Koh Phil-Ok, Cho Jae-Hyeon, Won Chung-Kil, Lee Hyo-Jong, Sung Jin-Hee, Kim Myeong-Ok
Department of Anatomy, College of Veterinary Medicine, Institute of Agriculture and Life Science, Gyeongsang National University, 900 Gajwa-dong, Jinju 660-701, South Korea.
Neurosci Lett. 2008 May 2;436(1):62-6. doi: 10.1016/j.neulet.2008.02.061. Epub 2008 Mar 2.
We previously showed that estradiol prevents neuronal cell death through the activation of Akt and its downstream targets Bad and FKHR. This study investigated whether estradiol modulates the survival pathway through other downstream targets of Akt, including mammalian target of rapamycin (mTOR) and p70S6 kinase. It is known that mTOR is a downstream target of Akt and a central regulator of protein synthesis, cell growth, and cell cycle progression. Adult female rats were ovariectomied and treated with estradiol prior to middle cerebral artery occlusion (MCAO). Brains were collected 24h after MCAO and infarct volumes were analyzed. We confirmed that estradiol significantly reduces infarct volume and decreases the number of positive cells for TUNEL staining in the cerebral cortex. Brain injury-induced a decrease in phospho-mTOR and phospho-p70S6 kinase. Estradiol prevented the injury-induced decrease in Akt activation and phosphorylation of mTOR and p70S6 kinases, and the subsequent decrease in S6 phosphorylation. Our findings suggest that estradiol plays a potent protective role against brain injury by preventing the injury-induced decrease of mTOR and p70S6 kinase phosphorylation.
我们之前的研究表明,雌二醇通过激活Akt及其下游靶点Bad和FKHR来防止神经元细胞死亡。本研究调查了雌二醇是否通过Akt的其他下游靶点(包括雷帕霉素哺乳动物靶点(mTOR)和p70S6激酶)来调节生存通路。已知mTOR是Akt的下游靶点,也是蛋白质合成、细胞生长和细胞周期进程的核心调节因子。成年雌性大鼠接受卵巢切除术,并在大脑中动脉闭塞(MCAO)前用雌二醇进行治疗。在MCAO后24小时收集大脑并分析梗死体积。我们证实,雌二醇显著减小梗死体积,并减少大脑皮质中TUNEL染色阳性细胞的数量。脑损伤导致磷酸化mTOR和磷酸化p70S6激酶减少。雌二醇可防止损伤诱导的Akt激活以及mTOR和p70S6激酶磷酸化的降低,以及随后S6磷酸化的降低。我们的研究结果表明,雌二醇通过防止损伤诱导的mTOR和p70S6激酶磷酸化降低,对脑损伤发挥强大的保护作用。