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Protective Effect of Arabinoxylan against Scopolamine-Induced Learning and Memory Impairment

  • Kim, Chang-Yul (Department of Pathology, College of Oriental Medicine, Daegu Haany University) ;
  • Lee, Gil-Yong (Department of Pathology, College of Oriental Medicine, Daegu Haany University) ;
  • Park, Gyu Hwan (Research Institute of Pharmaceutical Sciences, College of Pharmacy, Kyungpook National University) ;
  • Lee, Jongwon (Deparment of Biochemistry, School of Medicine, Catholic University of Daegu) ;
  • Jang, Jung-Hee (Department of Pharmacology, School of Medicine, Keimyung University)
  • Received : 2014.05.29
  • Accepted : 2014.07.08
  • Published : 2014.09.30

Abstract

The purpose of this study is to investigate the memory enhancing effect and underlying molecular mechanism of arabinoxylan (AX), a major component of dietary fiber in wheat against scopolamine (SCO)-induced amnesia in Sprague-Dawley (SD) rats. Diverse behavior tests including Y-maze, Morris water maze, and passive avoidance tests were performed to measure cognitive functions. SCO significantly decreased the spontaneous alterations in Y-maze test and step-through latency in passive avoidance test, whereas increased time spent to find the hidden platform in Morris water maze test compared with the sham control group. In contrast, oral administration of AX (25 mg/kg and 50 mg/kg) effectively reversed the SCO-induced cognitive impairments in SD rats. Furthermore, AX treatment up-regulated the expression of brain-derived neurotrophic factor (BDNF) in the cortex and hippocampus via promoting activation of cAMP response element binding protein (CREB). Therefore, our findings suggest that AX can improve SCO-induced learning and memory impairment possibly through activation of CREB and up-regulation of BDNF levels, thereby exhibiting a cognition-enhancing potential.

Keywords

References

  1. Asanuma, M., Nishibayashi, S., Iwata, E., Kondo, Y., Nakanishi, T., Vargas, M. G. and Ogawa, N. (1996) Alterations of cAMP response element-binding activity in the aged rat brain in response to administration of rolipram, a cAMP-specific phosphodiesterase inhibitor. Brain Res. Mol. Brain Res. 41, 210-215. https://doi.org/10.1016/0169-328X(96)00098-8
  2. Bitner, R. C. (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. https://doi.org/10.1016/j.bcp.2011.11.009
  3. Brenner, T., Nizri, E., Irony-Tur-Sinai, M., Hamra-Amitay, Y. and Wirguin, I. (2008) Acetylcholinesterase inhibitors and cholinergic modulation in myasthenia gravis and neuroinflammation. J. Neuroimmunol. 201-202, 121-127. https://doi.org/10.1016/j.jneuroim.2008.05.022
  4. Broekaert, W. F., Courtin, C. M., Verbeke, K., Wiele, T. V. D., Verstraete, W. and Delcour, J. A. (2011) Prebiotic and other health-related effects of cereal-derived arabinoxylans, arabinoxylan-oligosaccharides, and xylooligosaccharides. Crit. Rev. Food Sci. Nutr. 51, 178-194. https://doi.org/10.1080/10408390903044768
  5. Craig, L. A., Hong, N. S. and McDonald, R. J. (2011) Revisiting the cholinergic hypothesis in the development of Alzheimer's disease. Neurosci. Biobehav. Rev. 35, 1397-1409. https://doi.org/10.1016/j.neubiorev.2011.03.001
  6. Cunha, C., Brambilla, R. and Thomas, K. L. (2010) A simple role for BDNF in learning and memory? Front. Mol. Neurosci. 3, 1.
  7. Dienel, G. A., Liu, K. and Cruz, N. F. (2001) Local uptake of 14C-labeled acetate and butyrate in rat brain in vivo during spreading cortical depression. J. Neurosci. Res. 66, 812-820. https://doi.org/10.1002/jnr.10063
  8. Eidelberg, E., Fishman, J. and Hams, M. L. (1967) Penetration of sugars across the blood-brain barrier. J. Physiol. 191, 47-57. https://doi.org/10.1113/jphysiol.1967.sp008236
  9. Gebruers, K., Dornez, E., Boros, D., Fraś, A., Dynkowska, W., Bedo, Z., Rakszegi, M., Delcour, J. A. and Courtin, C. M. (2008) Variation in the content of dietary fiber and components thereof in wheats in the HEALTHGRAIN diversity screen. J. Agric. Food Chem. 56, 9740-9749. https://doi.org/10.1021/jf800975w
  10. Han, H. S., Jang, J. H., Jang, J. H., Choi, J. S., Kim, Y. J., Lee, C., Lim, S. H., Lee, H. K. and Lee, J. (2010) Water extract of Triticum aestivum L. and its components demonstrate protective effect in a model of vascular dementia. J. Med. Food 13, 572-578. https://doi.org/10.1089/jmf.2009.1242
  11. Hu, H., Zhang, R., Zhang, Y., Xia, Z. and Hu, Y. (2010) Role of CREB in the regulatory action of sarsasapogenin on muscarinic M1 receptor density during cell aging. FEBS Lett. 584, 1549-1552. https://doi.org/10.1016/j.febslet.2010.03.006
  12. Jang, J. H., Kim, C. Y., Lim, S. H., Yang, C. H., Song, K. S., Han, H. S., Lee, H. K. and Lee, J. (2010) Neuroprotective effects of Triticum aestivum L. against beta-amyloid cell death and memory impairments. Phytother. Res. 24, 76-84. https://doi.org/10.1002/ptr.2871
  13. Jin, C. H., Shin, E. J., Park, J. B., Jang, C. G., Li, Z., Kim, M. S., Koo, K. H., Yoon, H. J., Park, S. J., Choi, W. C., Yamada, K., Nabeshima, T. and Kim, H. C. (2009) Fustin flavonoid attenuates ${\beta}$-amyloid (1-42)-induced learning impairment. J. Neurosci. Res. 87, 3658-3670. https://doi.org/10.1002/jnr.22159
  14. Joh, E. H., Lee, I. A. and Kim, D. H. (2011) Kalopanaxsaponins A and B isolated from Kalopanax pictus ameliorate memory deficits in mice. Phytother. Res. 26, 546-551.
  15. Karran, E., Mercken, M. and De Strooper, B. (2011) The amyloid cascade hypothesis for Alzheimer's disease: an appraisal for the development of therapeutics. Nat. Rev. Drug Discov. 10, 698-712. https://doi.org/10.1038/nrd3505
  16. Kim, H. J., Leeds, P. and Chuang, D. M. (2009) The HDAC inhibitor, sodium butyrate, stimulates neurogenesis in the ischemic brain. J. Neurochem. 110, 1226-1240. https://doi.org/10.1111/j.1471-4159.2009.06212.x
  17. Lee, C., Park, G. H., Kim, C. Y. and Jang, J. H. (2011a) [6]-Gingerol attenuates ${\beta}$-amyloid-induced oxidative cell death via fortifying cellular antioxidant defense system. Food Chem. Toxicol. 49, 1261-1269. https://doi.org/10.1016/j.fct.2011.03.005
  18. Lee, C., Park, G. H. and Jang, J. H. (2011b) Cellular antioxidant adaptive survival response to 6-hydroxydopamine-induced nitrosative cell death in C6 glioma cells. Toxicology 283, 118-128. https://doi.org/10.1016/j.tox.2011.03.004
  19. Ward, J. L., Poutanen, K., Gebruers, K., Piironen, V., Lampi, A. M., Nystrom, L., Andersson, A. A., Aman, P., Boros, D., Rakszegi, M., Bedo, Z. and Shewry, P. R. (2008) The HEALTHGRAIN cereal diversity screen: concept, results, and prospects. J. Agric. Food Chem. 56, 9699-9709. https://doi.org/10.1021/jf8009574
  20. Wang, A., Si, H., Liu, D. and Jiang, H. (2012) Butyrate activates the cAMP-protein kinase A-cAMP response element-binding protein signaling pathway in Caco-2 cells. J. Nutr. 142, 1-6. https://doi.org/10.3945/jn.111.148155
  21. Xue, W., Hu, J. F., Yuan, Y. H., Sun, J. D., Li, B. Y., Zhang, D. M., Li, C. J. and Chen, N. H. (2009) Polygalasaponin XXXII from Polygala tenuifolia root improves hippocampal-dependent learning and memory. Acta Pharmacol. Sin. 30, 1211-1219. https://doi.org/10.1038/aps.2009.112
  22. Zhang, P., Zhang, Q. and Whistler, R. L. (2003) L-Arabinose release from arabinoxylan and arabinogalactan under potential gastric aciditities. Cereal Chem. 80, 252-254. https://doi.org/10.1094/CCHEM.2003.80.3.252
  23. Zhang, X., Odom, D. T., Koo, S. H., Conkright, M. D., Canettieri, G., Best, J., Chen, H., Jenner, R., Herbolsheimer, E., Jacobsen, E., Kadam, S., Ecker, J. R., Emerson, B., Hogenesch, J. B., Unterman, T., Young, R. A. and Montminy, M. (2005) Genome-wide analysis of cAMP-response element binding protein occupancy, phosphorylation, and target gene activation in human tissues. Proc. Natl. Acad. Sci. U.S.A. 102, 4459-4464. https://doi.org/10.1073/pnas.0501076102

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