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Temporary inactivation of the anterior part of the bed nucleus of the stria terminalis blocks alarm pheromone-induced defensive behavior in rats

机译:终端纹状体床核前部的暂时失活阻止了警报信息素诱导的大鼠防御行为

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摘要

Rats emit an alarm pheromone in threatening situations. Exposure of rats to this alarm pheromone induces defensive behaviors, such as head out behavior, and increases c-Fos expression in brain areas involved in the mediation of defensive behaviors. One of these brain areas is the anterior bed nucleus of the stria terminalis (aBNST). The goal of the present study was to investigate if pharmacological inactivation of the aBNST by local microinjections of the GABAA receptor-agonist muscimol modulates alarm pheromone-induced defensive behaviors. We first established the behavioral paradigm of alarm pheromone-induced defensive behaviors in Sprague-Dawley rats in our laboratory. In a second experiment, we inactivated the aBNST, then exposed rats to one of four different odors (neck odor, female urine, alarm pheromone, fox urine) and tested the effects of the aBNST inactivation on the behavior in response to these odors. Our data show that temporary inactivation of the aBNST blocked head out behavior in response to the alarm pheromone. This indicates that the aBNST plays an important role in the mediation of the alarm pheromone-induced defensive behavior in rats.
机译:在威胁情况下,老鼠会发出警报信息素。大鼠暴露于这种警报信息素会诱导防御行为,例如出头行为,并增加参与防御行为介导的大脑区域的c-Fos表达。这些大脑区域之一是末端纹状体(aBNST)的前床核。本研究的目的是研究通过局部微量注射GABAA受体激动剂麝香酚对aBNST的药理失活是否能调节警报信息素诱导的防御行为。我们首先在我们的实验室中建立了警报信息素诱导的Sprague-Dawley大鼠防御行为的行为范式。在第二个实验中,我们使aBNST失活,然后将大鼠暴露于四种不同的气味(颈部气味,女性尿液,警报信息素,狐狸尿液)之一,并测试了aBNST失活对响应这些气味的行为的影响。我们的数据表明aBNST的暂时失活阻止了响应警报信息素的抬头行为。这表明aBNST在调动警报信息素诱导的大鼠防御行为中起重要作用。

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