Romero-Márquez Jose M, Navarro-Hortal María D, Jiménez-Trigo Victoria, Vera-Ramírez Laura, Forbes-Hernández Tamara J, Esteban-Muñoz Adelaida, Giampieri Francesca, Bullón Pedro, Battino Maurizio, Sánchez-González Cristina, Quiles José L
Department of Physiology, Institute of Nutrition and Food Technology ''José Mataix Verdú", Biomedical Research Centre, University of Granada, Avda. del Conocimiento s.n, 18100, Armilla, Spain.
Department of Physiology, Institute of Nutrition and Food Technology ''José Mataix Verdú", Biomedical Research Centre, University of Granada, Avda. del Conocimiento s.n, 18100, Armilla, Spain; Department of Genomic Medicine, GENYO: Centre for Genomics and Oncology (Pfizer-University of Granada and Andalusian Regional Government), PTS Granada, 18016, Spain.
Food Chem Toxicol. 2022 Apr;162:112914. doi: 10.1016/j.fct.2022.112914. Epub 2022 Mar 8.
Olive tree-derived products have been associated with numerous benefits for health. The aim of the present study was to characterize an olive leaf extract enriched in oleuropein (OLE) concerning phenolic content and profile as well as antioxidant capacity. Short-term and long-term toxicity, including oxidative stress, was in vivo evaluated in the experimental model Caenorhabditis elegans. Moreover, the potential therapeutic effect of the extract against Aβ induced- and tau protein induced-toxicity was also evaluated in C. elegans. OLE treatment did not exert toxicity. On the contrary, the extract was able to ameliorate oxidative stress and proteotoxicity related to Aβ and tau aggregation. The potential molecular mechanisms present behind the observed results explored by RNAi technology revealed that DAF-16/FOXO and SKN-1/NRF2, elements of the insulin insulin-like signalling pathway, as well as HSP-16.2 overexpression were involved.
橄榄树衍生产品对健康有诸多益处。本研究旨在表征一种富含橄榄苦苷(OLE)的橄榄叶提取物的酚类含量、酚类谱以及抗氧化能力。在秀丽隐杆线虫实验模型中对短期和长期毒性,包括氧化应激进行了体内评估。此外,还在秀丽隐杆线虫中评估了该提取物对Aβ诱导毒性和tau蛋白诱导毒性的潜在治疗作用。OLE处理未产生毒性。相反,该提取物能够改善与Aβ和tau聚集相关的氧化应激和蛋白毒性。通过RNAi技术探索观察结果背后潜在的分子机制表明,胰岛素样信号通路的元件DAF-16/FOXO和SKN-1/NRF2以及HSP-16.2的过表达都参与其中。