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(Stroke. 2005;36:2468.)
© 2005 American Heart Association, Inc.
Original Contributions |
From the Department of Obstetrics and Gynecology (J.I.N., T. Ikeda, T. Ikenoue), Faculty of Medicine, University of Miyazaki, Miyazaki, and the Department of Neuropharmacology (K.M., N.A., S.O., N.E., K.I., M.F.), Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Correspondence to Tsuyomu Ikenoue, MD, Department of Obstetrics and Gynecology, Faculty of Medicine, University of Miyazaki, 5200 Kihara, Kiyotake, Miyazaki 889-1692, Japan. E-mail satomako{at}fc.miyazaki-med.ac.jp
Background and Purpose Edaravone (3-methyl-1-phenyl-2-pyrazolin-5-one) is a new free radical scavenger that is used for the treatment of adult acute cerebral infarction in Japan. We examined the effect of edaravone on the optimal duration of treatment, the long-term effect on the brain, and the effect on learning and memory disability in a rat model of neonatal hypoxicischemic encephalopathy.
Methods Seven-day-old Wistar rats were subjected to left common carotid artery ligation then 2 hours of hypoxicischemic insult or sham operation. Edaravone was administered intraperitoneally (9 mg/kg) after hypoxicischemic insult every 24 hours for 2, 5, or 10 consecutive days. The neuroprotective effect of edaravone was evaluated by behavioral test and histological analysis.
Results Two-day treatment with edaravone significantly gave protection to the learning and memory capability, as well as morphological recovery compared with control rats. Five-day treatment showed morphological improvement but no behavioral improvement. In contrast, 10-day treatment did not show either morphological or behavior improvement.
Conclusions These findings indicate that edaravone is a promising candidate as a treatment of choice for neonatal hypoxicischemic encephalopathy, when its use is limited to the acute phase after hypoxiaischemia.
Key Words: edaravone hypoxiaischemia learning impairment Levines model neonatal rat
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