Diallyl Disulfide Inhibits Cytochrome c-Mediated Apoptosis in H2O2 Induced Death of Neuronal-differentiated PC12 Cells.
- Author:
Seong Ho KOH
1
;
Hyugsung KWON
;
Younjoo PARK
;
Jun Gyou KIM
;
Kisok KIM
;
Chi Won SONG
;
Joo Hwan KIM
;
Juhan KIM
;
Myoung Ho KIM
;
Kyung Suk KIM
;
Hyun Jung YU
;
Hai Kwan JUNG
;
Seung Hyun KIM
Author Information
1. Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea. kimsh1@hanyang.ac.kr
- Publication Type:Original Article
- Keywords:
Diallyl disulfide;
Antioxidant;
Apoptosis;
Caspase-3;
PARP
- MeSH:
Animals;
Apoptosis*;
Blotting, Western;
Caspase 3;
Cytochromes c;
Cytochromes*;
Garlic;
Nerve Growth Factor;
Neurodegenerative Diseases;
Neuroprotective Agents;
Oxidative Stress;
PC12 Cells*
- From:Journal of the Korean Neurological Association
2004;22(4):375-381
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: The effects of diallyl disulfide (DADS), a garlic derived compound, on the viability and cell signaling- like the downstream signaling through cytochrome c, caspase-3, poly (ADP-ribose) polymerase (PARP) during an oxidative-stress induced injury were studied using H2O2 treated neuronal-differentiated PC12 cells by a nerve growth factor. METHODS: To evaluate the toxicity of the DADS itself, the viability of the differentiated PC12 cells treated with several concentrations of DADS was evaluated with 3, (4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assays. To evaluate the protective effect of the low concentration of DADS from oxidative stress, the viability of the cells (DADS pretreated vs. not pretreated) was evaluated following the exposure to 100 micro M H2O2. Additionally, the expression of caspase-3, PARP, and cytochrome c was examined using western blot analyses. RESULTS: The viability was not affected at low concentrations of DADS, up to 20 micro M, but, over this concentration, it was decreased. Compared with the cells treated with only 100 micro M H2O2, the pretreatment with low concentrations of DADS before exposure to 100 micro M H2O2 increased the viability and induced the inhibition of caspase-3 activation, PARP cleavage, and cytochrome c release. CONCLUSIONS: These results show that low concentrations of DADS shows neuroprotective effects by affecting the downstream signaling through cytochrome c, caspase-3, and PARP pathway and may be a new potential therapeutic strategy for neurodegenerative diseases associated with oxidative injury.
