Department of Pharmacology and Toxicology, Faculty of Pharmacy, Minia University, El-Minia 61111, Egypt.
Ministry of Health and Population, Undersecretary preventive sector, General administration viral hepatitis, Cairo, Egypt.
Can J Physiol Pharmacol. 2020 Aug;98(8):498-505. doi: 10.1139/cjpp-2019-0487. Epub 2020 Feb 21.
Nonalcoholic fatty liver disease (NAFLD) is an excessive accumulation of fats in the liver resulting in hepatic inflammation and fibrous tissue formation along with insulin resistance. This study was designed to investigate the possible protective effects of metformin alone and in combination with different phosphodiesterase inhibitors (PDEIs). Rats were fed a high-fat diet (HFD) for 16 weeks to induce NAFLD. Starting from week 12, rats received metformin alone or in combination with pentoxifylline, cilostazol, or sildenafil. HFD administration resulted in hepatic steatosis and inflammation in rats. In addition, liver index, body composition index, activities of liver enzymes, and serum lipids deviated from normal. Further, significant elevations were recorded compared to control in terms of serum glucose, insulin, and HOMA-IR (homeostasis model assessment index for insulin resistance), oxidative stress parameters, hepatic TNF-α and NF-κB gene expression, and iNOS protein expression. Rats treated with metformin showed a significant improvement in the aforementioned parameters. However, the addition of pentoxifylline to metformin treatment synergized its action and produced a fortified effect against HFD-induced NAFLD better than other PDEIs. Data from this study indicated that combined treatment of metformin and pentoxifylline had the most remarkable ameliorated effects against HFD-induced NAFLD; further clinical investigations are needed to approve PDEIs for NAFLD treatment.
非酒精性脂肪性肝病(NAFLD)是肝脏中脂肪的过度积累,导致肝炎症和纤维组织形成,同时伴有胰岛素抵抗。本研究旨在探讨单独使用二甲双胍以及与不同磷酸二酯酶抑制剂(PDEIs)联合使用的可能保护作用。大鼠喂食高脂肪饮食(HFD)16 周以诱导 NAFLD。从第 12 周开始,大鼠单独或联合使用己酮可可碱、西洛他唑或西地那非接受治疗。HFD 给药导致大鼠肝脂肪变性和炎症。此外,肝指数、身体成分指数、肝酶活性和血清脂质偏离正常。与对照组相比,血清葡萄糖、胰岛素和 HOMA-IR(胰岛素抵抗的稳态模型评估指数)、氧化应激参数、肝 TNF-α 和 NF-κB 基因表达以及 iNOS 蛋白表达均显著升高。用二甲双胍治疗的大鼠上述参数有显著改善。然而,将己酮可可碱加入二甲双胍治疗中会产生协同作用,并产生比其他 PDEIs 更强的强化作用,以对抗 HFD 诱导的 NAFLD。本研究数据表明,二甲双胍和己酮可可碱联合治疗对 HFD 诱导的 NAFLD 具有最显著的改善作用;需要进一步的临床研究来批准 PDEIs 用于治疗 NAFLD。