2020
DOI: 10.1007/s11033-020-05543-y
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Curcumin protects BV2 cells against lipopolysaccharide-induced injury via adjusting the miR-362-3p/TLR4 axis

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Cited by 11 publications
(5 citation statements)
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“…Investigation of the nitrite inhibitory effect in LPS-induced BV2 microglia and neuroprotective effects in glutamate-induced HT22 hippocampal cells revealed that intermedin B ( 4 ) and curcumin ( 9 ) exhibited the highest NO inhibitory and neuroprotective effects. However, numerous studies have reported the anti-inflammatory and antioxidant effects of curcumin ( 9 ) [ 45 , 46 , 47 , 48 ]. In this regard, intermedin B ( 4 ) was administered to LPS-induced BV2 microglia to investigate its inhibitory effect on the production of PGE2, an inflammatory cytokine.…”
Section: Resultsmentioning
confidence: 99%
“…Investigation of the nitrite inhibitory effect in LPS-induced BV2 microglia and neuroprotective effects in glutamate-induced HT22 hippocampal cells revealed that intermedin B ( 4 ) and curcumin ( 9 ) exhibited the highest NO inhibitory and neuroprotective effects. However, numerous studies have reported the anti-inflammatory and antioxidant effects of curcumin ( 9 ) [ 45 , 46 , 47 , 48 ]. In this regard, intermedin B ( 4 ) was administered to LPS-induced BV2 microglia to investigate its inhibitory effect on the production of PGE2, an inflammatory cytokine.…”
Section: Resultsmentioning
confidence: 99%
“…MiR-215-5p plays a protective role in the inflammatory injury of septic H9c2 by targeting ILF3 and LRRFIP1 [ 30 ]. Curcumin protects BV2 cells from LPS-induced damage by regulating the miR-362-3p/TLR4 axis [ 31 ]. Among the down-regulated genes, down-regulation of miR-122-5p in Huh7 cells suppressed exosome-induced macrophage activation and macrophage-related inflammation [ 32 ].…”
Section: Discussionmentioning
confidence: 99%
“…MiRNAs in this panel have known roles in cancer progression ( Che et al., 2019 ; Hsu et al., 2016 ; Huang et al., 2018 ; Kobayashi et al., 2012 ; Kohram et al., 2018 ; Li et al., 2011 , 2016 ; Ling et al., 2019 ; Lv et al., 2018 ; Mogilyansky and Rigoutsos, 2013 ), inflammation and inflammatory diseases ( Paraskevi et al., 2012 ; Reddycherla et al., 2015 ; Wu et al., 2011 ; Zheng et al., 2015 ), and neurodegeneration ( Basak et al, 2016 ; Denk et al., 2015 ; Jee et al., 2012b ; Khoo et al., 2012 ; Liu et al., 2017 ). These miRNAs have also been shown to target genes that have neuroinflammatory functions and roles in diseases with neuroinflammatory pathophysiology ( Cao et al., 2017 ; Lisha Chang et al., 2020 ; Gao et al., 2019 ; Gayen et al., 2020 ; Hu et al., 2019 ; Jee et al., 2012a ; Jiang et al., 2018 ; Ma et al., 2014 ; Mao et al., 2019 ; Martinez and Peplow, 2017 ; Naqvi et al., 2016 ; Navaderi et al., 2019 ; Peng and Ying, 2014 ; Shi et al., 2018 ; Sinha et al., 2012 ; Sujith et al., 2018 ; Thangaraj et al., 2021 ; Wang et al., 2021 ; Xie et al., 2020 ; Yang et al., 2018 ; Yao et al., 2014 ; Zhao et al., 2017 ; Zhong et al., 2021 ; Zhou et al., 2021 ). Post-hoc miRNA-gene network analyses further solidified the involvement of these nine miRNAs in mitochondrial processes and neuroinflammation (see Tables S6–S8 , Figures S6–S8 ).…”
Section: Discussionmentioning
confidence: 99%