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大鼠的母性攻击行为:氯氮卓和氟哌嗪的影响。

Maternal aggression in rats: effects of chlordiazepoxide and fluprazine.

作者信息

Olivier B, Mos J, van Oorschot R

出版信息

Psychopharmacology (Berl). 1985;86(1-2):68-76. doi: 10.1007/BF00431686.

DOI:10.1007/BF00431686
PMID:3927368
Abstract

Although maternal aggression in rats is confined to a restricted post-partum period, the high and stable aggression level and the constancy of its behavioural structure make it an attractive experimental procedure for studying the behavioural effects of psychotropic drugs. Female rats were tested against naive male intruder rats for 5 or 10 min on post-partum days 3-9, during which aggression is stable. Chlordiazepoxide (CDP; 5, 10 and 20 mg/kg, orally) had a biphasic effect on aggression; it increased aggression considerably at 5 and (to a lesser extent) at 10 mg/kg. At 20 mg/kg aggression returned to control level. CDP shortened the latency to the first attack at 5 mg/kg, but not at higher dosages. CDP enhanced aggression, particularly in the first 2 min of an encounter. It did not change the structure of the aggressive behaviour, but did induce a dose-dependent increase in feeding. Fluprazine (Flu; 5, 10 and 20 mg/kg IP), a specific antiaggressive (serenic) drug, induced a dose-dependent decrease in aggression and exerted its largest effect in the first 2 min of an encounter. In accordance with the reduced aggression, latencies to the first attack increased. Maternal aggression in rats represents an extension to other (male) aggression paradigms in psychopharmacology. First, it has no male counterpart. Secondly, the hormonal mechanisms underlying this behaviour differ from those of male aggression. Thirdly, the morphology of maternal aggression is different from that shown in male models of agonistic behaviour (e.g. resident-intruder). These features make maternal aggression an attractive paradigm for pharmacological studies of female behaviour.

摘要

虽然大鼠的母性攻击行为仅限于产后的一段特定时期,但攻击水平高且稳定,行为结构恒定,这使其成为研究精神药物行为效应的一个有吸引力的实验方法。在产后第3至9天,让雌性大鼠与未经验的雄性入侵者大鼠进行5或10分钟的测试,在此期间攻击行为是稳定的。氯氮卓(CDP;5、10和20毫克/千克,口服)对攻击行为有双相效应;在5毫克/千克时显著增加攻击行为,在10毫克/千克时(程度较轻)也有增加。在20毫克/千克时,攻击行为恢复到对照水平。CDP在5毫克/千克时缩短了首次攻击的潜伏期,但在较高剂量时则没有。CDP增强了攻击行为,尤其是在相遇的前2分钟。它没有改变攻击行为的结构,但确实引起了剂量依赖性的进食增加。氟哌嗪(Flu;5、10和20毫克/千克,腹腔注射),一种特定的抗攻击(镇静)药物,引起攻击行为的剂量依赖性减少,并在相遇的前2分钟发挥最大作用。随着攻击行为的减少,首次攻击的潜伏期增加。大鼠的母性攻击行为是精神药理学中其他(雄性)攻击范式的一种扩展。首先,它没有雄性对应行为。其次,这种行为背后的激素机制与雄性攻击行为的不同。第三,母性攻击行为的形态与雄性攻击行为模型(如定居者-入侵者)中显示的不同。这些特征使母性攻击行为成为研究雌性行为药理学的一个有吸引力的范式。

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Maternal aggression in rats: effects of chlordiazepoxide and fluprazine.大鼠的母性攻击行为:氯氮卓和氟哌嗪的影响。
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Psychopharmacology (Berl). 1988;95(4):476-81. doi: 10.1007/BF00172958.

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