Booth Id:
BMED032I
Category:
Biomedical Engineering
Year:
2015
Finalist Names:
Wu, Jinyu
Abstract:
The purpose of this study was to investigate the anti-amyloid and anti-inflammatory properties of CNI-1493 as a treatment for intracellular amyloid beta toxicity and chronic neuro-inflammation. Three types of studies were performed in this study: a cell free model of amyloid beta aggregates were treated with CNI-1493 to measure the formation of fibrils and oligomers; an in vitro analysis using human neuroblatoma cells and microglia cells to test for the presence of intracellular amyloid beta and effects of CNI-1493 on inflammation; an in vivo analysis using C. elegans strain CL2006, which genetically expresses human amyloid beta in its muscle wall and phenotypically expresses paralysis, to determine the effects of CNI-1493 on ntracellular amyloid beta plaque destruction. Data was analyzed using a student’s t-test where (p<.05). Results show that the drug directly interacts with amyloid beta. CNI-1493 reduced fibril and oligomer formation by 21.5% and 45.83% (p<.02) respectively. In a cell free system CNI-1493 changes the structure of soluble and insoluble amyloid beta aggregates. Additionally, CNI-1493 attenuates intracellular amyloid beta toxicity in vivo in the transgenic C. elegans strain CL2006 where worms treated with CNI-1493 had 50% of the population move over 79.722 units with only 43.64 units for the untreated group (p=.0017). Lastly, CNI-1493 significantly reduced inflammation levels in inflammatory microglia cell. By mitigating inflammation and amyloid beta aggregation, CNI-1493 targets two major pathways of AD. Taken together, CNI-1493 represents a future drug candidate to be repurposed for the treatment of a-beta-mediated inflammatory diseases.