Choi Songhwa, Snider Ashley J
Department of Medicine and Molecular and Cellular Biology, Stony Brook University, Stony Brook, NY 11794, USA ; Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY 11794, USA.
Department of Medicine and Molecular and Cellular Biology, Stony Brook University, Stony Brook, NY 11794, USA ; Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY 11794, USA ; Northport VA Medical Center, Northport, NY 11768, USA.
Mediators Inflamm. 2015;2015:520618. doi: 10.1155/2015/520618. Epub 2015 Nov 16.
Nutrient oversupply associated with a high fat diet (HFD) significantly alters cellular metabolism, and specifically including sphingolipid metabolism. Sphingolipids are emerging as bioactive lipids that play key roles in regulating functions, in addition to their traditional roles as membrane structure. HFD enhances de novo sphingolipid synthesis and turnover of sphingolipids via the salvage pathway, resulting in the generation of ceramide, and more specifically long chain ceramide species. Additionally, HFD elevates sphingomyelin and sphingosine-1 phosphate (S1P) levels in several tissues including liver, skeletal muscle, adipose tissue, and cardiovascular tissues. HFD-stimulated sphingolipid generation contributes to systemic insulin resistance, dysregulated lipid accumulation, and cytokine expression and secretion from skeletal muscle and adipose tissues, exacerbating obesity-related conditions. Furthermore, altered sphingolipid levels, particularly ceramide and sphingomyelin, are involved in obesity-induced endothelial dysfunction and atherosclerosis. In this review, HFD-mediated sphingolipid metabolism and its impact on HFD-induced biology and pathobiology will be discussed.
与高脂饮食(HFD)相关的营养物质供应过多会显著改变细胞代谢,尤其包括鞘脂代谢。鞘脂作为生物活性脂质正在崭露头角,除了其作为膜结构的传统作用外,还在调节功能中发挥关键作用。高脂饮食通过补救途径增强从头合成鞘脂以及鞘脂的周转,导致神经酰胺的生成,更具体地说是长链神经酰胺种类。此外,高脂饮食会提高包括肝脏、骨骼肌、脂肪组织和心血管组织在内的多个组织中的鞘磷脂和1-磷酸鞘氨醇(S1P)水平。高脂饮食刺激的鞘脂生成会导致全身胰岛素抵抗、脂质积累失调以及骨骼肌和脂肪组织中细胞因子的表达和分泌,加剧肥胖相关病症。此外,鞘脂水平的改变,特别是神经酰胺和鞘磷脂,与肥胖诱导的内皮功能障碍和动脉粥样硬化有关。在这篇综述中,将讨论高脂饮食介导的鞘脂代谢及其对高脂饮食诱导的生物学和病理生物学的影响。