Reda Doha, Elshopakey Gehad E, Mahgoub Hebatallah A, Risha Engy F, Khan Anmar A, Rajab Bodour S, El-Boshy Mohamed E, Abdelhamid Fatma M
Department of Clinical Pathology, Faculty of Veterinary Medicine, Mansoura University, Mansoura 35516, Egypt.
Department of Pathology, Faculty of Veterinary Medicine, Mansoura University, Mansoura 35516, Egypt.
Evid Based Complement Alternat Med. 2022 Aug 11;2022:3362005. doi: 10.1155/2022/3362005. eCollection 2022.
Metabolic syndrome (MS) is a serious health problem associated with an increase in risk factors for hepatic steatosis, which is the most common liver disease today. The goal of this study was to investigate the protective effects of resveratrol against metabolic alterations associated with a high-fat high-fructose diet (HFFD). Thirty-two male rats were randomly divided into four equal groups: control (cont.), metabolic syndrome (MS), resveratrol (Res), and metabolic syndrome treated with resveratrol (MS + Res). Resveratrol was administrated orally at a dose of 30 mg/kg·bw, daily. After 10 weeks, body weight, serum biochemical parameters, hepatic oxidative stress, inflammatory markers, as well as mRNA levels of hepatic genes related to lipid metabolism and insulin signaling were measured. In addition, the liver was examined histopathologically to detect lipid deposition. Increased body weight, hepatic dysfunction, dyslipidemia, hepatic insulin resistance, hepatic oxidative and inflammatory stress conditions, upregulation of mRNA expression level of sterol regulatory element binding protein 1-c (SREBP1-c), and downregulation of mRNA expression levels of peroxisome proliferated activated receptor alpha (PPAR) and insulin receptor substrate-2 (IR-S2) were all observed in the MS rats. Hepatic steatosis was confirmed by hematoxylin and eosin and Oil Red O staining. Administration of resveratrol reduced liver steatosis, oxidative stress, and inflammatory state. Also, it improved lipid profile as well as insulin sensitivity and reverted alterations in hepatic mRNA expression levels of the tested genes. Based on these findings, resveratrol could be proposed as a therapeutic approach for MS prevention.
代谢综合征(MS)是一个严重的健康问题,与肝脂肪变性风险因素增加相关,肝脂肪变性是当今最常见的肝脏疾病。本研究的目的是探讨白藜芦醇对与高脂高果糖饮食(HFFD)相关的代谢改变的保护作用。32只雄性大鼠被随机分为四组,每组数量相等:对照组(cont.)、代谢综合征组(MS)、白藜芦醇组(Res)和白藜芦醇治疗的代谢综合征组(MS + Res)。白藜芦醇以30 mg/kg·bw的剂量每日口服给药。10周后,测量体重、血清生化参数、肝脏氧化应激、炎症标志物以及与脂质代谢和胰岛素信号相关的肝脏基因的mRNA水平。此外,对肝脏进行组织病理学检查以检测脂质沉积。在MS大鼠中观察到体重增加、肝功能障碍、血脂异常、肝脏胰岛素抵抗、肝脏氧化和炎症应激状态、固醇调节元件结合蛋白1-c(SREBP1-c)的mRNA表达水平上调以及过氧化物酶体增殖物激活受体α(PPAR)和胰岛素受体底物-2(IR-S2)的mRNA表达水平下调。苏木精和伊红染色以及油红O染色证实了肝脂肪变性。白藜芦醇给药减轻了肝脏脂肪变性、氧化应激和炎症状态。此外,它改善了血脂谱以及胰岛素敏感性,并逆转了受试基因肝脏mRNA表达水平的改变。基于这些发现,白藜芦醇可被提议作为预防MS的一种治疗方法。