Reitman Marc L
Department of Metabolic Disorders, Merck Research Laboratories, Rahway, NJ 07065, USA.
Cell Metab. 2007 Jun;5(6):405-7. doi: 10.1016/j.cmet.2007.05.010.
A sufficient energy supply is essential for life; consequently, multiple mechanisms have evolved to ensure both energy availability and conservation during fasting and starvation. Two reports in this issue of Cell Metabolism (Badman et al., 2007; Inagaki et al., 2007) demonstrate that FGF21, a circulating protein produced in the liver in response to the PPARalpha transcription factor, is a "missing link" in the biology of fasting, inducing adipose tissue lipolysis, liver ketogenesis, and metabolic adaptation to the fasting state.
充足的能量供应对生命至关重要;因此,多种机制已经进化出来,以确保在禁食和饥饿期间能量的可获得性和保存。本期《细胞代谢》杂志上的两篇报道(Badman等人,2007年;Inagaki等人,2007年)表明,成纤维细胞生长因子21(FGF21)是一种在肝脏中响应PPARα转录因子而产生的循环蛋白,它是禁食生物学中的“缺失环节”,可诱导脂肪组织脂肪分解、肝脏生酮作用以及对禁食状态的代谢适应。