SAR110894, a potent histamine H3-receptor antagonist, displays disease-modifying activity in a transgenic mouse model of tauopathy

Author:

Delay-Goyet Philippe1,Blanchard Véronique1,Schussler Nathalie1,Lopez-Grancha Mati1,Ménager Jean1,Mary Véronique1,Sultan Eric2,Buzy Armelle3,Guillemot Jean-Claude3,Stemmelin Jeanne1,Bertrand Philippe1,Rooney Thomas1,Pradier Laurent1,Barnéoud Pascal1

Affiliation:

1. Neurodegeneration and Pain Unit; Sanofi R&D; Chilly-Mazarin France

2. Disposition, Safety and Animal Research; Sanofi R&D; Montpellier France

3. Translational Sciences Unit; Sanofi R&D; Chilly-Mazarin France

Publisher

Wiley

Subject

Psychiatry and Mental health,Clinical Neurology

Reference39 articles.

1. Discovery of histamine H3 antagonists for the treatment of cognitive disorders and Alzheimer's disease;Brioni;J Pharmacol Exp Ther,2011

2. The Akt/GSK-3β axis as a new signaling pathway of the histamine H3 receptor;Bongers;J Neurochem,2007

3. Activation of the histaminergic H3 receptor induces phosphorylation of the Akt/GSK-3β pathway in cultured cortical neurons and protects against neurotoxic insults;Mariottini;J Neurochem,2009

4. Cellular phosphorylation of tau by GSK-3β influences tau binding to microtubules and microtubule organisation;Wagner;J Cell Sci,1996

5. Specific tau phosphorylation sites correlate with severity of neuronal cytopathology in Alzheimer's disease;Augustinack;Acta Neuropathol,2002

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