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Amyloid tracers binding sites in autosomal dominant and sporadic Alzheimer's disease




TekijätNi Ruiqing, Gillberg Per-Göran, Bogdanovic Nenad, Viitanen Matti, Myllykangas Liisa, Nennesmo Inger, Långström Bengt, Nordberg Agneta

KustantajaElsevier

Julkaisuvuosi2016

JournalAlzheimer's and Dementia

Vuosikerta13

Numero4

Sivujen määrä12

ISSN1552-5260

eISSN1552-5279

DOIhttps://doi.org/10.1016/j.jalz.2016.08.006


Tiivistelmä
Introduction

Amyloid imaging has been integrated into diagnostic criteria for Alzheimer's disease (AD). How amyloid tracers binding differ for different tracer structures and amyloid-β aggregates in autosomal dominant AD (ADAD) and sporadic AD is unclear.

Methods

Binding properties of different amyloid tracers were examined in brain homogenates from six ADAD with APPswe, PS1 M146V, and PS1 EΔ9 mutations, 13 sporadic AD, and 14 control cases.

Results

3H-PIB, 3H-florbetaben, 3H-AZD2184, and BTA-1 shared a high- and a varying low-affinity binding site in the frontal cortex of sporadic AD. AZD2184 detected another binding site (affinity 33 nM) in the frontal cortex of ADAD. The 3H-AZD2184 and 3H-PIB binding were significantly higher in the striatum of ADAD compared to sporadic AD and control. Polyphenol resveratrol showed strongest inhibition on 3H-AZD84 binding followed by 3H-florbetaben and minimal on 3H-PIB.

Discussion

This study implies amyloid tracers of different structures detect different sites on amyloid-β fibrils or conformations.



Last updated on 2024-26-11 at 22:04