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雄性大鼠的攻击行为和性行为是否由相似的神经系统介导?来自c-Fos和药理学研究的见解。

Do similar neural systems subserve aggressive and sexual behaviour in male rats? Insights from c-Fos and pharmacological studies.

作者信息

Veening Jan G, Coolen Lique M, de Jong Trynke R, Joosten Henk W, de Boer Sietze F, Koolhaas Jaap M, Olivier Berend

机构信息

Department of Anatomy, University Medical Center St Radboud, Nijmegen, The Netherlands.

出版信息

Eur J Pharmacol. 2005 Dec 5;526(1-3):226-39. doi: 10.1016/j.ejphar.2005.09.041. Epub 2005 Nov 2.

Abstract

It is a common belief that male aggressive and sexual behaviour share many of the underlying neurobiological, neurological, pharmacological and neuroendocrine mechanisms. Therefore, we studied brain activation patterns in male rat after performance of aggressive and sexual behaviour and compared serotonergic pharmacology in the same paradigms to delineate possible similarities and differences. Patterns of Fos-immunoreactivity induced by aggressive and sexual encounters of Wild-type male Brown Norway rats were studied to localise the commonly activated (functionally shared) parts of the circuitry, and the specific (functionally different) parts of the neuronal circuitry. Some brain areas (caudal medial preoptic area and medial amygdala) were commonly activated, but other areas (e.g. posterodorsal parts of the medial amygdala, rostral preoptic and premammillary hypothalamus) showed remarkably specific differences in neural activation. 5-HT(1A) receptor agonists inhibit aggressive, but stimulate male sexual behaviour, whereas 5-HT(1B) receptor agonists inhibit both types of behaviour. Selective serotonin reuptake inhibitors share comparable inhibitory effects in aggression and sexual behaviour, although only at relatively high doses. We propose that separate hard-wired neural systems exist in the brain for aggressive and sexual behaviours, modulated via hierarchically 'higher-level' brain areas that are involved in the integration (gating) of the behavioural outcome of an organism.

摘要

人们普遍认为,雄性的攻击行为和性行为具有许多共同的潜在神经生物学、神经学、药理学和神经内分泌机制。因此,我们研究了雄性大鼠在表现出攻击行为和性行为后脑的激活模式,并比较了相同范式下的血清素能药理学,以确定可能的异同。研究了野生型雄性挪威棕色大鼠在攻击和性接触后诱导的Fos免疫反应模式,以定位神经回路中共同激活(功能共享)的部分以及神经元回路中特定(功能不同)的部分。一些脑区(尾内侧视前区和内侧杏仁核)被共同激活,但其他区域(如内侧杏仁核的后背部、视前区前部和乳头体前下丘脑)在神经激活方面表现出明显的特异性差异。5-HT(1A)受体激动剂抑制攻击行为,但刺激雄性性行为,而5-HT(1B)受体激动剂抑制这两种行为。选择性5-羟色胺再摄取抑制剂在攻击行为和性行为中具有类似的抑制作用,尽管仅在相对高剂量时才有此作用。我们提出,大脑中存在独立的、硬连线的神经系统来控制攻击行为和性行为,这些系统通过参与生物体行为结果整合(控制)的“更高层次”脑区进行调节。

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