Yang X, Criswell H E, Simson P, Moy S, Breese G R
UNC Neuroscience Center, University of North Carolina School of Medicine at Chapel Hill, North Carolina, USA.
J Pharmacol Exp Ther. 1996 Jul;278(1):114-24.
An extracellular electrophysiological approach was used to determine the effect of ethanol on responses to N-methyl-D-aspartate (NMDA) across several brain regions in urethane-anesthetized rats. The results indicated that, in most brain regions, ethanol inhibited the NMDA-induced increases in firing rate for some, but not all, spontaneously active neurons. Ethanol functioned as an NMDA antagonist for some neurons in the medial septum, red nucleus, deep mesencephalic nucleus, substantia nigra reticulata, ventral tegmental area and cerebellum. In the hippocampus, ethanol inhibited NMDA responses from all neurons. However, ethanol was not found to be active against NMDA responses in the lateral septum, suggesting that there is a degree of regional specificity for ethanol inhibition of NMDA responses. It was then established in unanesthetized rats that ethanol also antagonized responses to NMDA in some, but not all, neurons in the medial septum and cortex, indicating that the differential action of ethanol on NMDA responses obtained in the urethane-anesthetized rats was not due to the anesthetic. Based on an earlier study showing that the effects of ifenprodil and ethanol on NMDA responses were correlated, the ability of ethanol to inhibit NMDA responses was compared with changes produced by ifenprodil on the same neurons, where ethanol did or did not affect NMDA responses. In the several brain regions investigated, ethanol inhibited NMDA responses in a subgroup of neurons in which ifenprodil inhibited NMDA-induced increases in firing. For all neurons investigated, if a cell was insensitive to ifenprodil antagonism of NMDA responses then ethanol also was ineffective against the response to NMDA. These results suggest that ethanol acts on an ifenprodil-sensitive NMDA receptor subtype. Given that previous investigations have suggested that the NMDA receptor type 2B subunit is essential for the action of ifenprodil, the positive relationship between the actions of ifenprodil and ethanol on responses to NMDA is consistent with the hypothesis that the combination of specific receptor subunits forming an NMDA receptor on a neuron determines the ability of ethanol to antagonize an NMDA response.
采用细胞外电生理方法,测定乙醇对氨基甲酸乙酯麻醉大鼠多个脑区N-甲基-D-天冬氨酸(NMDA)反应的影响。结果表明,在大多数脑区,乙醇抑制了部分(而非全部)自发活动神经元由NMDA诱导的放电频率增加。在中隔内侧、红核、中脑深核、黑质网状部、腹侧被盖区和小脑中,乙醇对部分神经元起到了NMDA拮抗剂的作用。在海马体中,乙醇抑制了所有神经元的NMDA反应。然而,未发现乙醇对外侧隔区的NMDA反应有作用,这表明乙醇对NMDA反应的抑制存在一定程度的区域特异性。随后在未麻醉的大鼠中证实,乙醇也拮抗了中隔内侧和皮质中部分(而非全部)神经元对NMDA的反应,这表明在氨基甲酸乙酯麻醉大鼠中观察到的乙醇对NMDA反应的差异作用并非由麻醉剂引起。基于早期一项显示艾芬地尔和乙醇对NMDA反应的影响具有相关性的研究,将乙醇抑制NMDA反应的能力与艾芬地尔对相同神经元产生的变化进行了比较,这些神经元中乙醇对NMDA反应有或没有影响。在所研究的几个脑区中,乙醇在艾芬地尔抑制NMDA诱导的放电增加的神经元亚组中抑制了NMDA反应。对于所有研究的神经元,如果一个细胞对艾芬地尔对NMDA反应的拮抗不敏感,那么乙醇对NMDA反应也无效。这些结果表明,乙醇作用于对艾芬地尔敏感的NMDA受体亚型。鉴于先前的研究表明NMDA 2B型受体亚基对艾芬地尔的作用至关重要,艾芬地尔和乙醇对NMDA反应的作用之间的正相关关系与以下假设一致:神经元上形成NMDA受体的特定受体亚基组合决定了乙醇拮抗NMDA反应的能力。