Current time in Korea 01:15 Feb 29 (Sat) Year 2020 KCS KCS Publications
KCS Publications
My Journal Log In Register
HOME > Search > Browsing(BKCS) > Archives

Bulletin of the Korean Chemical Society (BKCS)

ISSN 0253-2964(Print)
ISSN 1229-5949(Online)
Volume 29, Number 12
BKCSDE 29(12)
December 20, 2008 

The Reaction of Salsolinol with Ferritin Induces DNA Strand Breakage
Jung Hoon Kang
Salolinol, Ferritin, DNA, Hydroxyl radical
Iron released from ferritin may trigger oxidative stress leading to progressive degeneration of brains from patients with neurodegenerative diseases. Previous studies have shown that oxidative damage of proteins and DNA was induced by catechol neurotoxin such as salsolinol (1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline). In the present study, we have investigated oxidative damage of DNA induced by the reaction of salsolinol with ferritin. When DNA was incubated with ferritin and salsolinol, DNA strand breakage increased in a time-dependent manner. Hydroxyl radical scavengers, such as azide, mannitol and dimethyl sulfoxide, effectively inhibited the salsolinol/ferritin system-mediated DNA cleavage, whereas Cu,Zn-superoxide dismutase did not suppress DNA cleavage. Catalase significantly inhibited the salsolinol/ferritin system-mediated DNA cleavage. Iron specific chelator, deferoxamine, also inhibited DNA cleavage. Spectrophotometric study using a color reagent showed that the release of iron from salsolinol-treated ferritin was increased in a time dependent manner. These results suggest that DNA strand breakage is mediated in the reaction of salsolinol with ferritin via the generation of hydroxyl radicals by the Fenton-like reaction of free iron ions released from oxidatively damaged ferritin.
2395 - 2398
Full Text