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激活三磷酸腺苷敏感性钾通道是中药 MLC901 抗缺氧葡萄糖剥夺神经保护作用的一个因素。

Activation of ATP-sensitive potassium channels as an element of the neuroprotective effects of the Traditional Chinese Medicine MLC901 against oxygen glucose deprivation.

机构信息

Institut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique (CNRS, UMR6097), Université de Nice Sophia Antipolis, 660 Route des Lucioles, 06560 Valbonne, France.

出版信息

Neuropharmacology. 2012 Sep;63(4):692-700. doi: 10.1016/j.neuropharm.2012.05.035. Epub 2012 May 30.

Abstract

NeuroAid (MLC601 and MLC901), a Traditional Medicine used in China for patients after stroke has been reported in preclinical models of ischemia to induce neuroprotection and neuroplasticity. This work shows the effects of MLC901 on an in vitro model of oxygen glucose deprivation (OGD). MLC901 prevents neuronal death induced by 120 min OGD and decreases the exaggerated Ca²⁺ entry in mature cortical neurons exposed to 120 min OGD. The neuroprotective effect of MLC901 is associated with a large hyperpolarization of ∼20 mV which is antagonized by glibenclamide, the specific inhibitor of K(ATP) channels. In addition MLC901 strengthens the activation of K(ATP) channels. MLC901 has been directly shown to act as an activator of K(ATP) channels as potent as the classical K(ATP) channel opener. The capacity of MLC901 to produce a large hyperpolarization, particularly in neurons that have suffered from energy deprivation probably plays an important role in the neuroprotective effects of this traditional medicine that comes in addition to its previously demonstrated neuroregenerative properties.

摘要

神经辅助剂(MLC601 和 MLC901)是一种在中国用于中风后患者的传统药物,已在缺血的临床前模型中被报道具有诱导神经保护和神经可塑性的作用。本研究显示了 MLC901 对体外氧葡萄糖剥夺(OGD)模型的影响。MLC901 可预防 120 分钟 OGD 诱导的神经元死亡,并降低成熟皮质神经元在 120 分钟 OGD 暴露下过度的 Ca²⁺内流。MLC901 的神经保护作用与约 20 mV 的超极化有关,该超极化被 K(ATP)通道的特异性抑制剂格列本脲拮抗。此外,MLC901 还增强了 K(ATP)通道的激活。已经直接证明 MLC901 作为 K(ATP)通道的激活剂,其作用与经典的 K(ATP)通道 opener 一样有效。MLC901 产生大超极化的能力,特别是在经历能量剥夺的神经元中,可能在这种传统药物的神经保护作用中发挥重要作用,除了其先前证明的神经再生特性。

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