Department of Internal Medicine, Division of Endocrinology, Fraternal Order of Eagles Diabetes Research Center, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA; email:
Department of Nutrition and Integrative Physiology and the Diabetes and Metabolism Research Center, University of Utah, Salt Lake City, Utah 84112, USA; email:
Annu Rev Physiol. 2021 Feb 10;83:303-330. doi: 10.1146/annurev-physiol-031620-093815. Epub 2020 Nov 6.
The global prevalence of metabolic diseases such as type 2 diabetes mellitus, steatohepatitis, myocardial infarction, and stroke has increased dramatically over the past two decades. These obesity-fueled disorders result, in part, from the aberrant accumulation of harmful lipid metabolites in tissues not suited for lipid storage (e.g., the liver, vasculature, heart, and pancreatic beta-cells). Among the numerous lipid subtypes that accumulate, sphingolipids such as ceramides are particularly impactful, as they elicit the selective insulin resistance, dyslipidemia, and ultimately cell death that underlie nearly all metabolic disorders. This review summarizes recent findings on the regulatory pathways controlling ceramide production, the molecular mechanisms linking the lipids to these discrete pathogenic events, and exciting attempts to develop therapeutics to reduce ceramide levels to combat metabolic disease.
在过去的二十年中,全球范围内代谢性疾病(如 2 型糖尿病、脂肪性肝炎、心肌梗死和中风)的患病率急剧上升。这些由肥胖引起的疾病部分是由于有害脂质代谢物在不适合脂质储存的组织(如肝脏、血管、心脏和胰岛β细胞)中的异常积累所致。在积累的众多脂质亚型中,神经酰胺等鞘脂类特别有影响,因为它们引起几乎所有代谢性疾病的选择性胰岛素抵抗、血脂异常和最终的细胞死亡。这篇综述总结了最近关于控制神经酰胺产生的调节途径、将脂质与这些特定病理事件联系起来的分子机制,以及令人兴奋的尝试开发降低神经酰胺水平以对抗代谢性疾病的治疗方法的发现。