1
Return

Pharmacokinetic Studies of Amyloid-Targeting Bis(styryl)benzene Agents for Alzheimer’s Disease

delete2026-06-22
delete0
PRE
AI
K
Kerui Xu
J
Jennifer A. Salaiza
H
Hammed Adeoye
S
Saumitra Bhowmik
T
Tarek El Sayed
M
Monika Rana
L
Liviu M. Mirica *
DOI:10.1021/acschemneuro.6c00361delete
deleteOriginal
deleteOriginal request for help
deleteShare
deleteSave
Abstract

Abstract

En 中文
The pharmacokinetics (PK) and biodistribution of radiolabeled amyloid-β (Aβ)-targeting probes have been extensively characterized in the context of Alzheimer’s disease (AD), whereas the corresponding nonradiolabeled scaffolds remain largely unexplored in vivo. Herein, we report in vivo PK studies of the widely used amyloid probe methoxy-X04 (MeX04) in transgenic 5xFAD and wild-type (WT) mice. In plasma, MeX04 shows comparable exposure between 5xFAD and WT mice, indicating no major genotype-dependent differences in systemic clearance. In contrast, brain exposure was markedly increased in 5xFAD mice, with higher brain Cmax and AUC parameters and slower washout, consistent with Aβ-dependent sequestration and retention in the AD brain tissue. Notably, fluorescence microscopy revealed that the fluorescence intensity of amyloid plaque-bound MeX04 closely mirrored the total brain concentration, and we employed ex vivo fluorescence intensity quantification to evaluate the PK of a related bis(styryl)benzene compound, LS-4, which is proposed to exhibit increased affinity for soluble Aβ aggregates. We then performed age-dependent ex vivo staining of compound-bound Aβ aggregates in 5xFAD brains, and LS-4 exhibits appreciable amyloid-bound fluorescence intensity in younger 5xFAD mice, consistent with its higher affinity for Aβ oligomers, whereas MeX04 exhibited stronger fluorescence intensity in older mice. Consequently, we propose an efficient approach to track temporal changes in the PK of Aβ-binding compounds by ex vivo evaluation of their amyloid-bound fluorescence intensity, providing a rapid assessment of the general PK trends of newly developed amyloid-binding probes.
Keywords:
Central nervous system
Fluorescence
Nervous system diseases
Peptides and proteins
Rodent models
Alzheimer’s disease (AD)
amyloid-targeting compounds
pharmacokinetics (PK)
noncompartmental analysis (NCA)

Journal

ACS Chemical Neuroscience cover
ACS Chemical Neuroscience
IF:
3.9
Papers:
4.5K
Citations:
1.3W

Organization

U
university of illinois urbana-champaign
Scholars:
2.0K
Papers: 1.1K
Citations: 0
Cited Papers

Cited Papers

Citing Papers

Citing Papers