Effects of Anemarrhena asphodeloides on Focal Ischemic Brain Injury Induced by Middle Cerebral Artery Occlusion in Rats
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- Oh Jin Kyung
- Department of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University
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- Hyun Seung Ye
- Department of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University
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- Oh Hye Rim
- Department of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University
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- Jung Ji Wook
- Department of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University
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- Park Chan
- Department of Anatomy, College of Medicine, Kyung Hee University
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- Lee Sun-Young
- Graduate School of East-West Medical Science, Kyung Hee University
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- Park Ji Ho
- Graduate School of East-West Medical Science, Kyung Hee University
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- Kim Sun Yeou
- Graduate School of East-West Medical Science, Kyung Hee University
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- Kim Ki Hoon
- Department of Forest Products, College of Forest Science, Kookmin University
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- Kim Young Kyun
- Department of Forest Products, College of Forest Science, Kookmin University
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- Ryu Jong Hoon
- Department of Oriental Pharmaceutical Science, College of Pharmacy, Kyung Hee University
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The preventive effect of Anemarrhena asphodeloides BUNGE (Liliaceae), a traditional Chinese medicine, on ischemia-reperfusion-induced brain injury was evaluated in the rat brain. Ischemia was induced by intraluminal occlusion of the right middle cerebral artery for 2 h and reperfusion was continued for 22 h. Water extract of Anemarrhena asphodeloides (WEAA) was orally administered promptly prior to and 2 h after reperfusion. Total infarct volume and edema in the ipsilateral hemispheres of ischemia-reperfusion rats were significantly reduced by treatment with WEAA in a dose-dependent manner (p<0.05). The therapeutic time window of WEAA was 3 h in this ischemia-reperfusion rat model. WEAA also significantly inhibited increased neutrophil infiltration of ischemic brain tissue as estimated by myeloperoxidase (MPO) activity and immunohistochemical analysis. MPO-positive cells were markedly reduced by WEAA administration in striatal and cortical areas. These findings suggest that WEAA plays a crucial protective role in ischemia-induced brain injury, and suggest that WEAA could serve as a lead medicinal herb for the development of neuroprotective agents following transient focal ischemic brain injury.
収録刊行物
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- Biological & Pharmaceutical Bulletin
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Biological & Pharmaceutical Bulletin 30 (1), 38-43, 2007
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390282679603668992
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- NII論文ID
- 110006153263
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- NII書誌ID
- AA10885497
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- ISSN
- 13475215
- 09186158
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- NDL書誌ID
- 8589952
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
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- 抄録ライセンスフラグ
- 使用不可