Wang Guan, Amato Stephen, Gilbert James, Man Heng-Ye
Department of Biology, Boston University, Boston, MA 02215, USA.
Department of Biology, Boston University, Boston, MA 02215, USA.
Neuropharmacology. 2015 Aug;95:144-53. doi: 10.1016/j.neuropharm.2015.03.003. Epub 2015 Mar 17.
Resveratrol is a phytoalexin that confers overall health benefits including positive regulation in brain function such as learning and cognition. However, whether and how resveratrol affects synaptic activity remains largely unknown. α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) are glutamatergic receptors that mediate the majority of fast excitatory transmission and synaptic plasticity, and thus play a critical role in higher brain functions, including learning and memory. We find that in rat primary neurons, resveratrol can rapidly increase AMPAR protein level, AMPAR synaptic accumulation and the strength of excitatory synaptic transmission. The resveratrol effect on AMPAR protein expression is independent of sirtuin 1 (SIRT1), the conventional downstream target of resveratrol, but rather is mediated by AMP-activated protein kinase (AMPK) and subsequent downstream phosphoinositide 3-kinase (PI3K)/Akt signaling. Application of the AMPK specific activator 5-aminoimidazole-4-carboxamide-1-β-d-ribofuranoside (AICAR) mimics the effects of resveratrol on both signaling and AMPAR expression. The resveratrol-induced increase in AMPAR expression results from elevated protein synthesis via regulation of the eukaryotic initiation factor (eIF) 4E/4G complex. Disruption of the translation initiation complex completely blocks resveratrol-dependent AMPAR up-regulation. These findings indicate that resveratrol may regulate brain function through facilitation of AMPAR biogenesis and synaptic transmission.
白藜芦醇是一种植物抗毒素,具有多种健康益处,包括对大脑功能如学习和认知的正向调节作用。然而,白藜芦醇是否以及如何影响突触活动在很大程度上仍不清楚。α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPARs)是谷氨酸能受体,介导大部分快速兴奋性传递和突触可塑性,因此在包括学习和记忆在内的高级脑功能中起关键作用。我们发现,在大鼠原代神经元中,白藜芦醇可快速增加AMPAR蛋白水平、AMPAR突触聚集以及兴奋性突触传递的强度。白藜芦醇对AMPAR蛋白表达的影响不依赖于其传统下游靶点沉默调节蛋白1(SIRT1),而是由AMP激活的蛋白激酶(AMPK)及其下游的磷酸肌醇3-激酶(PI3K)/Akt信号通路介导。应用AMPK特异性激活剂5-氨基咪唑-4-甲酰胺-1-β-D-呋喃核糖苷(AICAR)可模拟白藜芦醇对信号传导和AMPAR表达的影响。白藜芦醇诱导的AMPAR表达增加是通过调节真核生物起始因子(eIF)4E/4G复合物提高蛋白质合成所致。翻译起始复合物的破坏完全阻断了白藜芦醇依赖性的AMPAR上调。这些发现表明,白藜芦醇可能通过促进AMPAR的生物合成和突触传递来调节脑功能。