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脑靶向雷帕霉素治疗大鼠癫痫的疗效

[Efficacy of brain-targeted rapamycin for treatment of epilepsy in rats].

作者信息

Zhang Yuanyuan, Wang Qingmei, Dong Jingyin, Zhang Binbin, Liu Luna, Zhu Feng, Zeng Linghui

机构信息

School of Medicine, Zhejiang University City College, Hangzhou 310015, China.

出版信息

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2018 May 25;47(5):457-464. doi: 10.3785/j.issn.1008-9292.2018.10.03.

Abstract

OBJECTIVE

To investigate the efficacy of brain-targeted rapamycin (T-Rap) in treatment of epilepsy in rats.

METHODS

Rapamycin nanoparticles targeting brain were prepared. The epilepsy model was induced by injection of pilocarpine in rats. The rats with pilocarpine-induced epilepsy were treated with rapamycin (Rap group) or brain-targeted rapamycin (T-Rap group). Seizure activity was observed by electroencephalography; the effect on mTOR signaling pathway was detected by Western blot; neuronal death and moss fiber sprouting were analyzed by Fluoro-Jade B (FJB) and Timm's staining, respectively.

RESULTS

Electroencephalography showed that both preparation of rapamycin significantly reduced the frequency of spontaneous seizures in rats, and the effect of T-Rap was stronger than that of conventional rapamycin (<0.05). Western blot showed that the phosphorylation levels of S6K and S6 in T-Rap group were lower than those in Rap group (all <0.05), indicating that T-Rap had a stronger inhibitory effect on mTOR signaling pathway. FJB staining showed that T-Rap significantly decreased neuronal death, but there was no significant difference as compared with Rap group. Timm's staining showed that both preparations of rapamycin significantly reduced the germination of mossy fibers, while the effect of T-Rap was more pronounced than Rap group (<0.05). The inhibition of body weight gain of T-Rap group was less than that of Rap group (<0.05).

CONCLUSIONS

T-Rap has a better therapeutic effect on epilepsy than conventional rapamycin with a less adverse effects in rats.

摘要

目的

探讨脑靶向雷帕霉素(T-Rap)治疗大鼠癫痫的疗效。

方法

制备脑靶向雷帕霉素纳米粒。通过向大鼠注射匹罗卡品诱导癫痫模型。用雷帕霉素(Rap组)或脑靶向雷帕霉素(T-Rap组)治疗匹罗卡品诱导癫痫的大鼠。通过脑电图观察癫痫发作活动;用蛋白质免疫印迹法检测对mTOR信号通路的影响;分别用氟玉髓B(FJB)染色和Timm染色分析神经元死亡和苔藓纤维出芽情况。

结果

脑电图显示,两种雷帕霉素制剂均显著降低大鼠自发性癫痫发作频率,且T-Rap的效果强于传统雷帕霉素(<0.05)。蛋白质免疫印迹法显示,T-Rap组中S6K和S6的磷酸化水平低于Rap组(均<0.05),表明T-Rap对mTOR信号通路具有更强的抑制作用。FJB染色显示,T-Rap显著降低神经元死亡,但与Rap组相比无显著差异。Timm染色显示,两种雷帕霉素制剂均显著减少苔藓纤维出芽,而T-Rap的效果比Rap组更明显(<0.05)。T-Rap组对体重增加的抑制作用小于Rap组(<0.05)。

结论

在大鼠中,T-Rap对癫痫的治疗效果优于传统雷帕霉素,且不良反应较少。

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