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背侧海马体参与坦度螺酮抗焦虑作用的介导,坦度螺酮是一种5-羟色胺1A激动剂类抗焦虑药。

Involvement of the dorsal hippocampus in mediation of the antianxiety action of tandospirone, a 5-hydroxytryptamine1A agonistic anxiolytic.

作者信息

Kataoka Y, Shibata K, Miyazaki A, Inoue Y, Tominaga K, Koizumi S, Ueki S, Niwa M

机构信息

Department of Pharmacology, Nagasaki University School of Medicine, Japan.

出版信息

Neuropharmacology. 1991 May;30(5):475-80. doi: 10.1016/0028-3908(91)90009-z.

Abstract

The effect of tandospirone, a 5-hydroxytryptamine (5-HT)1A agonist/anxiolytic, injected directly into dorsal hippocampus, on Vogel-type conflict behavior in rats was investigated and the findings were compared with the effects of diazepam and zopiclone. Tandospirone (30 micrograms/2 microliters and 60 micrograms/2 microliters) and diazepam (40 micrograms/2 microliters) but not zopiclone (20 micrograms/2 microliters), produced a potent anticonflict action in rats. The anticonflict action of tandospirone (30 micrograms/2 microliters), injected into the dorsal hippocampus, was significantly blocked by (-)-propranolol (5 mg/kg i.p.). The present findings provide evidence that suggests that tandospirone has an antianxiety action, presumably by stimulating 5-HT1A receptors in the dorsal hippocampus.

摘要

研究了直接注射到大鼠背侧海马体中的5-羟色胺(5-HT)1A激动剂/抗焦虑药坦度螺酮对大鼠Vogel型冲突行为的影响,并将结果与地西泮和佐匹克隆的作用进行了比较。坦度螺酮(30微克/2微升和60微克/2微升)和地西泮(40微克/2微升),而非佐匹克隆(20微克/2微升),在大鼠中产生了有效的抗冲突作用。注射到背侧海马体中的坦度螺酮(30微克/2微升)的抗冲突作用被(-)-普萘洛尔(5毫克/千克,腹腔注射)显著阻断。目前的研究结果提供了证据,表明坦度螺酮具有抗焦虑作用,可能是通过刺激背侧海马体中的5-HT1A受体实现的。

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