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Chronic Intermittent Hypobaric Hypoxia Pretreatment Ameliorates Ischemia-Induced Cognitive Dysfunction Through Activation of ERK1/2-CREB-BDNF Pathway in Anesthetized Mice

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Abstract

Chronic intermittent hypobaric hypoxia (CIHH) has protective effects on heart and brain against ischemia injury through mobilizing endogenous adaptive mechanisms. However, whether CIHH prevents against cognitive impairment was not elucidated. The present study aimed to investigate the effect and mechanism of CIHH treatment on ischemia/reperfusion (IR)-induced cognitive dysfunction. Mice were randomly divided into 8 groups: Control, Sham, CIHH (simulating 5000 m high-altitude for 28 days, 6 h per day), IR (three 16-min occlusions of bilateral common carotid arteries interrupted by two 10-min intervals), CIHH + IR, PD98059 (inhibitor of MEK1/2) + CIHH + IR, PD98059 + Sham and PD98059 + IR group. Morris water maze and step-down passive avoidance tests were performed to evaluate the capability of learning and memory 1 month after ischemia. Thionine dyeing was to examine histological manifestations of pyramidal neurons in hippocampus CA1 region. Western blotting assay was for measurement of the protein expressions in ERK1/2-CREB-BDNF signaling pathway. There were a shorter escape latency and a longer percentage of time retaining in the target quadrant in Morris water maze test, fewer times of errors in the step-down avoidance test and a higher neuronal density of the hippocampal CA1 subfield in CIHH + IR group than in IR group. CIHH upregulated the expressions of BDNF, phosphorylated CREB, ERK1/2 and TrkB with or without ischemia. The protective effects of CIHH were abolished by PD98059 administration 15 min before ischemia. CIHH ameliorated ischemia-induced cognitive dysfunction through activation of ERK1/2-CREB-BDNF signaling pathway.

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References

  1. Lei Y, Guo Q, Li Y, Jiang H, Ni W, Gu Y (2014) Characteristics of cognitive impairment in adults with cerebral ischemia. Zhonghua Yi Xue Za Zhi 94:984–989

    PubMed  Google Scholar 

  2. Briones TL, Woods J, Wadowska M (2014) Chronic neuroinflammation and cognitive impairment following transient global cerebral ischemia: role of fractalkine/CX3CR1 signaling. J Neuroinflammation 11:13. doi:10.1186/1742-2094-11-13

    Article  PubMed  PubMed Central  Google Scholar 

  3. Lee YS, Silva AJ (2009) The molecular and cellular biology of enhanced cognition. Nat Rev Neurosci 10:126–140. doi:10.1038/nrn2572

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Lipsky RH, Marini AM (2007) Brain-derived neurotrophic factor in neuronal survival and behavior-related plasticity. Ann N Y Acad Sci 1122:130–143. doi:10.1196/annals.1403.009

    Article  CAS  PubMed  Google Scholar 

  5. Okuyama S, Morita M, Sawamoto A, Terugo T, Nakajima M, Furukawa Y (2015) Edaravone enhances brain-derived neurotrophic factor production in the ischemic mouse brain. Pharmaceuticals (Basel) 8:176–185. doi:10.3390/ph8020176

    Article  CAS  Google Scholar 

  6. Buckley PF, Pillai A, Howell KR (2011) Brain-derived neurotrophic factor: findings in schizophrenia. Curr Opin Psychiatry 24:122–127. doi:10.1097/YCO.0b013e3283436eb7

    Article  PubMed  Google Scholar 

  7. Niitsu T, Shirayama Y, Matsuzawa D, Hasegawa T, Kanahara N, Hashimoto T, Shiraishi T, Shiina A, Fukami G, Fujisaki M, Watanabe H, Nakazato M, Asano M, Kimura S, Hashimoto K, Iyo M (2011) Associations of serum brain-derived neurotrophic factor with cognitive impairments and negative symptoms in schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 35:1836–1840. doi:10.1016/j.pnpbp.2011.09.004

    Article  CAS  PubMed  Google Scholar 

  8. Asevedo E, Gadelha A, Noto C, Mansur RB, Zugman A, Belangero SI, Berberian AA, Scarpato BS, Leclerc E, Teixeira AL, Gama CS, Bressan RA, Brietzke E (2013) Impact of peripheral levels of chemokines, BDNF and oxidative markers on cognition in individuals with schizophrenia. J Psychiatr Res 47:1376–1382. doi:10.1016/j.jpsychires.2013.05.032

    Article  PubMed  Google Scholar 

  9. Guo X, Chen ZH, Wang HL, Liu ZC, Wang XP, Zhou BH, Yang C, Zhang XP, Xiao L, Shu C, Chen JX, Wang GH (2015) WSKY, a traditional Chinese decoction, rescues cognitive impairment associated with NMDA receptor antagonism by enhancing BDNF/ERK/CREB signaling. Mol Med Rep 11:2927–2934. doi:10.3892/mmr.2014.3086

    CAS  PubMed  Google Scholar 

  10. Bekinschtein P, Cammarota M, Igaz LM, Bevilaqua LR, Izquierdo I, Medina JH (2007) Persistence of long-term memory storage requires a late protein synthesis- and BDNF-dependent phase in the hippocampus. Neuron 53:261–277. doi:10.1016/j.neuron.2006.11.025

    Article  CAS  PubMed  Google Scholar 

  11. Callaghan CK, Kelly AM (2012) Differential BDNF signaling in dentate gyrus and perirhinal cortex during consolidation of recognition memory in the rat. Hippocampus 22:2127–2135. doi:10.1002/hipo.22033

    Article  CAS  PubMed  Google Scholar 

  12. Almeida RD, Manadas BJ, Melo CV, Gomes JR, Mendes CS, Graos MM, Carvalho RF, Carvalho AP, Duarte CB (2005) Neuroprotection by BDNF against glutamate-induced apoptotic cell death is mediated by ERK and PI3-kinase pathways. Cell Death Differ 12:1329–1343. doi:10.1038/sj.cdd.4401662

    Article  CAS  PubMed  Google Scholar 

  13. Cunha C, Brambilla R, Thomas KL (2010) A simple role for BDNF in learning and memory? Front Mol Neurosci 3:1. doi:10.3389/neuro.02.001.2010

    PubMed  PubMed Central  Google Scholar 

  14. Scott Bitner R (2012) Cyclic AMP response element-binding protein (CREB) phosphorylation: a mechanistic marker in the development of memory enhancing Alzheimer’s disease therapeutics. Biochem Pharmacol 83:705–714. doi:10.1016/j.bcp.2011.11.009

    Article  CAS  PubMed  Google Scholar 

  15. Roels B, Bentley DJ, Coste O, Mercier J, Millet GP (2007) Effects of intermittent hypoxic training on cycling performance in well-trained athletes. Eur J Appl Physiol 101:359–368. doi:10.1007/s00421-007-0506-8

    Article  PubMed  Google Scholar 

  16. Serebrovskaya TV, Manukhina EB, Smith ML, Downey HF, Mallet RT (2008) Intermittent hypoxia: cause of or therapy for systemic hypertension? Exp Biol Med (Maywood) 233:627–650. doi:10.3181/0710-mr-267

    Article  CAS  Google Scholar 

  17. Zhang Y, Yang HT, Zhou ZN (2007) The cardioprotection of intermittent hypoxic adaptation. Sheng Li Xue Bao 59:601–613

    CAS  PubMed  Google Scholar 

  18. Guan Y, Gao L, Ma HJ, Li Q, Zhang H, Yuan F, Zhou ZN, Zhang Y (2010) Chronic intermittent hypobaric hypoxia decreases beta-adrenoceptor activity in right ventricular papillary muscle. Am J Physiol Heart Circ Physiol 298:H1267–H1272. doi:10.1152/ajpheart.00410.2009

    Article  CAS  PubMed  Google Scholar 

  19. Zhu XH, Yan HC, Zhang J, Qu HD, Qiu XS, Chen L, Li SJ, Cao X, Bean JC, Chen LH, Qin XH, Liu JH, Bai XC, Mei L, Gao TM (2010) Intermittent hypoxia promotes hippocampal neurogenesis and produces antidepressant-like effects in adult rats. J Neurosci 30:12653–12663. doi:10.1523/jneurosci.6414-09.2010

    Article  CAS  PubMed  Google Scholar 

  20. Gong SJ, Chen LY, Zhang M, Gong JX, Ma YX, Zhang JM, Wang YJ, Hu YY, Sun XC, Li WB, Zhang Y (2012) Intermittent hypobaric hypoxia preconditioning induced brain ischemic tolerance by up-regulating glial glutamate transporter-1 in rats. Neurochem Res 37:527–537. doi:10.1007/s11064-011-0639-3

    Article  CAS  PubMed  Google Scholar 

  21. Rybnikova E, Mironova V, Pivina S, Tulkova E, Ordyan N, Nalivaeva N, Turner A, Samoilov M (2007) Involvement of the hypothalamic–pituitary–adrenal axis in the antidepressant-like effects of mild hypoxic preconditioning in rats. Psychoneuroendocrinology 32:813–823. doi:10.1016/j.psyneuen.2007.05.010

    Article  CAS  PubMed  Google Scholar 

  22. Yang Y, Zhang X, Cui H, Zhang C, Zhu C, Li L (2014) Apelin-13 protects the brain against ischemia/reperfusion injury through activating PI3K/Akt and ERK1/2 signaling pathways. Neurosci Lett 568:44–49. doi:10.1016/j.neulet.2014.03.037

    Article  CAS  PubMed  Google Scholar 

  23. Wang H (2014) Establishment of an animal model of vascular dementia. Exp Ther Med 8:1599–1603. doi:10.3892/etm.2014.1926

    PubMed  PubMed Central  Google Scholar 

  24. Kato H, Liu Y, Araki T, Kogure K (1991) Temporal profile of the effects of pretreatment with brief cerebral ischemia on the neuronal damage following secondary ischemic insult in the gerbil: cumulative damage and protective effects. Brain Res 553:238–242

    Article  CAS  PubMed  Google Scholar 

  25. Kirino T, Tamura A, Sano K (1986) A reversible type of neuronal injury following ischemia in the gerbil hippocampus. Stroke 17:455–459

    Article  CAS  PubMed  Google Scholar 

  26. Levine BD (2002) Intermittent hypoxic training: fact and fancy. High Alt Med Biol 3:177–193. doi:10.1089/15270290260131911

    Article  PubMed  Google Scholar 

  27. Zhuang J, Zhou Z (1999) Protective effects of intermittent hypoxic adaptation on myocardium and its mechanisms. Biol Signals Recept 8:316–322

    Article  CAS  PubMed  Google Scholar 

  28. Zhang Y, Zhou ZN (2012) Beneficial effects of intermittent hypobaric hypoxia on the body. Zhongguo Ying Yong Sheng Li Xue Za Zhi 28:504–9

    CAS  PubMed  Google Scholar 

  29. Udayabanu M, Kumaran D, Nair RU, Srinivas P, Bhagat N, Aneja R, Katyal A (2008) Nitric oxide associated with iNOS expression inhibits acetylcholinesterase activity and induces memory impairment during acute hypobaric hypoxia. Brain Res 1230:138–149. doi:10.1016/j.brainres.2008.06.081

    Article  CAS  PubMed  Google Scholar 

  30. Wu L, Feng XT, Hu YQ, Tang N, Zhao QS, Li TW, Li HY, Wang QB, Bi XY, Cai XK (2015) Global gene expression profile of the hippocampus in a rat model of vascular dementia. Tohoku J Exp Med 237:57–67. doi:10.1620/tjem.237.57

    Article  CAS  PubMed  Google Scholar 

  31. Treves A, Tashiro A, Witter MP, Moser EI (2008) What is the mammalian dentate gyrus good for? Neuroscience 154:1155–1172. doi:10.1016/j.neuroscience.2008.04.073

    Article  CAS  PubMed  Google Scholar 

  32. Lee KY, Jeong EJ, Huh J, Cho N, Kim TB, Jeon BJ, Kim SH, Kim HP, Sung SH (2012) Cognition-enhancing and neuroprotective activities of the standardized extract of Betula platyphylla bark and its major diarylheptanoids. Phytomedicine 19:1315–1320. doi:10.1016/j.phymed.2012.09.012

    Article  CAS  PubMed  Google Scholar 

  33. Debette S (2013) Vascular risk factors and cognitive disorders. Rev Neurol (Paris) 169:757–764. doi:10.1016/j.neurol.2013.07.022

    Article  CAS  Google Scholar 

  34. Mou L, Heldt SA, Ressler KJ (2011) Rapid brain-derived neurotrophic factor-dependent sequestration of amygdala and hippocampal GABA(A) receptors via different tyrosine receptor kinase B-mediated phosphorylation pathways. Neuroscience 176:72–85. doi:10.1016/j.neuroscience.2010.12.041

    Article  CAS  PubMed  Google Scholar 

  35. Aleisa AM, Alzoubi KH, Gerges NZ, Alkadhi KA (2006) Chronic psychosocial stress-induced impairment of hippocampal LTP: possible role of BDNF. Neurobiol Dis 22:453–462. doi:10.1016/j.nbd.2005.12.005

    Article  CAS  PubMed  Google Scholar 

  36. Kim J, Kwon JT, Kim HS, Josselyn SA, Han JH (2014) Memory recall and modifications by activating neurons with elevated CREB. Nat Neurosci 17:65–72. doi:10.1038/nn.3592

    Article  CAS  PubMed  Google Scholar 

  37. Kim DH, Kim JM, Park SJ, Cai M, Liu X, Lee S, Shin CY, Ryu JH (2012) GABA(A) receptor blockade enhances memory consolidation by increasing hippocampal BDNF levels. Neuropsychopharmacology 37:422–433. doi:10.1038/npp.2011.189

    Article  CAS  PubMed  Google Scholar 

  38. Kim HJ, Kim W, Kong SY (2013) Antidepressants for neuro-regeneration: from depression to Alzheimer’s disease. Arch Pharm Res 36:1279–1290. doi:10.1007/s12272-013-0238-8

    Article  CAS  PubMed  Google Scholar 

  39. Nagahara AH, Merrill DA, Coppola G, Tsukada S, Schroeder BE, Shaked GM, Wang L, Blesch A, Kim A, Conner JM, Rockenstein E, Chao MV, Koo EH, Geschwind D, Masliah E, Chiba AA, Tuszynski MH (2009) Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer’s disease. Nat Med 15:331–337. doi:10.1038/nm.1912

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Tao X, Finkbeiner S, Arnold DB, Shaywitz AJ, Greenberg ME (1998) Ca2+ influx regulates BDNF transcription by a CREB family transcription factor-dependent mechanism. Neuron 20:709–726

    Article  CAS  PubMed  Google Scholar 

  41. Lonze BE, Ginty DD (2002) Function and regulation of CREB family transcription factors in the nervous system. Neuron 35:605–623

    Article  CAS  PubMed  Google Scholar 

  42. Sakamoto K, Karelina K, Obrietan K (2011) CREB: a multifaceted regulator of neuronal plasticity and protection. J Neurochem 116:1–9. doi:10.1111/j.1471-4159.2010.07080.x

    Article  CAS  PubMed  Google Scholar 

  43. Shakil H, Saleem S (2013) Genetic deletion of prostacyclin IP receptor exacerbates transient global cerebral ischemia in aging mice. Brain Sci 3:1095–108

    Article  PubMed  PubMed Central  Google Scholar 

  44. Wang J, Ming H, Chen R, Ju JM, Peng WD, Zhang GX, Liu CF (2015) CIH-induced neurocognitive impairments are associated with hippocampal Ca(2+) overload, apoptosis, and dephosphorylation of ERK1/2 and CREB that are mediated by overactivation of NMDARs. Brain Res 1625:64–72. doi:10.1016/j.brainres.2015.08.012

    Article  CAS  PubMed  Google Scholar 

  45. Alonso M, Medina JH, Pozzo-Miller L (2004) ERK1/2 activation is necessary for BDNF to increase dendritic spine density in hippocampal CA1 pyramidal neurons. Learn Mem 11:172–178. doi:10.1101/lm.67804

    Article  PubMed  PubMed Central  Google Scholar 

  46. Choi YS, Cho HY, Hoyt KR, Naegele JR, Obrietan K (2008) IGF-1 receptor-mediated ERK/MAPK signaling couples status epilepticus to progenitor cell proliferation in the subgranular layer of the dentate gyrus. Glia 56:791–800. doi:10.1002/glia.20653

    Article  PubMed  PubMed Central  Google Scholar 

  47. Iida N, Namikawa K, Kiyama H, Ueno H, Nakamura S, Hattori S (2001) Requirement of Ras for the activation of mitogen-activated protein kinase by calcium influx, cAMP, and neurotrophin in hippocampal neurons. J Neurosci 21:6459–6466

    CAS  PubMed  Google Scholar 

  48. Ying SW, Futter M, Rosenblum K, Webber MJ, Hunt SP, Bliss TV, Bramham CR (2002) Brain-derived neurotrophic factor induces long-term potentiation in intact adult hippocampus: requirement for ERK activation coupled to CREB and upregulation of Arc synthesis. J Neurosci 22:1532–1540

    CAS  PubMed  Google Scholar 

  49. Jeon SJ, Rhee SY, Seo JE, Bak HR, Lee SH, Ryu JH, Cheong JH, Shin CY, Kim GH, Lee YS, Ko KH (2011) Oroxylin A increases BDNF production by activation of MAPK-CREB pathway in rat primary cortical neuronal culture. Neurosci Res 69:214–222. doi:10.1016/j.neures.2010.11.008

    Article  CAS  PubMed  Google Scholar 

  50. Bath KG, Akins MR, Lee FS (2012) BDNF control of adult SVZ neurogenesis. Dev Psychobiol 54:578–589. doi:10.1002/dev.20546

    Article  CAS  PubMed  Google Scholar 

  51. Arany I, Megyesi JK, Reusch JE, Safirstein RL (2005) CREB mediates ERK-induced survival of mouse renal tubular cells after oxidant stress. Kidney Int 68:1573–1582. doi:10.1111/j.1523-1755.2005.00569.x

    Article  PubMed  Google Scholar 

  52. Schulte JH, Schramm A, Klein-Hitpass L, Klenk M, Wessels H, Hauffa BP, Eils J, Eils R, Brodeur GM, Schweigerer L, Havers W, Eggert A (2005) Microarray analysis reveals differential gene expression patterns and regulation of single target genes contributing to the opposing phenotype of TrkA- and TrkB-expressing neuroblastomas. Oncogene 24:165–177. doi:10.1038/sj.onc.1208000

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

This work was supported by Natural Science Foundation of Hebei Province, China (C2014206363) and Hebei Province Students innovative and entrepreneurial project (201510089016).

Author Contributions

Designed experiment and wrote manuscript: YL. Performed experiment: JW, ZL, XW. Analyzed data: HuijuanMa. Wrote manuscript: SZ. Reviewed and approved the final version of the manuscript: SW, YZ.

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Correspondence to Yixian Liu.

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Wang, J., Zhang, S., Ma, H. et al. Chronic Intermittent Hypobaric Hypoxia Pretreatment Ameliorates Ischemia-Induced Cognitive Dysfunction Through Activation of ERK1/2-CREB-BDNF Pathway in Anesthetized Mice. Neurochem Res 42, 501–512 (2017). https://doi.org/10.1007/s11064-016-2097-4

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