Targeted Medicine Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongwon, Chungbuk 363–883, Korea.
Biol Pharm Bull. 2013;36(7):1167-73. doi: 10.1248/bpb.b13-00152. Epub 2013 Apr 12.
Diacylglycerol acyltransferase 2 (DGAT2) is one of two distinct DGAT enzymes that catalyze the last step in triacylglycerol (TG) synthesis. Findings from previous studies suggest that inhibition of DGAT2 is a promising strategy for the treatment of hepatic steatosis and insulin resistance. Here, we identified compound 122 as a potent and selective inhibitor of human DGAT2, which appeared to act competitively against oleoyl-CoA in vitro. The selective inhibition of DGAT2 was also confirmed by the reductions in enzymatic activity and de novo TG synthesis in DGAT2-overexpressing HEK293 cells and hepatic cells HepG2. Compound 122, as a newly identified inhibitor of DGAT2, will be useful for the research on DGAT2-related lipid metabolism as well as the development of therapeutic drug for several metabolic diseases.
二酰基甘油酰基转移酶 2(DGAT2)是两种截然不同的 DGAT 酶之一,它催化三酰基甘油(TG)合成的最后一步。先前的研究结果表明,抑制 DGAT2 是治疗肝脂肪变性和胰岛素抵抗的一种很有前途的策略。在这里,我们鉴定出化合物 122 是一种有效的、选择性的人 DGAT2 抑制剂,它似乎在体外对油酰基辅酶 A 表现出竞争性抑制作用。DGAT2 的选择性抑制作用也在 DGAT2 过表达的 HEK293 细胞和肝细胞 HepG2 中的酶活性和从头 TG 合成的降低中得到了证实。作为一种新发现的 DGAT2 抑制剂,化合物 122 将有助于研究 DGAT2 相关的脂质代谢,以及开发几种代谢性疾病的治疗药物。