• 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