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Glutamate in CNS disorders as a target for drug development: an update.中枢神经系统疾病中的谷氨酸作为药物开发靶点:最新进展
Drug News Perspect. 1998 Nov;11(9):523-69. doi: 10.1358/dnp.1998.11.9.863689.
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Chemistry and pharmacology of compounds related to 4-(4-hydroxy-4-phenyl-piperidino)-butyrophenone. IV. Influence of haloperidol (R 1625) and of chlorpromazine on the behaviour of rats in an unfamiliar "open field" situation.与4-(4-羟基-4-苯基-哌啶基)-丁酰苯相关化合物的化学与药理学。IV. 氟哌啶醇(R 1625)和氯丙嗪对大鼠在陌生“旷场”环境中行为的影响。
Psychopharmacologia. 1960 Sep 13;1:389-92. doi: 10.1007/BF00441186.
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Anxiolytic-like effects of the prototypical metabotropic glutamate receptor 5 antagonist 2-methyl-6-(phenylethynyl)pyridine in rodents.典型的代谢型谷氨酸受体5拮抗剂2-甲基-6-(苯乙炔基)吡啶对啮齿动物的抗焦虑样作用。
J Pharmacol Exp Ther. 2000 Dec;295(3):1267-75.
4
Effect of chronic antidepressant or electroconvulsive shock treatment on mGLuR1a immunoreactivity expression in the rat hippocampus.慢性抗抑郁药或电休克治疗对大鼠海马中代谢型谷氨酸受体1a免疫反应性表达的影响。
Pol J Pharmacol. 1999 Nov-Dec;51(6):539-41.
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Potential anti-anxiety, anti-addictive effects of LY 354740, a selective group II glutamate metabotropic receptors agonist in animal models.LY 354740(一种选择性II组代谢型谷氨酸受体激动剂)在动物模型中的潜在抗焦虑、抗成瘾作用。
Neuropharmacology. 1999 Dec;38(12):1831-9. doi: 10.1016/s0028-3908(99)00066-0.
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Potentiation of NMDA and AMPA responses by the specific mGluR5 agonist CHPG in spinal cord motoneurons.脊髓运动神经元中特异性代谢型谷氨酸受体5激动剂CHPG对N-甲基-D-天冬氨酸(NMDA)和α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)反应的增强作用。
Neuropharmacology. 1999 Oct;38(10):1569-76. doi: 10.1016/s0028-3908(99)00095-7.
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2-Methyl-6-(phenylethynyl)-pyridine (MPEP), a potent, selective and systemically active mGlu5 receptor antagonist.2-甲基-6-(苯乙炔基)吡啶(MPEP),一种强效、选择性且具有全身活性的代谢型谷氨酸受体5(mGlu5)拮抗剂。
Neuropharmacology. 1999 Oct;38(10):1493-503. doi: 10.1016/s0028-3908(99)00082-9.
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Antidepressants for the new millennium.面向新千年的抗抑郁药。
Eur J Pharmacol. 1999 Jun 30;375(1-3):31-40. doi: 10.1016/s0014-2999(99)00330-1.
9
SIB-1757 and SIB-1893: selective, noncompetitive antagonists of metabotropic glutamate receptor type 5.SIB - 1757和SIB - 1893:代谢型谷氨酸受体5型的选择性非竞争性拮抗剂。
J Pharmacol Exp Ther. 1999 Jul;290(1):170-81.
10
Glycine and N-methyl-D-aspartate receptors: physiological significance and possible therapeutic applications.甘氨酸和N-甲基-D-天冬氨酸受体:生理意义及潜在治疗应用
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MPEP(一种强效、选择性且具有全身活性的mGlu5受体拮抗剂)潜在的抗焦虑和抗抑郁样作用。

Potential anxiolytic- and antidepressant-like effects of MPEP, a potent, selective and systemically active mGlu5 receptor antagonist.

作者信息

Tatarczyńska E, Klodzińska A, Chojnacka-Wójcik E, Palucha A, Gasparini F, Kuhn R, Pilc A

机构信息

Institute of Pharmacology, Polish Academy of Sciences, 31-343 Kraków, Smetna 12, Poland.

出版信息

Br J Pharmacol. 2001 Apr;132(7):1423-30. doi: 10.1038/sj.bjp.0703923.

DOI:10.1038/sj.bjp.0703923
PMID:11264235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1572682/
Abstract
  1. Several lines of evidence suggest a crucial involvement of glutamate in the mechanism of action of anxiolytic and/or antidepressant drugs. The involvement of group I mGlu receptors in anxiety and depression has also been proposed. Given the recent discovery of a selective and brain penetrable mGlu5 receptor antagonists, the effect of 2-methyl-6-(phenylethynyl)-pyridine (MPEP), i.e. the most potent compound described, was evaluated in established models of anxiety and depression. 2. Experiments were performed on male Wistar rats or male Albino Swiss or C57BL/6J mice. The anxiolytic-like effects of MPEP was tested in the conflict drinking test and the elevated plus-maze test in rats as well as in the four-plate test in mice. The antidepressant-like effect was estimated using the tail suspension test in mice and the behavioural despair test in rats. 3. MPEP (1 - 30 mg kg(-1)) induced anxiolytic-like effects in the conflict drinking test and the elevated plus-maze test in rats as well as in the four-plate test in mice. MPEP had no effect on locomotor activity or motor coordination. MPEP (1 - 20 mg kg(-1)) did shorten the immobility time in a tail suspension test in mice, however it was inactive in the behavioural despair test in rats. 4. These data suggest that selective mGlu5 receptor antagonists may play a role in the therapy of anxiety and/or depression, further studies are required to identify the sites and the mechanism of action of MPEP.
摘要
  1. 多条证据表明谷氨酸在抗焦虑和/或抗抑郁药物的作用机制中起关键作用。也有人提出I组代谢型谷氨酸受体(mGlu受体)参与焦虑和抑郁过程。鉴于最近发现了一种选择性且可穿透血脑屏障的mGlu5受体拮抗剂,因此在已建立的焦虑和抑郁模型中评估了2-甲基-6-(苯乙炔基)吡啶(MPEP)(即所描述的最有效化合物)的作用效果。2. 实验在雄性Wistar大鼠、雄性白化瑞士小鼠或C57BL/6J小鼠身上进行。在大鼠的冲突饮水试验和高架十字迷宫试验以及小鼠的四板试验中测试了MPEP的抗焦虑样作用。使用小鼠的悬尾试验和大鼠的行为绝望试验评估其抗抑郁样作用。3. MPEP(1 - 30 mg·kg⁻¹)在大鼠的冲突饮水试验和高架十字迷宫试验以及小鼠的四板试验中诱导出抗焦虑样作用。MPEP对运动活性或运动协调性无影响。MPEP(1 - 20 mg·kg⁻¹)确实缩短了小鼠悬尾试验中的不动时间,然而在大鼠的行为绝望试验中无活性。4. 这些数据表明选择性mGlu5受体拮抗剂可能在焦虑和/或抑郁治疗中发挥作用,需要进一步研究以确定MPEP的作用位点和作用机制。