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7-硝基吲唑是一种一氧化氮合酶抑制剂,在焦虑探索模型中具有抗焦虑样特性。

7-Nitroindazole, a nitric oxide synthase inhibitor, has anxiolytic-like properties in exploratory models of anxiety.

作者信息

Volke V, Soosaar A, Kõks S, Bourin M, Männistö P T, Vasar E

机构信息

Department of Physiology, University of Tartu, Estonia.

出版信息

Psychopharmacology (Berl). 1997 Jun;131(4):399-405. doi: 10.1007/s002130050309.

Abstract

The action of the novel nitric oxide synthase (NOS) inhibitor 7-nitroindazole (7-NI) was studied in different exploratory models of anxiety. In the rat plus-maze test, 7-NI potently increased time spent on open arms and percentage of open arm visits in a dose dependent manner with the minimal effective dose of 40 mg/kg. 7-NI caused an anxiolytic-like effect in the rat social interaction test. The minimal dose increasing social interaction time was 20 mg/kg. However, the drug also produced a clear sedative effect occurring even at smaller doses (10 mg/kg) in the open field test. 7-NI also showed an anxiolytic-like profile in the mouse light-dark compartment test and in the elevated plus-maze test, but the doses required were higher (80-120 mg/kg) than in rat models. Also, the sedative effect occurred at these doses in open field. We failed to demonstrate any effect of L-arginine either in the rat elevated plus-maze test or in the open field test at doses up to 600 mg/kg IP. These results indicate that there are no major interspecies differences between rats and mice in respect of action of 7-NI. The clear anxiolytic-like action of the nitric oxide synthase inhibitor in four different models shows that nitric oxide is involved in the process of anxiety and that NOS could be a new target in developing anxiolytic drugs.

摘要

新型一氧化氮合酶(NOS)抑制剂7-硝基吲唑(7-NI)在不同的焦虑探索模型中的作用得到了研究。在大鼠高架迷宫试验中,7-NI以剂量依赖性方式显著增加了在开放臂上花费的时间和开放臂访问的百分比,最小有效剂量为40mg/kg。在大鼠社交互动试验中,7-NI产生了类似抗焦虑的作用。增加社交互动时间的最小剂量为20mg/kg。然而,在旷场试验中,该药物即使在较小剂量(10mg/kg)时也会产生明显的镇静作用。7-NI在小鼠明暗箱试验和高架迷宫试验中也表现出类似抗焦虑的特征,但所需剂量(80-120mg/kg)高于大鼠模型。此外,在这些剂量下,旷场试验中也出现了镇静作用。在腹腔注射高达600mg/kg的剂量时,我们未能在大鼠高架迷宫试验或旷场试验中证明L-精氨酸有任何作用。这些结果表明,在7-NI的作用方面,大鼠和小鼠之间没有主要的种间差异。一氧化氮合酶抑制剂在四种不同模型中明显的类似抗焦虑作用表明,一氧化氮参与了焦虑过程,并且NOS可能是开发抗焦虑药物的一个新靶点。

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