Neuroprotective Effects of a Butanol Fraction of Rosa hybrida Petals in a Middle Cerebral Artery Occlusion Model

被引:15
|
作者
Yang, Goeun [1 ]
Park, Dongsun [1 ]
Lee, Sun Hee [1 ]
Bae, Dae-Kwon [1 ]
Yang, Yun-Hui [1 ]
Kyung, Jangbeen [1 ]
Kim, Dajeong [1 ]
Choi, Ehn-Kyoung [1 ]
Hong, Jin Tae [2 ]
Jeong, Heon-Sang [3 ]
Kim, Hee Jung [4 ]
Jang, Su Kit [4 ]
Joo, Seong Soo [4 ]
Kim, Yun-Bae [1 ]
机构
[1] Chungbuk Natl Univ, Coll Vet Med, Cheongju 361763, South Korea
[2] Chungbuk Natl Univ, Coll Pharm, Cheongju 361763, South Korea
[3] Chungbuk Natl Univ, Dept Food Sci & Technol, Cheongju 361763, South Korea
[4] Gangneung Wonju Natl Univ, Coll Life Sci, Dept Marine Mol Biotechnol, Kangnung 210702, South Korea
基金
新加坡国家研究基金会;
关键词
Ischemic brain injury; Middle cerebral artery occlusion; Glial fibrillary acidic protein; Rosa hybrida; Antioxidation; Anti-inflammation; ISCHEMIC BRAIN-INJURY; NITRIC-OXIDE SYNTHASE; HEXANE FRACTION; GENE-EXPRESSION; STROKE; EXTRACT; FLOWER; DAMAGE; RATS; REPERFUSION;
D O I
10.4062/biomolther.2013.067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The neuroprotective effects of a butanol fraction of white rose petal extract (WRPE-BF) were investigated in a middle cerebral artery occlusion (MCAO) model. Seven week-old male rats were orally administered WRPE-BF for 2 weeks and subjected to MCAO for 2 h, followed by reperfusion. Twenty-four h later, MCAO-induced behavioral dysfunctions were markedly improved in a dose-dependent manner by pretreatment with WRPE-BF. Moreover, higher dose of WRPE-BF not only decreased infarction area but also effectively reduced astrogliosis. The expression of inducible nitric oxide synthase, cyclooxygenase-2, and glial fibrillary acidic protein in MCAO model were markedly inhibited by WRPE-BF treatment. Notably, WRPE-BF decreased nitric oxide and nnalondialdehyde levels in the striatum and subventricular zone of stroke-challenged brains. These data suggested that WRPE-BF may exert its neuroprotective effects via anti-oxidative and anti-inflammatory activities against ischemia-reperfusion brain injury and could be a good candidate as a therapeutic target for ischemic stroke.
引用
收藏
页码:454 / 461
页数:8
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