“…These types of anti‐inflammatory drugs exert their pharmacological effect at the genomic level, either through binding to glucocorticoid recognition elements (GRE) in DNA, inducing the transcription and translation of anti‐inflammatory proteins (Charmandari, 2012) or by suppressing the expression of pro‐inflammatory genes, by inhibiting transcription factors, such as NF‐κB (Biddie et al, 2012), thus avoiding the synthesis of pro‐inflammatory mediators, such as TNF‐α, as well as the expression of COX‐2, with the subsequent inhibition of the synthesis of PGE 2 (Muñoz‐Carrillo et al, 2017a). Various studies have shown that glucocorticoids are effective for the treatment of pulp inflammation (Gallinari et al, 2019), as well as for the reduction of the periapical inflammatory response after endodontic treatment (Holland, 1996; Marshall, 2002). The results agree with that reported in the literature since, in the present study, treatment with dexamethasone significantly decreased (* p < .05) the levels of PGE 2 and TNF‐α at the systemic level, both at 14 and 18 hours, after pulp damage.…”