A groundbreaking study by Lancaster University reveals a novel drug, RI-AG03, that targets two key areas of the Tau protein, preventing its buildup and potentially slowing Alzheimer’s disease progression.
Key Findings:
- RI-AG03 prevents Tau protein aggregation in lab and fruit fly models.
- Dual-targeting approach addresses both aggregation-promoting hotspots.
- Peptide-based treatment may reduce side effects.
Study Details:
- International collaboration involving Lancaster, Southampton, Nottingham Trent, Tokyo Metropolitan, and Texas Southwestern universities.
- Published in Alzheimer’s & Dementia: The Journal of the Alzheimer’s Association.
Expert Insights:
“Our research represents an important step toward creating treatments that prevent Alzheimer’s progression.” – Dr. Anthony Aggidis
Tau Protein’s Role in Alzheimer’s:
- Malfunctioning Tau proteins clump, forming neurofibrillary tangles.
- Tangles clog neurons, leading to cognitive decline.
The Dual-Targeting Approach:
- RI-AG03 targets two aggregation hotspots on the Tau protein.
- Current treatments target only one hotspot.
Advantages of Peptide-Based Treatment:
- More targeted approach reduces potential side effects.
- Safer treatment option for neurodegenerative diseases.
Implications:
- Potential breakthrough in Alzheimer’s treatment.
- Further research needed to confirm human efficacy.
Reference:
” Dual-targeting peptide inhibitor of Tau aggregation” (Alzheimer’s & Dementia: The Journal of the Alzheimer’s Association, 2024)
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