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논문 기본 정보

자료유형
학술저널
저자정보
Kang, Jun-Mo (Department of Neuroscience and Medical Research Institute, School of Medicine, Ewha Womans University) Jung, Jae-Chul (Department of Neuroscience and Medical Research Institute, School of Medicine, Ewha Womans University) Kim, Hee-Jeong (Department of Neuroscience and Medical Research Institute, School of Medicine, Ewha Womans University) Lim, Hee-Na (Department of Neuroscience and Medical Research Institute, School of Medicine, Ewha Womans University) Jang, So-Yong (Department of Neuroscience and Medical Research Institute, School of Medicine, Ewha Womans University) Oh, Sei-Kwan (Department of Neuroscience and Medical Research Institute, School of Medicine, Ewha Womans University)
저널정보
대한약학회 Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea 제31권 제9호
발행연도
2008.1
수록면
1,098 - 1,107 (10page)

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In this study, we investigated the neuroprotective effect of a benzylideneacetophenone derivative, JC3, in a mouse model of l-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson's disease (PD). C57BL/6 mice were treated with MPTP (30 mg/kg, i.p.) for 5 consecutive days. JC3 (10 mg/kg, i.p.) treatment was initiated 2 h after the first administration of MPTP and then at 24-h intervals for 3 consecutive days. The mice were sacrificed for analyses 7 days after the last MPTP injection. Immunohistochemistry and Western blot were used to determine the expression levels of tyrosine hydroxylase (TH), dopamine transporter (DAT), OX-42 (a marker of microglial activation), and glial fibrillary acid protein (GFAP, a marker of astrocyte activation) in the substantia nigra (SN) and striatum (ST). The results of these experiments demonstrated that JC3 restored the decreased TH-immunoreactivity (IR) and DAT and JC3 attenuated the increase in OX-42, GFAP, and COX-2 on the SN and ST on day 7 post-MPTP injection. These results suggest that JC3 can be a neuroprotective agent in an MPTP-induced model of PD.

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