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. 2019 Nov 18;24(22):4176. doi: 10.3390/molecules24224176

Figure 1.

Figure 1

Figure 1

The cytotoxic effects of CdCl2 on normal kidney epithelial (NKE) cells and the protective effect of carnosic acid (CA) as estimated by cell viability, image, and flow cytometry analyses. (A) Concentration dependent cytotoxic effect of CdCl2. Data were represented as the mean ± SD, n (number of plates) = 3. (B) Effect on the cell viability in the absence (CdCl2) and presence of CA (CdCl2 + CA) on NKE cells. (C) Hoechst staining of NKE cells in the absence (CdCl2) and presence of CA (CdCl2 + CA). Percentage of viable cells is represented by histogram. (D) Flow cytometry analyses of NKE cells the absence (CdCl2) and presence of CA (CdCl2 + CA). Annexin V–fluorescein isothiocyanate (FITC) positive and propidium iodide (PI) negative cells were in the early stage of apoptosis and both annexin V–FITC and PI positive cells were in the end stage of apoptosis. Percentage of apoptotic cells is represented by histogram. Data were represented as the mean ± SD, n (number of plates) = 3. # Values significantly (p < 0.01) differed from the vehicle-treated group. * Values significantly (p < 0.05) differed from only the CdCl2-treated group. ** Values significantly (p < 0.01) differed from only the CdCl2-treated group.