Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1999-4-1
pubmed:abstractText
Amyloid beta-peptide (A beta), the major constituent of the senile plaques in the brains of patients with Alzheimer's disease, is cytotoxic to neurons and has a central role in the pathogenesis of the disease. Previous studies have suggested that oxidative stress is involved in the mechanisms of A beta-induced neurotoxicity in vitro. In the present study, we examined whether oxidative stress contributes to learning and memory deficits caused by continuous intracerebroventricular infusion of A beta-(1-42). In the A beta-(1-42)-infused rats, spontaneous alternation behaviour in a Y-maze and spatial memory in a water maze task were significantly impaired, as compared with A beta-(40-1)-infused control rats. The retention of passive avoidance learning was also significantly impaired by treatment with A beta-(1-42). Potent antioxidants idebenone and alpha-tocopherol prevented the behavioural deficits in Y-maze and water maze, but not passive avoidance, tasks in A beta-(1-42)-infused rats when they were repeatedly administered by mouth once a day from 3 days before the start of A beta infusion to the end of behavioural experiments. Lipid peroxide levels in the hippocampus and cerebral cortex of A beta-(1-42)-infused rats did not differ from those in control animals, and neither idebenone nor alpha-tocopherol affected the lipid peroxide levels. These results suggest that treatment with antioxidants such as idebenone and alpha-tocopherol prevents learning and memory deficits caused by A beta.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0953-816X
pubmed:author
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
83-90
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:9987013-Alzheimer Disease, pubmed-meshheading:9987013-Amyloid beta-Peptides, pubmed-meshheading:9987013-Animals, pubmed-meshheading:9987013-Antioxidants, pubmed-meshheading:9987013-Avoidance Learning, pubmed-meshheading:9987013-Benzoquinones, pubmed-meshheading:9987013-Brain Chemistry, pubmed-meshheading:9987013-Drug Interactions, pubmed-meshheading:9987013-Injections, Intraventricular, pubmed-meshheading:9987013-Lipid Peroxidation, pubmed-meshheading:9987013-Locomotion, pubmed-meshheading:9987013-Male, pubmed-meshheading:9987013-Maze Learning, pubmed-meshheading:9987013-Memory, pubmed-meshheading:9987013-Nerve Degeneration, pubmed-meshheading:9987013-Neurotoxins, pubmed-meshheading:9987013-Oxidative Stress, pubmed-meshheading:9987013-Peptide Fragments, pubmed-meshheading:9987013-Rats, pubmed-meshheading:9987013-Rats, Wistar, pubmed-meshheading:9987013-Ubiquinone, pubmed-meshheading:9987013-Vitamin E
pubmed:year
1999
pubmed:articleTitle
Protective effects of idebenone and alpha-tocopherol on beta-amyloid-(1-42)-induced learning and memory deficits in rats: implication of oxidative stress in beta-amyloid-induced neurotoxicity in vivo.
pubmed:affiliation
Department of Neuropsychopharmacology and Hospital Pharmacy, Nagoya University School of Medicine, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't