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自噬抑制剂3-甲基腺嘌呤削弱创伤性脑损伤中度低温的神经保护作用。

Autophagy Inhibitor 3-MA Weakens Neuroprotective Effects of Posttraumatic Brain Injury Moderate Hypothermia.

作者信息

Jin Yichao, Lei Jin, Lin Yingying, Gao Guo-Yi, Jiang Ji-Yao

机构信息

Department of Neurosurgery, Renji Hospital, Shanghai Jiaotong University, School of Medicine, Shanghai, People's Republic of China.

Department of Neurosurgery, Renji Hospital, Shanghai Jiaotong University, School of Medicine, Shanghai, People's Republic of China.

出版信息

World Neurosurg. 2016 Apr;88:433-446. doi: 10.1016/j.wneu.2015.10.055. Epub 2015 Nov 4.

Abstract

OBJECTIVE

The role of autophagy in moderate hypothermia in posttraumatic brain injury (post-TBI) remains elusive. In this study, we evaluated the protective role of autophagy in post-TBI moderate hypothermia.

METHODS

Adult male Sprague-Dawley rats were randomly divided into 3 groups (n = 36/group): TBI with hypothermia group (sham), TBI with hypothermia and a single intracerebroventricular injection of saline (saline, 5 μL), and TBI with hypothermia and a single intracerebroventricular injection of 3-methyladenine (600 nmol, diluted in 0.9% saline to a final volume of 5 μL). All rats, except those in the behavioral tests, were killed at 24 hours after fluid percussion TBI. Immunohistochemistry staining, western blot, and transmission electron microscopy were performed to assess changes in apoptosis and autophagy after injection of 3-methyladenine. Motor function (beam-walk test) and spatial learning/memory (Morris water maze) were assessed on postoperative days 1-5 and 11-15, respectively.

RESULTS

Our results showed downregulation of the expression level of microtubule-associated protein 1 light chain 3 and Beclin-1, aggravation of behavioral outcome, and increase of apoptosis.

CONCLUSION

Our results suggest that the autophagy pathway is involved in the neuroprotective effect of post-TBI hypothermia and negative modulation of apoptosis may be 1 possible mechanism.

摘要

目的

自噬在创伤性脑损伤(TBI)后中度低温中的作用仍不明确。在本研究中,我们评估了自噬在TBI后中度低温中的保护作用。

方法

成年雄性Sprague-Dawley大鼠随机分为3组(每组n = 36):TBI伴低温组(假手术组)、TBI伴低温且脑室内单次注射生理盐水组(生理盐水组,5 μL)、TBI伴低温且脑室内单次注射3-甲基腺嘌呤组(600 nmol,用0.9%生理盐水稀释至最终体积5 μL)。除行为测试组外,所有大鼠在流体冲击性TBI后24小时处死。进行免疫组织化学染色、蛋白质印迹法和透射电子显微镜检查,以评估注射3-甲基腺嘌呤后凋亡和自噬的变化。分别在术后第1 - 5天和第11 - 15天评估运动功能(横梁行走试验)和空间学习/记忆(莫里斯水迷宫试验)。

结果

我们的结果显示微管相关蛋白1轻链3和Beclin-1表达水平下调、行为结果恶化以及凋亡增加。

结论

我们的结果表明自噬途径参与了TBI后低温的神经保护作用,对凋亡的负向调节可能是一种可能的机制。

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