نتایج جستجو برای: amyloid β

تعداد نتایج: 204360  

2011
Loes C. A. Rutten-Jacobs Frank-Erik de Leeuw Lenny Geurts-van Bon Marije C. Gordinou de Gouberville Annelieke N. Schepens-Franke P. Jos Dederen Wim G. M. Spliet Pieter Wesseling Amanda J. Kiliaan

Population-based studies have investigated the relation between β-amyloid levels in cerebrospinal fluid or plasma and white matter lesions (WMLs). However, these circulating levels of β-amyloid in cerebrospinal fluid or plasma may not reliably reflect the actual degree of amyloid present in the brain. Therefore, we investigated the relation between WMLs and β-amyloid plaques and amyloid angiopa...

Journal: :Brain : a journal of neurology 2017
Blaine R Roberts Monica Lind Aaron Z Wagen Alan Rembach Tony Frugier Qiao-Xin Li Timothy M Ryan Catriona A McLean James D Doecke Christopher C Rowe Victor L Villemagne Colin L Masters

We fractionated frontal cortical grey matter from human Alzheimer's disease and control subjects into four biochemically defined pools that represent four distinct compartments: soluble/cytosolic, peripheral membrane/vesicular cargo, integral lipid/membranous pools and aggregated/insoluble debris. Most of the readily extractable amyloid-β remains associated with a lipid/membranous compartment. ...

2015
Damian M. Cummings Wenfei Liu Erik Portelius Sevinç Bayram Marina Yasvoina Sui-Hin Ho Hélène Smits Shabinah S. Ali Rivka Steinberg Chrysia-Maria Pegasiou Owain T. James Mar Matarin Jill C. Richardson Henrik Zetterberg Kaj Blennow John A. Hardy Dervis A. Salih Frances A. Edwards

Detecting and treating Alzheimer's disease, before cognitive deficits occur, has become the health challenge of our time. The earliest known event in Alzheimer's disease is rising amyloid-β. Previous studies have suggested that effects on synaptic transmission may precede plaque deposition. Here we report how relative levels of different soluble amyloid-β peptides in hippocampus, preceding plaq...

Journal: :Brain : a journal of neurology 2011
Wenlin Hao Yang Liu Shirong Liu Silke Walter Marcus O Grimm Amanda J Kiliaan Botond Penke Tobias Hartmann Claudia E Rübe Michael D Menger Klaus Fassbender

Alzheimer's disease is characterized by extracellular deposits of amyloid β peptide in the brain. Increasing evidence suggests that amyloid β peptide injures neurons both directly and indirectly by triggering neurotoxic innate immune responses. Myeloid differentiation factor 88 is the key signalling molecule downstream to most innate immune receptors crucial in inflammatory activation. For this...

2015
Nina Jährling Klaus Becker Bettina M. Wegenast-Braun Stefan A. Grathwohl Mathias Jucker Hans-Ulrich Dodt Javier Vitorica

Alzheimer´s disease (AD) is the most common neurodegenerative disorder. AD neuropathology is characterized by intracellular neurofibrillary tangles and extracellular β-amyloid deposits in the brain. To elucidate the complexity of AD pathogenesis a variety of transgenic mouse models have been generated. An ideal imaging system for monitoring β-amyloid plaque deposition in the brain of these anim...

Journal: :Brain : a journal of neurology 2014
Frank Dohler Diego Sepulveda-Falla Susanne Krasemann Hermann Altmeppen Hartmut Schlüter Diana Hildebrand Inga Zerr Jakob Matschke Markus Glatzel

Alzheimer's disease is the most common form of dementia and the generation of oligomeric species of amyloid-β is causal to the initiation and progression of it. Amyloid-β oligomers bind to the N-terminus of plasma membrane-bound cellular prion protein (PrP(C)) initiating a series of events leading to synaptic degeneration. Composition of bound amyloid-β oligomers, binding regions within PrP(C),...

Journal: :Journal of neurochemistry 2014
Diane M Wuest Kelvin H Lee

Intravenous immunoglobulin (IVIG) contains anti-amyloid-β antibodies as well as antibodies providing immunomodulatory effects that may modify chronic inflammation in Alzheimer's disease. Answers to important questions about IVIG transport into the central nervous system and assessments of any impact amyloid-β has on this transport can be provided by in vitro models of the blood-brain barrier. I...

Journal: :Brain : a journal of neurology 2014
Sarah K Fritschi Franziska Langer Stephan A Kaeser Luis F Maia Erik Portelius Dorothea Pinotsi Clemens F Kaminski David T Winkler Walter Maetzler Kathy Keyvani Philipp Spitzer Jens Wiltfang Gabriele S Kaminski Schierle Henrik Zetterberg Matthias Staufenbiel Mathias Jucker

The soluble fraction of brain samples from patients with Alzheimer's disease contains highly biologically active amyloid-β seeds. In this study, we sought to assess the potency of soluble amyloid-β seeds derived from the brain and cerebrospinal fluid. Soluble Alzheimer's disease brain extracts were serially diluted and then injected into the hippocampus of young, APP transgenic mice. Eight mont...

2017
Jekaterina Krishtal Olga Bragina Kristel Metsla Peep Palumaa Vello Tõugu

The progression of Alzheimer's disease is causatively linked to the accumulation of amyloid-β aggregates in the brain, however, it is not clear how the amyloid aggregates initiate the death of neuronal cells. The in vitro toxic effects of amyloid peptides are most commonly examined using the human neuroblastoma derived SH-SY5Y cell line and here we show that differentiated neuron-like SH-SY5Y c...

Journal: :American journal of physiology. Endocrinology and metabolism 2013
Kathryn Aston-Mourney Shoba L Subramanian Sakeneh Zraika Thanya Samarasekera Daniel T Meier Lynn C Goldstein Rebecca L Hull

The dipeptidyl peptidase-4 (DPP-4) inhibitor sitagliptin is an attractive therapy for diabetes, as it increases insulin release and may preserve β-cell mass. However, sitagliptin also increases β-cell release of human islet amyloid polypeptide (hIAPP), the peptide component of islet amyloid, which is cosecreted with insulin. Thus, sitagliptin treatment may promote islet amyloid formation and it...

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