Suppr超能文献

四种N-甲基-D-天冬氨酸受体拮抗剂对小鼠抗抑郁样和抗焦虑样作用以及认知和运动副作用的研究。

Investigation of antidepressant-like and anxiolytic-like actions and cognitive and motor side effects of four N-methyl-D-aspartate receptor antagonists in mice.

作者信息

Refsgaard Louise K, Pickering Darryl S, Andreasen Jesper T

机构信息

Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Behav Pharmacol. 2017 Feb;28(1):37-47. doi: 10.1097/FBP.0000000000000266.

Abstract

Evidence suggests that N-methyl-D-aspartate receptor (NMDAR) antagonists could be efficacious in treating depression and anxiety, but side effects constitute a challenge. This study evaluated the antidepressant-like and anxiolytic-like actions, and cognitive and motor side effects of four NMDAR antagonists. MK-801, ketamine, S-ketamine, RO 25-6981 and the positive control, citalopram, were tested for antidepressant-like and anxiolytic-like effects in mice using the forced-swim test, the elevated zero maze and the novelty-induced hypophagia test. Side effects were assessed using a locomotor activity test, the modified Y-maze and the rotarod test. All compounds increased swim distance in the forced-swim test. In the elevated zero maze, the GluN2B subtype-selective RO 25-6981 affected none of the measured parameters, whereas all other compounds showed anxiolytic-like effects. In the novelty-induced hypophagia test, citalopram and MK-801 showed anxiogenic-like action. All NMDAR antagonists induced hyperactivity. The high doses of ketamine and MK-801 impaired performance in the modified Y-maze test, whereas S-ketamine and RO 25-6891 showed no effects in this test. Only MK-801 impaired rotarod performance. The study supports that NMDARs could be a possible therapeutic target for treating depression and anxiety. However, selective antagonism of GluN2B subunit-containing NMDARs showed no effect on anxiety-like behaviours in this study.

摘要

有证据表明,N-甲基-D-天冬氨酸受体(NMDAR)拮抗剂可能对治疗抑郁症和焦虑症有效,但副作用构成了一项挑战。本研究评估了四种NMDAR拮抗剂的抗抑郁样和抗焦虑样作用,以及认知和运动副作用。使用强迫游泳试验、高架零迷宫试验和新奇诱导性摄食减少试验,对MK-801、氯胺酮、S-氯胺酮、RO 25-6981以及阳性对照西酞普兰在小鼠体内的抗抑郁样和抗焦虑样作用进行了测试。使用自发活动试验、改良Y迷宫试验和转棒试验评估副作用。所有化合物在强迫游泳试验中均增加了游泳距离。在高架零迷宫试验中,GluN2B亚型选择性拮抗剂RO 25-6981对所测参数均无影响,而所有其他化合物均表现出抗焦虑样作用。在新奇诱导性摄食减少试验中,西酞普兰和MK-801表现出致焦虑样作用。所有NMDAR拮抗剂均诱导活动亢进。高剂量的氯胺酮和MK-801在改良Y迷宫试验中损害了小鼠的行为表现,而S-氯胺酮和RO 25-6891在该试验中无影响。只有MK-801损害了转棒试验中的表现。该研究支持NMDAR可能是治疗抑郁症和焦虑症的一个潜在治疗靶点。然而,在本研究中,对含GluN2B亚基的NMDAR的选择性拮抗作用对焦虑样行为没有影响。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验