Schiffmann Raphael
Institute of Metabolic Disease, Baylor Research Institute, 3812 Elm Street, Dallas, TX, USA,
J Inherit Metab Dis. 2015 Jan;38(1):77-84. doi: 10.1007/s10545-014-9758-8. Epub 2014 Aug 28.
A new therapy based on substrate synthesis reduction in sphingolipidoses is showing promise. The consequences of decreasing sphingolipid synthesis depend on the level at which synthetic blockage occurs and on the extent of the blockage. Complete synthetic blockage may be lethal if it includes all sphingolipids, such as in a global knockout of serine palmitoyltransferase. Partial inhibition of sphingolipid synthetic pathways is usually benign and may have beneficial effects in a number of lysosomal diseases and in more common pathologies, as seen in animal models for atherosclerosis, polycystic kidney disease, diabetes, and asthma. Studies of various forms of sphingolipid synthesis reduction serve to highlight not only the cellular role of these lipids but also the potential risks and therapeutic benefits of pharmacological agents to be used in therapy for human diseases.
一种基于减少鞘脂病中底物合成的新疗法显示出了前景。鞘脂合成减少的后果取决于合成阻断发生的水平以及阻断的程度。如果完全阻断包括所有鞘脂,如丝氨酸棕榈酰转移酶的整体敲除,可能是致命的。鞘脂合成途径的部分抑制通常是良性的,并且在一些溶酶体疾病以及更常见的病症中可能具有有益作用,如在动脉粥样硬化、多囊肾病、糖尿病和哮喘的动物模型中所见。对各种形式的鞘脂合成减少的研究不仅有助于突出这些脂质的细胞作用,还能凸显用于人类疾病治疗的药物的潜在风险和治疗益处。