Fluorescent 1,4-Naphthoquinones To Visualize Diffuse and Dense-Core Amyloid Plaques in APP/PS1 Transgenic Mouse Brains.
Naewoo Neo ShinHanna JeonYoungeun JungSeungyeop BaekSejin LeeHee Chan YooGi Hun BaeKeunwan ParkSeung-Hoon YangJung Min HanIkyon KimYoung Soo KimPublished in: ACS chemical neuroscience (2019)
Recent clinical approvals of brain imaging radiotracers targeting amyloid-β provided clinicians the tools to detect and confirm Alzheimer's disease pathology without autopsy or biopsy. While current imaging agents are effective in postsymptomatic Alzheimer's patients, there is much room for improvement in earlier diagnosis, hence prompting a need for new and improved amyloid imaging agents. Here we synthesized 41 novel 1,4-naphthoquinone derivatives and initially discovered 14 antiamyloidogenic compounds via in vitro amyloid-β aggregation assay; however, qualitative analyses of these compounds produced conflicting results and required further investigation. Follow-up docking and biophysical studies revealed that four of these compounds penetrate the blood-brain barrier, directly bind to amyloid-β aggregates, and enhance fluorescence properties upon interaction. These compounds specifically stain both diffuse and dense-core amyloid-β plaques in brain sections of APP/PS1 double transgenic Alzheimer's mouse models. Our findings suggest 1,4-naphthoquinones as a new scaffold for amyloid-β imaging agents for early stage Alzheimer's.
Keyphrases
- high grade
- low grade
- high resolution
- early stage
- cognitive decline
- systematic review
- end stage renal disease
- newly diagnosed
- white matter
- molecular dynamics
- ejection fraction
- drug delivery
- chronic kidney disease
- squamous cell carcinoma
- high throughput
- lymph node
- peritoneal dialysis
- sentinel lymph node
- patient reported outcomes
- single cell
- energy transfer
- cancer therapy
- fine needle aspiration