PI3K/AKT/mTOR通路
神经保护
蛋白激酶B
沃特曼宁
药理学
医学
细胞凋亡
冲程(发动机)
自噬
LY294002型
细胞生物学
再灌注损伤
癌症研究
化学
生物化学
工程类
机械工程
作者
Houcai Huang,Rongling Zhong,Zhi Xia,Jie Song,Liang Feng
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2014-07-30
卷期号:19 (8): 11196-11210
被引量:51
标识
DOI:10.3390/molecules190811196
摘要
Rhynchophylline (Rhy) is an alkaloid isolated from Uncaria which has long been recommended for the treatment of central nervous diseases. In our study, the neuroprotective effect of Rhy was investigated in a stroke model, namely permanent middle cerebral artery occlusion (pMCAO). Rats were injected intraperitoneally once daily for four consecutive days before surgery and then received one more injection after surgery. The protein and mRNA levels of p-Akt, p-mTOR, apoptosis-related proteins (p-BAD and cleaved caspase-3), TLR2/4/9, NF-κB, MyD88, BDNF and claudin-5 were examined. Following pMCAO, Rhy treatment not only ameliorated neurological deficits, infarct volume and brain edema, but also increased claudin-5 and BDNF expressions (p < 0.05). Moreover, Rhy could activate PI3K/Akt/mTOR signaling while inhibiting TLRs/NF-κB pathway. Wortmannin, a selective PI3K inhibitor, could abolish the neuroprotective effect of Rhy and reverse the increment in p-Akt, p-mTOR and p-BAD levels. In conclusion, we hypothesize that Rhy protected against ischemic damage, probably via regulating the Akt/mTOR pathway.
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