
To investigate the effects of N‐acetyl cysteine (NAC), Biodentine, ProRoot MTA, and their combinations, on cell viability, mitochondrial reactive oxygen species (mtROS) production, mineralization, and on the expression of genes related to inflammatory cytokine production, mitochondrial dynamics and cell apoptosis of lipopolysaccharide (LPS)‐induced human dental pulp cells (hDPCs).
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