Struys E A, Gibson K M, Jakobs C
VU University Medical Centre, Clinical Chemistry, Metabolic Unit, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
J Inherit Metab Dis. 2007 Oct;30(5):690-3. doi: 10.1007/s10545-007-0697-5. Epub 2007 Sep 17.
Employing lymphoblasts derived from two non related patients with L-2-HG aciduria, we examined the origin of L-2-hydroxyglutaric acid (L-2-HG) through incubation with [(13)C6]glucose and [(2)H5]glutamic acid. Formation of labelled 2-ketoglutaric acid (2-KG), citric acid and L-2-HG was determined by GC-MS. The quantitative and qualitative isotopomer pattern following incubation with [(13)C6]glucose was identical for all end-products. Incubations with [(2)H5]glutamic acid as precursor revealed the formation of identical isotopomers for 2-KG and L-2-HG. Our data indicate that 2-KG is the metabolic precursor of L-2-HG, adding to previous studies which revealed that 2-KG is the metabolic precursor of D-2-HG. These data suggest that 2-KG has a pathophysiological role in combined D/L-2-HG aciduria.
我们使用来自两名非亲缘关系的L-2-羟基戊二酸尿症患者的淋巴母细胞,通过与[¹³C₆]葡萄糖和[²H₅]谷氨酸孵育来研究L-2-羟基戊二酸(L-2-HG)的来源。通过气相色谱-质谱联用仪(GC-MS)测定标记的2-酮戊二酸(2-KG)、柠檬酸和L-2-HG的形成。用[¹³C₆]葡萄糖孵育后,所有终产物的定量和定性同位素异构体模式均相同。以[²H₅]谷氨酸作为前体进行孵育,结果显示2-KG和L-2-HG形成相同的同位素异构体。我们的数据表明,2-KG是L-2-HG的代谢前体,这补充了之前揭示2-KG是D-2-HG代谢前体的研究。这些数据表明,2-KG在合并的D/L-2-HG酸尿症中具有病理生理作用。