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. 2015 Apr 8;35(6):1741–1746. doi: 10.3892/ijmm.2015.2176

Figure 3.

Figure 3

Effect of hydrogen sulfide (H2S) on histone deacetylase (HDAC) and histone acetyltransferase (HAT) activity. (A) HDAC activity in THP-1 extracts treated with various concentrations of sodium hydrosulfide (NaHS) for 30 min. Trichostatin (TSA; C) was used as a positive control. (B) HDAC activity was measured in the THP-1 cells pre-treated with NaHS for 30 min, followed by a challenge with lipopolysaccharide (LPS) (1 μg/ml) for 4 h. Note the lack of effect of NaHS alone (A), in contrast to the effect of NaHS pre-treatment (B), when applied prior to LPS challenge. (C) HAT activity was measured in THP-1 cells pretreated with NaHS for 30 min, followed by a challenge with LPS (1 μg/ml) for 4 h. *p<0.05 vs. C+, 0.01 and 0.1 mM; #p<0.05 vs. all groups; **p<0.05 vs. 0 mM.

HHS Vulnerability Disclosure