Die Funktion der Blut-Hirn-Schranke für die Pathogenese der Alzheimer-Demenz--Implikationen für immunologische Therapien zur Plaqueauflösung.

Translated title of the contribution: The role of blood-brain barrier in the pathogenesis of Alzheimer dementia--implications for immunological therapies for plaque dissolution

J. Pahnke*, M. Krohn, K. Scheffler

*Corresponding author for this work
3 Citations (Scopus)

Abstract

Alzheimer's disease (AD) is a devastating neurodegenerative disorder affecting more than 27 million people worldwide and leading to severe social-economic problems. One characteristic hallmark of AD--the amyloid plaques--are still being discussed to be one important triggering factor. However, current animal and autopsy studies refer to soluble and highly toxic A block oligomers as the deadly agent for the neurons. Current therapies mainly rely on the abatement of symptoms without antagonizing the etiology of the disease. Potential new approaches address reduced production, increased degradation and/or evacuation of toxic A block peptides from the brain. Among others one important group of target-proteins are the ABC transporters of the blood-brain barrier which contribute importantly to the detoxification of the brain. Changes of specific transport functions evoke important alterations for the known pathogenesis and future therapies of AD, especially approaches that target plaque dissolution and plaque reduction. (c) Georg Thieme Verlag KG Stuttgart-New York.

Translated title of the contributionThe role of blood-brain barrier in the pathogenesis of Alzheimer dementia--implications for immunological therapies for plaque dissolution
Original languageGerman
JournalFortschritte der Neurologie-Psychiatrie
Volume77 Suppl 1
Pages (from-to)S21-24
Number of pages4
ISSN0720-4299
DOIs
Publication statusPublished - 08.2009

Research Areas and Centers

  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

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