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雷帕霉素靶蛋白通路的药理学抑制可抑制获得性癫痫。

Pharmacological inhibition of the mammalian target of rapamycin pathway suppresses acquired epilepsy.

机构信息

Center for Neuropharmacology and Neuroscience, Albany Medical College, Albany, NY 12208, USA.

出版信息

Neurobiol Dis. 2010 Oct;40(1):193-9. doi: 10.1016/j.nbd.2010.05.024. Epub 2010 May 26.

Abstract

Inhibition of mTOR by rapamycin has been shown to suppress seizures in TSC/PTEN genetic models. Rapamycin, when applied immediately before or after a neurological insult, also prevents the development of spontaneous recurrent seizures (epileptogenesis) in an acquired model. In the present study, we examined the mTOR pathway in rats that had already developed chronic spontaneous seizures in a pilocarpine model. We found that mTOR is aberrantly activated in brain tissues from rats with chronic seizures. Furthermore, inhibition of mTOR by rapamycin treatment significantly reduces seizure activity. Finally, mTOR inhibition also significantly suppresses mossy fiber sprouting. Our findings suggest the possibility for a much broader window for intervention for some acquired epilepsies by targeting the mTOR pathway.

摘要

雷帕霉素抑制 mTOR 的作用已被证明可抑制 TSC/PTEN 遗传模型中的癫痫发作。雷帕霉素在神经损伤前后立即应用,也可防止获得性模型中自发性复发性癫痫(癫痫发生)的发展。在本研究中,我们检查了已经在匹鲁卡品模型中发生慢性自发性癫痫的大鼠的 mTOR 通路。我们发现,慢性癫痫大鼠脑组织中的 mTOR 异常激活。此外,雷帕霉素抑制 mTOR 治疗可显著降低癫痫发作活动。最后,mTOR 抑制也显著抑制苔藓纤维发芽。我们的研究结果表明,通过靶向 mTOR 通路,针对某些获得性癫痫的干预时间窗可能会更宽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/418f/2926303/59ff639d32b4/nihms-210649-f0001.jpg

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