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山奈酚通过刺激腺苷 A2A 受体诱导皮质神经元表达脑源性神经营养因子:在神经保护中的可能作用。

Oroxylin A Induces BDNF Expression on Cortical Neurons through Adenosine A2A Receptor Stimulation: A Possible Role in Neuroprotection.

机构信息

Department of Pharmacology, College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 151-742 ; Neuroscience Research Center, Institute for Advanced Biomedical Sciences.

出版信息

Biomol Ther (Seoul). 2012 Jan;20(1):27-35. doi: 10.4062/biomolther.2012.20.1.027.

Abstract

Oroxylin A is a flavone isolated from a medicinal herb reported to be effective in reducing the inflammatory and oxidative stresses. It also modulates the production of brain derived neurotrophic factor (BDNF) in cortical neurons by the transactivation of cAMP response element-binding protein (CREB). As a neurotrophin, BDNF plays roles in neuronal development, differentiation, synaptogenesis, and neural protection from the harmful stimuli. Adenosine A2A receptor colocalized with BDNF in brain and the functional interaction between A2A receptor stimulation and BDNF action has been suggested. In this study, we investigated the possibility that oroxylin A modulates BDNF production in cortical neuron through the regulation of A2A receptor system. As ex-pected, CGS21680 (A2A receptor agonist) induced BDNF expression and release, however, an antagonist, ZM241385, prevented oroxylin A-induced increase in BDNF production. Oroxylin A activated the PI3K-Akt-GSK-3β signaling pathway, which is inhibited by ZM241385 and the blockade of the signaling pathway abolished the increase in BDNF production. The physiological roles of oroxylin A-induced BDNF production were demonstrated by the increased neurite extension as well as synapse formation from neurons. Overall, oroxylin A might regulate BDNF production in cortical neuron through A2A receptor stimulation, which promotes cellular survival, synapse formation and neurite extension.

摘要

山奈素 A 是一种从药用植物中分离出来的黄酮类化合物,据报道它可以有效减轻炎症和氧化应激。它还通过 cAMP 反应元件结合蛋白 (CREB) 的转激活调节皮质神经元中脑源性神经营养因子 (BDNF) 的产生。作为一种神经营养因子,BDNF 在神经元发育、分化、突触形成和神经保护方面发挥作用,免受有害刺激的影响。在大脑中,腺苷 A2A 受体与 BDNF 共定位,并且已经提出了 A2A 受体刺激和 BDNF 作用之间的功能相互作用。在这项研究中,我们研究了山奈素 A 是否通过调节 A2A 受体系统来调节皮质神经元中 BDNF 的产生。正如预期的那样,CGS21680(A2A 受体激动剂)诱导了 BDNF 的表达和释放,然而,拮抗剂 ZM241385 阻止了山奈素 A 诱导的 BDNF 产生增加。山奈素 A 激活了 PI3K-Akt-GSK-3β 信号通路,该通路被 ZM241385 抑制,阻断该信号通路会消除 BDNF 产生的增加。山奈素 A 诱导的 BDNF 产生增加了神经元的突起延伸和突触形成,证明了其具有生理作用。总的来说,山奈素 A 可能通过 A2A 受体刺激调节皮质神经元中 BDNF 的产生,从而促进细胞存活、突触形成和突起延伸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3464/3792198/a51fea58d143/ooomb4-20-27-g001.jpg

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