Journal
ACS CHEMICAL NEUROSCIENCE
Volume 9, Issue 12, Pages 2880-2885Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acschemneuro.8b00203
Keywords
Alzheimer's disease; ASS234; neuroinflammation; multitarget small compounds; gene expression; signaling pathways
Funding
- MINECO [SAF2012-33304, SAF2015-6.5586-R]
- Camilo Jose Cela University
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There is clear evidence that neuroinflammation plays a crucial role in the pathogenesis of Alzheimer's disease. Consequently, modulating the inflammatory environment in brain has become a powerful and attractive strategy to deal with Alzheimer's disease physiopathology. In spite of the neuroprotective capacity shown by ASS234, a multitarget propargylamine targeted for Alzheimer's disease, its regulation of inflammation in the brain still remains unexplored. Therefore, we aimed to characterize possible anti-inflammatory effects of ASS234, counteracting induced inflammatory effects in RAW 264.7 cells and evaluating seven neuroinflammation related genes expression profiling (IL-6, IL-10, ILI beta NF-kappa B, TNF-alpha, TNFR1, and TGF-beta), after ASS234 (5 mu M) treatment in SH-SYSY cells. The analysis of the obtained fold changes lead us to conclude that ASS234 may play an important role facing the neuroinflammatory environment in Alzheimer's disease pathology.
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