Zeatin supplement improves scopolamine-induced memory impairment in mice

Bioscience, Biotechnology and Biochemistry

Volumn 72, Issue 2, 2008, Pages 577-581

  Kim, Mi Jeong ^a,d   Choi, Soo Jung ^b   Lim, Seung Taik ^b   Kim, Hye Kyung ^c   Kim, Young Jun ^b   Yoon, Ho Geun ^d   Shin, Dong Hoon ^b  

^a Yonsei University   (South Korea)

^b Korea University   (South Korea)

^c Hanseo University   (South Korea)

^d Yonsei University College of Medicine   (South Korea)

Author keywords

Acetylcholinesterase; Alzheimer's disease; Cognitive function; Scopolamine; Zeatin 6 (4 hydroxy 3 methyl trans 2 butenylamino) purine

Indexed keywords

BIOACTIVITY; DISEASES; ENZYMES; LIVING SYSTEMS STUDIES; PLANTS (BOTANY);

ALZHEIMER'S DISEASE; COGNITIVE FUNCTIONS; SCOPOLAMINE;

HORMONES;

CHOLINERGIC RECEPTOR BLOCKING AGENT; SCOPOLAMINE; ZEATIN;

ANIMAL; ARTICLE; MEMORY DISORDER; MOUSE;

ANIMALS; CHOLINERGIC ANTAGONISTS; MEMORY DISORDERS; MICE; SCOPOLAMINE; ZEATIN;

MUS;

EID: 40449140007     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.70480     Document Type: Article

References (21)

1. Roger, M. L., Miia, K., and Nigel, H. G., Acetylcholinesterase and its inhibition in Alzheimer's disease. Clin. Neuropharmacol., 27, 141-149 (2004).
2. Heo, H. J., Hong, S. C., Cho, H. Y., Bumshik, H., Kim, H. K., Kim, E. K., and Shin, D. H., Inhibitory effect of Zeatin, isolated from Fiatoua villosa, on acetylcholinesterase activity from PC12 cells. Mol. Cells, 13, 113-117 (2001).
3. Jaime, N., Jimmy, A. H., Yaned, M. C., and Oscar, M. M., In vitro inhibition of acetylcholinesterase by crude plant extracts from Colombian flora. Mem. Inst. Oswaldo Cruz., Rio de Janeiro, 101, 783-785 (2006).
4. Heo, H. J., Kim, M. J., Lee, J. M., Choi, S. J., Cho, H. Y., Bumshik, H., Kim, H. K., Eunki, K., and Shin, D. H., Naringenin from Citrus junos has an inhibitory effect on acetylcholinesterase and a mitigating effect on amnesia. Dement. Geriatr. Cogn. Disord., 17, 151-157 (2004).
5. Pulok, K. M., Venkatesan, K., Mainmak, M., and Peter, J. H., Acetylcholinesterase inhibitors form plants. Phytomedicine, 14, 289-300 (2007).
6. Mani, V., and Milind, P., Pharmacological evidence for the potential of Daucus carota in the management of Cognitive dyfunctions. Biol. Pharm. Bull., 29, 1154-1161 (2006).
7. Shen, Z., Wang, G., and Lin, S. Z., Two-way shuttle box avoidance conditioning and brain NADH in rats. Physiol. Behav., 48, 515-517 (1990).
8. Yamaguchi, Y., and Kawashima, S., Effects of amyloid-β-(25-35) on passive avoidance, radial-arm maze learning and choline acetyltransferase activity in the rat. Eur. J. Pharmacol., 421, 256-272 (2001).
9. Heo, H. J., Kim, M. J., Suh, Y. M., Choi, S. J., Mun, N. S., Kim, H. K., Kim, E. K., and Shin, D. H., Protective effects of daidzein on oxidative stress-induced neurotoxicity and scopolaine-mediated cognitive defect. J. Food Sci., 70, S91-S94 (2005).
10. Ellman, G. L., Courtney, K. D., Andres, V., Jr., and featherstone, R. M., A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol., 7, 88-95 (1961).
11. Kim, J. H., Ha, H. C., Lee, M. S., Kang, J. I., Kim, H. S., Lee, S. Y., Pyun, K. H., and Insop, S., Effect of Tremella fucoformis on the neurite outgrowth of PC 12 cells and the improvement of memory in rats. Biol. Pharm. Bull., 30, 708-714 (2007).
12. Bartus, R. T., Dean, R. L., Pontecorvo, M. J., and Flicker, C., The cholinergic hypothesis: a histological overview, current perspective, and future directions. Ann. NY Acad. Sci., 444, 332-358 (1985).
13. Giacobin, E., Cholinergic foundations of Alzheimer's disease therapy. J. Physiol. (Paris), 92, 283-287 (1998).
14. Hagan, J. J., Salamon, J. D., Simpsin, S., Iversen, S. D., and Morris, R. G. M., Place navigation in rats is impaired by lesion of medial septum and diagonal band but not nucleus basalis magnocellularis. Behav. Brain Res., 27, 9-20 (1998).
15. Julio, R., Haixia, D., Mengjuan, G., Ximmin, L., Shi-lin, C., and Gustavo, F. G., Aqueous and hydroalcholic extracts of Black Maca (Lepidium meyenii) improve scopolamine-induced memory impairment in mice. Food Chem. Toxicol., in press.
16. Kim, D. H., Kim, D. Y., Kim, Y. C., Jung, J. W., Seungjoo, L., Yoon, B. H., Cheong, J. H., Kim, Y. S., Kang, S. S., Ko, K. H., and Ryu, J. H., Nodakenin, a coumarin compound, ameliorates scopolamine-induced memory disruption in mice. Life Sci., 80, 1944-1950 (2007).
17. Nelson, J. L., Sidny, M. H., Folke, S., and Ruth, Y. S., Cytokinins: synthesis, mass spectra, and biological activity of compounds related to zeatin. Proc. Natl. Acad. Sci. USA, 63, 175-182 (1969).
18. Sidney, M. H., Fray, B. R., Dieter, W., and Hawrelak, S. D., On the "activation" of cytokinins. J. Biol. Chem., 25, 7343-7351 (1975).
19. Kareal, D., Igora, P., Vladimir, K., Lukáš, S., Martina, F., Jan, H., René, L., Thomas, S., and Miroslav, S., Preparation and biological activity of 6-benzylaminopurine derivatives in plants and human cancer cells. Bioorg. Med. Chem., 14, 875-884 (2006).
20. Abraham, P. T., Acqyarone, M., Andersen, A., Asensi, A., Bellé, R., Beger, F., Bergounioux, C., Brunn, G., Buquet-Fagot, C., Fagot, D., Clab, N., Goudeau, H., Goudeau, M., Guerrier, P., Houghoton, P., Hedrikx, H., Kloareg, B., Lippai, M., Marie, D., Maro, B., Meijer, L., Mester, J., Mulner-Lorillon, O., Poulet, S. A., Shierenberg, E., Shutte, B., Vaulot, D., and Verlhac, M. H., Cellular effects of olomoucine, an inhibitor of cyclin-dependent kinase. Biol. Cell, 83, 105-120 (1995).
21. Zavaleta-Mancera, H. A., López-Delgado, H., Loza-Tavera, H., Mora-Herrera, M., Trevilla-Gracia, C., Vagas-Suárez, M., and Helen, O., Cytokinin promotes catalase and ascorbate peroxidase activities and preserves the chloroplast integrity during dark-senescence. J. Plant Physiol., in press.