References
- Annunziato, L., Amoroso, S., Pannaccione, A., Cataldi, M., Pignataro, G., D'Alessio, A., Sirabella, R., Secondo, A., Sibaud, L. and Di Renzo, G. F. (2003). Apoptosis induced in neuronal cells by oxidative stress: role played by caspases and intracellular calcium ions. Toxicol. Lett. 139, 125-133 https://doi.org/10.1016/S0378-4274(02)00427-7
- Balazs, L. and Leon, M. (1994). Evidence of an oxidative challenge in the Alzheimer's brain. Neurochem. Res. 19, 1131-1137 https://doi.org/10.1007/BF00965146
- Barnes, C. A., Danysz, W. and Parsons, C. G. (1996). Effects of the uncompetitive NMDA receptor antagonist memantine on hippocampal long-term potentiation, short-term exploratory modulation and spatial memory in awake, freely moving rats. Eur. J. Neurosci. 8, 565-571 https://doi.org/10.1111/j.1460-9568.1996.tb01241.x
- Bassett, C. N. and Montine, T. J. (2003). Lipoproteins and lipid peroxidation in Alzheimer's disease. J. Nutr. Health Aging 7, 446-451
- Bejar, C., Wang, R. H. and Weinstock, M. (1999). Effect of rivastigmine on scopolamine-induced memory impairment in rats. Eur. J. Pharmacol 3, 231-240 https://doi.org/10.1016/S0014-2999(99)00643-3
- Blokland, A., Geraerts, E. and Been, M. (2004). A detailed analysis of rats' spatial memory in a probe trial of a Morris task. Behav. Brain Res. 154, 71-75 https://doi.org/10.1016/j.bbr.2004.01.022
- Cruz, R., Almaguer Melian, W. and Bergado Rosado, J. A. (2003). Glutathione in cognitive function and neurodegeneration. Rev. Neurol. 36, 877-886
- Cruz-Aguado, R., Fernandez-Verdecia, C. I., Diaz-Suarez, C. M., Gonzalez-Monzon, O., Antunez-Potashkina, I. and Bergado-Rosado, J. (1998). Effects of nerve growth factor on brain glutathione-related enzymes from aged rats. Fundam. Clin. Pharmacol. 12, 538-545 https://doi.org/10.1111/j.1472-8206.1998.tb00983.x
- Dhingra, D., Parle, M. and Kalkarni, S. K. (2004). Memory enhancing activity of Glycyrrhiza glabra in mice. J. Ethnopharmacol. 91, 361-365 https://doi.org/10.1016/j.jep.2004.01.016
- Ellman, G. L., Courtney, K. D., Andres, V. Jr. and Feather-Stone, R. M. (1961). A new and rapid colormetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 7, 88-95 https://doi.org/10.1016/0006-2952(61)90145-9
- El-Sherbiny, D. A., Khalifa, A. E., Attia, A. S. and Eldenshary, Eel-D. (2003). Hypericum perforatum extract demonstrates antioxidant properties against elevated rat brain oxidative status induced by amnesic dose of scopolamine. Pharmacol. Biochem. Behav. 76, 525-533 https://doi.org/10.1016/j.pbb.2003.09.014
- Fan, Y., Hu, J., Li, J., Yang, Z., Xin, X., Wang, J., Ding, J. and Geng, M. (2005). Effect of acidic oligosaccharide sugar chain on scopolamine-induced memory impairment in rats and its related mechanisms. Neurosci. Lett. 374, 222-226 https://doi.org/10.1016/j.neulet.2004.10.063
- Hayashi, K., Nagamatsu, T., Ito, M. and Hattori, T. (1994). Acteoside, a component of Stachys sieboldii MIQ, may be a promising antinephritic agent (2): Effect of acteoside on leukocyte accumulation in the glomeruli of nephritic rats. Jpn. J. Pharmacol. 66, 47-52 https://doi.org/10.1254/jjp.66.47
- He, Z. D., Lau, K. M., Xu, H. X., Li, P. C. and Pui-Hay But, P. (2000). Antioxidant activity of phenylethanoid glycosides from Brandisia hancei. J. Ethnopharmacol. 71, 483-486 https://doi.org/10.1016/S0378-8741(00)00189-6
- Ilic, T. V., Jovanovic, M., Jovicic, A. and Tomovic, M. (1999). Oxidative stress indicators are elevated in de novo Parkinson's disease patients. Funct. Neurol. 14, 141-147
- Jung, K., Lee, B., Han, S. J., Ryu, J. H. and Kim, D. H. (2009). Mangiferin ameliorates scopolamine-induced learning deficits in mice. Biol. Pharm. Bull. 32, 242-246 https://doi.org/10.1248/bpb.32.242
- Kim, D. H., Hung, T. M., Bae, K. H., Jung, J. W., Lee, S., Yoon, B. H., Cheong, J. H., Ko, K. H. and Ryu, J. H. (2006). Gomisin A improves scopolamine-induced memory impairment in mice. Eur. J. Pharmacol. 542, 129-135 https://doi.org/10.1016/j.ejphar.2006.06.015
- Kristensen, M. (1990). Neurotransmitters in Alzheimer's disease. Ugeskr. Laeg. 152, 2165-2168
- Lee, K. Y., Jeong, E. J., Lee, H. S. and Kim, Y. C. (2006). Acteoside of Callicarpa dichotoma attenuate scopolamine-induced memory impairments. Biol. Pharm. Bull. 29, 71-74. https://doi.org/10.1248/bpb.29.71
- Marcus, D. L., Thomas, C., Rodriguez, C., Simberkoff, K., Tsai, J. S., Strafaci, J. A. and Freedman, M. L. (1998). Increased peroxidation and reduced antioxidant enzyme activity in Alzheimer's disease. Exp. Neurol. 150, 40-44 https://doi.org/10.1006/exnr.1997.6750
- Misane, I. and Ogren, S. O. (2003). Selective 5-HT1A antagonists WAY 100635 and NAD-299 attenuate the impairment of passive avoidance caused by scopolamine in the rat. Neuropsychopharmacology. 28, 253-264 https://doi.org/10.1038/sj.npp.1300024
- Morris, R. G. (1984). Development of a water maze procedure for studying spatial learning in the rat. J. Neurosci. Methods. 11, 47-60 https://doi.org/10.1016/0165-0270(84)90007-4
- Nishibe, S., Okabe, K., Tsukamoto, H., Sakushima, A. and Hisada, S. (1982). The Structure of Forsythiaside isolated from Forsythia suspense. Chem. Pharm. Bull. 30, 1048-1050
- Palmer, A. M. (1999). The activity of the pentose phosphate pathway is increased in response to oxidative stress in Alzheimer's disease. J. Neural Transm. 106, 317-328 https://doi.org/10.1007/s007020050161
- Perry, E., Walker, M., Grace, J. and Perry, R. (1999). Acetylcholine in mind: a neurotransmitter correlate of consciousness? Trends Neurosci. 22, 273-280 https://doi.org/10.1016/S0166-2236(98)01361-7
- Qu, H., Zhang, Y., Wang, Y., Li, B. and Sun, W. (2008). Antioxidant and antibacterial activity of two compounds (forsythiaside and forsythin) isolated from Forsythia suspensa. J. Pharm. Pharmacol. 60, 261-266 https://doi.org/10.1211/jpp.60.2.0016
- Sahpaz, S., Garbacki, N., Tits, M. and Bailleul, F. (2002). Isolation and pharmacological activity of phenylpropanoid esters from Marrubium vulgare. J. Ethnopharmacol. 79, 389-392 https://doi.org/10.1016/S0378-8741(01)00415-9
- Singh, A., Naidu, P. S. and Kulkarni, S. K. (2003). Reversal of aging and chronic ethanol-induced cognitive dysfunction by quercetin a bioflavonoid. Free Radic. Res. 37, 1245-1252 https://doi.org/10.1080/10715760310001616014
- Vitor, R. F., Mota-Filipe, H., Teixeira, G., Broges, C., Rodrigues, A. I., Teixeira, A. and Paulo, A. (2004). Flavonoids of an extract of Pterospartum tridentatum showing endothelial protection against oxidative injury. J. Ethnopharmacol 93, 363-370 https://doi.org/10.1016/j.jep.2004.04.003
- Weinstock, M. and Shoham, S. (2004). Rat models of dementia based on reductions in regional glucose metabolism, cerebral blood flow and cytochrome oxidase activity. J. Neural Transm. 111, 347-366 https://doi.org/10.1007/s00702-003-0058-y
- Xiong, Q., Hase, K., Tezuka, Y., Tani, T., Namba, T. and Kadota, S. (1998). Hepatoprotective activity of phenylethanoids from Cistanche deserticola. Planta Med. 64, 120-125 https://doi.org/10.1055/s-2006-957387
- Zhu, Y. P. (1998). Chinese Materia Medica Chemistry, Pharmacology and Applications. pp. 176-180. Harwood Academic Publishers, The Netherlands
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