P3‐011: Biochemical characterization of the TG2576 mouse model: Age‐dependent levels of Amyloid‐beta species and other APP processing fragments in plasma and brain

Appelkvist, Paulina; Fabre, Susanne Froelich; Eketjäll, Susanna; Bogstedt, Anna; Nilsson, Karolina; Bergstedt, Karin Dillner

doi:10.1016/j.jalz.2011.05.1450

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“…The additional dataset consisted of Aβ levels measured in Tg2576 mice of various ages, between 3.5 and 26 months at termination. Details of those data can be found in Appelkvist et al ( 2011 ). In total, data from 71 preclinical studies were used.…”

Section: Methodsmentioning

confidence: 99%

Modeling of age‐dependent amyloid accumulation and γ‐secretase inhibition of soluble and insoluble Aβ in a transgenic mouse model of amyloid deposition

Parkinson

Ploeger

Appelkvist

et al. 2013

Pharmacology Res & Perspec

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According to the “amyloid hypothesis,” accumulation of amyloid beta (Aβ) peptides in the brain is linked to the development of Alzheimer's disease. The aims of this investigation were to develop a model for the age-dependent amyloid accumulation and to quantify the age- and treatment-duration-dependent efficacy of the γ-secretase inhibitor MRK-560 in the Tg2576 transgenic mouse model of amyloid deposition. Soluble and insoluble Aβ40 and Aβ42 brain concentrations were compiled from multiple naïve, vehicle, and MRK-560-treated animals. The age of Tg2576 mice in the studies ranged between 3.5 and 26 months. Single doses of MRK-560 inhibited soluble Aβ40 levels in animals up to 9 months old. In contrast, MRK-560 did not cause significant acute effects on soluble Aβ40 levels in animals older than 13 months. Absolute levels of Aβ variants increased exponentially over age and reached a plateau at ∼20 months. In the final model, it was assumed that MRK-560 inhibited the Aβ production rate with an Aβ level-dependent IC50.The age-dependent increase in Aβ levels was best described by a logistic model that stimulated the production rate of soluble Aβ. The increase in insoluble Aβ was defined as a function of soluble Aβ by using a scaling factor and a different turnover rate. The turnover half-life for insoluble Aβ was estimated at 30 days, explaining that at least a 4-week treatment in young animals was required to demonstrate a reduction in insoluble Aβ. Taken together, the derived knowledge could be exploited for an improved design of new experiments in Tg2576 mice.

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Section: Methodsmentioning

confidence: 99%