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Article: The herbal medicine Dipsacus asper Wall extract reduces the cognitive deficits and overexpression of β-amyloid protein induced by aluminum exposure

TitleThe herbal medicine Dipsacus asper Wall extract reduces the cognitive deficits and overexpression of β-amyloid protein induced by aluminum exposure
Authors
KeywordsAluminum
Alzheimer's disease
Dipsacus asper
Passive avoidance task
Rat
Vitamin E
β-amyloid protein
Issue Date2003
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescie
Citation
Life Sciences, 2003, v. 73 n. 19, p. 2443-2454 How to Cite?
AbstractExcess aluminum (Al) exposure impairs neurocognitive function in humans and animals. Epidemiologic studies have shown a potential link between chronic Al exposure and Alzheimer's disease. In the present study, we sought to evaluate the protective effects of the herbal medicine Dipsacus asper extract against the cognitive impairment and overexpression of hippocampal β-amyloid protein (Aβ) induced by chronic Al exposure in rats. Vitamin E (VE) was used as a positive control. Following exposure to 0.3% aluminum chloride (AlCl 3) solution for 90 days in their drinking water, animals displayed a striking decrease (>80%) in step-through latency in the passive avoidance task and a significant increase (123%) in the number of Aβ immunoreactive cells in the hippocampus compared to controls. Al-exposed animals were then randomly assigned to receive vehicle, Dipsacus asper extract (4 g/kg), or VE (40 mg/kg) treatment up to 5 months. Both Dipsacus asper extract and VE significantly ameliorated animal's performance impairment in the passive avoidance task and suppressed the overexpression of hippocampal Aβ immunoreactivity. The effects of Dipsacus asper extract, but not VE, increased with time of treatment. The present results suggest that Dipsacus asper extract may possess therapeutic effects against Alzheimer's disease. © 2003 Elsevier Inc. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/179417
ISSN
2021 Impact Factor: 6.780
2020 SCImago Journal Rankings: 1.131
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhang, ZJen_US
dc.contributor.authorQian, YHen_US
dc.contributor.authorHu, HTen_US
dc.contributor.authorYang, Jen_US
dc.contributor.authorYang, GDen_US
dc.date.accessioned2012-12-19T09:56:18Z-
dc.date.available2012-12-19T09:56:18Z-
dc.date.issued2003en_US
dc.identifier.citationLife Sciences, 2003, v. 73 n. 19, p. 2443-2454en_US
dc.identifier.issn0024-3205en_US
dc.identifier.urihttp://hdl.handle.net/10722/179417-
dc.description.abstractExcess aluminum (Al) exposure impairs neurocognitive function in humans and animals. Epidemiologic studies have shown a potential link between chronic Al exposure and Alzheimer's disease. In the present study, we sought to evaluate the protective effects of the herbal medicine Dipsacus asper extract against the cognitive impairment and overexpression of hippocampal β-amyloid protein (Aβ) induced by chronic Al exposure in rats. Vitamin E (VE) was used as a positive control. Following exposure to 0.3% aluminum chloride (AlCl 3) solution for 90 days in their drinking water, animals displayed a striking decrease (>80%) in step-through latency in the passive avoidance task and a significant increase (123%) in the number of Aβ immunoreactive cells in the hippocampus compared to controls. Al-exposed animals were then randomly assigned to receive vehicle, Dipsacus asper extract (4 g/kg), or VE (40 mg/kg) treatment up to 5 months. Both Dipsacus asper extract and VE significantly ameliorated animal's performance impairment in the passive avoidance task and suppressed the overexpression of hippocampal Aβ immunoreactivity. The effects of Dipsacus asper extract, but not VE, increased with time of treatment. The present results suggest that Dipsacus asper extract may possess therapeutic effects against Alzheimer's disease. © 2003 Elsevier Inc. All rights reserved.en_US
dc.languageengen_US
dc.publisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/lifescieen_US
dc.relation.ispartofLife Sciencesen_US
dc.subjectAluminum-
dc.subjectAlzheimer's disease-
dc.subjectDipsacus asper-
dc.subjectPassive avoidance task-
dc.subjectRat-
dc.subjectVitamin E-
dc.subjectβ-amyloid protein-
dc.subject.meshAdministration, Oralen_US
dc.subject.meshAluminum Compounds - Toxicityen_US
dc.subject.meshAmyloid Beta-Peptides - Biosynthesisen_US
dc.subject.meshAnimalsen_US
dc.subject.meshAvoidance Learning - Drug Effectsen_US
dc.subject.meshChlorides - Toxicityen_US
dc.subject.meshDrugs, Chinese Herbal - Pharmacologyen_US
dc.subject.meshHippocampus - Drug Effects - Metabolismen_US
dc.subject.meshMaleen_US
dc.subject.meshRatsen_US
dc.subject.meshRats, Sprague-Dawleyen_US
dc.subject.meshVitamin E - Pharmacologyen_US
dc.titleThe herbal medicine Dipsacus asper Wall extract reduces the cognitive deficits and overexpression of β-amyloid protein induced by aluminum exposureen_US
dc.typeArticleen_US
dc.identifier.emailZhang, ZJ: zhangzj@hkucc.hku.hken_US
dc.identifier.authorityZhang, ZJ=rp01297en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/S0024-3205(03)00649-0en_US
dc.identifier.pmid12954453-
dc.identifier.scopuseid_2-s2.0-0041828392en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0041828392&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume73en_US
dc.identifier.issue19en_US
dc.identifier.spage2443en_US
dc.identifier.epage2454en_US
dc.identifier.isiWOS:000185224200005-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridZhang, ZJ=8061473900en_US
dc.identifier.scopusauthoridQian, YH=8061474000en_US
dc.identifier.scopusauthoridHu, HT=35305074400en_US
dc.identifier.scopusauthoridYang, J=8928087300en_US
dc.identifier.scopusauthoridYang, GD=8627524400en_US
dc.identifier.issnl0024-3205-

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