Cannabinoid CB2 receptor stimulation attenuates brain edema and neurological deficits in a germinal matrix hemorrhage rat model

被引:20
作者
Tao, Yihao [1 ]
Tang, Jun [1 ]
Chen, Qianwei [1 ]
Guo, Jing [1 ]
Li, Lin [1 ]
Yang, Liming [1 ]
Feng, Hua [1 ]
Zhu, Gang [1 ]
Chen, Zhi [1 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Neurosurg, Chongqing 400038, Peoples R China
基金
中国国家自然科学基金;
关键词
Germinal matrix hemorrhage; Cannabinoid receptor; Brain edema; Inflammation; NEONATAL HYPOXIA-ISCHEMIA; INTRACEREBRAL HEMORRHAGE; INTRAVENTRICULAR HEMORRHAGE; SUBARACHNOID HEMORRHAGE; NEURONAL DEATH; WATER-MAZE; INJURY; ACTIVATION; INVOLVEMENT; INHIBITION;
D O I
10.1016/j.brainres.2015.01.025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Germinal matrix hemorrhage (GMH) is one of the most common and devastating cerebrovascular events that affect premature infants, resulting in a significant socioeconomic burden. However, GMH has been largely unpreventable, and clinical treatments are mostly inadequate. In the present study, we tested the hypothesis that JWH133, a selective CB2 receptor agonist, could attenuate brain injury and neurological deficits in a clostridial collagenase VII induced GMH model in seven-day-old (P7) S-D rat pups. Up to 1 h post-injury, the administration of JWH133 (1 mg/kg, intraperitoneal injection) significantly attenuated brain edema at 24 h post-GMH, which was reversed by a selective CB2R antagonist, SR144528 (3 mg/kg, intraperitoneal injection). Long-term brain morphology and neurofunctional outcomes were also improved. In contrast, JWH133 did not have a noticeable effect on the hematoma volume during the acute phase. These data also showed that microglia activation and inflammatory cytokine (TNF-alpha) release were significantly inhibited by JWH133 after GMH. This current study suggests a potential clinical utility for CB2R agonists as a potential therapy to reduce neurological injury and improve patient outcomes after GMH. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
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