Neuroprotective effects of dexmedetomidine combined with targeted temperature management on brain edema in traumatic brain injury

创伤性脑损伤 右美托咪定 神经保护 莫里斯水上航行任务 麻醉 医学 H&E染色 脑水肿 水肿 脑水肿 目标温度管理 内科学 海马体 免疫组织化学 镇静 心肺复苏术 复苏 自然循环恢复 精神科
作者
Hongjie Huang,Lijing Ding,Nana Zhang,Cheng Yang,Yi Tailong,Nuo Yan,Jie Gao,Hui Li,Shuchao Guo,Sai Zhang,Shixiang Cheng
出处
期刊:Chinese Journal of Behavioral Medicine and Brain Science [Chinese Medical Association]
卷期号:26 (4): 311-315
标识
DOI:10.3760/cma.j.issn.1674-6554.2017.04.005
摘要

Objective To explore the neuroprotective effects of dexmedetomidine (Dex) combined with targeted temperature management (TTM) on brain edema in traumatic brain injury (TBI) mice. Methods A total of 132 male C57BL/6 mice were randomly divided into normal group, sham-operation (Sham) group, traumatic brain injury (TBI) group, targeted temperature management (TTM) group, dexmedetomidine (Dex) group, and combination with TTM and Dex (DT) group, respectively (n=22 per group). The TBI animal model was established by electric controlled cortical impactor (eCCI), and then settled promptly on a mild hypothermic blanket (targeted temperature of (32±1)℃) for 6 h, or intraperitoneal injection of Dex (20 μl/kg) at 0, 2 and 4 h after TBI. Neurological function and spatial learning and memory ability were evaluated by modified neurological severity scores (mNSS) and Morris water maze (MWM), respectively. Then, mice were sacrificed at 24 h after TBI and stained using hematoxylin and eosin (H & E). Additionally, the cerebral edema was evaluated from the water content of the brain tissue using the wet-to-dry weight ratio, and the expression of aquaporin 4 (AQP4) was measured by Western blot assay. Results Compared with the Sham group, TBI mice showed neurologic deficits ((13.2±3.0) vs (0.5±0.7))(P<0.01), spatial learning and memory capacity decline((2.9±1.0) vs (7.4±1.3))( P<0.05), and the brain water content and the expression of AQP4 were increased ((79.81±0.80)% vs (75.98±0.62)%): ((1.60±0.07) vs (0.73±0.03))(all P<0.01). However, Dex or TTM could improve the neurological function(Dex: (10.3±2.8), TTM: (10.0±2.9)), reduce the brain water content(Dex: (78.50±0.40)%, TTM: (78.10±0.45)%), and significantly decrease the expression of AQP4 compared with the TBI group(Dex: (1.40±0.04), TTM: (1.15±0.12)) (all P<0.05), especially that of DT group ((9.2±2.5) , (5.4±1.8) , (77.67±0.30)%, (0.93±0.09)) (all P<0.01). Conclusion These finding suggests that Dex combined with targeted temperature management can reduce cerebral edema and improve neurological outcome in mice after TBI to exert neuroprotection effect, which may be related with the down-regulation of AQP4 protein. Key words: Traumatic brain injury; Dexmedetomidine; Targeted temperature management; Brain edema
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