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苯二氮䓬受体配体对激动行为的调节作用。

Modulatory actions of benzodiazepine receptor ligands on agonistic behaviour.

作者信息

Mos J, Olivier B, van der Poel A M

机构信息

Duphar B.V., Department of Pharmacology, Weesp, Holland.

出版信息

Physiol Behav. 1987;41(3):265-78. doi: 10.1016/0031-9384(87)90363-5.

Abstract

Several experiments were conducted to establish the role of benzodiazepine (BDZ) receptor ligands in aggressive behaviour in male and female rats. In particular, the pro-aggressive effects of BDZ agonists was subject of investigation. Predatory aggression (mouse killing) was facilitated by chlordiazepoxide (CDP) when tested in naive female rats, but CDP was unable to induce muricide in non-killing rats with extensive experience with mice. In experiments on maternal aggression in rats a post-hoc analysis revealed that the pro-aggressive action of CDP on maternal aggression was base line dependent: the increase in aggression in spontaneously low aggressive females was significantly higher than in females with a higher base line level. A further study aimed at unravelling the underlying factors contributing to this pro-aggressive action by determining the role of opponent size on the effects induced by CDP. Normally large opponents evoke less aggression from lactating females than smaller opponents and CDP exerted its pro-aggressive effect particularly strongly in the 'large opponent' situation. An ethological analysis was made of lateral display--an ambivalent posture frequently occurring in agonistic behaviour--to establish whether CDP indirectly increases aggression by reducing fear by means of its anxiolytic properties. The data partly support this hypothesis. These findings stress the importance of environmental and experiential factors in the possible outcome of CDP effects on aggression. Moreover, they point to possible explanations of seemingly contradictory data. In two final experiments an inverse benzodiazepine receptor agonist (beta-CCE) was tested in maternal aggression. beta-CCE reduced aggression, although not in a completely specific way. A neutral BDZ-receptor antagonist (Ro 15-1788) was tried in an attempt to antagonize the pro-aggressive effects of CDP in maternal aggression. Ro 15-1788 did not counteract the pro-aggressive action of CDP, but antagonized CDP effects on exploration. The modulatory role of the benzodiazepine receptor complex in aggression remains an intriguing area of research in which many subtleties in testing conditions play a role and in which more BDZ agonists, inverse agonists and antagonists have to be tested.

摘要

进行了多项实验以确定苯二氮卓(BDZ)受体配体在雄性和雌性大鼠攻击行为中的作用。特别是,BDZ激动剂的促攻击作用是研究的主题。当在未接触过的雌性大鼠中进行测试时,氯氮卓(CDP)促进了掠食性攻击(捕杀小鼠),但CDP无法在对小鼠有丰富经验的非捕杀大鼠中诱导杀鼠行为。在大鼠母性攻击实验中,事后分析表明,CDP对母性攻击的促攻击作用取决于基线:自发低攻击性雌性的攻击性增加明显高于基线水平较高的雌性。进一步的研究旨在通过确定对手大小对CDP诱导的效应的作用来揭示促成这种促攻击作用的潜在因素。通常,大型对手比小型对手引起哺乳期雌性的攻击性更小,而CDP在“大型对手”情况下尤其强烈地发挥其促攻击作用。对侧向展示——一种在争斗行为中经常出现的矛盾姿势——进行了行为学分析,以确定CDP是否通过其抗焦虑特性减轻恐惧来间接增加攻击性。数据部分支持了这一假设。这些发现强调了环境和经验因素在CDP对攻击性影响的可能结果中的重要性。此外,它们指出了看似矛盾的数据的可能解释。在最后两项实验中,对一种反向苯二氮卓受体激动剂(β-CCE)进行了母性攻击测试。β-CCE降低了攻击性,尽管不是完全特异性的。尝试使用一种中性BDZ受体拮抗剂(Ro 15-1788)来拮抗CDP在母性攻击中的促攻击作用。Ro 15-1788没有抵消CDP的促攻击作用,但拮抗了CDP对探索的影响。苯二氮卓受体复合物在攻击中的调节作用仍然是一个有趣的研究领域,其中测试条件中的许多细微差别都起作用,并且必须测试更多的BDZ激动剂、反向激动剂和拮抗剂。

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