Chen Jinying, Pu Yuzhi, Pei Heying, He Linhong, Fu Suhong, Chen Lijuan
State Key Laboratory of Biotherapy, West China Hospital, West China Medical, Sichuan University, Chengdu, P. R. China.
Arch Pharm (Weinheim). 2014 Dec;347(12):908-22. doi: 10.1002/ardp.201400227. Epub 2014 Sep 15.
A series of tert-butyl-5-methylpyrimidin-piperazine derivatives were synthesized and their anti-obesity activities were evaluated. Compounds 4g and 5j were found to have significant effects in down-regulating the triglyceride level of 3T3-L1 adipocytes. 5j exhibited remarkable therapeutic effects on the diet-induced obesity (DIO) mouse model at 20 mg kg(-1) day(-1) for 4 weeks by decreasing the weights of body, liver, and fat. 5j also regulated serum biomarkers to appropriate ranges, exerted therapeutic activity of steatosis in liver tissue and ameliorated the obese-related symptoms. In addition, 5j significantly decreased the blood glucose levels in oral glucose tolerance tests and improved the insulin sensitivity in insulin tolerance tests. These results suggest that 5j could be a candidate for obesity treatment.
合成了一系列叔丁基-5-甲基嘧啶-哌嗪衍生物,并评估了它们的抗肥胖活性。发现化合物4g和5j在下调3T3-L1脂肪细胞的甘油三酯水平方面具有显著作用。5j在20 mg kg(-1) 天(-1) 的剂量下对饮食诱导肥胖(DIO)小鼠模型进行为期4周的治疗时,通过降低体重、肝脏重量和脂肪重量表现出显著的治疗效果。5j还将血清生物标志物调节至适当范围,对肝组织中的脂肪变性发挥治疗活性,并改善肥胖相关症状。此外,5j在口服葡萄糖耐量试验中显著降低血糖水平,并在胰岛素耐量试验中提高胰岛素敏感性。这些结果表明5j可能是肥胖治疗的候选药物。