Sundaresan Arjunan, Radhiga Thangaiyan, Pugalendi Kodukkur Viswanathan
Faculty of Science, Department of Biochemistry and Biotechnology, Annamalai University, Annamalainagar 608002, Tamilnadu, India.
Faculty of Science, Department of Biochemistry and Biotechnology, Annamalai University, Annamalainagar 608002, Tamilnadu, India.
Eur J Pharmacol. 2014 Oct 15;741:297-303. doi: 10.1016/j.ejphar.2014.07.032. Epub 2014 Aug 19.
This study investigated the combined effect of ursolic acid (UA) and Rosiglitazone (RSG) on lipid regulatory genes in high fat diet (HFD)-fed mice. Male C57BL/6J mice were fed either normal diet or HFD for 10 weeks, after which animals in each dietary group were divided into following six groups, (normal diet, normal diet plus UA and RSG, HFD alone, HFD plus UA, HFD plus RSG, and HFD plus UA and RSG), for the next 5 weeks. UA (5mg/kg BW) and RSG (4mg/kg BW) were administered as suspensions directly into the stomach using a gastric tube. At the end of the study (106th day), their liver was analyzed for lipid content. RT-PCR and western blotting methods were used to analyze lipid regulatory genes. HFD-fed mice showed increased activities of hepatic marker enzymes (aspartate aminotransferase and alanine aminotransferase) in plasma and an increased concentration of total cholesterol, triglyceride and free fatty acid in liver. These results were confirmed by upregulated mRNA expression of lipogenic genes such as sterol-regulatory-element-binding protein-1c, fatty acid synthase and acetyl-CoA carboxylase and downregulated mRNA expression of fatty acid oxidative genes such as carnitine palmitoyltransferase-1, acetyl-CoA carboxylase and peroxisome proliferator activated receptor-α in HFD-fed mice. Combined treatment (UA/RSG) significantly reduced the hepatic marker enzyme activities and decreased the lipid accumulation in liver. Furthermore, combination treatment (UA/RSG) down-regulated lipogenic genes and upregulated fatty acid oxidative genes in HFD-fed mice. This study suggests that UA in combination with RSG reduced lipid accumulation in liver.
本研究调查了熊果酸(UA)和罗格列酮(RSG)对高脂饮食(HFD)喂养小鼠脂质调节基因的联合作用。雄性C57BL/6J小鼠分别给予正常饮食或高脂饮食10周,之后将每个饮食组的动物分为以下六组(正常饮食、正常饮食加UA和RSG、单纯高脂饮食、高脂饮食加UA、高脂饮食加RSG、高脂饮食加UA和RSG),持续5周。UA(5mg/kg体重)和RSG(4mg/kg体重)以悬浮液形式通过胃管直接灌入胃中。在研究结束时(第106天),分析它们肝脏中的脂质含量。采用逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法分析脂质调节基因。高脂饮食喂养的小鼠血浆中肝标志物酶(天冬氨酸转氨酶和丙氨酸转氨酶)活性增加,肝脏中总胆固醇、甘油三酯和游离脂肪酸浓度升高。这些结果通过高脂饮食喂养小鼠中脂质生成基因如固醇调节元件结合蛋白-1c、脂肪酸合酶和乙酰辅酶A羧化酶的mRNA表达上调以及脂肪酸氧化基因如肉碱棕榈酰转移酶-1、乙酰辅酶A羧化酶和过氧化物酶体增殖物激活受体-α的mRNA表达下调得到证实。联合治疗(UA/RSG)显著降低了肝标志物酶活性,并减少了肝脏中的脂质积累。此外,联合治疗(UA/RSG)下调了高脂饮食喂养小鼠中的脂质生成基因,并上调了脂肪酸氧化基因。本研究表明,UA与RSG联合使用可减少肝脏中的脂质积累。