Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Biochem J. 2010 Dec 1;432(2):249-54. doi: 10.1042/BJ20101225.
GSD-1 (glycogen storage disease type 1) is caused by an inherited defect in glucose-6-phosphatase activity, resulting in a massive accumulation of hepatic glycogen content and an induction of de novo lipogenesis. The chlorogenic acid derivative S4048 is a pharmacological inhibitor of the glucose 6-phosphate transporter, which is part of glucose-6-phosphatase, and allows for mechanistic studies concerning metabolic defects in GSD-1. Treatment of mice with S4048 resulted in an ~60% reduction in blood glucose, increased hepatic glycogen and triacylglycerol (triglyceride) content, and a markedly enhanced hepatic lipogenic gene expression. In mammals, hepatic expression of lipogenic genes is regulated by the co-ordinated action of the transcription factors SREBP (sterol-regulatory-element-binding protein)-1c, LXRα (liver X receptor α) and ChREBP (carbohydrate-response-element-binding protein). Treatment of Lxra-/- mice and Chrebp-/- mice with S4048 demonstrated that ChREBP, but not LXRα, mediates the induction of hepatic lipogenic gene expression in this murine model of GSD-1. Thus ChREBP is an attractive target to alleviate derangements in lipid metabolism observed in patients with GSD-1.
GSD-1(糖原贮积症 1 型)是由葡萄糖-6-磷酸酶活性的遗传缺陷引起的,导致肝糖原含量大量积累,并诱导新的脂肪生成。绿原酸衍生物 S4048 是葡萄糖 6-磷酸转运蛋白的药理学抑制剂,葡萄糖 6-磷酸转运蛋白是葡萄糖-6-磷酸酶的一部分,允许对 GSD-1 中的代谢缺陷进行机制研究。用 S4048 治疗小鼠可使血糖降低约 60%,肝糖原和三酰基甘油(甘油三酯)含量增加,并显著增强肝脂肪生成基因表达。在哺乳动物中,肝脂肪生成基因的表达受转录因子 SREBP(固醇调节元件结合蛋白)-1c、LXRα(肝 X 受体 α)和 ChREBP(碳水化合物反应元件结合蛋白)的协调作用调节。用 S4048 治疗 Lxra-/-小鼠和 Chrebp-/-小鼠表明,ChREBP 而不是 LXRα,介导了这种 GSD-1 小鼠模型中肝脂肪生成基因表达的诱导。因此,ChREBP 是一种有吸引力的靶标,可以缓解 GSD-1 患者脂质代谢紊乱。