Program in Neuroscience, Washington State University, Pullman, Washington 99164, USA.
J Neurosci. 2011 Dec 14;31(50):18453-63. doi: 10.1523/JNEUROSCI.3824-11.2011.
The nucleus accumbens shell (NAc) is a key brain region mediating emotional and motivational learning. In rodent models, dynamic alterations have been observed in synaptic NMDA receptors (NMDARs) within the NAc following incentive stimuli, and some of these alterations are critical for acquiring new emotional/motivational states. NMDARs are prominent molecular devices for controlling neural plasticity and memory formation. Although synaptic NMDARs are predominately located postsynaptically, recent evidence suggests that they may also exist at presynaptic terminals and reshape excitatory synaptic transmission by regulating presynaptic glutamate release. However, it remains unknown whether presynaptic NMDARs exist in the NAc and contribute to emotional and motivational learning. In an attempt to identify presynaptically located NMDARs in the NAc, the present study uses slice electrophysiology combined with pharmacological and genetic tools to examine the physiological role of the putative presynaptic NMDARs in rats. Our results show that application of glycine, the glycine-site agonist of NMDARs, potentiated presynaptic release of glutamate at excitatory synapses on NAc neurons, whereas application of 5,7-dichlorokynurenic acid or 7-chlorokynurenic acid, the glycine-site antagonists of NMDARs, produced the opposite effect. However, these seemingly presynaptic NMDAR-mediated effects could not be prevented by application of d-APV, the glutamate-site NMDAR antagonist, and were still present in the mice in which NMDAR NR1 or NR3 subunits were genetically deleted. Thus, rather than suggesting the existence of presynaptic NMDARs, our results support the idea that an unidentified type of glycine-activated substrate may account for the presynaptic effects appearing to be mediated by NMDARs.
伏隔核壳(NAc)是调节情绪和动机学习的关键大脑区域。在啮齿动物模型中,激励刺激后 NAc 中的突触 NMDA 受体(NMDARs)会观察到动态改变,其中一些改变对于获得新的情绪/动机状态至关重要。NMDARs 是控制神经可塑性和记忆形成的主要分子装置。尽管突触 NMDARs 主要位于突触后,但最近的证据表明,它们也可能存在于突触前末梢,并通过调节突触前谷氨酸释放来重塑兴奋性突触传递。然而,突触前 NMDARs 是否存在于 NAc 中并参与情绪和动机学习仍不清楚。为了鉴定 NAc 中的突触前 NMDARs,本研究使用切片电生理学结合药理学和遗传学工具来检查大鼠中假定的突触前 NMDARs 的生理作用。我们的结果表明,应用甘氨酸(NMDAR 的甘氨酸位点激动剂)可增强 NAc 神经元上兴奋性突触前谷氨酸的释放,而应用 5,7-二氯犬尿氨酸或 7-氯犬尿氨酸(NMDAR 的甘氨酸位点拮抗剂)则产生相反的效果。然而,这些看似突触前 NMDAR 介导的效应不能通过应用谷氨酸位点 NMDAR 拮抗剂 d-APV 来阻止,并且在 NMDAR NR1 或 NR3 亚基被基因删除的小鼠中仍然存在。因此,我们的结果支持这样一种观点,即一种未识别的甘氨酸激活底物可能解释了看似由 NMDAR 介导的突触前效应,而不是表明存在突触前 NMDARs。