ACS Omega· 2026Q1
Passiflora edulis Tohum Ekstraktı ve Piceatannol'ün Hiperglisemi ve Oksidatif Stresi Azaltmadaki Etkinliği
Evaluation of Passiflora edulis Seed Extract and Piceatannol in Attenuating Hyperglycemia and Oxidative Stress Using Human and Nonhuman Antidiabetic Enzymes, Human Neutrophil Oxidative Burst, and Embryonic Zebrafish Hyperglycemia Model
- 0atıf
- Q1SCImago
- 2026yıl
Kısa özet
Passiflora edulis tohum ekstraktı (PESE) ve bileşeni piceatannol (PIC), birden fazla mekanizma aracılığıyla hiperglisemi ve oksidatif stresi önemli ölçüde azaltır; PESE, PIC'den daha düşük embriyotoksisite gösterir.
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Ana noktalar
- Piceatannol (PIC), α-glukosidazı (IC50 = 3.1 μg/mL) ve α-amilazı (IC50 = 11.8 μg/mL) inhibe ederek α-glukosidaza karşı akarbosdan daha üstün performans göstermiştir.
- Passiflora edulis tohum ekstraktı (PESE), PIC tarafından etkilenmeyen PTP1B'yi (IC50 = 29.8 μg/mL) inhibe etmiştir.
- Hem PESE hem de PIC, insan nötrofillerde ROS üretimini azaltmış, PIC yüksek potens göstermiştir (IC50 = 0.12 μg/mL).
- Hiperglisemik zebrafish embriyolarında, hem PESE hem de PIC glukoz ve oksidan aktiviteyi önemli ölçüde azaltmıştır (p ≤ 0.05).
- PESE, PIC'ye kıyasla daha düşük embriyotoksisite (LC50 = 39.3 μg/mL) göstermiştir (LC50 = 6.2 μg/mL).
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
Abstract Passiflora edulis seeds are frequently discarded as agro-industrial residues despite being a source of bioactive compounds such as piceatannol (PIC). Their valorization through ethanolic extraction aligns with circular economy principles and enables the investigation of antioxidant, anti-inflammatory, and antidiabetic potential relevant to metabolic disorders associated with oxidative stress, inflammation, and impaired glucose homeostasis. Therefore, this study compared the biological activities and toxicological profiles of P. edulis seed ethanol extract (PESE) and PIC using in vitro and in vivo assays, including human and nonhuman models, and hyperglycemia induced during embryogenesis. The zebrafish procedures were approved by the Animal Use Ethics Committee (CEUA; protocol No. 13/2022). LC–MS identified PIC among the main constituents of PESE, which exhibited a high total phenolic content and relevant antioxidant capacity. PIC showed greater antioxidant potency than PESE against DPPH•, HOCl, and O2•–. It also inhibited α-amylase and α-glucosidase, with IC50 values of 11.8 and 3.1 μg/mL, respectively, outperforming acarbose against α-glucosidase, and activated glucokinase. In contrast, PESE inhibited PTP1B (IC50 = 29.8 μg/mL), an effect not observed with PIC alone. Both samples reduced ROS production in human neutrophils, with PIC displaying high potency in the luminol assay (IC50 = 0.12 μg/mL). In zebrafish embryos, PESE was less embryotoxic than PIC, with LC50 values of 39.3 and 6.2 μg/mL, respectively. In the hyperglycemic zebrafish model, both samples significantly reduced total free glucose and oxidant activity (p ≤ 0.05) and induced distinct antioxidant gene-expression responses: PESE upregulated nfe2l2a, sod1, sod2, and cat, whereas PIC upregulated nfe2l2a, gpx1a, and cat. These findings demonstrate that PESE and PIC act through multiple complementary mechanisms to counteract hyperglycemia and oxidative stress, highlighting the therapeutic potential of an underutilized byproduct while emphasizing the importance of developmental toxicity assessment for the safe advancement of plant-derived agents.
Yazarların özeti; kaynağından alınmıştır. ACS Omega, 2026 · DOI ↗
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