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慢性焦虑和“无畏”的动物模型。

Animal models of chronic anxiety and "fearlessness".

作者信息

Marczynski T J, Urbancic M

机构信息

Department of Pharmacology, University of Illinois, College of Medicine, Chicago 60612.

出版信息

Brain Res Bull. 1988 Sep;21(3):483-90. doi: 10.1016/0361-9230(88)90163-3.

DOI:10.1016/0361-9230(88)90163-3
PMID:2850844
Abstract

Three behavioral animal models have been described: a feline and a rodent model of chronic anxiety, and a rodent model of "fearless" behavior. The models have been obtained by pre- or perinatal exposure to diazepam (DZ) or RO 15-1788 which produced enduring postnatal deficits or enrichment, respectively, of brain benzodiazepine (BDZ) receptors. The receptor-deficient one-year-old cat progenies showed hyperarousal, unabated restless behavior, delayed acquisition of instrumentally conditioned behavior, bizarre escape responses and absence or reduced alpha-like EEG activity. The receptor-deficient rat progencies, studied at the age of 5-6 months, showed a reduction of time spent in deep slow wave sleep, and inability to habituate to novel environment, such as the radial arm maze. In the maze, the behavior of these progenies was characterized by delayed and incomplete exploratory activity often terminated by sudden escape, numerous fecal deposits and significantly more frequent than normal errors of "working memory." On the other hand, in all aspects, the receptor-enriched progenies were superior to the control animals as well as to the receptor-deficient group, particularly when the animals were challenged by novel and "intimidating" visual and/or auditory stimuli. In addition, 12 out of 51 receptor-deficient rats reared for 18 months developed mammary fibroadenomas, while no such tumors were found in the group of 44 vehicle-exposed control animals. Increased density and affinity of BDZ brain receptors was also observed after adult rats were treated with RO 15-1788 administered water for 7 or 14 days.

摘要

已描述了三种行为动物模型

一种慢性焦虑的猫科动物模型和啮齿动物模型,以及一种“无畏”行为的啮齿动物模型。这些模型是通过产前或围产期接触地西泮(DZ)或RO 15-1788获得的,它们分别导致出生后大脑苯二氮䓬(BDZ)受体持久缺乏或富集。受体缺乏的一岁猫后代表现出过度觉醒、持续的不安行为、工具性条件行为习得延迟、奇异的逃避反应以及α波样脑电图活动缺失或减少。对5-6个月大的受体缺乏大鼠后代进行研究发现,它们在深度慢波睡眠中花费的时间减少,并且无法适应新环境,如放射状臂迷宫。在迷宫中,这些后代的行为特点是探索活动延迟且不完整,常因突然逃避而终止,有大量粪便沉积,且“工作记忆”错误比正常情况频繁得多。另一方面,在各个方面,受体富集的后代均优于对照动物以及受体缺乏组,尤其是当动物受到新颖和“吓人”的视觉和/或听觉刺激挑战时。此外,在51只饲养18个月的受体缺乏大鼠中,有12只发生了乳腺纤维腺瘤,而在44只接受赋形剂处理的对照动物组中未发现此类肿瘤。在用RO 15-1788处理成年大鼠7天或14天后,还观察到BDZ脑受体的密度和亲和力增加。

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Animal models of chronic anxiety and "fearlessness".慢性焦虑和“无畏”的动物模型。
Brain Res Bull. 1988 Sep;21(3):483-90. doi: 10.1016/0361-9230(88)90163-3.
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