DocumentCode
2090258
Title
Salsolinol, a Dopamine-derived Tetrahydroisoquinoline, Occur in Dopaminergic SH-SY5Y Cells Induced by Dopamine
Author
Wang, Ran ; Yang, Wei ; Luan, Yujing ; Mao, Jian ; Qing, Hong ; Deng, Yulin
Author_Institution
Beijing Inst. of Technol., Beijing
fYear
2007
fDate
23-27 May 2007
Firstpage
1404
Lastpage
1408
Abstract
The dopamine-derived salsolinol (Sal), 1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, has been considered a potential endogenous neurotoxin involved in the etiology of PD. In the present study, 150 muM dopamine (DA) was applied to be the treatment concentration on account of that 150 muM DA decreased cell viability to 44.8%. The level of salsolinol in human dopaminergic SH-SY5Y cells treated with 150 muM DA for 24 h was measured using high-performance liquid chromatography with electrochemical detection (HPLC-ECD), and the possible mechanism of salsolinol formation in SH-SY5Y cells was discussed. DA significantly increased the production of hydroxyl radicals quantitatively measured after derivatization as 2, 3-and 2, 5-DHBA by reaction with salicylic acid, and malonaldehyde (MDA), a marker of lipid peroxidation. Salsolinol increased remarkably in DA-induced cells compared to control cells. These results suggest that DA incubation and oxidative stress induced by excessive dopamine contribute to the synthesis of salsolinol in SH-SH5Y cells.
Keywords
cellular biophysics; diseases; drugs; molecular biophysics; neurophysiology; organic compounds; toxicology; HPLC-ECD; Parkinson disease; cell viability; dopaminergic SH-SY5Y cells; electrochemical detection; endogenous neurotoxin; hydroxyl radicals; lipid peroxidation; liquid chromatography; malonaldehyde; salicylic acid; salsolinol; tetrahydroisoquinoline; Chemical analysis; Humans; In vitro; Lipidomics; Neurons; Parkinson´s disease; Pathogens; Production; Radio access networks; Stress;
fLanguage
English
Publisher
ieee
Conference_Titel
Complex Medical Engineering, 2007. CME 2007. IEEE/ICME International Conference on
Conference_Location
Beijing
Print_ISBN
978-1-4244-1077-4
Electronic_ISBN
978-1-4244-1078-1
Type
conf
DOI
10.1109/ICCME.2007.4381975
Filename
4381975
Link To Document