首页> 外文期刊>Journal of Pharmacological and Toxicological Methods >Comparison of pro-amnesic efficacy of scopolamine, biperiden, and phencyclidine by using passive avoidance task in CD-1 mice
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Comparison of pro-amnesic efficacy of scopolamine, biperiden, and phencyclidine by using passive avoidance task in CD-1 mice

机译:通过在CD-1小鼠中使用被动避免任务的汽油胺,双链和苯磺酸纤维的亲惰性效果的比较

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Introduction: Memory disorders accompany numerous diseases and therapies, and this is becoming a growing medical issue worldwide. Currently, various animal models of memory impairments are available; however, many of them require high financial outlay and/or are time-consuming. A simple way to achieve an efficient behavioral model of cognitive disorders is to inject defined drug that has pro-amnesic properties. Since the involvement of cholinergic and glutamatergic neurotransmission in cognition is well established, the utilization of a nonselective muscarinic receptor antagonist, scopolamine (SCOP), a selective M1 muscarinic receptor antagonist, biperiden (BIP), and a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist, phencyclidine (PCP) seems to be reliable tools to induce amnesia. As the determination of their effective doses remains vague and the active doses vary significantly in laboratory settings and in mouse species being tested, the aim of this study was to compare these three models of amnesia in CD-1 mice.
机译:简介:内存障碍伴随着众多疾病和治疗,这正成为全球越来越多的医学问题。目前,可以使用各种内存损伤的动物模型;然而,其中许多人需要高金融支出和/或耗时。实现认知障碍有效行为模型的简单方法是注入具有促进性质的定义的药物。由于胆碱能和谷氨酸神经传递在认知中的参与度,因此利用非选择性毒蕈碱受体拮抗剂,Scopolamine(SCOP),选择性M1毒蕈碱受体拮抗剂,双层(BIP)和非竞争性N-甲基-D - 海滩酸盐(NMDA)受体拮抗剂,PhenyClidine(PCP)似乎是诱导胃癌的可靠工具。由于其有效剂量的测定仍然模糊而活性剂量在实验室环境中显着变化,并且在测试的小鼠物种中,本研究的目的是将这三种模型的CD-1小鼠进行比较。

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