Curcumin was demonstrated to be an active ingredient with anti-inflammatory effects. This research was to investigate the effects of curcumin. We found that curcumin promoted cell viability and suppressed cell apoptosis. Meanwhile, curcumin decreased the level of cleaved caspase-3 and the release of TNF-α, IL-1β, IL-6, but increased IL-10 release in LPS-treated BV2 cells. miR-362-3p expression was upregulated by curcumin, while TLR4 expression was downregulated. Besides, we observed that the cytoprotective effects of curcumin were lost when miR-362-3p was silenced. TLR4 was a direct target gene of miR-362-3p. Moreover, miR-362-3p deletion attenuated the cytoprotective effects of curcumin by regulating TLR4 expression in LPS-induced BV2 cells. Furthermore, curcumin suppressed p-p65 expression via regulating miR-362-3p/TLR4 axis. We discovered that curcumin exhibited protective effects against LPS-triggered cell injury via modulating miR-362-3p/TLR4 axis through NF-κB pathway.
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This study was supported by the Fundamental Research Funds for the Central Universities (Grant No. 2042017kf0139), Innovative Seed Funds of Medical College of Wuhan University (Grant No. TFZZ2018027), Natural Science Foundation of Hubei Province (Grant No. 2019CFB457) and Wuhan Medical Research Project (Youth Project) (Grant No. WZ19Q02).
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Xie, P., Deng, M., Sun, Q. et al. Curcumin protects BV2 cells against lipopolysaccharide-induced injury via adjusting the miR-362-3p/TLR4 axis. Mol Biol Rep 47, 4199–4208 (2020). https://doi.org/10.1007/s11033-020-05543-y
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