Evaluation of Copper Chelation Therapy in a Transgenic Rat Model of Cerebral Amyloid Angiopathy.
Ashwin AmbiAleksandra StanisavljevicTiffany W VictorAdam W LoweryJudianne DavisWilliam E Van NostrandLisa M MillerPublished in: ACS chemical neuroscience (2023)
Cerebral amyloid angiopathy (CAA) is characterized by the accumulation of the amyloid β (Aβ) protein in blood vessels and leads to hemorrhages, strokes, and dementia in elderly individuals. Recent reports have shown elevated copper levels colocalized with vascular amyloid in human CAA and Alzheimer's disease patients, which have been suggested to contribute to cytotoxicity through the formation of reactive oxygen species. Here, we treated a transgenic rat model of CAA (rTg-DI) with the copper-specific chelator, tetrathiomolybdate (TTM), via intraperitoneal (IP) administration for 6 months to determine if it could lower copper content in vascular amyloid deposits and modify CAA pathology. Results showed that TTM treatment led to elevated Aβ load in the hippocampus of the rTg-DI rats and increased microbleeds in the wild type (WT) animals. X-ray fluorescence microscopy was performed to image the distribution of copper and revealed a surprising increase in copper colocalized with Aβ aggregates in TTM-treated rTg-DI rats. Unexpectedly, we also found an increase in the copper content in unaffected vessels of both rTg-DI and WT animals. These results show that IP administration of TTM was ineffective in removing copper from vascular Aβ aggregates in vivo and increased the development of disease pathology in CAA.
Keyphrases
- oxide nanoparticles
- reactive oxygen species
- end stage renal disease
- high resolution
- newly diagnosed
- biofilm formation
- endothelial cells
- escherichia coli
- machine learning
- chronic kidney disease
- wild type
- single molecule
- computed tomography
- stem cells
- mild cognitive impairment
- cognitive decline
- peritoneal dialysis
- cystic fibrosis
- pseudomonas aeruginosa
- combination therapy
- amino acid
- staphylococcus aureus
- induced pluripotent stem cells
- cell therapy
- electronic health record