| Literature DB >> 17965547 |
Nakashi Sasano1, Atsushi Enomoto, Yoshio Hosoi, Yosuke Katsumura, Yoshihisa Matsumoto, Kenshiro Shiraishi, Kiyoshi Miyagawa, Hiroshi Igaki, Keiichi Nakagawa.
Abstract
Edaravone, a clinical drug used widely for the treatment of acute cerebral infarction, is reported to scavenge free radicals. In the present study, we investigated the radioprotective effect of edaravone on X-ray-induced apoptosis in MOLT-4 cells. Apoptosis was determined by the dye exclusion test, Annexin V binding assay, cleavage of caspase, and DNA fragmentation. We found that edaravone significantly suppressed the X-ray-induced apoptosis. The amount of intracellular ROS production was determined by the chloromethyl-2',7'-dichlorodihydro-fluorescein diacetate system. We found that the intracellular ROS production by X-irradiation was completely suppressed by the addition of edaravone. The accumulation and phosphorylation of p53 and the expression of p21(WAF1), a target protein of p53, which were induced by X-irradiation, were also suppressed by adding edaravone. We conclude that the free radical scavenger edaravone suppresses X-ray-induced apoptosis in MOLT-4 cells by inhibiting p53.Entities:
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Year: 2007 PMID: 17965547 DOI: 10.1269/jrr.07061
Source DB: PubMed Journal: J Radiat Res ISSN: 0449-3060 Impact factor: 2.724