References
- Kar S, Slowikowski SP, Westaway D, Mount HT. Interactions between beta-amyloid and central cholinergic neurons: implications for Alzheimer's disease. J Psychiatry Neurosci 2004;29:427-41.
- Ibach B, Haen E. Acetylcholinesterase inhibition in Alzheimer's Disease. Curr Pharm Des 2004;10:231-51. https://doi.org/10.2174/1381612043386509
- Golde TE. Disease modifying therapy for AD? J Neurochem 2006;99:689-707. https://doi.org/10.1111/j.1471-4159.2006.04211.x
- Perini G, Della-Bianca V, Politi V, Della Valle G, Dal-Pra I, Rossi F, Armato U. Role of p75 neurotrophin receptor in the neurotoxicity by beta-amyloid peptides and synergistic effect of inflammatory cytokines. J Exp Med 2002;195:907-18. https://doi.org/10.1084/jem.20011797
- Giovannini MG, Scali C, Prosperi C, Bellucci A, Vannucchi MG, Rosi S, Pepeu G, Casamenti F. Beta-amyloid-induced inflammation and cholinergic hypofunction in the rat brain in vivo: involvement of the p38MAPK pathway. Neurobiol Dis 2002;11:257-74. https://doi.org/10.1006/nbdi.2002.0538
- Toro VC, Tehranian R, Zetterstrom M, Eriksson G, Langel U, Bartfai T, Iverfeld K. Increased gene expression of interleukin-1alpha and interleukin-6 in rat primary glial cells induced by beta-amyloid fragment. J Mol Neurosci 2001;17:341-50.
- Mrak RE, Griffin WS. Interleukin-1, neuroinflammation, and Alzheimer's disease. Neurobiol Aging 2001;22:903-8. https://doi.org/10.1016/S0197-4580(01)00287-1
- Rubio-Perez JM, Morillas-Ruiz JM. A review: inflammatory process in Alzheimer's disease, role of cytokines. Scientific World Journal 2012;2012:756357.
- de Craen AJ, Gussekloo J, Vrijsen B, Westendorp RG. Meta-analysis of nonsteroidal antiinflammatory drug use and risk of dementia. Am J Epidemiol 2005;161:114-20. https://doi.org/10.1093/aje/kwi029
- Vlad SC, Miller DR, Kowall NW, Felson DT. Protective effects of NSAIDs on the development of Alzheimer disease. Neurology 2008;70:1672-7. https://doi.org/10.1212/01.wnl.0000311269.57716.63
- McGeer PL, McGeer EG. NSAIDs and Alzheimer disease: epidemiological, animal model and clinical studies. Neurobiol Aging 2007;28:639-47. https://doi.org/10.1016/j.neurobiolaging.2006.03.013
- Moon M, Kim HG, Choi JG, Oh H, Lee PK, Ha SK, Kim SY, Park Y, Huh Y, Oh MS. 6-Shogaol, an active constituent of ginger, attenuates neuroinflammation and cognitive deficits in animal models of dementia. Biochem Biophys Res Commun 2014;449:8-13. https://doi.org/10.1016/j.bbrc.2014.04.121
- Lee B, Jung K, Kim DH. Timosaponin AIII, a saponin isolated from Anemarrhena asphodeloides, ameliorates learning and memory deficits in mice. Pharmacol Biochem Behav 2009;93:121-7. https://doi.org/10.1016/j.pbb.2009.04.021
- Kim J, Kim SH, Lee DS, Lee DJ, Kim SH, Chung S, Yang HO. Effects of fermented ginseng on memory impairment and b-amyloid reduction in Alzheimer's disease experimental models. J Ginseng Res 2013;37:100-7. https://doi.org/10.5142/jgr.2013.37.100
- Cho IH. Effects of Panax ginseng in neurodegenerative diseases. J Ginseng Res 2012;36:342-53. https://doi.org/10.5142/jgr.2012.36.4.342
- Zhao Z, Kim YW, Wu Y, Zhang J, Lee JH, Li X, Cho IJ, Park SM, Jung DH, Yang CH, et al. Korean Red Ginseng attenuates anxiety-like behavior during ethanol withdrawal in rats. J Ginseng Res 2014;15:256-63.
- Wan DB, Jiao LL, Yang HM, Liu SY. Structural characterization and immunological activities of the water-soluble oligosaccharides isolated from the Panax ginseng roots. Planta 2012;235:1289-97. https://doi.org/10.1007/s00425-011-1574-x
- Jiao L, Wan D, Zhang X, Li B, Zhao H, Liu S. Characterization and immunostimulating effects on murine peritoneal macrophages of oligosaccharide isolated from Panax ginseng C.A. Meyer. J Ethnopharmacol 2012;144:490-6. https://doi.org/10.1016/j.jep.2012.09.004
- Jiao L, Zhang X, Li B, Liu Z, Wang M, Liu S. Anti-tumour and immunomodulatory activities of oligosaccharides isolated from Panax ginseng C.A. Meyer. Int J Biol Macromol 2014;65:229-33. https://doi.org/10.1016/j.ijbiomac.2014.01.039
- Wang Y, Jiang RZ, Li GR, Chen YH, Luo HM, Gao Y, Gao QP. Structural and enhanced memory activity studies of extracts from Panax ginseng root. Food Chem 2010;119:969-73. https://doi.org/10.1016/j.foodchem.2009.07.061
- Han RW, Zhang RS, Chang M, Peng YL, Wang P, Hu SQ, Choi CL, Yin M, Wang R, Han YF. Reversal of scopolamine-induced spatial and recognition memory deficits in mice by novel multifunctional dimers bis-cognitins. Brain Res 2012;1470:59-68. https://doi.org/10.1016/j.brainres.2012.06.015
- Paxinos G, Franklin KBJ. The mouse brain in stereotaxic coordinates. Waltham, MA: Academic Press; 2001.
- Zhang CX, Zhang H, Xu HY, Li MX, Wang S. The lateral habenula is a common target of cocaine and dexamethasone. Neurosci Lett 2013;555:12-7. https://doi.org/10.1016/j.neulet.2013.09.019
- Fan Y, Hu J, Li J, Yang Z, Xin X, Wang J, Ding J, Geng M. Effect of acidic oligosaccharide sugar chain on scopolamine-induced memory impairment in rats and its related mechanisms. Neurosci Lett 2005;374:222-6. https://doi.org/10.1016/j.neulet.2004.10.063
- Rose M, Dudas B, Cornelli U, Hanin I. Protective effect of the heparin-derived oligosaccharide C3, on AF64A-induced cholinergic lesion in rats. Neurobiol Aging 2003;24:481-90. https://doi.org/10.1016/S0197-4580(02)00093-3
- Yao J, Ho D, Calingasan NY, Pipalia NH, Lin MT, Beal MF. Neuroprotection by cyclodextrin in cell and mouse models of Alzheimer disease. J Exp Med 2012;209:2501-13. https://doi.org/10.1084/jem.20121239
- Vukic V, Callaghan D, Walker D, Lue LF, Liu QY, Couraud PO, Romero IA, Weksler B, Stanimirovic DB, Zhang W. Expression of inflammatory genes induced by beta-amyloid peptides in human brain endothelial cells and in Alzheimer's brain is mediated by the JNK-AP1 signaling pathway. Neurobiol Dis 2009;34:95-106. https://doi.org/10.1016/j.nbd.2008.12.007
- Schwab C, McGeer PL. Inflammatory aspects of Alzheimer disease and other neurodegenerative disorders. J Alzheimer's Dis 2008;13:359-69. https://doi.org/10.3233/JAD-2008-13402
- Millington C, Sonego S, Karunaweera N, Rangel A, Aldrich-Wright JR, Campbell IL, Gyengesi E, Munch G. Chronic neuroinflammation in Alzheimer's disease: new perspectives on animal models and promising candidate drugs. Biomed Res Int 2014;2014:309129.
- Lee B, Shim I, Lee H, Hahm DH. Rehmannia glutinosa ameliorates scopolamine-induced learning and memory impairment in rats. J Microbiol Biotechnol 2011;21:874-83. https://doi.org/10.4014/jmb.1104.04012
- Ma Q, Dudas B, Daud A, Iqbal O, Hoppensteadt D, Jeske W, Cornelli U, Lee J, Lorens S, Mervis R, et al. Molecular and biochemical profiling of a heparin-derived oligosaccharide, C3. Thromb Res 2002;105:303-9. https://doi.org/10.1016/S0049-3848(01)00413-3
- Guo X, Xin X, Gan L, Nie Q, Geng M. Determination of the accessibility of acidic oligosaccharide sugar chain to blood-brain barrier using surface plasmon resonance. Biol Pharm Bull 2006;29:60-3. https://doi.org/10.1248/bpb.29.60
- Guo X, Geng M, Du G. Glucose transporter 1, distribution in the brain and in neural disorders: its relationship with transport of neuroactive drugs through the blood-brain barrier. Biochem Genet 2005;43:175-87. https://doi.org/10.1007/s10528-005-1510-5
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