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速激肽NK2受体拮抗剂沙瑞杜坦在基础和应激相关条件下情绪障碍实验模型中的行为效应。

Behavioral effects of saredutant, a tachykinin NK2 receptor antagonist, in experimental models of mood disorders under basal and stress-related conditions.

作者信息

Micale Vincenzo, Tamburella Alessandra, Leggio Gian Marco, Mazzola Carmen, Li Volsi Valentina, Drago Filippo

机构信息

Department of Experimental and Clinical Pharmacology, University of Catania Medical School, Viale A. Doria 6 95125 Catania, Italy.

出版信息

Pharmacol Biochem Behav. 2008 Sep;90(3):463-9. doi: 10.1016/j.pbb.2008.04.003. Epub 2008 Apr 12.

Abstract

The present study was made to investigate the role of tachykinin NK2 receptors in the expression of stress-related behaviors in animals. Under basal conditions, intraperitoneal (i.p.) administration of the selective tachykinin NK2 receptor antagonist, saredutant (1 and 3 mg/kg) or diazepam (1 mg/kg) exerted anxiolytic-like effects in rodents, as they reduced grooming score of Wistar male rats tested in the novelty-induced grooming sampling test (NGT) and increased percentage of time and entries in open arms of Swiss male mice tested in the elevated plus maze (EPM) test. After previous exposure to stress-related conditions, as induced by a 2-min forced swim made 5 min prior to the EPM test, saredutant but not diazepam, exhibited anxiolytic-like effects in mice. To study the antidepressant-like activity of tachykinin NK2 receptor antagonist under basal conditions, different groups of rats were injected i.p. with saredutant (2.5, 5 and 10 mg/kg) or the tricyclic antidepressant, clomipramine (50 mg/kg) and tested in the forced swim test (FST), a widely used antidepressant-responsive test. The influence of stress-related conditions was studied in rats subjected to electric foot-shocks (1 mA, 1 s) 24, 5 and 1 h prior to FST, after drugs injection. In the FST, clomipramine decreased the immobility time only under basal conditions, but not after application of acute foot-shocks. To the contrary, saredutant-treated rats also exhibited more active behavior in FST after previous exposure to stressors. These results give further support to the hypothesis that tachykinin NK2 receptors may be a therapeutic target for pharmacological treatment of stress-related diseases, such as anxiety and depression.

摘要

本研究旨在探讨速激肽NK2受体在动物应激相关行为表达中的作用。在基础条件下,腹腔注射选择性速激肽NK2受体拮抗剂沙瑞肽坦(1和3mg/kg)或地西泮(1mg/kg)对啮齿动物具有抗焦虑样作用,因为它们降低了在新奇诱导梳理采样试验(NGT)中测试的Wistar雄性大鼠的梳理得分,并增加了在高架十字迷宫(EPM)试验中测试的瑞士雄性小鼠在开放臂中的停留时间和进入次数百分比。在先前暴露于应激相关条件后,如在EPM试验前5分钟进行2分钟强迫游泳所诱导的,沙瑞肽坦而非地西泮在小鼠中表现出抗焦虑样作用。为了研究基础条件下速激肽NK2受体拮抗剂的抗抑郁样活性,不同组的大鼠腹腔注射沙瑞肽坦(2.5、5和10mg/kg)或三环类抗抑郁药氯米帕明(50mg/kg),并在强迫游泳试验(FST)中进行测试,这是一种广泛使用的抗抑郁反应性试验。在注射药物后,在FST前24、5和1小时对大鼠施加电足部电击(1mA,1s),研究应激相关条件的影响。在FST中,氯米帕明仅在基础条件下缩短了不动时间,但在施加急性足部电击后没有。相反,先前暴露于应激源后,沙瑞肽坦处理的大鼠在FST中也表现出更活跃的行为。这些结果进一步支持了以下假设:速激肽NK2受体可能是焦虑和抑郁等应激相关疾病药物治疗的治疗靶点。

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