Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
Neurosci Biobehav Rev. 2012 Mar;36(3):989-1000. doi: 10.1016/j.neubiorev.2011.12.011. Epub 2012 Jan 2.
N-methyl-D-aspartate receptors (NMDARs) are key components of neural signaling, playing roles in synaptic transmission and in the synaptic plasticity thought to underlie learning and memory. NMDAR activation can also have neurotoxic consequences contributing to several forms of neurodegeneration. Additionally, NMDARs can modulate neuronal function and regulate the ability of synapses to undergo synaptic plasticity. Evidence gathered over the past 20 years strongly supports the idea that untimely activation of NMDARs impairs the induction of long-term potentiation (LTP) by a form of metaplasticity. This metaplasticity can be triggered by multiple stimuli including physiological receptor activation, and metabolic and behavioral stressors. These latter findings raise the possibility that NMDARs contribute to cognitive dysfunction associated with neuropsychiatric disorders. This paper examines NMDAR metaplasticity and its potential role in cognition. Recent studies using NMDAR antagonists for therapeutic purposes also raise the possibility that metaplasticity may contribute to clinical effects of certain drugs.
N-甲基-D-天冬氨酸受体(NMDARs)是神经信号传递的关键组成部分,在突触传递和被认为是学习和记忆基础的突触可塑性中发挥作用。NMDAR 的激活也可能具有神经毒性后果,导致几种形式的神经退行性变。此外,NMDAR 可以调节神经元功能并调节突触经历突触可塑性的能力。过去 20 年收集的证据强烈支持这样一种观点,即 NMDAR 的过早激活会损害长时程增强(LTP)的诱导,这是一种形式的变构调节。这种变构可以由多种刺激触发,包括生理受体激活以及代谢和行为应激源。这些发现提出了一种可能性,即 NMDARs 与神经精神障碍相关的认知功能障碍有关。本文研究了 NMDAR 变构调节及其在认知中的潜在作用。最近使用 NMDAR 拮抗剂进行治疗的研究也提出了这样一种可能性,即变构调节可能有助于某些药物的临床效果。