首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Musk Ketone Induces Neural Stem Cell Proliferation and Differentiation in Cerebral Ischemia via Activation of the PI3K/Akt Signaling Pathway
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Musk Ketone Induces Neural Stem Cell Proliferation and Differentiation in Cerebral Ischemia via Activation of the PI3K/Akt Signaling Pathway

机译:麝香酮通过激活PI3K / AKT信号通路诱导脑缺血中的神经干细胞增殖和分化

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Traditional Chinese medicine has been reported to influence the proliferation and differentiation of neural stem cells (NSCs) that may be protective against nervous system diseases. Recent evidence indicates the importance of musk ketone in nerve recovery and preventing secondary damage after cerebral ischemic injury. A middle cerebral artery occlusion (MCAO) rat model was established by a transient filament model, and rats were treated with musk ketone (0.9 or 1.8 mu M). Next, an in vitro oxygen-glucose deprivation (OGD) cell model was established to study the effect of musk ketone on the proliferation and differentiation of NSCs. To determine the potential mechanisms of musk ketone involved in activities of NSCs, the effect of musk ketone on the PI3K/Akt signaling pathway activation was assessed. Furthermore, NSCs were treated with musk ketone in the presence of PI3K/Akt inhibitor Akti-1/2 to examine their roles on NSC proliferation and differentiation. Musk ketone reduced cerebral ischemic injury in a dose-dependent manner in rats. In addition, NSCs treated with musk ketone showed enhanced proliferation and differentiation along with increased PI3K/Akt signaling pathway activation. The effects of muck ketone were reversed by Akti-1/2. Altogether, musk ketone promoted NSC proliferation and differentiation and protected against cerebral ischemia by activating the PI3K/Akt signaling pathway, highlighting the potential of musk ketone as a physiologically validated approach for the treatment of cerebral ischemia. (C) 2020 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:据报道,中药据报道,影响神经干细胞(NSC)的增殖和分化,这可能对神经系统疾病进行保护。最近的证据表明麝香酮在神经恢复和脑缺血性损伤后预防二次损害的重要性。通过瞬态灯丝模型建立中脑动脉闭塞(MCAO)大鼠模型,并用麝香酮(0.9或1.8μm)处理大鼠。接下来,建立体外氧 - 葡萄糖剥夺(OGD)细胞模型,以研究麝香酮对NSCs的增殖和分化的影响。为了确定参与NSC的活动的麝香酮的潜在机制,评估了麝香酮对PI3K / AKT信号传导途径激活的影响。此外,在PI3K / AKT抑制剂AKTI-1/2存在下用麝香酮处理NSCs,以检查它们对NSC增殖和分化的作用。麝香酮以依赖于大鼠的剂量依赖性的方式降低脑缺血性损伤。此外,用麝香酮处理的NSCs显示出增强的增殖和分化以及增加的PI3K / AKT信号通路激活。通过Akti-1/2逆转蒙克酮的效果。共用麝香酮促进了NSC的增殖和分化,并通过激活PI3K / AKT信号通路来保护脑缺血,突出麝香酮的潜力作为治疗脑缺血的生理学验证的方法。 (c)2020年度IBRO。 elsevier有限公司出版。保留所有权利。

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