首页> 美国卫生研究院文献>Journal of Neurotrauma >Inhibition of Src Family Kinases Protects Hippocampal Neurons and Improves Cognitive Function after Traumatic Brain Injury
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Inhibition of Src Family Kinases Protects Hippocampal Neurons and Improves Cognitive Function after Traumatic Brain Injury

机译:Src家族激酶的抑制保护海马神经元和改善认知功能的颅脑外伤后。

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摘要

Traumatic brain injury (TBI) is often associated with intracerebral and intraventricular hemorrhage. Thrombin is a neurotoxin generated at bleeding sites fater TBI and can lead to cell death and subsequent cognitive dysfunction via activation of Src family kinases (SFKs). We hypothesize that inhibiting SFKs can protect hippocampal neurons and improve cognitive memory function after TBI. To test these hypotheses, we show that moderate lateral fluid percussion (LFP) TBI in adult rats produces bleeding into the cerebrospinal fluid (CSF) in both lateral ventricles, which elevates oxyhemoglobin and thrombin levels in the CSF, activates the SFK family member Fyn, and increases Rho-kinase 1(ROCK1) expression. Systemic administration of the SFK inhibitor, PP2, immediately after moderate TBI blocks ROCK1 expression, protects hippocampal CA2/3 neurons, and improves spatial memory function. These data suggest the possibility that inhibiting SFKs after TBI might improve clinical outcomes.
机译:脑外伤(TBI)通常与脑内和脑室内出血有关。凝血酶是在TBI加油的出血部位产生的神经毒素,可通过激活Src家族激酶(SFK)导致细胞死亡和随后的认知功能障碍。我们假设抑制SFKs可以保护TBI后的海马神经元并改善认知记忆功能。为了检验这些假设,我们显示成年大鼠中度的外侧fluid击(LFP)TBI会导致两个侧脑室的脑脊液(CSF)出血,这会升高CSF中的氧合血红蛋白和凝血酶水平,激活SFK家族成员Fyn,并增加Rho激酶1(ROCK1)的表达。在中度TBI阻断后,立即全身给药SFK抑制剂PP2,可阻止ROCK1表达,保护海马CA2 / 3神经元,并改善空间记忆功能。这些数据表明在TBI后抑制SFKs可能会改善临床结局的可能性。

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