Attenuation of ROS/Chloride Efflux-Mediated NLRP3 Inflammasome Activation Contributes to Alleviation of Diabetic Cardiomyopathy in Rats after Sleeve Gastrectomy

Figure 6

Chloride intracellular channel-dependent chloride efflux induced pyroptosis mediated by NLRP3 inflammasomes in H9c2 cells. (a) Protein expression of CLIC1 and CLIC4 in heart tissues. (b) Relative mRNA expression of Clic1 and Clic4 in hearts. (c) IAA-94 was used to block chloride efflux, and the intracellular chloride was measured with MQAE, a chloride-sensitive dye. (d) Chloride concentrations in supernatants. (e) The LDH release measured by a colorimetric assay. (f) Caspase-1 activity. (g) E42 staining indicated the membrane integrity. (h) TUNEL staining of H9c2 cells. (i) Protein levels of NLRP3-related molecules. (j) The ratio of caspase-1 p12/procaspase-1 and (k) the ratio of phospho-NF-κB/total NF-κB. (l) Relative mRNA expression of Nlrp3-related molecules in H9c2 cells, Tubb3 as the internal reference. Data are presented as . CON vs. HG; ^## HG+IAA-94 vs. HG. in each group.

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