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下丘脑前部的血管加压素调节叙利亚仓鼠青春期接触可卡因的攻击刺激作用。

Anterior hypothalamic vasopressin modulates the aggression-stimulating effects of adolescent cocaine exposure in Syrian hamsters.

作者信息

Jackson D, Burns R, Trksak G, Simeone B, DeLeon K R, Connor D F, Harrison R J, Melloni R H

机构信息

Behavioral Neuroscience Program, Department of Psychology, 125 Nightingale Hall, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, USA.

出版信息

Neuroscience. 2005;133(3):635-46. doi: 10.1016/j.neuroscience.2005.02.047.

Abstract

Repeated low-dose cocaine treatment (0.5 mg/kg/day) during adolescence induces offensive aggression in male Syrian hamsters (Mesocricetus auratus). This study examines the hypothesis that adolescent cocaine exposure predisposes hamsters to heightened levels of aggressive behavior by increasing the activity of the anterior hypothalamic-vasopressinergic neural system. In a first experiment, adolescent male hamsters were treated with low-dose cocaine and then scored for offensive aggression in the absence or presence of vasopressin receptor antagonists applied directly to the anterior hypothalamus. Adolescent cocaine-treated hamsters displayed highly escalated offensive aggression that could be reversed by blocking the activity of vasopressin receptors within the anterior hypothalamus. In a second set of experiments, adolescent hamsters were administered low-dose cocaine or vehicle, tested for offensive aggression, and then examined for differences in vasopressin innervation patterns and expression levels in the anterior hypothalamus, as well as the basal- and stimulated-release of vasopressin in this same brain region. Aggressive, adolescent cocaine-treated hamsters showed no differences in vasopressin afferent innervation and/or peptide levels in the anterior hypothalamus compared with non-aggressive, saline-treated littermates. Conversely, significant increases in stimulated, but not basal, vasopressin release were detected from the anterior hypothalamus of aggressive, cocaine-treated animals compared with non-aggressive, saline-treated controls. Together, these data suggest that adolescent cocaine exposure increases aggression by increasing stimulated release of vasopressin in the anterior hypothalamus, providing direct evidence for a causal role of anterior hypothalamic-vasopressin activity in adolescent cocaine-induced offensive aggression. A model for how alterations in anterior hypothalamic-vasopressin neural functioning may facilitate the development of the aggressive phenotype in adolescent-cocaine exposed animals is presented.

摘要

青春期反复给予低剂量可卡因(0.5毫克/千克/天)会诱发雄性叙利亚仓鼠(金仓鼠)的攻击性攻击行为。本研究检验了这样一个假说,即青春期接触可卡因会通过增强下丘脑前部加压素能神经系统的活性,使仓鼠更容易出现高水平的攻击行为。在第一个实验中,对青春期雄性仓鼠给予低剂量可卡因治疗,然后在直接向下丘脑前部施加或不施加加压素受体拮抗剂的情况下,对其攻击性攻击行为进行评分。接受青春期可卡因治疗的仓鼠表现出高度升级的攻击性攻击行为,而通过阻断下丘脑前部加压素受体的活性可以逆转这种行为。在第二组实验中,对青春期仓鼠给予低剂量可卡因或赋形剂,测试其攻击性攻击行为,然后检查下丘脑前部加压素神经支配模式和表达水平的差异,以及同一脑区加压素的基础释放和刺激释放情况。与非攻击性、接受生理盐水治疗的同窝仓鼠相比,攻击性的、接受青春期可卡因治疗的仓鼠在下丘脑前部加压素传入神经支配和/或肽水平上没有差异。相反,与非攻击性、接受生理盐水治疗的对照组相比,在攻击性的、接受可卡因治疗的动物的下丘脑前部检测到刺激后加压素释放显著增加,但基础释放没有增加。这些数据共同表明,青春期接触可卡因通过增加下丘脑前部加压素的刺激释放来增强攻击性,为下丘脑前部加压素活性在青春期可卡因诱发的攻击性攻击行为中的因果作用提供了直接证据。本文还提出了一个模型,说明下丘脑前部加压素神经功能的改变可能如何促进青春期接触可卡因的动物攻击性行为表型的发展。

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