Protective Effect of Sulforaphane against Dopaminergic Cell Death
 

Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on January 26, 2007; DOI: 10.1124/jpet.106.110866


PubMed Citation
Articles by Han, J. M.
Articles by Hwang, O.

NEUROPHARMACOLOGY

Protective Effect of Sulforaphane against Dopaminergic Cell Death
Ji Man Han, Yong Jin Lee, So Yeon Lee, Eun Mee Kim, Younghye Moon, Ha Won Kim, and Onyou Hwang
Department of Biochemistry and Molecular Biology, University of Ulsan College of Medicine, Seoul, Korea (J.M.H., Y.J.L., S.Y.L., E.M.K., Y.M., O.H.); and Department of Life Science, University of Seoul, Seoul, Korea (Y.J.L., H.W.K.)


Parkinson's disease (PD) is a progressive neurodegenerative disorder with a selective loss of dopaminergic neurons in the substantia nigra. Evidence suggests oxidation of dopamine (DA) to DA quinone and consequent oxidative stress as a major factor contributing to this vulnerability. We have previously observed that exposure to or induction of NAD(P)H:quinone reductase (QR1), the enzyme that catalyzes the reduction of quinone, effectively protects DA cells. Sulforaphane (SF) is a drug identified as a potent inducer of QR1 in various non-neuronal cells. In the present study, we show that SF protects against compounds known to induce DA quinone production (6-hydroxydopamine and tetrahydrobiopterin) in DAergic cell lines CATH.a and SK-N-BE(2)C as well as in mesencephalic DAergic neurons. SF leads to attenuation of the increase in protein-bound quinone in tetrahydrobiopterin-treated cells, but this does not occur in cells that have been depleted of DA, suggesting involvement of DA quinone. SF pretreatment prevents membrane damage, DNA fragmentation, and accumulation of reactive oxygen species. SF causes increases in mRNA levels and enzymatic activity of QR1 in a dose-dependent manner. Taken together, these results indicate that SF causes induction of QR1 gene expression, removal of intracellular DA quinone, and protection against toxicity in DAergic cells. Thus, this major isothiocyanate found in cruciferous vegetables may serve as a potential candidate for development of treatment and/or prevention of PD.

(Brocco sprouts are a good source of sulforaphane--organic food stores carry them, and i have also found them at our area Kroger's market)



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Received July 14, 2006; accepted January 25, 2007.

It also works vs cancer in a similar way to a chemo drug, but it's kinder to healthy cells.

I'm going to grow broccoli sprouts if I can find some safe seeds.