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Neuroprotection of Dexmedetomidine against Cerebral Ischemia-Reperfusion Injury in Rats: Involved in Inhibition of NF-kappa B and Inflammation Response

    作者

    Wang, LJ;Liu, HY;Zhang, LG;Wang, GM;Zhang, MY;Yu, YH

    作者单位

    [Wang, Lijun; Liu, Haiyan; Yu, Yonghui] Shandong Univ, Dept Pediat, Shandong Prov Hosp, Jinan 250021, Peoples R China.;-;[Zhang, Ligong; Wang, Gongming; Zhang, Mengyuan] Shandong Univ, Dept Anesthesia, Shandong Prov Hosp, Jinan 250021, Peoples R China.

    摘要

    Dexmedetomidine is an alpha 2-adrenergic receptor agonist that exhibits a protective effect on ischemia-reperfusion injury of the heart, kidney, and other organs. In the present study, we examined the neuroprotective action and potential mechanisms of dexmedetomidine against ischemia-reperfusion induded cerebral injury. Transient focal cerebral ischemia-reperfusion injury was induced in Sprague-Dawley rats by middle cerebral artery occlusion. After the ischemic insult, animals then received intravenous dexmedetomidine of 1 mu g/kg load dose, followed by 0.05 mu g/kg/min infusion for 2 h. After 24 h of reperfusion, neurological function, brain edema, and the morphology of the hippocampal CA1 region were evaluated. The levels and mRNA expressions of interleukin-1 beta, interleukin-6 and tumor nevrosis factor-alpha as well as the protein expression of inducible nitric Oxide synthase, cyclooxygenase-2, nuclear factor-kappa Bp65, inhibitor of kappa B alpha and phosphorylated of kappa B alpha in hippocampus were asessed. We found that dexmedetomidine reduced focal cerebral ischemia-reperfusion injury in rats by inhibiting the expression and release of inflammatory cytokines and mediators. Inhibition of the nuclear factor-kappa B pathway may be a mechanism underlying the neuroprotective action of dexmedetomidine against focal cerebral I/R injury.

    关键词

    GLOBAL-ISCHEMIA; BRAIN-INJURY; SIGNALING PATHWAY; OXIDATIVE STRESS; ARTERY OCCLUSION; NEONATAL-RATS; EXPRESSION; TRANSIENT; ACTIVATION; NEURODEGENERATION
基本信息

  • 所属机构:儿科新生儿

    归属医师: 于永慧 王公明 刘海燕 张立功 张孟元 王立俊

    PMID:27871154

    UT:000404947800006

    刊名:BIOMOLECULES & THERAPEUTICS

    年,卷(期):2017年25卷4期

    页码:383-389

    DOI:10.4062/biomolther.2015.180

    附件: pdf

    收录:   SCIE