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Neuroprotection of hydroxysafflor yellow A in the transient focal ischemia: Inhibition of protein oxidation/nitration, 12/15-lipoxygenase and blood-brain barrier disruption
被引:63
作者:
Sun, Li
[1
]
Yang, Li
[1
]
Xu, Yan-Wei
[1
]
Liang, Hao
[1
]
Han, Jing
[1
]
Zhao, Rui-Jie
[1
]
Cheng, Yan
[1
]
机构:
[1] Tianjin Med Univ, Tianjin Key Lab Injuries Variat & Regenerat Nervo, Tianjin Neurol Inst,Minist Educ,Gen Hosp, Key Lab Posttrauma Neurorepair & Regenerat Cent N, Tianjin 300052, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Hydroxysafflor yellow A;
Ischemia/reperfusion;
Protein carbonylation;
Nitrotyrosine;
12/15-Lipoxygenase;
Blood-brain barrier;
OXIDATIVE STRESS;
TYROSINE NITRATION;
CEREBRAL-ISCHEMIA;
NITRIC-OXIDE;
REPERFUSION INJURY;
PEROXYNITRITE FORMATION;
DAMAGE;
RATS;
TARGETS;
STROKE;
D O I:
10.1016/j.brainres.2012.07.047
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Hydroxysafflor yellow A (HSYA) is the main component of the safflower yellow pigments, the aqueous extract of safflower florets. We report here an experimental study for evaluating HSYA for their neuroprotective qualities on rats subjected to middle cerebral artery occlusion (60 min) and reperfusion (24 h), an experimental model in which excessive production of reactive oxygen and nitrogen species has been found. In our data, biochemical analysis of tissue proteins showed that cerebral ischemia/reperfusion (I/R) injury resulted in significant elevation of carbonyl groups and nitrotyrosine in the brain of I/R in comparison to sham controls, indicating the occurrence of oxidative/nitrative modification to brain proteins. I-ISYA-treatment (1, 5 and 10 mg/kg) inhibited I/R-induced protein oxidation and nitration. 12/15-Lipoxygenase (12/15-LOX), the enzyme implicated in oxidative stress of cerebral I/R, displayed overexpression in I/R rats. Elevated 12/15-LOX activity, estimated by the level of its metabolite 15-hydroxyeicosate-traenoic acid (15-HETE), was also induced by the challenge of cerebral I/R Administration of HSYA 1, 5 and 10 mg/kg reduced the upregulation of 12/15-LOX expression and activity in a dose-dependent manner. Moreover, the increase in blood-brain barrier (BBB) permeability evaluated by IgG leakage, Evans blue extravasation, and brain water content, respectively, was markedly alleviated by HSYA, indicating its protection against BBB disruption and brain edema following I/R insult. Taken together, these results demonstrate the neuroprotective properties of HSYA, which may be at least in part due to its potential to reduce protein oxidation and nitration, inhibit the upregulation of 12/15-LOX, and attenuate BBB breakdown. (C) 2012 Elsevier B.V. All rights reserved.
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页码:227 / 235
页数:9
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