Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy.
Prof. Antonio Imbesi Foundation, Messina, Italy.
Food Funct. 2024 Sep 30;15(19):9941-9953. doi: 10.1039/d4fo02538e.
Consumption of high-fat diets (HFDs) is a contributing factor to obesity, insulin resistance and non-alcoholic fatty liver disease (NAFLD). Several studies suggested the protective role of bioactives present in fruits against the above mentioned chronic metabolic conditions. In this study, we evaluated if a flavonoid-rich extract of (bergamot) juice (BJe) could inhibit HFD-induced intestinal permeability and endotoxemia and, through this mechanism, mitigate the associated hepatic damage in C57BL/6J mice. After 12 weeks of the treatment, HFD consumption caused high body weight (BW) gain, hyperinsulinemia, hyperglycemia, and dyslipidemia, which were mitigated by BJe (50 mg per kg BW) supplementation. Furthermore, supplementation with BJe prevented HFD-induced liver alterations, including increased plasma alanine aminotransferase (ALT) activity, increased hepatic lipid deposition, high NAS, and fibrosis. Mice fed a HFD for 12 weeks showed (i) a decrease in small intestine tight junction protein levels (ZO-1, occludin, and claudin-1), (ii) increased intestinal permeability, and (iii) endotoxemia. All these adverse events were mitigated by BJe supplementation. Linking the capacity of BJe to prevent HFD-associated endotoxemia, supplementation with this extract decreased the HFD-induced overexpression of hepatic TLR-4, downstream signaling pathways (MyD88, NF-κB and MAPK), and the associated inflammation, evidenced by increased MCP-1, TNF-α, IL-6, iNOS, and F4/80 levels. Overall, we suggest that BJe could mitigate the harmful consequences of western style diet consumption on liver physiology by protecting the gastrointestinal tract from permeabilization and associated metabolic endotoxemia.
高脂肪饮食(HFD)的摄入是肥胖、胰岛素抵抗和非酒精性脂肪性肝病(NAFLD)的一个促成因素。几项研究表明,水果中存在的生物活性物质对上述慢性代谢疾病具有保护作用。在这项研究中,我们评估了富含(佛手柑)果汁的类黄酮提取物(BJe)是否可以抑制 HFD 诱导的肠道通透性和内毒素血症,并通过这种机制减轻 C57BL/6J 小鼠相关的肝损伤。在治疗 12 周后,HFD 摄入导致体重(BW)增加、高胰岛素血症、高血糖和血脂异常,BJe(50mg/kg BW)补充可减轻这些症状。此外,BJe 补充可预防 HFD 诱导的肝脏改变,包括增加血浆丙氨酸氨基转移酶(ALT)活性、肝脂质沉积增加、NAS 升高和纤维化。喂养 HFD 12 周的小鼠表现出(i)小肠紧密连接蛋白水平(ZO-1、occludin 和 claudin-1)降低,(ii)肠道通透性增加,(iii)内毒素血症。BJe 补充可减轻所有这些不良事件。BJe 预防 HFD 相关内毒素血症的能力表明,这种提取物的补充可降低 HFD 诱导的肝 TLR-4、下游信号通路(MyD88、NF-κB 和 MAPK)的过度表达,以及相关炎症,这表现为 MCP-1、TNF-α、IL-6、iNOS 和 F4/80 水平增加。总体而言,我们认为 BJe 通过保护胃肠道免受通透性和相关代谢内毒素血症的影响,可减轻西式饮食摄入对肝脏生理的有害影响。