Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute (CSIR-CDRI), Lucknow 226 001, India.
J Med Chem. 2012 Mar 22;55(6):2769-79. doi: 10.1021/jm201697v. Epub 2012 Mar 2.
Hypolipidemic and antiobesity effects of the newly synthesized indole-based fibrates were evaluated in Triton WR-1339 and high fat diet (HFD)-induced hyperlipidemic rats. Preliminary screening of all the synthesized compounds was done by using an acute model (Triton model), in which compounds 3f and 3l showed significant antidyslipidemic activity. Furthermore, these compounds 3f and 3l were found to induce significant weight loss in the visceral fat mass of HFD-fed hyperlipidemic rats without affecting the normal feeding behavior. Histological examination of the liver of rats supplemented with 3f and 3l revealed a significant decrease in steatosis when compared to the effect of the standard drug fenofibrate. Additional effects such as an increase in lecithin cholesterol acyl-transferase (LCAT) enzyme level and increased receptor mediated catabolism of I(131)-low density lipoproteins (LDL) confirm and reinforce the efficacy of both of these compounds as a new class of dual-acting hypolipidemic and antiobesity agents.
我们评估了新合成的基于吲哚的纤维酸酯类降脂和抗肥胖作用在 Triton WR-1339 和高脂饮食(HFD)诱导的高血脂大鼠中的效果。所有合成化合物的初步筛选都是通过使用急性模型(Triton 模型)进行的,其中化合物 3f 和 3l 显示出显著的抗血脂异常活性。此外,这些化合物 3f 和 3l 被发现可在不影响正常进食行为的情况下,诱导 HFD 喂养的高血脂大鼠内脏脂肪质量的显著体重减轻。与标准药物非诺贝特的效果相比,补充 3f 和 3l 的大鼠肝脏组织学检查显示脂肪变性显著减少。其他作用,如卵磷脂胆固醇酰基转移酶(LCAT)酶水平的增加和受体介导的 I(131)-低密度脂蛋白(LDL)的代谢增加,证实并加强了这两种化合物作为新型双重作用降脂和抗肥胖剂的功效。