Baker IDI Heart and Diabetes Institute, Melbourne, Australia.
Baker IDI Heart and Diabetes Institute, Melbourne, Australia.
Trends Endocrinol Metab. 2015 Oct;26(10):538-550. doi: 10.1016/j.tem.2015.07.006.
In obesity and dyslipidemia, the oversupply of fat to tissues not suited for lipid storage induces cellular dysfunction that underlies diabetes and cardiovascular disease (i.e., lipotoxicity). Of the myriad lipids that accrue under these conditions, sphingolipids such as ceramide or its metabolites are amongst the most deleterious because they disrupt insulin sensitivity, pancreatic β cell function, vascular reactivity, and mitochondrial metabolism. Remarkably, inhibiting ceramide biosynthesis or catalyzing ceramide degradation in rodents ameliorates many metabolic disorders including diabetes, cardiomyopathy, insulin resistance, atherosclerosis, and steatohepatitis. Herein we discuss and critically assess studies that identify sphingolipids as major contributors to the tissue dysfunction underlying metabolic pathologies, highlighting the need to further decipher the full array of benefits elicited by ceramide depletion.
在肥胖和血脂异常中,过多的脂肪供应给不适合储存脂质的组织会导致细胞功能障碍,从而引发糖尿病和心血管疾病(即脂毒性)。在这些情况下积累的无数脂质中,神经酰胺等鞘脂或其代谢物是最具危害性的,因为它们会破坏胰岛素敏感性、胰岛β细胞功能、血管反应性和线粒体代谢。值得注意的是,在啮齿动物中抑制神经酰胺的生物合成或催化神经酰胺的降解可以改善许多代谢紊乱,包括糖尿病、心肌病、胰岛素抵抗、动脉粥样硬化和脂肪性肝炎。本文中,我们讨论并批判性地评估了将鞘脂鉴定为代谢病理基础组织功能障碍的主要贡献者的研究,强调需要进一步阐明神经酰胺耗竭所带来的全部益处。