首页> 外文期刊>Aggressive behavior: A multidisciplinary journal devoted to the experimental and observational analysis of conflict in humans and animals >Behavioral profile of L-655,708, a selective ligand for the benzodiazepine site of GABA-A receptors which contain the α5 subunit, in social encounters between male mice
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Behavioral profile of L-655,708, a selective ligand for the benzodiazepine site of GABA-A receptors which contain the α5 subunit, in social encounters between male mice

机译:在雄性小鼠之间的社交交往中,L-655,708(一种包含α5亚基的GABA-A受体的苯二氮卓类位点的选择性配体)的行为特征

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摘要

GABA-A receptor is a transmembrane hetero-oligomeric protein which consists of five subunits, the combination of which confers unique pharmacological properties to the receptor. It is well-known that the GABAergic system is involved in the modulation of aggression. However, the role of α5/GABA-A receptors has not been explored. In this study, we examined the effect of L-655,708 (0.625-5 mg/kg), a selective ligand for the benzodiazepine site of GABA-A receptors which contain the α5 subunit, on agonistic behavior elicited by isolation in male mice. Individually housed mice were exposed to an anosmic standard opponent 30 min after drug administration, and the encounters were videotaped and evaluated using an ethologically based analysis. L-655,708 (5 mg/kg) exhibited an ethopharmacological profile characterized by a marked reduction of the time spent in offensive behavior (threat and attack) without affecting immobility, accompanied by a significant increase of avoidance/flee and nonsocial exploration behaviors, suggesting that the antiaggressive effect of the drug is unselective. Overall, this behavioral profile might indicate the existence of an anxiogenic-like activity of L-655,708 in mice.
机译:GABA-A受体是一种跨膜异源寡聚蛋白,它由五个亚基组成,这些亚基的结合赋予该受体独特的药理特性。众所周知,GABA能系统参与了攻击的调节。然而,尚未探索α5/ GABA-A受体的作用。在这项研究中,我们研究了L-655,708(0.625-5 mg / kg)对雄性小鼠隔离引起的激动行为的影响,L-655,708(0.625-5 mg / kg)是包含α5亚基的GABA-A受体的苯二氮卓类位点的选择性配体。在给药后30分钟,将单独饲养的小鼠暴露于一个厌氧的标准对手中,并对相遇进行录像,并使用基于行为学的分析进行评估。 L-655708(5 mg / kg)具有人体药理学特征,其进攻行为(威胁和攻击)所花费的时间显着减少,而不会影响固定性,同时回避/逃逸和非社会探索行为也显着增加,这表明该药物的抗攻击作用是非选择性的。总体而言,这种行为模式可能表明小鼠中存在L-655708的类似焦虑的活性。

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