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新型抗精神病药物氨磺必利和阿立哌唑对大鼠母性行为的影响。

Effects of novel antipsychotics, amisulpiride and aripiprazole, on maternal behavior in rats.

作者信息

Li Ming, Budin Radek, Fleming Alison S, Kapur Shitij

机构信息

Centre for Addiction and Mental Health, Clarke Site 250 College Street, Toronto, Ontario, M5R 1T8, Canada.

出版信息

Psychopharmacology (Berl). 2005 Sep;181(3):600-10. doi: 10.1007/s00213-005-0091-7. Epub 2005 Oct 12.

Abstract

RATIONALE

Rat maternal behavior, which entails complex motivational and social factors, is disrupted by the currently available typical and atypical antipsychotics. It is thought that this disruption reflects a side effect of antipsychotics, modeling the neuroleptic-induced negative or deficit state. Amisulpiride and aripiprazole are new atypical antipsychotics with mechanisms of action distinct from the current typical and atypical antipsychotics. The effects of these drugs on maternal behavior have not been explored.

OBJECTIVE

In the present study, we systematically examined the behavioral effects of amisulpiride and aripiprazole on maternal behavior in postpartum female rats.

METHODS

Various components of maternal behavior (pup retrieval, pup licking, nest building and pup nursing) were examined repeatedly over a period of 24 h after a single injection of three doses of amisulpiride (10, 30, and 100 mg/kg s.c.) and aripiprazole (3, 10, and 30 mg/kg).

RESULTS

Amisulpiride at the lower doses (10 and 30 mg/kg) enhanced pup licking, and only at the highest dose disrupted the active components of maternal behavior such as pup retrieval and nest building. Its effect was delayed in onset and prolonged as compared to other antipsychotics. Aripiprazole, even at the highest dose (30 mg/kg) did not impair pup retrieval or pup licking. However, it did disrupt nest building and led to enhanced pup nursing.

CONCLUSIONS

The unique effects of these two drugs may be due to their unique actions at the mesolimbic dopamine synapses. The sparing of the major components of maternal behavior by aripiprazole may be related to its partial agonist effects, whereas the enhancement of pup licking by amisulpiride may be related to its dose-dependent preferential effect on the presynaptic autoreceptors. The potential clinical implications of these findings are discussed.

摘要

理论依据

大鼠的母性行为涉及复杂的动机和社会因素,目前可用的典型和非典型抗精神病药物会破坏这种行为。人们认为这种破坏反映了抗精神病药物的副作用,模拟了神经阻滞剂诱发的阴性或缺陷状态。氨磺必利和阿立哌唑是新型非典型抗精神病药物,其作用机制与目前的典型和非典型抗精神病药物不同。尚未探讨这些药物对母性行为的影响。

目的

在本研究中,我们系统地研究了氨磺必利和阿立哌唑对产后雌性大鼠母性行为的行为学影响。

方法

在单次注射三种剂量的氨磺必利(10、30和100mg/kg皮下注射)和阿立哌唑(3、10和30mg/kg)后的24小时内,反复检查母性行为的各个组成部分(幼崽找回、幼崽舔舐、筑巢和幼崽护理)。

结果

较低剂量(10和30mg/kg)的氨磺必利增强了幼崽舔舐行为,仅在最高剂量时才破坏母性行为的积极组成部分,如幼崽找回和筑巢。与其他抗精神病药物相比,其作用起效延迟且持续时间延长。阿立哌唑即使在最高剂量(30mg/kg)时也不会损害幼崽找回或幼崽舔舐行为。然而,它确实破坏了筑巢行为并导致幼崽护理增加。

结论

这两种药物的独特作用可能归因于它们在中脑边缘多巴胺突触处的独特作用。阿立哌唑对母性行为主要组成部分的保留可能与其部分激动剂作用有关;而氨磺必利对幼崽舔舐行为的增强可能与其对突触前自身受体的剂量依赖性优先作用有关。讨论了这些发现的潜在临床意义。

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