Simvastatin strongly reduces levels of Alzheimer's disease β-amyloid peptides Aβ42 and Aβ40 <i>in vitro</i> and <i>in vivo</i>

Klaus Faßbender(Heidelberg University), Mikael Simons(Heidelberg University), Christine Bergmann(Heidelberg University), Mark Stroick(Heidelberg University), Dieter Lütjohann(Heidelberg University), Patrick Keller(Heidelberg University), Heiko Runz(Heidelberg University), Sandra Kühl(Heidelberg University), Thomas Bertsch(Heidelberg University), Klaus von Bergmann(Heidelberg University), M.G. Hennerici(Heidelberg University), Konrad Beyreuther(Heidelberg University), Tobias Hartmann(Heidelberg University)
Proceedings of the National Academy of Sciences
April 10, 2001
Cited by 1,088Open Access
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Abstract

Recent epidemiological studies show a strong reduction in the incidence of Alzheimer's disease in patients treated with cholesterol-lowering statins. Moreover, elevated Abeta42 levels and the varepsilon4 allele of the lipid-carrier apolipoprotein E are regarded as risk factors for sporadic and familial Alzheimer's disease. Here we demonstrate that the widely used cholesterol-lowering drugs simvastatin and lovastatin reduce intracellular and extracellular levels of Abeta42 and Abeta40 peptides in primary cultures of hippocampal neurons and mixed cortical neurons. Likewise, guinea pigs treated with high doses of simvastatin showed a strong and reversible reduction of cerebral Abeta42 and Abeta40 levels in the cerebrospinal fluid and brain homogenate. These results suggest that lipids are playing an important role in the development of Alzheimer's disease. Lowered levels of Abeta42 may provide the mechanism for the observed reduced incidence of dementia in statin-treated patients and may open up avenues for therapeutic interventions.


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