An In Vivo Pharmacological Screen Identifies Cholinergic Signaling as a Therapeutic Target in Glial-Based Nervous System Disease.
Liqun WangTracy L HagemannAlbee MessingMel B FeanyPublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2016)
Despite the urgent need for better treatments for neurological diseases, drug development for these devastating disorders has been challenging. The effectiveness of traditional large-scale in vitro screens may be limited by the lack of the appropriate molecular, cellular, and structural environment. Using a simple Drosophila model of Alexander disease, we performed a moderate throughput chemical screen of FDA-approved drugs and natural compounds, and found that reducing muscarinic cholinergic signaling ameliorated clinical symptoms and oxidative stress in Alexander disease model flies and mice. Our work demonstrates that small animal models are valuable screening tools for therapeutic compound identification in complex human diseases and that existing drugs can be a valuable resource for drug discovery given their known pharmacological and safety profiles.
Keyphrases
- drug discovery
- oxidative stress
- high throughput
- randomized controlled trial
- endothelial cells
- systematic review
- genome wide
- gene expression
- dna damage
- skeletal muscle
- physical activity
- high intensity
- spinal cord injury
- spinal cord
- single molecule
- insulin resistance
- diabetic rats
- heat stress
- blood brain barrier
- wild type