DOI QR코드

DOI QR Code

Anti-amnesic and Antioxidant Effect of Yeongkyekamjotanggayonggolmoryo Aqueous Extracts on Scopolamine-induced Memory Impairment in Mice

Scopolamine 유발 기억력손상 흰 쥐에서 영계감조탕가용골모려(笭桂甘棗湯加龍骨牡蠣)의 인지기능개선과 항산화 효과

  • Kim, Dae-eok (Department of Oriental Neuropsychiatry, College of Korean Medicine, Daegu Hanny University) ;
  • Han, Da-young (Department of Oriental Neuropsychiatry, College of Korean Medicine, Daegu Hanny University) ;
  • Kim, Sang-ho (Department of Oriental Neuropsychiatry, College of Korean Medicine, Daegu Hanny University) ;
  • Chung, Dae-kyoo (Department of Oriental Neuropsychiatry, College of Korean Medicine, Daegu Hanny University)
  • 김대억 (대구한의대학교 한의과대학 신경정신과교실) ;
  • 한다영 (대구한의대학교 한의과대학 신경정신과교실) ;
  • 김상호 (대구한의대학교 한의과대학 신경정신과교실) ;
  • 정대규 (대구한의대학교 한의과대학 신경정신과교실)
  • Received : 2018.07.26
  • Accepted : 2018.09.15
  • Published : 2018.09.30

Abstract

Objectives: The purpose of this in vivo study is to observe anti-amnesic effects of Yeongkyekamjotanggayonggolmoryo (YGYM), a novel mixed herbal prescription, Ossis Mastodi and Ostreae Testa added Yeongkyekamjo-tang, on scopolamine induced amnesia in C57BL/6 mice through acetylcholine (ACh) and acetylcholinesterase (AChE) activity, Choline acetyltransferase (ChAT) mRNA expression, and antioxidant effects. Methods: Six groups, total 20 intact or 100 Sco treated mice were used in this study after one week of acclimatization period. Half the animals were used for passive avoidance task tests and hippocampus ACh content, AChE activity, and ChAT mRNA expression were measured. The other half was subjected to an underwater maze test and then the cerebral cortex antioxidant defense system was measured. Results: In the passive avoidance experiment, there was significant decrease in residence time in the bright room and in the underwater maze test, escape latency to escape from the esophagus significantly increased compared with the normal control group. At the final sacrifice, ACh content and ChAT mRNA expression decreased, AChE activity increased, and cerebral cortical MDA increased GSH content, SOD and CAT activity in Sco control mice, as compared to intact vehicle control mice. However, these Sco treatment-related memory loss through AChE activation destroyed the cerebral cortex antioxidant defense system, and was inhibited dose-dependently by 28 days consecutive oral pretreatments of YGYM extracts 500, 250, 125 mg/kg. Conclusions: In the above results, YGYM extract that oral administration of YGYM extracts alleviates the antioxidant defense system, through preservation of ACh mediated by upregulation of ChAT mRNA expression, and increase of AChE inhibition and brain antioxidant defense systems.

Keywords

References

  1. Chuong NN, Trung BH, Luan TC, Hung TM, Dang NH, Dat NT. Anti-amnesic effect of alkaloid fraction from Lycopodiella cernua (L.) Pic. Serm. on scopolamine-induced memory impairment in mice. Neurosci Lett. 2014;575:42-6. https://doi.org/10.1016/j.neulet.2014.05.031
  2. Taraschenko OD, Barnes WG, Herrick-Davis K, Yokoyama Y, Boyd DL, Hough LB. Actions of tacrine and galanthamine on histamine-N-methyl transferase. Methods Find Exp Clin Pharmacol. 2005;27:161-5. https://doi.org/10.1358/mf.2005.27.3.890872
  3. Choi WH, Um MY, Ahn JY, Kim SR, Kang MH and Ha TY. Acetylcholinestarase inhibitory activity and protctive effect against cytotoxicity of perilla seed methanol extraract. J Korean Food Sci TECHNOL 2004;36:1026-31.
  4. Nordberg A. Mechanisms behind the neuroprotective actions of cholinesterase inhibitors in Alzheimer disease. Alzheimer Dis Assoc Disord. 2006;20(2):12-8. https://doi.org/10.1097/01.wad.0000213804.59187.2d
  5. Park SM, Ki SH, Han NR, Cho IJ, Ku SK, Kim SC, Zhao RJ, Kim YW. Tacrine, an oral acetylcholinesterase inhibitor, induced hepatic oxidative damage, which was blocked by liquiritigenin through GSK3-beta inhibition. Biol Pharm Bull. 2015;38:184-92. https://doi.org/10.1248/bpb.b14-00430
  6. Watkins PB, Zimmerman HJ, Knapp MJ, Gracon SI, Lewis KW. Hepatotoxic effects of tacrine administration in patients with Alzheimer's disease. JAMA. 1994;271:992-8. https://doi.org/10.1001/jama.1994.03510370044030
  7. Dunn NR, Pearce GL, Shakir SA. Adverse effects associated with the use of donepezil in general practice in England. J Psychopharmacol. 2000;14:406-8. https://doi.org/10.1177/026988110001400410
  8. Oh MH, Houghton PJ, Whang WK, Cho JH. Screening of Korean herbal medicines used to improve cognitive function for anti-cholinesterase activity. Phytomedicine. 2004; 11(6):544-8. https://doi.org/10.1016/j.phymed.2004.03.001
  9. Chae IS. Sanghanronyeokjeon. Seoul:Komoonsa 1995:62.
  10. Rho EJ, Kang HE. Gufangleiju. Seoul:Publshing Gobang 2011:200-2.
  11. Ha JH, Lee MG, Chang SM, Lee JT. In vivo characterization of sedative activities of Fossilia Mastodi OSSIS. Biol Pharm Bull. 2006;29:1414-7. https://doi.org/10.1248/bpb.29.1414
  12. Hong MW. Pharmaceutical investigation of fossil shell Crassostrea gravitesta eoilensis Kim et Noda. Korean J Pharmacog. 1973;4:9-17.
  13. Yun JH, Study of boiled extract LMK02 on acute oral toxicity in SD rat and effectiveness on $A{\beta}$(1-42)level and $\beta$-amyloid deposition in the brain of Tg-APPswe/PS1dE9 mouse model of Alzheimer disease, Graduate School of Oriental Medicine Won Kwang University. a doctor's thesis. 2010;37.
  14. Seo JH, The Enhancing effect of Herbal Mixture (HT008-1) on Memory and Cognitive Function. Graduate School of Oriental Medicine Kyung Hee University. a master's thesis. 2008;21.
  15. Hung TM, Na M, Dat NT, Ngoc TM, Youn U, Kim HJ, Min BS, Lee J, Bae K. Cholinesterase inhibitory and anti-amnesic activity of alkaloids from Corydalis turtschaninovii. J Ethnopharmacol. 2008;119:74-80. https://doi.org/10.1016/j.jep.2008.05.041
  16. Morris R. Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods.1984;11:47-60. https://doi.org/10.1016/0165-0270(84)90007-4
  17. Del Rio D, Stewart AJ, Pellegrini N. A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutr Metab Cardiovasc Dis. 2005;15:316-28. https://doi.org/10.1016/j.numecd.2005.05.003
  18. Lee S, Kim J, Seo SG, Choi BR, Han JS, Lee KW, Kim J. Sulforaphane alleviates scopolamine-induced memory impairment in mice. Pharmacol Res. 2014;85:23-32. https://doi.org/10.1016/j.phrs.2014.05.003
  19. Jamall IS, Smith JC. Effects of cadmium on glutathione peroxidase, superoxidase dismutase and lipid peroxidation in the rat heart: a possible mechanism of cadmium cardiotoxicity. Toxicol Appl Pharmacol. 1985;80: 33-42. https://doi.org/10.1016/0041-008X(85)90098-5
  20. Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ: Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:265-75.
  21. Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Anal Biochem. 1968;25:192-205. https://doi.org/10.1016/0003-2697(68)90092-4
  22. Aebi H. Catalase. In: Bergmeyer HU (Ed.), Methods in Enzymatic Analysis. New York: Academic Press, 1974;673-86.
  23. Sun Y, Larry WO, Ying L. A simple method for clinical assay of superoxide dismutase. Clin Chem. 1988;34:497-500.
  24. Levene A. Pathological factors influencing excision of tumours in the head and neck. Part I. Clin Otolaryngol Allied Sci. 1981;6:145-51. https://doi.org/10.1111/j.1365-2273.1981.tb01800.x
  25. Ludbrook J. Update: microcomputer statistics packages. A personal view. Clin Exp Pharmacol Physiol. 1997;24.
  26. Kang SJ, Lee JE, Lee EK, Jung DH, Song CH, Park SJ, Choi SH, Han CH, Ku SK, Lee YJ. Fermentation with Aquilariae Lignum enhances the anti-diabetic activity of green tea in type II diabetic db/db mouse. Nutrients. 2014;6:3536-71. https://doi.org/10.3390/nu6093536
  27. Hwang EW, Kim JH. Oriental Medicine Psychiatry. Seoul:Hyundae Medical Books.1989:135.
  28. Davies P, Maloney AJF. Selective loss of central cholinergic neurons in Alzheimer's disease. Lancet. 1976;2:1403.
  29. Giacobini E, Becker R. Present progress and future development in the therapy for Alzheimer's disease. 1989:1122.
  30. Giacobini E. The cholinergic system in Alzheimer disease. Prog Brain Res. 1990;84:321-32.
  31. Bachurin SO. Medicinalchemistry approaches for the treatment and prevention of Alzheimer's disease. Med Res Rev. 2003.
  32. Nam Y, Lee D. Ameliorating effects of constituents from Cortex Acanthopanacis Radicis on memory impairment in mice induced by scopolamine. J Tradit Chin Med. 2014;34:57-62. https://doi.org/10.1016/S0254-6272(14)60055-8
  33. Lee JH, Jung CH. Yaozheng. Seoul: Cheonghong 2006:228.
  34. Park JH, Lee GE, Lyu YS, Bae DB, Baek DG, Shin YJ, Kang HW, Lyu YS. The clinical study of 3 menopausal disorder patients with palpitation and depression treated by Yeongkyekamjo-tang. J Oriental Neuropsychiatry. 2012;23:67-84. https://doi.org/10.7231/JON.2012.23.2.067
  35. LeDoux JE. Emotional memory systems in the brain. Behav Brain Res. 1993;58:69-79. https://doi.org/10.1016/0166-4328(93)90091-4
  36. Blusztajn JK, Wurtman RJ. Choline and cholinergic neurons. Science. 1983;221:614-20. https://doi.org/10.1126/science.6867732
  37. Brandon EP, Mellott T, Pizzo DP, Coufal N, D'Amour KA, Gobeske K, Lortie M, Lopez-Coviella I, Berse B, Thal LJ, Gage FH, Blusztajn JK. Choline transporter 1 maintains cholinergic function in choline acetyltransferase haploinsufficiency. J Neurosci. 2004;24:5459-66. https://doi.org/10.1523/JNEUROSCI.1106-04.2004
  38. Mohapel P, Leanza G, Kokaia M, Lindvall O. Forebrain acetylcholine regulates adult hippocampal neurogenesis and learning. Neurobiol Aging. 2005;26:939-46. https://doi.org/10.1016/j.neurobiolaging.2004.07.015
  39. Eichenbaum H. How does the brain organize memories? Science. 1997;277:330-2. https://doi.org/10.1126/science.277.5324.330
  40. Giacobini E. Cholinesterase inhibitors: new roles and therapeutic alternatives. Pharmacol Res. 2004;50:433-40. https://doi.org/10.1016/j.phrs.2003.11.017
  41. Oda Y. Choline acetyltransferase: the structure, distribution and pathologic changes in the central nervous system. Pathol Int. 1999;49:921-37. https://doi.org/10.1046/j.1440-1827.1999.00977.x
  42. Zambrzycka A, Alberghina M, Strosznajder JB. Effects of aging and amyloid-beta peptides on choline acetyltransferase activity in rat brain. Neurochem Res. 2002;27:277-81. https://doi.org/10.1023/A:1014951010834
  43. Dawson GR, Heyes CM, Iversen SD. Pharmacological mechanisms and animal models of cognition. Behav Pharmacol. 1992;3:285-97.
  44. Wattanathorn J, Jittiwat J, Tongun T, Muchimapura S, Ingkaninan K. Zingiber officinale mitigates brain damage and improves memory impairment in focal cerebral ischemic rat. Evid Based Complement Alternat Med. 2011;2011:429-505.
  45. Rao KS. Free radical induced oxidative damage to DNA: relation to brain aging and neurological disorders. Indian J Biochem Biophys. 2009;46:9-15.
  46. Ghumatkar PJ, Patil SP, Jain PD, Tambe RM, Sathaye S. Nootropic, neuroprotective and neurotrophic effects of phloretin in scopolamine induced amnesia in mice. Pharmacol Biochem Behav. 2015;135:182-91. https://doi.org/10.1016/j.pbb.2015.06.005
  47. Kumar H, Kim BW, Song SY, Kim JS, Kim IS, Kwon YS, Koppula S, Choi DK. Cognitive enhancing effects of alpha asarone in amnesic mice by influencing cholinergic and antioxidant defense mechanisms. Biosci Biotechnol Biochem. 2012;76:1518-22. https://doi.org/10.1271/bbb.120247
  48. Mattson MP, Pedersen WA, Duan W, Culmsee C, Camandola S. Cellular and molecular mechanisms underlying perturbed energy metabolism and neuronal degeneration in Alzheimer's and Parkinson's diseases. Ann N Y Acad Sci. 1999;893:154-75. https://doi.org/10.1111/j.1749-6632.1999.tb07824.x
  49. Nam Y, Lee D. Ameliorating effects of constituents from Cortex Acanthopanacis Radicis on memory impairment in mice induced by scopolamine. J Tradit Chin Med. 2014;34:57-62. https://doi.org/10.1016/S0254-6272(14)60055-8
  50. Raichle ME. The pathophysiology of brain ischemia. Ann Neurol. 1983;13:2-10. https://doi.org/10.1002/ana.410130103
  51. Odabasoglu F, Cakir A, Suleyman H, Aslan A, Bayir Y, Halici M, Kazaz C. Gastroprotective and antioxidant effects of usnic acid on indomethacin-induced gastric ulcer in rats. J Ethnopharmacol. 2006;103:59-65. https://doi.org/10.1016/j.jep.2005.06.043
  52. Zhan C, Yang J. Protective effects of isoliquiritigenin in transient middle cerebral artery occlusion-induced focal cerebral ischemia in rats. Pharmacol Res. 2006;53:303-9. https://doi.org/10.1016/j.phrs.2005.12.008
  53. Hu D, Cao Y, He R, Han N, Liu Z, Miao L, Yin J. Schizandrin, an antioxidant lignin from Schisandra chinensis, ameliorates $A{\beta}1$-42-induced memory impairment in mice. Oxid Med Cell Longev. 2012;2012:721.

Cited by

  1. Scrophularia buergeriana Extract (Brainon) Improves Scopolamine-Induced Neuronal Impairment and Cholinergic Dysfunction in Mice through CREB-BDNF Signaling Pathway vol.11, pp.9, 2021, https://doi.org/10.3390/app11094286