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Effects of aspartame on migration, <t>endothelial</t> function, apoptosis, and caspase-3 expression in corpus <t>cavernosum</t> endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.
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Effects of aspartame on migration, <t>endothelial</t> function, apoptosis, and caspase-3 expression in corpus <t>cavernosum</t> endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.
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Effects of aspartame on migration, <t>endothelial</t> function, apoptosis, and caspase-3 expression in corpus <t>cavernosum</t> endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.
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Effects of aspartame on migration, <t>endothelial</t> function, apoptosis, and caspase-3 expression in corpus <t>cavernosum</t> endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.
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Effects of aspartame on migration, <t>endothelial</t> function, apoptosis, and caspase-3 expression in corpus <t>cavernosum</t> endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.
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Effects of aspartame on migration, <t>endothelial</t> function, apoptosis, and caspase-3 expression in corpus <t>cavernosum</t> endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.
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Effects of aspartame on migration, endothelial function, apoptosis, and caspase-3 expression in corpus cavernosum endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.

Journal: Frontiers in Nutrition

Article Title: Aspartame may promote erectile dysfunction via DPP4-mediated endothelial dysfunction and apoptosis: evidence from network toxicology, molecular dynamics simulation, and experimental validation

doi: 10.3389/fnut.2026.1841453

Figure Lengend Snippet: Effects of aspartame on migration, endothelial function, apoptosis, and caspase-3 expression in corpus cavernosum endothelial cells. (A) RT-qPCR analysis of DPP4 mRNA expression in CCECs treated with different concentrations of aspartame. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (B) Representative images of the wound healing assay in the NC, HG, Aspartame, and Aspartame + Saxagliptin groups at 0 h and 48 h. (C) Representative western blot bands of DPP4, p-eNOS, eNOS, Bcl-2, Bax, and β-actin in each group. (D) Quantitative analysis of DPP4, Bax, Bcl-2, p-eNOS, eNOS and p-eNOS/eNOS protein expression. Data are presented as mean ± SD. ns, Not significant; * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. (E) Flow cytometric analysis of apoptosis in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups using Annexin V-FITC/PI staining. (F) Flow cytometric analysis of caspase-3 expression in CCECs from the NC, HG, Aspartame, and Aspartame + Saxagliptin groups.

Article Snippet: Penile corpus cavernosum endothelial cells (CCECs; catalog no. CP-R133) were purchased from Procell (China).

Techniques: Migration, Expressing, Quantitative RT-PCR, Wound Healing Assay, Western Blot, Staining