Skip to main content
Top
Published in: Journal of Natural Medicines 3-4/2011

01-07-2011 | Original Paper

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

Authors: Yanjing Bai, Chihiro Tohda, Shu Zhu, Masao Hattori, Katsuko Komatsu

Published in: Journal of Natural Medicines | Issue 3-4/2011

Login to get access

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.
Literature
1.
go back to reference Deyama T, Nishibe D, Nakazawa Y (2001) Constituents and pharmacological effects of Eucommia and Siberian ginseng. Acta Pharmacol Sin 22:1057–1070PubMed Deyama T, Nishibe D, Nakazawa Y (2001) Constituents and pharmacological effects of Eucommia and Siberian ginseng. Acta Pharmacol Sin 22:1057–1070PubMed
2.
go back to reference 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 56:567–572CrossRef 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 56:567–572CrossRef
3.
go back to reference 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 97:375–381PubMedCrossRef 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 97:375–381PubMedCrossRef
4.
go back to reference 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 107:329–339PubMedCrossRef 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 107:329–339PubMedCrossRef
6.
go back to reference Dickson TC, Vichkers JC (2001) The morphological phenotype of beta-amyloid plaques and associated neuritic changes in Alzheimer’s disease. Neuroscience 105:99–107PubMedCrossRef Dickson TC, Vichkers JC (2001) The morphological phenotype of beta-amyloid plaques and associated neuritic changes in Alzheimer’s disease. Neuroscience 105:99–107PubMedCrossRef
7.
go back to reference Kuboyama T, Tohda C, Komatsu K (2006) Withanoside IV and its active metabolite, sominone, attenuate Aβ(25–35)-induced neurodegeneration. Eur J Neurosci 23:1417–1427PubMedCrossRef Kuboyama T, Tohda C, Komatsu K (2006) Withanoside IV and its active metabolite, sominone, attenuate Aβ(25–35)-induced neurodegeneration. Eur J Neurosci 23:1417–1427PubMedCrossRef
8.
go back to reference 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 175:96–103PubMedCrossRef 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 175:96–103PubMedCrossRef
9.
go back to reference Kurkin VA (2003) Phenylpropanoids from medicinal plants: distribution, classification, structural analysis, and biological activity. Chem Nat Compd 39:123–153CrossRef Kurkin VA (2003) Phenylpropanoids from medicinal plants: distribution, classification, structural analysis, and biological activity. Chem Nat Compd 39:123–153CrossRef
10.
go back to reference Kuboyama T, Tohda C, Komatsu K (2005) Neuritic regeneration and synaptic reconstruction induced by withanolide A. Br J Pharmacol 144:961–971 Kuboyama T, Tohda C, Komatsu K (2005) Neuritic regeneration and synaptic reconstruction induced by withanolide A. Br J Pharmacol 144:961–971
11.
go back to reference 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 26:1014–1017PubMedCrossRef 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 26:1014–1017PubMedCrossRef
12.
go back to reference 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 15:231–234PubMedCrossRef 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 15:231–234PubMedCrossRef
13.
go back to reference 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 38:1763–1765PubMed 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 38:1763–1765PubMed
14.
go back to reference Ryu J, Son D, Kang J, Kim HS, Kim BK, Sanghyun L (2004) A benzenoid from the stem of Acanthopanax senticosus. Arch Pharm Res 27:912–914PubMedCrossRef Ryu J, Son D, Kang J, Kim HS, Kim BK, Sanghyun L (2004) A benzenoid from the stem of Acanthopanax senticosus. Arch Pharm Res 27:912–914PubMedCrossRef
15.
go back to reference Kim DK, Lim JP, Kim JW, Park HW, Eun JS (2005) Antitumor and anti-inflammatory constituents from Celtis sinensis. Arch Pharm Res 28:39–43PubMedCrossRef Kim DK, Lim JP, Kim JW, Park HW, Eun JS (2005) Antitumor and anti-inflammatory constituents from Celtis sinensis. Arch Pharm Res 28:39–43PubMedCrossRef
16.
go back to reference Tsukamoto H, Hisada S, Nishibe S (1985) Coumarins from bark of Fraxinus japonica and F. mandshurica var. japonica. Chem Pharm Bull 33:4069–4073 Tsukamoto H, Hisada S, Nishibe S (1985) Coumarins from bark of Fraxinus japonica and F. mandshurica var. japonica. Chem Pharm Bull 33:4069–4073
17.
go back to reference 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 49:4067–4072CrossRef 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 49:4067–4072CrossRef
18.
go back to reference 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 10:122–126PubMedCrossRef 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 10:122–126PubMedCrossRef
19.
go back to reference 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 50:136–145PubMed 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 50:136–145PubMed
20.
go back to reference 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 22:89–95PubMedCrossRef 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 22:89–95PubMedCrossRef
21.
go back to reference 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 56:414–420PubMedCrossRef 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 56:414–420PubMedCrossRef
22.
go back to reference 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 29:860–868PubMedCrossRef 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 29:860–868PubMedCrossRef
23.
go back to reference Thoda C, Tamura T, Matsuyama S, Komatsu K (2006) Promotion of axonal maturation and inhibition of dementia by Astragalus mongholicus. Br J Pharmacol 149:532–541CrossRef Thoda C, Tamura T, Matsuyama S, Komatsu K (2006) Promotion of axonal maturation and inhibition of dementia by Astragalus mongholicus. Br J Pharmacol 149:532–541CrossRef
24.
go back to reference Patrick JD, Lamprecht JH (1999) Plant sterols and sterolins: a review of their immune-modulating properties. Altern Med Rev 4:170–177 Patrick JD, Lamprecht JH (1999) Plant sterols and sterolins: a review of their immune-modulating properties. Altern Med Rev 4:170–177
25.
go back to reference 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 18:693–700CrossRef 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 18:693–700CrossRef
26.
go back to reference 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 55:1291–1295PubMedCrossRef 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 55:1291–1295PubMedCrossRef
Metadata
Title
Active components from Siberian ginseng (Eleutherococcus senticosus) for protection of amyloid β(25–35)-induced neuritic atrophy in cultured rat cortical neurons
Authors
Yanjing Bai
Chihiro Tohda
Shu Zhu
Masao Hattori
Katsuko Komatsu
Publication date
01-07-2011
Publisher
Springer Japan
Published in
Journal of Natural Medicines / Issue 3-4/2011
Print ISSN: 1340-3443
Electronic ISSN: 1861-0293
DOI
https://doi.org/10.1007/s11418-011-0509-y

Other articles of this Issue 3-4/2011

Journal of Natural Medicines 3-4/2011 Go to the issue