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1.
Guochuan Tsai Hsien-Yuan Lane Pinchen Yang Mian-Yoon Chong Nicholas Lange 《Neuropsychopharmacology》2004,55(5):452-456
BACKGROUND: Hypofunction of N-methyl-D-aspartate glutamate receptor had been implicated in the pathophysiology of schizophrenia. Treatment with D-serine or glycine, endogenous full agonists of the glycine site of N-methyl-D-aspartate receptor, or D-cycloserine, a partial agonist, improve the symptoms of schizophrenia. N-methylglycine (sarcosine) is an endogenous antagonist of glycine transporter-1, which potentiates glycine's action on N-methyl-D-aspartate glycine site and can have beneficial effects on schizophrenia. METHODS: Thirty-eight schizophrenic patients were enrolled in a 6-week double-blind, placebo-controlled trial of sarcosine (2 g/d), which was added to their stable antipsychotic regimens. Twenty of them received risperidone. Measures of clinical efficacy and side effects were determined every other week. RESULTS: Patient who received sarcosine treatment revealed significant improvements in their positive, negative, cognitive, and general psychiatric symptoms. Similar therapeutic effects were observed when only risperidone-treated patients were analyzed. Sarcosine was well-tolerated, and no significant side effect was noted. CONCLUSIONS: Sarcosine treatment can benefit schizophrenic patients treated by antipsychotics including risperidone. The significant improvement with the sarcosine further supports the hypothesis of N-methyl-D-aspartate receptor hypofunction in schizophrenia. Glycine transporter-1 is a novel target for the pharmacotherapy to enhance N-methyl-D-aspartate function. 相似文献
2.
In the cortex only a few of the available NMDA receptors must be activated to evoke maximal release of adenosine. In fact, maximal adenosine release occurs at 30 μM NMDA, a concentration at which noradrenaline release is only 20% maximal. NMDA-evoked noradrenaline release appears to require the generation of propagated action potentials, while adenosine release does not. Noncompetitive block of NMDA-evoked release of adenosine, but not noradrenaline, can be overcome by increasing NMDA concentrations. The above findings are consistent with the possibility that there are spare receptors for NMDA-evoked adenosine release, but not for nor-adrenaline release. These spare receptors are not due to elevated levels of glycine in the vicinity of those NMDA receptors mediating adenosine release. Functionally, it appears that low level NMDA receptor activation provides a purinergic inhibitory threshold against higher level NMDA receptor mediated processes. This could provide inhibitory tone and selectivity for critical functions, such as learning, memory, and synaptic plasticity in the cortex. © 1993 Wiley-Liss, Inc. 相似文献
3.
F. Mennicken M. Savasta R. Peretti-Renucci C. Feuerstein 《Journal of neural transmission (Vienna, Austria : 1996)》1992,4(1):1-14
Summary The firing rate and terminal excitability of identified nigrostriatal dopamine (DA) neurons was determined before, and over a 10–15 min period following, direct intrastriatal administration of the glutamate (GLU) agonist NMDA, or saline. NMDA (0.025 and 0.075 mol) produced a short latency increase in DA cell firing rate. In 7/8 cases, this increase in firing rate was accompanied by a profound reduction in terminal excitability. The decrease in excitability usually outlasted the increase in firing rate (sometimes by more than 8 min), and was superseded at a later stage by a marked increase in excitability. None of these effects were seen with saline (n=5), and they could all be blocked by preadministration of the competitive NMDA antagonist AP-7 (0.025 mol; n=6). The sequence of events leading to the observed results is argued to be as follows; NMDA initially excites striatal efferents to the DA cell, which through disinhibition and direct stimulation increase DA cell firing rate. Increased firing rate leads to enhanced striatal DA release. Dopamine's inhibitory influence pre-empts any effect NMDA itself may have on the terminals of nigrostriatal neurons, and counteracts NMDA's stimulatory effect on striatal output cells. Furthermore, the marked reduction in terminal excitability suggests that DA becomes the dominant influence in the striatum for a time. Hence, the net outcome of the injection is augmented striatal DA tone. Later, the effect of residual NMDA becomes predominant once more. 相似文献
4.
O. N. Koreshonkov P. V. Perestenko M. A. Dumpis L. B. Piotrovskii 《Bulletin of experimental biology and medicine》1992,113(6):749-751
Institute of Experimental Medicine, Russian Academy of Medical Sciences, St. Petersburg. (Presented by Academician of the Russian Academy of Medical Sciences A. N. Klimov.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 113, No. 6, pp. 563–565, June, 1992. 相似文献
5.
Bengt Nellgård Tadeusz Wieloch 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1992,92(2):259-266
Summary Excitatory amino acids are implicated in the development of neuronal cell damage following periods of reversible cerebral ischemia or insulin-induced hypoglycemic coma. To explore the importance of glutamate receptor activation in the posthypoglycemic phase, we exposed rats to 20 min of insulin-induced severe hypoglycemia. The rats were treated immediately after the hypoglycemic insult with four regimes of glutamate receptor antagonists: (1) the AMPA (-amino-3-hydroxy-5-methyl-4-isoxazole propriate)-receptor antagonist NBQX [2.3-dihydroxy-6-nitro-7-sulfamoyl-benzo (F) quinoxaline] given as a bolus dose of 30 mg · kg-1 i.p., followed by an i.v. infusion of 225 g · kg-1 · min-1 for 6 h; (2) the non-competitive NMDA-receptor antagonist, dizocilpine (MK-801) 1 mg · kg-1 given i.v.; (3) a combined NBQX treatment, (a bolus dose of 10 mg · kg-1 i.p., followed by an i.v. infusion of 225 g · kg-1 · min-1 for 6 h), with dizocilpine 0.33 mg · kg-1 given twice i.p. at 0 and 15 min after recovery and (4) the competitive NMDA-receptor blocker CGP 40116 [D-(E)-2-amino-4-methyl-5-phosphono-3-pentenoic acid] 10 mg · kg-1 given i.p.. In the striatum, all glutamate receptor blockers significantly decreased neuronal damage by approximately 30%. An approximately 50% decrease in neuronal damage was demonstrated in neocortex and hippocampus following the combined treatment with NBQX and dizocilpine, while protection was variable following the treatment with a single glutamate-receptor antagonist. We conclude that neuronal damage continues to develop in the striatum and in cortical brain regions in the posthypoglycemic period and that both NMDA- and AMPA-receptors contribute to this process, possibly by a change in the cellular response to both AMPA- and NMDA-receptor stimulation. 相似文献
6.
综述了近年来N-甲基-D-天冬氨酸受体拮抗剂治疗脑缺血的应用进展,并从不同作用位点分别对各类药物特点作了阐述。 相似文献
7.
8.
二苯乙烯苷对脑缺血再灌注沙土鼠学习记忆功能及NMDA受体亲合力的影响 总被引:7,自引:2,他引:7
目的:研究2,3,5,4'-四羟基二苯乙烯-2-O-β-D-葡萄糖苷(2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucoside,简称二苯乙烯苷)对脑缺血再灌注沙土鼠学习记忆功能和对N-甲基-D-天冬氨酸(NMDA)受体亲合力的影响.方法:夹闭沙土鼠双侧颈总动脉10min,然后撤去动脉夹实现再灌注,7d后通过水迷宫测定学习记忆功能的改变,随后处死,测定前脑组织NMDA受体与[3H]MK801的亲合力.结果:Morris水迷宫实验显示,模型组游出时间和游泳距离比假手术组明显延长,二苯乙烯苷治疗组的游出时间和游泳距离均比模型组缩短.受体亲合情况测定结果显示,模型组的NMDA受体与[3H]MK801的亲和力比假手术组明显升高,而二苯乙烯苷治疗组可以降低模型动物的NMDA受体亲合力.结论:二苯乙烯苷能够改善缺血再灌注所导致的学习记忆功能障碍,降低NMDA受体与[3H]MK801亲合力,可能具有脑保护作用. 相似文献
9.
长时程增强(LTP)与学习记忆机制关系密切.长时程增强的产生依赖于钙离子通道的活动特性,Ca2+经不同的钙离子通道内流引发的长时程增强对应不同的记忆作用.综述了通过N-甲基-D-天门冬氨酸(NMDA)受体钙离子通道和电压依赖性钙离子通道(VDCC)活动产生LTP及其各自对应的记忆作用,还介绍了以低频刺激方式产生长时程增强的研究实例. 相似文献
10.
Effects of intrathecal NMDA and AMPA receptors agonists or antagonists on antinociception of propofol 总被引:7,自引:0,他引:7
AIM: To study the effects of intrathecal (it) agonists and antagonists of N-methyl-D-aspartate (NMDA) and alpha amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptors and NMDAR1 antisense oligodeoxynucleotides (AS ODN) on the antinociception of propofol. METHODS: Hot-plate test (HPPT) and acetic acid-induced writhing test were used to measure the nociceptive thresholds in mice. The effects of intrathecal NMDA, 相似文献