n-methyl-d-aspartate      n-甲基-d-天冬氨酸(98) n-甲基-d-天门冬氨酸(46) n-甲基-d-门冬氨酸(20) n甲基d天冬氨酸(8) n-甲基-d-天门冬氨酸(0)   n-甲基-d-天冬氨酸     Effect of D-serine on N-methyl-D-aspartateinduced efflux  of cGMP from rat hippocampus     D-丝氨酸对N-甲基-D-天冬氨酸诱导大鼠海马cGMP释放作用的影响 短句来源     Suppression of morphine withdrawal signs by low doses of ketamine, a N-methyl-D-aspartate receptor antagonist     N-甲基-D-天冬氨酸受体拮抗剂氯胺酮抑制大鼠吗啡戒断症状的表达 短句来源     Protection of propofol on cultured PC12 cells impaired by N-methyl-D-aspartate     丙泊酚对N-甲基-D-天冬氨酸所致PC12细胞损伤的保护作用 短句来源     Regulation of Excitatory Amino Acid Release by N-Methyl-D-Aspartate Receptors in Rat Hippocampus     N-甲基-D-天冬氨酸受体对清醒大鼠海马谷氨酸释放的调节作用 短句来源     Effects of the blocker of N-methyl-D-aspartate receptor MK801 on the electrophysiological changes of CA1 neurons during hypoxia in isolated hippocampal slices of rats     离体海马脑片CA1区锥体细胞缺氧期间电生理指标变化与N-甲基-D-天冬氨酸受体阻断剂MK801干预后的变化(英文) 短句来源 更多          n-甲基-d-天门冬氨酸     Reversing effect of histamine on neuron death induced by N-methyl-D-aspartate     组胺对N-甲基-D-天门冬氨酸诱发的神经元损伤的改善作用 短句来源     Ketamine is a non-competitive antagonist of N-methyl-D-aspartate (NMDA) receptor.     氯胺酮(ketamine,Ket)属N-甲基-D-天门冬氨酸(N-methyl-D-aspartate,NMDA)受体非竞争性拮抗剂。 短句来源     Memantine hydrochloride is an amantadine derivative. It is a moderate affinity, non-competitive N-methyl-D-aspartate (NMDA) antagonist.     盐酸美金胺是盐酸金刚烷胺衍生物,它是具有中等亲和力的非竞争性的N-甲基-D-天门冬氨酸(NMDA)受体拮抗剂。 短句来源     They inhibit NMDA (N-methyl-D-aspartate) receptors; moreover,different conantokin species present different NMDA receptor subunit specificity. It can induce sleep-like symptoms in young mice when delivered intracranially.     芋螺睡眠肽是一类非竞争性的N-甲基-D-天门冬氨酸(N-methyl-D-aspartate,NMDA)受体的选择性抑制剂,并且具有受体亚型特异性,颅内注射芋螺睡眠肽后,实验鼠会呈现一种睡眠样症状。 短句来源   n-甲基-d-门冬氨酸     Protection of risperidone against N-methyl-D-aspartate induced injury in rat cortical neuronal cultures     利培酮对N-甲基-D-门冬氨酸诱导的大鼠皮层神经细胞损伤保护作用的研究 短句来源     N-methyl-D-aspartate (NMDA) receptors play an important role in the pathological processes of ischemic neuron injury.     兴奋性氨基酸受体N-甲基-D-门冬氨酸(NMDA)受体在脑缺血损伤的病理过程中起重要作用。 短句来源     MK-801 (Dizocilpine) is a non-competitive antagonist of N-methyl-D-aspartate (NMDA) receptor, which can easily penetrate blood-brain barrier[1] .     MK-801[(+)-5-methyl-10，11-dibenzol a,d-cyclohepten-5，10-imine meleate]，中文名地佐西平，是一种化学合成的非竞争性NMDA(N-甲基-D-门冬氨酸)受体拮抗剂，其作用强、易透过血脑屏障。 短句来源     Objective To explore the effect of risperidone on N-methyl-D-aspartate (NMDA)-induced injury in rat cortical neuronal cultures.     目的探讨利培酮对N-甲基-D-门冬氨酸(NMDA)诱导的大鼠皮层神经细胞损伤的作用。 短句来源     The discovery of novel classes of ion channels and their mechanisms of analgesia has provided pharma-ceutical researches with a large number of novel targets for pain therapy, including: tetrodotoxin-resistant (TTXr) Na+ ionchannel blockers, N-type Ca2+ ion channel blockers, acid-sensitive ion channel (ASICs) blockers, nicotinic acetylcholinereceptor (nAChRs) agonists, N-methyl-D- aspartate (NMDA) receptor antagonists, g-aminobutyric acid receptor subtypeA (GABAA) receptor agonists, P2X receptor antagonists and vanilloid receptor (VR) regulators.     新型离子通道及镇痛机理的发现,为药学研究提供了大量镇痛新靶点,包括河豚毒抗性-Na+(TTXr-Na+)通道阻滞剂、N-型Ca2+通道阻滞剂、酸敏离子通道(ASICs)阻滞剂、烟碱型乙酰胆碱受体(nAChRs)激动剂、N-甲基-D-门冬氨酸(NMDA)受体拮抗剂、g-氨基丁酸A亚型(GABAA)受体激动剂、P2X受体拮抗剂和香草素受体(VR)调节剂。 短句来源 更多          n甲基d天冬氨酸     Objective: To elucidate whether ketamine, a non-competitive antagonist of the N-methyl-D-aspartate(NMDA) receptor, could suppress the withdrawal signs of morphine when it has no effect on the motor functions in rats.     目的 :观察N 甲基 D 天冬氨酸 (N methyl D aspartate ,NMDA)受体拮抗剂氯胺酮 (ketamine)在不影响运动功能的条件下 ,是否能抑制吗啡依赖大鼠的戒断症状。 短句来源     AIM To investigate the potential neuroprotective effect of haloperidol on oxygen/glucose deprivation (OGD)- and N-methyl-D-aspartate (NMDA)-induced injuries on rat hippocampal slices in vitro and hippocampal neurons in primary culture, and the possible mechanism.     目的　观察氟哌啶醇对大鼠离体海马脑片和原代神经元的缺糖 缺氧 (OGD)和N 甲基 D 天冬氨酸 (N methyl D aspartate ,NMDA)损伤的潜在保护作用及其机制。 短句来源     ObjectiveTo study the protective effect of memantine on the regulation of N-methyl-D-aspartate(NMDA) receptor in dichlo rvos-poisoned rat brain,and to understand the mechanism of its role in organoph osphate poisoning.     目的　研究美金刚对敌敌畏染毒大鼠脑组织N 甲基 D 天冬氨酸 (NMDA)受体的保护作用及其治疗有机磷农药中毒的机制。 短句来源     Objective To observe the influence of propofol on amino acid levels in cultured PC12 cells impaired by N-methyl-D-aspartate, and explore the possible protective action mechanism of anesthetic propofol.     目的观察静脉麻醉药异丙酚对N甲基D天冬氨酸(NMDA)致PC12细胞损伤时氨基酸水平的影响,并探讨异丙酚细胞保护作用的可能机制。 短句来源     查询“n-methyl-d-aspartate”译词为其他词的双语例句 n-甲基-d-天门冬氨酸   查询“n-methyl-d-aspartate”译词为用户自定义的双语例句     我想查看译文中含有：的双语例句 为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法，我们为您准备了出自英文原文的大量英语例句，供您参考。   n-methyl-d-aspartate The effects of intracerebroventricular (icv) agonists and antagonists of N-methyl-D-aspartate (NMDA) and alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA) receptors on the general anesthesia of propofol were studied. 例句来源       It has been demonstrated that the key target of these peptides are N-methyl-D-aspartate glutamate receptors. 例句来源       Activation of rat cerebellum granule cells by N-methyl-D-aspartate (NMDA, 10-4-10-3 M) results in progressive increase in reactive oxygen species (ROS) and suppression of the ouabain-sensitive part of Na/K-ATPase activity. 例句来源       Objective: To study the effect of glycine site/NMDA (N-methyl-D-aspartate) receptor antagonist MRZ2/576 on the conditioned place preference (CPP) and locomotor activity induced by morphine in mice. 例句来源       Background and purpose A low-affinity, use-dependent N-Methyl-D-Aspartate (NMDA) antagonist AR-R15896AR has neuroprotective properties in animal models of ischaemic stroke. 例句来源       更多                    The ability of tetrandrine (Tet),as a Ca2+ antagonist isolated from a traditionalChinese herb,to reduce cortical neuronal injury was quantitatively examined in cell cultures derivedfrom fetal rats by measurement of lactate dehydrogenase(LDH)released to the extracellular bathingmedia.Cell cultures exposed to excitotoxins-glutamate(Glu),N-methyl-D-aspartate(NMDA),β-N-oxalylamino-L-alanine(BOAA, on non-NMDA receptors)and β-N-methyla...             兴奋性氨基酸类神经毒剂与粉防己碱（Ｔｅｔ）共同作用于原代培养胎鼠大脑皮层神经元２４ｈ，发现１０－７，１０－６ｍｏｌ·Ｌ－１Ｔｅｔ明显降低谷氨酸（Ｇｌｕ），β－Ｎ－ｏｘａｌｙｌａｍｉｎｏ－Ｌ－ａｌａｎｉｎｅ（ＢＯＡＡ）和β－Ｎ－ｍｅｔｈｙｌａｍｉｎｏ－Ｌ－ａｌａｎｉｎｅ（ＢＭＡＡ）导致的培养液乳酸脱氢酶（ＬＤＨ）活性增高，细胞形态损害减轻，细胞数量增加。对ＮＭＤＡＡ介导的神经元损伤改变无影响。提示Ｔｅｔ对某些Ｇｌｕ类神经毒剂引起的胎鼠大脑皮层神经元损伤有一定保护作用，其机制可能是抑制细胞膜Ｎａ＋通道开放，阻止膜去极化而影响电压依赖性Ｃａ２＋通道启动。对ＮＭＤＡ受体可能亦有一定作用。 文摘来源          The microdialysis technique was utilized to study the effects of exogenous D-serine on the cGMP level in the perfusate of rat hippocampus. Addition of N-methyl-D-aspartate (NMDA) 250 μmol·L1 to the perfusate resulted in a striking increase of cGMP in perfusate. The cGMP response elicited by NMDA was prevented by 7-chlorokynurenic acid (7CKA), a selective antagonist at the glycine site of the NMDA receptor. Dserine completely reversed the antagonis...             Ｄ┐丝氨酸对Ｎ┐甲基┐Ｄ┐天冬氨酸诱导大鼠海马ｃＧＭＰ释放作用的影响金英刘晓娟王化洲（锦州医学院药理学教研室，锦州１２１００１）很久以来，人们一直认为高级脊椎动物几乎不产生也不利用Ｄ－氨基酸系列［１］．然而，最近越来越多的实验表明在成年哺乳动物包括人... 文摘来源          Cultured neurons obtained from rat cortex were used to examine the protective effect of (-) S·R daurisoline (Dau) against N methyl D aspartate (NMDA) induced neurotoxicity. Cell viability was estimated by using trypan blue dye exclusion and MTT assay.Intracellular free Ca 2+ concentration ([Ca 2+ ] i ) was measured by using AR CM MIC cation measurement system with Fura 2/AM as Ca 2+ senstive fluorecent indicator. It was ...             蝙蝠葛苏林碱（ｄａｕｒｉｓｏｌｉｎｅ，Ｄａｕ）是从防己科植物蝙蝠葛根茎中提取的生物碱，（－）－Ｓ·Ｒ－Ｄａｕ是其人工合成非对映异构体．研究表明它的药理活性比天然品强很多［１］．我们最近报道（－）－Ｓ·Ｒ－Ｄａｕ能抑制谷氨酸（Ｇｌｕ）对原代培养的大鼠皮... 文摘来源   << 更多相关文摘         相关查询:  对查询结果不满意

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