Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/93039
Title: The diphenylpyrazole compound anle138b blocks Aβ channels and rescues disease phenotypes in a mouse model for amyloid pathology
Authors: Hernandez, Ana Martinez
Urbanke, Hendrik
Gillman, Alan L.
Lee, Joon
Ryazanov, Sergey
Agbemenyah, Hope Y.
Benito, Eva
Jain, Gaurav
Kaurani, Lalit
Grigorian, Gayane
Leonov, Andrei
Rezaei-Ghaleh, Nasrollah
Wilken, Petra
Teran Arce, Fernando
Wagner, Jens
Fuhrman, Martin
Caruana Grech Perry, Mario
Camilleri, Angelique
Vassallo, Neville
Zweckstetter, Markus
Benz, Roland
Giese, Armin
Schneider, Anja
Korte, Martin
Lal, Ratnesh
Griesinger, Christian
Eichele, Gregor
Fischer, Andre
Keywords: Alzheimer's disease -- Pathophysiology
Alzheimer's disease -- Treatment
Amyloid beta-protein
Nervous system -- Degeneration
Plaque, amyloid -- Physiopathology
Issue Date: 2018
Publisher: EMBOpress
Citation: Martinez Hernandez, A., Urbanke, H., Gillman, A. L., Lee, J., Ryazanov, S., Agbemenyah, H. Y.,... Fischer, A. (2018). The diphenylpyrazole compound anle138b blocks Aβ channels and rescues disease phenotypes in a mouse model for amyloid pathology. EMBO Molecular Medicine, 10(1), 32-47.
Abstract: Alzheimer’s disease is a devastating neurodegenerative disease eventually leading to dementia. An effective treatment does not yet exist. Here we show that oral application of the compound anle138b restores hippocampal synaptic and transcriptional plasticity as well as spatial memory in a mouse model for Alzheimer’s disease, when given orally before or after the onset of pathology. At the mechanistic level, we provide evidence that anle138b blocks the activity of conducting Ab pores without changing the membrane embedded Ab-oligomer structure. In conclusion, our data suggest that anle138b is a novel and promising compound to treat AD-related pathology that should be investigated further.
URI: https://www.um.edu.mt/library/oar/handle/123456789/93039
Appears in Collections:Scholarly Works - FacHScFSEH



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