Yasmin Tahmina, Menon Sreelakshmi N, Pandey Ajay, Siddiqua Shahnaz, Kuddus Syed Abdul, Rahman Md Mizanur, Khan Ferdous, Hoque Nazia, Rana Md Sohel, Subhan Nusrat, Habibi Emran, Ramezani Fatemeh, Sarker Satyajit D, Nahar Lutfun, Alam Md Ashraful, Hasan Raquibul
Department of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Department of Pharmacy, Jahangirnagar University, Dhaka, Bangladesh.
Sci Rep. 2025 Jul 11;15(1):25162. doi: 10.1038/s41598-025-08450-z.
This study evaluated the protective effects of resveratrol against high-fat diet (HFD)-induced hepatic dysfunction and intestinal mucus layer depletion with a focus on antioxidant and anti-inflammatory mechanisms. HFD-fed rats were treated with resveratrol for 8 weeks, and various metabolic, molecular, and histological parameters were assessed. Resveratrol therapy significantly reduced body weight gain and adiposity, lowered plasma and hepatic oxidative stress markers, and restored endogenous antioxidant enzyme activity. Liver function markers including ALT, AST, and ALP were normalized in treated animals. RT-PCR analysis showed enhanced expression of lipid-metabolizing and antioxidant genes including PPARα, CPT-1, Nrf2, and HO-1. Histological analysis revealed that resveratrol attenuated hepatic steatosis, collagen deposition, and fibrosis. Importantly, it preserved the goblet cell population within both intestinal crypts and villi, thereby maintaining the integrity of the gut-mucus barrier. These findings demonstrate that resveratrol exerts a multi-organ protective effect by simultaneously preserving intestinal mucus, improving hepatic antioxidant defenses, and reducing fibrosis. This study highlights a novel gut-liver axis mechanism for resveratrol action that extends beyond its well-known anti-obesity and mitochondrial benefits.
本研究评估了白藜芦醇对高脂饮食(HFD)诱导的肝功能障碍和肠道黏液层消耗的保护作用,重点关注抗氧化和抗炎机制。给喂食HFD的大鼠用白藜芦醇治疗8周,并评估各种代谢、分子和组织学参数。白藜芦醇治疗显著降低了体重增加和肥胖程度,降低了血浆和肝脏氧化应激标志物,并恢复了内源性抗氧化酶活性。治疗动物的肝功能标志物包括谷丙转氨酶(ALT)、谷草转氨酶(AST)和碱性磷酸酶(ALP)恢复正常。逆转录聚合酶链反应(RT-PCR)分析显示,脂质代谢和抗氧化基因包括过氧化物酶体增殖物激活受体α(PPARα)、肉碱棕榈酰转移酶-1(CPT-1)、核因子E2相关因子2(Nrf2)和血红素加氧酶-1(HO-1)的表达增强。组织学分析表明,白藜芦醇减轻了肝脏脂肪变性、胶原沉积和纤维化。重要的是,它保留了肠道隐窝和绒毛内的杯状细胞数量,从而维持了肠道黏液屏障的完整性。这些发现表明,白藜芦醇通过同时保护肠道黏液、改善肝脏抗氧化防御和减少纤维化发挥多器官保护作用。本研究突出了白藜芦醇作用的一种新的肠-肝轴机制,该机制超出了其众所周知的抗肥胖和线粒体益处。