Xie Bingjie, Lin Fankai, Ullah Kaleem, Peng Lei, Ding Wei, Dai Rongji, Qing Hong, Deng Yulin
School of Life Science, Beijing Institute of Technology, No. 5 Zhongguancun Nandajie, Haidian District, Beijing 100081, People's Republic of China.
Biochem Biophys Res Commun. 2015 Apr 10;459(3):361-6. doi: 10.1016/j.bbrc.2015.02.069. Epub 2015 Mar 3.
Diabetes is associated with an increased risk of Parkinson's disease (PD). Number of studies have suggested that methylglyoxal (MGO) induced by diabetes is related to PD. However, very little is known about its molecular mechanism. On other hand, 1-acetyl-6, 7- dihydroxyl-1, 2, 3, 4- Tetrahydroisoquinoline(ADTIQ) is a dopamine (DA)-derived tetrahydroisoquinoline (TIQ), a novel endogenous neurotoxins, which was first discovered in frozen Parkinson's disease human brain tissue. While ADTIQ precursor methylglyoxal was also found in diabetic patients related to the glucose metabolism and diabetic patients.
LC-MS/MS, 1H NMR and infrared spectroscopy identified the structure of ADTIQ. The Annexin V-FITC/PI, MTT and western blot analysis were used to measure the neurotoxicity of ADTIQ. The levels of ADTIQ and methylglyoxal were detected by LC-MS/MS.
Here we report the chemical synthesis of ADTIQ, demonstrate its biosynthesis in SH-SY5Y neuroblastoma cell line and investigate its role in the pathogenesis of PD. In addition, a significant increase in the level of ADTIQ was detected in the brains of transgenic mice expressing mutant forms (A53T or A30P) of α-synuclein. ADTIQ also reduced the cell viability and induced mitochondrial apoptosis in dopaminergic cells, suggesting that ADTIQ acts as an endogenous neurotoxin and potentially involved in the pathogenesis of PD. Methylglyoxal, a major byproduct of glucose metabolism and abnormalities in glucose metabolism could influence the levels of ADTIQ. Consistent with the hypothesis, increased levels of ADTIQ and methylglyoxal were detected in the striatum of diabetic rats and SH-SY5Y cells cultured in the presence of high glucose concentrations.
Increased levels of ADTIQ could be related with Hyperglycemia and death of dopaminergic neurons.
The increased levels of ADTIQ could be a reason of dopamine neuron dysfunction in diabetes. Therefore, ADTIQ may play a key role in increasing the risk for PD in patients with diabetes.
糖尿病与帕金森病(PD)风险增加相关。多项研究表明,糖尿病诱导产生的甲基乙二醛(MGO)与PD有关。然而,其分子机制却鲜为人知。另一方面,1-乙酰基-6,7-二羟基-1,2,3,4-四氢异喹啉(ADTIQ)是一种源自多巴胺(DA)的四氢异喹啉(TIQ),是一种新型内源性神经毒素,最初在冷冻的帕金森病患者脑组织中被发现。而ADTIQ的前体甲基乙二醛在糖尿病患者中也与糖代谢及糖尿病患者相关。
采用液相色谱-串联质谱法(LC-MS/MS)、核磁共振氢谱(1H NMR)和红外光谱法鉴定ADTIQ的结构。运用膜联蛋白V-异硫氰酸荧光素/碘化丙啶(Annexin V-FITC/PI)、噻唑蓝(MTT)和蛋白质免疫印迹分析来检测ADTIQ的神经毒性。通过LC-MS/MS检测ADTIQ和甲基乙二醛的水平。
在此我们报告了ADTIQ的化学合成,证实了其在人神经母细胞瘤细胞系SH-SY5Y中的生物合成,并研究了其在PD发病机制中的作用。此外,在表达α-突触核蛋白突变形式(A53T或A30P)的转基因小鼠大脑中检测到ADTIQ水平显著升高。ADTIQ还降低了多巴胺能细胞的活力并诱导其线粒体凋亡,表明ADTIQ作为一种内源性神经毒素,可能参与了PD的发病机制。甲基乙二醛作为糖代谢的主要副产物,糖代谢异常可能会影响ADTIQ的水平。与该假设一致,在高糖浓度培养条件下的糖尿病大鼠纹状体和SH-SY5Y细胞中检测到ADTIQ和甲基乙二醛水平升高。
ADTIQ水平升高可能与高血糖及多巴胺能神经元死亡有关。
ADTIQ水平升高可能是糖尿病中多巴胺神经元功能障碍的一个原因。因此,ADTIQ可能在增加糖尿病患者患PD的风险中起关键作用。