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Neurobiol Aging ; 51: 19-30, 2017 03.
Article in English | MEDLINE | ID: mdl-28033505

ABSTRACT

Impaired cholinergic neurotransmission associated with cognitive dysfunction occurs in various mental disorders of different etiologies including Alzheimer's disease and postalcoholic dementia and others. To address the question whether there exists a common endophenotype with a defined genetic and/or epigenetic signature causing mental dysfunction in these disorders, we investigated 2 generations of offspring born to alcohol-treated mothers. Here, we show that memory impairment and reduced synthesis of acetylcholine occurs in both F1 (exposed to ethanol in utero) and F2 generation (never been exposed to ethanol). Effects in the F2 generation are most likely consequences of transgenerationally transmitted epigenetic modifications in stem cells induced by alcohol. This clearly documents the role of ancestral history of drug abuse on the brain development of subsequent generations. The results further suggest an epigenetic trait for an anticholinergic endophenotype associated with cognitive dysfunction which might be relevant to our understanding of mental impairment in neurodegenerative disorders such as Alzheimer's disease and related disorders.


Subject(s)
Acetylcholine/biosynthesis , Cognition Disorders/genetics , Endophenotypes , Ethanol/adverse effects , Memory Disorders/genetics , Prenatal Exposure Delayed Effects/chemically induced , Prenatal Exposure Delayed Effects/genetics , Alzheimer Disease/genetics , Animals , Epigenesis, Genetic , Female , Fetal Alcohol Spectrum Disorders/genetics , Maternal-Fetal Exchange , Pregnancy , Rats
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