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. 2022 May 6;15:847440. doi: 10.3389/fnmol.2022.847440

Table 3.

Selected noncoding RNAs involving NLRP3 inflammasome in cerebral I/R injury.

ncRNA TUG1 NEAT1 MiR-139 MiR-668
Target miR-200a-3p miR-22-3p c-Jun Mitochondrial function
Expression Upregulation Upregulation Downregulation Upregulation
Species Adult C57BL/6 mice Male Sprague–Dawley rats Human neuroblastoma cells and mouse microglia cells Male Sprague-Dawley rats
Model MCAO MCAO OGD/R MCAO
Treatment Knockdown of TET2 Gastrodin MiR-139 mimics MiR-668 inhibitor
Pathway TUG1/miR-200a-3p/NLRP3 NEAT1/miR-22-3p Axis c-Jun/NLRP3 inflammasome MiR-668/NLRP3
Therapeutic effect Attenuate I/R-induced inflammatory response and brain injuries Improve the neurological scores of rats, reduce the area of cerebral infarction, and inhibit pyroptosis Inhibit NLRP3 inflammasome-mediated pyroptosis and inflammatory response Modulate mitochondrial function and regulate NLRP3 signaling
Yin et al., 2021 Zhang et al., 2021 Wang Q.-S et al., 2020 He and Zhang, 2020
References