de Almeida Rosa Maria M, Benini Quelin, Betat Juliana S, Hipólide Débora C, Miczek Klaus A, Svensson Anders I
Laboratório de Neurociências, Centro 2, UNISINOS, Av. Unisinos, 950, 93022-000 São Leopoldo, RS, Brazil.
Psychopharmacology (Berl). 2008 Apr;197(2):309-18. doi: 10.1007/s00213-007-1031-5. Epub 2007 Dec 14.
Higher doses of benzodiazepines induce sedation. However, in low to moderate doses, benzodiazepines can increase aggressive behavior both after acute and chronic administration. The determinants for increasing aggression after chronic intake of flunitrazepam, a so-called date rape drug, in violence-prone individuals are incompletely understood.
The aim of this study is to assess the effects of acute and chronic treatment with flunitrazepam on male aggression in resident rats. We also examined possible changes in binding to benzodiazepine receptors throughout the brain of rats that display aggressive behavior after repeated flunitrazepam treatment using quantitative receptor autoradiography.
The behaviors of the male Wistar resident rats (n = 35) toward a male intruder were recorded for 10 min twice a week. The salient aggressive and non-aggressive elements in the resident rat's behavior were analyzed. Initially, the dose-dependent effects of flunitrazepam (0.01, 0.03, 0.1, 0.18, and 0.3 mg/kg) or vehicle were determined in all rats; subsequently, 0.3 mg/kg per day flunitrazepam was administered for 42 days (n = 15), and a parallel group was treated with vehicle (n = 20). After the chronic treatment, the flunitrazepam (0, 0.01, 0.03, 0.1, 0.18, and 0.3 mg/kg) effects were again assessed.
The most significant finding is the escalation of aggression after chronic treatment with flunitrazepam. A previously sedative 0.3 mg/kg dose of flunitrazepam engendered very high levels of attack bites, sideways threats, and aggressive postures (total aggression) after 6 weeks of daily administration. Individual differences emerged, and these were associated with decreased binding to benzodiazepine receptors, mainly in the limbic structures such as the cingulate cortex (cingulate areas 1 and 2) and caudate-putamen (posterior part) of aggressive animals, suggesting that these areas are pivotal in the control of emotional and aggressive behavior.
Chronic flunitrazepam produces changes in receptor binding in discrete areas of the cingulate cortex and caudate-putamen that are proposed to be part of the mechanisms for increased expression of aggressive behavior.
高剂量的苯二氮䓬类药物会引起镇静作用。然而,低至中等剂量的苯二氮䓬类药物在急性和慢性给药后均可增加攻击性行为。对于暴力倾向个体长期摄入氟硝西泮(一种所谓的迷奸药)后攻击性行为增加的决定因素,目前尚不完全清楚。
本研究旨在评估氟硝西泮急性和慢性治疗对雄性成年大鼠攻击性行为的影响。我们还使用定量受体放射自显影技术,研究了在反复给予氟硝西泮后表现出攻击性行为的大鼠全脑苯二氮䓬受体结合的可能变化。
每周两次记录雄性Wistar成年大鼠(n = 35)对雄性入侵者10分钟的行为。分析成年大鼠行为中显著的攻击和非攻击成分。最初,在所有大鼠中确定氟硝西泮(0.01、0.03、0.1、0.18和0.3 mg/kg)或溶剂的剂量依赖性效应;随后,每天给予0.3 mg/kg氟硝西泮,持续42天(n = 15),并设一组平行组给予溶剂(n = 20)。慢性治疗后,再次评估氟硝西泮(0、0.01、0.03、0.1、0.18和0.3 mg/kg)的效应。
最显著的发现是氟硝西泮慢性治疗后攻击性行为加剧。在每天给药6周后,之前具有镇静作用的0.3 mg/kg剂量的氟硝西泮引发了非常高水平的攻击撕咬、侧向威胁和攻击姿势(总攻击行为)。出现了个体差异,这些差异与苯二氮䓬受体结合减少有关,主要在攻击动物的边缘结构,如扣带回皮质(扣带区1和2)和尾状核 - 壳核(后部),这表明这些区域在控制情绪和攻击行为中起关键作用。
慢性给予氟硝西泮会使扣带回皮质和尾状核 - 壳核的离散区域的受体结合发生变化,这些变化被认为是攻击行为表达增加机制的一部分。