スダ サトシ
SUDA Satoshi
須田 智 所属 埼玉医科大学 医学部 国際医療センター 神経内科・脳卒中内科 職種 教授 |
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論文種別 | 学術雑誌(原著) |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Neuroprotective effects of clarithromycin against neuronal damage in cerebral ischemia and in cultured neuronal cells after oxygen-glucose deprivation |
掲載誌名 | 正式名:LIFE SCIENCES ISSNコード:0024-3205/1879-0631 |
出版社 | PERGAMON-ELSEVIER SCIENCE LTD |
巻・号・頁 | 168,7-15頁 |
著者・共著者 | Yasuo Katayama,Toshiki Inaba,Chikako Nito,Satoshi Suda,Masayuki Ueda |
発行年月 | 2017/01 |
概要 | Aims: Rats subjected to transient focal ischemia and cultured neuronal cells subjected to oxygen-glucose deprivation (OGD) were treated with clarithromycin (CAM) to evaluate the effects of CAM in protecting against neuronal damage. Main methods: Sprague-Dawley rats were subjected to middle cerebral artery occlusion (MCAO) for 90 min and then reperfused. Each animal was given an oral dose clarithromycin (CAM, 100 mg/kg) or vehicle alone just after the ischemia was commenced. The infarct volume, edema index and neurological performance were assessed after 24 and 72 h of reperfusion. The cerebral blood flow (CBF) was measured with an MRI system at 90 min after MCAO. After 24 and 72 h, oxidative stress (4-HNE, 8-OHdG) and inflammation (lba-1,TNF-alpha) were assessed by immunohistochemical analyses and degenerative cells were assessed in the cortex by Fluoro-Jade C (FJC) labeling. The cultured neuronal cells were also used to examine the effects of CAM exposure on the viability of the cells after OGD. Key findings: CBF was unchanged between the two groups. Significant reductions of the infarct volume and edema index, an improved neurological deficit score, a significant suppression of 4-HNE and 8-OHdG expression, marked reductions of lba-1 and TNF-alpha expression, and a significant reduction of FJC-positive cells were also observed in the CAM-treated animals at both time points. Treatment with 10 mu M and 100 mu M CAM in vitro significantly reduced cell death after OGD. Significance: CAM appears to provide antioxidant and anti-inflammatory effects and protect against neuronal damage after cerebral ischemia and OGD. (C) 2016 Elsevier Inc. All rights reserved. |
DOI | 10.1016/j.ifs.2016.11.004 |
PMID | 27825902 |