Lund University, Lund, Sweden.
Hepatol Res. 2013 Feb;43(2):131-8. doi: 10.1111/j.1872-034X.2012.01085.x. Epub 2012 Sep 20.
The role of cannabinoids in fatty liver disease has been increasingly acknowledged in recent years, and it has been suggested that drugs targeting peripheral cannabinoid receptors could have therapeutic use. Development of such drugs would require a good understanding of the mechanisms of fat accumulation caused by cannabinoid receptor activation. This review describes in detail the enzymatic steps that lead from the stimulation of cannabinoid 1 receptor to steatosis. It identifies several signaling pathways that activate sterol regulatory element-binding protein 1c (SREBP-1c), the key transcription factor causing fatty liver. The downstream effects of SREBP-1c leading to increased fatty acid synthesis and decreased fatty acid oxidation are also described.
近年来,大麻素在脂肪性肝病中的作用得到了越来越多的认可,并且有人提出,靶向外周大麻素受体的药物可能具有治疗用途。开发此类药物需要很好地了解大麻素受体激活引起脂肪堆积的机制。这篇综述详细描述了从刺激大麻素 1 受体到脂肪变性的酶促步骤。它确定了几种激活固醇调节元件结合蛋白 1c(SREBP-1c)的信号通路,SREBP-1c 是导致脂肪肝的关键转录因子。还描述了导致脂肪酸合成增加和脂肪酸氧化减少的 SREBP-1c 的下游效应。