Vieira Taynara Aparecida, Seloto Danielle Gabriel, Rizzi Joyce Santana, Peixoto Paloma Vitória Lima, Corrêa Giulia Vitória Betoni, Siqueira Juliana Silva, Grandini Nubia Alves, Nakandakare-Maia Erika Tiemi, Valente Letícia Cardoso, Francisqueti-Ferron Fabiane Valentini, Ferron Artur Junio Togneri, Baron Giovanna, Aldini Giancarlo, Correa Camila Renata, Pereira Lilian Cristina, Romualdo Guilherme Ribeiro
Medical School, São Paulo State University (UNESP), Botucatu 18618-687, Brazil.
Integrated Colleges of Bauru (FIB), Bauru 17056-100, Brazil.
Antioxidants (Basel). 2025 Apr 30;14(5):543. doi: 10.3390/antiox14050543.
Oxidative stress is involved in pathophysiological mechanisms associated with a myriad of liver diseases. Bergamot () leaves yield a high level of antioxidant polyphenolic compounds that may hinder the development of liver diseases, while their potential is yet to be fully explored. Thus, the aim of the study was to test the effects of bergamot leaf extract (BLE) on hepatic and mitochondrial oxidative stress in different models. In vivo study: Wistar rats were distributed into two groups: control diet (C) and high-sugar-fat diet (HSF) for twenty weeks. Afterward, the animals were redivided to initiate a ten-week treatment with BLE: C, HSF, and HSF+BLE. In vitro study: Rat hepatic mitochondria were isolated by differential centrifugation and used to assess safety and efficacy of the BLE. Hepatocyte monolayer and spheroids were applied to evaluate the safety of physiologically plausible BLE concentrations and their effects on hydrogen peroxide-induced cytotoxicity. The results showed that BLE improved metabolic parameters, reduced hepatic triglyceride levels, malondialdehyde, and increased catalase activity in vivo. In vitro, BLE decreased lipid peroxidation and increased the ratio of reduced and oxidized glutathione in chemically challenged mitochondria. BLE did not exert cytotoxicity in the hepatocyte monolayer and spheroids, while attenuated oxidative stress-induced cytotoxicity. Data indicate that in vivo and in vitro hepatic oxidative stress is modulated by BLE, reinforcing that BLE may act as an agent against chronic liver diseases.
氧化应激参与了与多种肝脏疾病相关的病理生理机制。佛手柑叶富含高水平的抗氧化多酚类化合物,可能会阻碍肝脏疾病的发展,但其潜力尚未得到充分探索。因此,本研究的目的是在不同模型中测试佛手柑叶提取物(BLE)对肝脏和线粒体氧化应激的影响。体内研究:将Wistar大鼠分为两组:对照组饮食(C)和高糖高脂饮食(HSF),持续20周。之后,将动物重新分组,开始用BLE进行为期10周的治疗:C组、HSF组和HSF+BLE组。体外研究:通过差速离心法分离大鼠肝脏线粒体,用于评估BLE的安全性和有效性。应用肝细胞单层和球体来评估生理上合理的BLE浓度的安全性及其对过氧化氢诱导的细胞毒性的影响。结果表明,BLE改善了体内代谢参数,降低了肝脏甘油三酯水平、丙二醛,并提高了过氧化氢酶活性。在体外,BLE降低了化学刺激线粒体中的脂质过氧化,并增加了还原型谷胱甘肽与氧化型谷胱甘肽的比例。BLE在肝细胞单层和球体中未表现出细胞毒性,同时减轻了氧化应激诱导的细胞毒性。数据表明,体内和体外肝脏氧化应激均受到BLE的调节,这进一步证明BLE可能作为一种抗慢性肝病的药物发挥作用。