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. 2024 Mar 4;15:1368853. doi: 10.3389/fendo.2024.1368853

Figure 1.

Figure 1

MUFAs/PUFAs improve the cell viability damage induced by SFAs in INS-1E cells. (A) Effects of 24 h treatment of PA (100 μM~800 μM) on the viability of INS-1E cells. (B) Effects of 24 h treatments of SA (100 μM~800 μM) on the viability of INS-1E cells. (C) The cell viability of INS-1E treated with 100 μM PA at different time points. (D) The cell viability of INS-1E treated with 100 μM SA at different time points. (E) Effects of 24 h treatment of OA (100 μM~800 μM) on the viability of INS-1E cells. (F) Effects of 24 h treatment of EPA (6 μM~50 μM) on the viability of INS-1E cells. (G) Effects of 24 h treatment of DHA (6 μM~50 μM) on the viability of INS-1E cells. (H) Effects of 24 h treatment of AA (1.5 μM~25 μM) on the viability of INS-1E cells. (I) Effects of 200 μM OA, 25 μM EPA, DHA, and AA combined with 200 μM PA respectively, on the viability of INS-1E cells. ## P<0.01, ### P<0.001, #### P<0.0001 vs. Control/Vehicle group. **** P <0.0001 vs. PA group. Data are expressed as mean ± SD, (n≥3).