Skip to main content

Advertisement

Log in

Active components from Siberian ginseng (Eleutherococcus senticosus) for protection of amyloid β(25–35)-induced neuritic atrophy in cultured rat cortical neurons

  • Original Paper
  • Published:
Journal of Natural Medicines Aims and scope Submit manuscript

Abstract

Not only neuronal death but also neuritic atrophy and synaptic loss underlie the pathogenesis of Alzheimer’s disease as direct causes of the memory deficit. Extracts of Siberian ginseng (the rhizome of Eleutherococcus senticosus) were shown to have protective effects on the regeneration of neurites and the reconstruction of synapses in rat cultured cortical neurons damaged by amyloid β (Aβ)(25–35), and eleutheroside B was one of the active constituents. In this study, a comprehensive evaluation of constituents was conducted to explore active components from Siberian ginseng which can protect against neuritic atrophy induced by Aβ(25–35) in cultured rat cortical neurons. The ethyl acetate, n-butanol and water fractions from the methanol extract of Siberian ginseng showed protective effects against Aβ-induced neuritic atrophy. Twelve compounds were isolated from the active fractions and identified. Among them, eleutheroside B, eleutheroside E and isofraxidin showed obvious protective effects against Aβ(25–35)-induced atrophies of axons and dendrites at 1 and 10 μM.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Deyama T, Nishibe D, Nakazawa Y (2001) Constituents and pharmacological effects of Eucommia and Siberian ginseng. Acta Pharmacol Sin 22:1057–1070

    PubMed  CAS  Google Scholar 

  2. Gaffeny BT, Hügel HM, Rich PA (2001) Panax ginseng and Eleutherococcus senticosus may exaggerate an already existing biphasic response to stress via inhibition of enzymes which limit the binding of stress hormones to their receptors. Med Hypotheses 56:567–572

    Article  Google Scholar 

  3. Fujikawa T, Miguchi S, Kanada N, Nakai N, Ogata M, Suzuki I, Nakashima K (2005) Acanthopanax senticosus Harms as a prophylactic for MPTP-induced Parkinson’s disease in rats. J Ethnopharmacol 97:375–381

    Article  PubMed  Google Scholar 

  4. Tohda C, Ichimura M, Bai YJ, Tanaka K, Zhu S, Komatsu K (2008) Inhibitory effects of Eleutherococcus senticosus extracts on amyloid β(25–35)-induced neuritic atrophy and synaptic loss. J Pharmacol Sci 107:329–339

    Article  PubMed  CAS  Google Scholar 

  5. Seltzer B (2007) Donepezil: an update. Expert Opin Pharmacother 8:1011–1023

    Article  PubMed  CAS  Google Scholar 

  6. Dickson TC, Vichkers JC (2001) The morphological phenotype of beta-amyloid plaques and associated neuritic changes in Alzheimer’s disease. Neuroscience 105:99–107

    Article  PubMed  CAS  Google Scholar 

  7. Kuboyama T, Tohda C, Komatsu K (2006) Withanoside IV and its active metabolite, sominone, attenuate Aβ(25–35)-induced neurodegeneration. Eur J Neurosci 23:1417–1427

    Article  PubMed  Google Scholar 

  8. Evans NA, Facci L, Owen DE (2008) Abeta(1–42) reduces synapse number and inhibits neurite outgrowth in primary cortical and hippocampal neurons: a quantitative analysis. J Neurosci Methods 175:96–103

    Article  PubMed  CAS  Google Scholar 

  9. Kurkin VA (2003) Phenylpropanoids from medicinal plants: distribution, classification, structural analysis, and biological activity. Chem Nat Compd 39:123–153

    Article  CAS  Google Scholar 

  10. Kuboyama T, Tohda C, Komatsu K (2005) Neuritic regeneration and synaptic reconstruction induced by withanolide A. Br J Pharmacol 144:961–971

    Google Scholar 

  11. Kiem PV, Minh CV, Dat NT, Cai XF, Lee JJ, Kim YH (2003) Two new phenylpropanoid glycosides from the stem bark of Acanthopanax trifoliatus. Arch Pharm Res 26:1014–1017

    Article  PubMed  CAS  Google Scholar 

  12. Gaffney BT, Hugel HM, Rich PA (2004) The chromatographic co-elution of dihydrodehydrodiconiferyl alcohol monopyranose with eleutheroside E in Eleutherococcus senticosus: implications for eleutheroside E assays. Phytochem Anal 15:231–234

    Article  PubMed  CAS  Google Scholar 

  13. Nishibe S, Kinoshita H, Takeda H, Okano G (1990) Phenolic compounds from stem bark of Acanthopanax senticosus and their pharmacological effect in chronic swimming stressed rats. Chem Pharm Bull 38:1763–1765

    PubMed  CAS  Google Scholar 

  14. Ryu J, Son D, Kang J, Kim HS, Kim BK, Sanghyun L (2004) A benzenoid from the stem of Acanthopanax senticosus. Arch Pharm Res 27:912–914

    Article  PubMed  CAS  Google Scholar 

  15. Kim DK, Lim JP, Kim JW, Park HW, Eun JS (2005) Antitumor and anti-inflammatory constituents from Celtis sinensis. Arch Pharm Res 28:39–43

    Article  PubMed  CAS  Google Scholar 

  16. Tsukamoto H, Hisada S, Nishibe S (1985) Coumarins from bark of Fraxinus japonica and F. mandshurica var. japonica. Chem Pharm Bull 33:4069–4073

    CAS  Google Scholar 

  17. Damrong K, Juraithip W, Wanchai DE (2008) Biosynthesis of β-sitosterol and stigmasterol proceeds exclusively via the mevalonate pathway in cell suspension cultures of Croton stellatopilosus. Tetrahedron Lett 49:4067–4072

    Article  Google Scholar 

  18. Whitehouse PJ, Price DL, Clark AW, Coyle JT, Delong MR (1981) Alzheimer disease: evidence for selective loss of cholinergic neurons in the nucleus basalis. Ann Neurol 10:122–126

    Article  PubMed  CAS  Google Scholar 

  19. Rogers SL, Farlow MR, Doody RS, Mohs R, Friedhoff LT (1998) A 24-week, double-blind, placebo-controlled trial of donepezil in patients with Alzheimer’s disease. Donepezil Study Group. Neurology 50:136–145

    PubMed  CAS  Google Scholar 

  20. Ogura H, Kosasa T, Yamanishi Y (2000) Donepezil, a centrally acting acetylcholinesterase inhibitor, alleviates learning deficits in hypocholinergic models in rats. Methods Find Exp Clin Pharmacol 22:89–95

    Article  PubMed  CAS  Google Scholar 

  21. Bobinski M, Wegiel J, Tarnawski M, Bobinski M, Reisberg B, Leon MJ (1997) Relationships between regional neuronal loss and neurofibrillary changes in the hippocampal formation and duration and severity of Alzheimer’s disease. J Neuropathol Exp Neurol 56:414–420

    Article  PubMed  CAS  Google Scholar 

  22. Tohda C, Matsumoto N, Zou K, Meselhy R, Komatsu K (2004) Aβ (25–35)-induced memory impairment, axonal atrophy, and synaptic loss are ameliorated by M1, a metabolite of protopanaxadiol-type saponins. Neuropsychopharmacology 29:860–868

    Article  PubMed  CAS  Google Scholar 

  23. Thoda C, Tamura T, Matsuyama S, Komatsu K (2006) Promotion of axonal maturation and inhibition of dementia by Astragalus mongholicus. Br J Pharmacol 149:532–541

    Article  Google Scholar 

  24. Patrick JD, Lamprecht JH (1999) Plant sterols and sterolins: a review of their immune-modulating properties. Altern Med Rev 4:170–177

    Google Scholar 

  25. Boulic PJD, Etsebeth S, Liebengerg RW (1996) Beta-sitosterol and beta-sitosterol glucoside stimulate human peripheral blood lymphocyte proliferation: implications for their use as an immunomodulatory vitamin combination. Int J Immunopharmacol 18:693–700

    Article  Google Scholar 

  26. Sun H, Lv H, Zhang Y-M, Wang X-J, Bi K-S, Cao H-X (2007) Pharmacokinetics of isofraxidin in rat plasma after oral administration of the extract of Acanthopanax senticosus using HPLC with solid phase extraction method. Chem Pharm Bull 55:1291–1295

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by a Grant-in-Aid for Scientific Research (B), No. 21406004 in 2009–2010, from the Japan Society for the Promotion of Science and by Expansion Program, Regional Innovation Cluster Program, Global Type (II), “Hokuriku Innovation Cluster for Health Science” from the Ministry of Education, Culture, Sports, Science and Technology, Japan.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Katsuko Komatsu.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bai, Y., Tohda, C., Zhu, S. et al. Active components from Siberian ginseng (Eleutherococcus senticosus) for protection of amyloid β(25–35)-induced neuritic atrophy in cultured rat cortical neurons. J Nat Med 65, 417–423 (2011). https://doi.org/10.1007/s11418-011-0509-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11418-011-0509-y

Keywords

Navigation