Cordycepin attenuates traumatic brain injury-induced impairments of blood-brain barrier integrity in rats

被引:42
|
作者
Yuan, Jing [1 ]
Wang, Aihua [1 ]
He, Yan [1 ]
Si, Zhihua [1 ]
Xu, Shan [1 ]
Zhang, Shanchao [1 ]
Wang, Kun [2 ]
Wang, Dawei [3 ]
Liu, Yiming [4 ]
机构
[1] Shandong Univ, Qianfoshan Hosp, Dept Neurol, 16766 Jingshi Rd, Jinan 250014, Peoples R China
[2] Shandong Univ, Qianfoshan Hosp, Dept Gen Surg, 16766 Jingshi Rd, Jinan 250014, Peoples R China
[3] Shandong Univ, Shandong Prov Hosp, Dept Orthoped, 324 Jingwu Rd, Jinan 250021, Peoples R China
[4] Shandong Univ, Qilu Hosp, Dept Neurol, 107 West Wenhua Rd, Jinan 250012, Peoples R China
基金
中国国家自然科学基金;
关键词
Cordycepin; Traumatic brain injury; Blood-brain barrier integrity; Neuroprotective; Anti-oxidative; Anti-inflammatory; CEREBRAL-ISCHEMIA; TIGHT JUNCTION; OCCLUDIN; PATHWAY; MICE; PERMEABILITY; DYSFUNCTION; DEFICITS; STRESS;
D O I
10.1016/j.brainresbull.2016.09.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Loss of blood-brain barrier (BBB) integrity is a downstream event caused by traumatic brain injury (TBI). BBB integrity is affected by certain physiological conditions, including inflammation and oxidative stress. Cordycepin is a susbtance with anti-inflammatory and anti-oxidative effects. Therefore, it is necessary to investigate whether cordycepin affects TBI-induced impairments of BBB integrity. Using TBI rats as the in vivo model and applying multiple techniques, including stroke severity evaluation, Evans blue assessment, quantitative real-time PCR, Western blotting and ELISA, we investigated the dose-dependent protective effects of cordycepin on the TBI-induced impairments of BBB integrity. Cordycepin treatment attenuated the TBI-induced impairments in a dose-dependent manner, and played a role in protecting BBB integrity. Cordycepin was able to alleviate TBI-induced loss of tight junction proteins zonula occludens protein-1 (ZO-1) and occludin, which are important for BBB integrity. Moreover, cordycepin suppressed pro-inflammatory factors, including IL-1 beta, iNOS, MPO and MMP-9, and promoted anti-inflammation-associated factors arginase 1 and IL-10. Furthermore, cordycepin inhibited NADPH oxidase (NOX) expression and activity following TBI, probably through NOX1, but not NOX2 and NOX4. Cordycepin has protective effects against brain damages induced by TBI. The protection of cordycepin on BBB integrity was probably achieved through recovery of tight junction proteins, inhibition of local inflammation, and prevention of NOX activity. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:171 / 176
页数:6
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