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An Intrinsic Therapy of Gold Nanoparticles in Focal Cerebral Ischemia-Reperfusion Injury in Rats
被引:44
|作者:
Liu, Zhengxia
[1
]
Shen, Yujie
[1
]
Wu, Yucheng
[1
]
Yang, Yujiao
[1
]
Wu, Jin
[1
]
Zhou, Ping
[1
]
Lu, Xiang
[1
]
Guo, Zhirui
[1
]
机构:
[1] Nanjing Med Univ, Affiliated Hosp 2, Dept Geriatr, Nanjing 210029, Jiangsu, Peoples R China
基金:
美国国家科学基金会;
关键词:
Ischemia-Reperfusion Injury;
Stroke;
Gold Nanoparticles;
Inflammation;
Apoptosis;
DNA FRAGMENTATION;
MAGNETIC NANOPARTICLES;
GLOBAL-ISCHEMIA;
SIZE;
CYTOTOXICITY;
MITOCHONDRIA;
TOXICITY;
BIOLOGY;
STRESS;
STROKE;
D O I:
10.1166/jbn.2013.1597
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Ischemic stroke is a leading cause of death and disability, and the treatment options are limited. Recent studies demonstrated that the promising applications of gold nanoparticles (Au-NPs) as intrinsic therapeutics; however, little is known about the effect of Au-NPs on cerebral ischemia-reperfusion (I/R) injury. In this paper, the role of Au-NPs on cerebral I/R injury in the rat middle cerebral artery occlusion (MCAO) model was investigated using citrate-capped 5 nm and 20 nm Au-NPs. It was found that 20 nm Au-NPs administration led to remarkable amelioration of neurologic deficits and infarction volumes. Further research revealed that 20 nm Au-NPs elevated the production of anti-inflammatory cytokines, as well as inhibited I/R induced activation of astrocytes and microglias. Moreover, the expressions of anti-apoptotic proteins were up-regulated and the pro-apoptotic molecules were down-regulated in the post-ischemic brains. These effects were opposite in 5 nm group. The above results showed that the neuroprotection of 20 nm Au-NPs was attributable to its anti-inflammatory and anti-apoptotic effect. This study could provide a novel strategy for the treatment of cerebral I/R injury.
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页码:1017 / 1028
页数:12
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