)
- Topics
- Health Sciences › Medicine › Rehabilitation › Exercise and Physiological Responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Keywords
- exerkines, neurodegenerative diseases, myokines, skeletal muscle, physical activity, muscle-brain axis, apelin, kynurenic acid, lactate, neuroprotection
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