Department of Psychiatry and Behavioral Sciences, The University of Texas Health Science Center Houston, Houston, TX, USA.
Psychopharmacology (Berl). 2010 Jul;210(4):521-31. doi: 10.1007/s00213-010-1851-6. Epub 2010 Apr 21.
The serotonin 1(B/D) (5-HT1(B/D)) receptor has shown potential as a target for decreasing aggression. The 5-HT1(B/D) agonist zolmitriptan's ability to reduce aggressive behavior in humans and its interaction with the well-known aggression-enhancing drug alcohol were examined.
Our objective was to investigate zolmitriptan's potential to modify human aggression in a laboratory paradigm across a range of alcohol doses. Alcohol has been consistently associated with aggression and violence, thus we hoped to expand current understanding of alcohol's role in aggressive behavior via manipulation of the serotonin (5-HT) system.
Eleven social drinkers, seven male, were recruited to participate in a research study lasting 3-4 weeks. Aggression was measured using the point-subtraction aggression paradigm (PSAP), a laboratory model widely used in human aggression studies. Subjects were administered 5-mg zolmitriptan and placebo capsules along with alcohol doses of 0.0, 0.4 and 0.8 g/kg in a within-subject, counterbalanced dosing design. Data were analyzed as the ratio of aggressive/monetary-earning responses, to account for possible changes in overall motor function due to alcohol.
There was a significant alcohol by zolmitriptan interaction on the aggressive/monetary response ratio. Specifically, compared to placebo, zolmitriptan decreased the aggressive/monetary ratio at the 0.4- and 0.8-g/kg alcohol doses.
A 5-mg dose of zolmitriptan effectively reduced alcohol-related aggression in an acute dosing protocol, demonstrating an interaction of 5-HT and alcohol in human aggressive behavior.
血清素 1(B/D)(5-HT1(B/D))受体已显示出作为降低攻击性的靶点的潜力。本文研究了 5-HT1(B/D)激动剂佐米曲坦减少人类攻击性行为的能力及其与众所周知的增强攻击性药物酒精的相互作用。
我们的目的是在一系列酒精剂量下,通过实验室范式研究佐米曲坦降低人类攻击性的潜力。酒精与攻击和暴力一直存在关联,因此我们希望通过操纵血清素(5-HT)系统来扩展对酒精在攻击性行为中作用的现有认识。
招募了 11 名社交饮酒者(7 名男性)参与为期 3-4 周的研究。使用点减法攻击范式(PSAP)测量攻击性,这是一种广泛用于人类攻击性行为研究的实验室模型。在一个基于个体的、平衡剂量设计中,受试者服用 5 毫克佐米曲坦和安慰剂胶囊,同时给予 0.0、0.4 和 0.8 g/kg 的酒精剂量。数据分析为攻击性/货币收益反应的比值,以考虑由于酒精导致的整体运动功能的可能变化。
在攻击性/货币反应比上,酒精与佐米曲坦存在显著的相互作用。具体来说,与安慰剂相比,佐米曲坦在 0.4 和 0.8 g/kg 酒精剂量下降低了攻击性/货币比值。
在急性给药方案中,5 毫克佐米曲坦有效降低了与酒精相关的攻击性,表明 5-HT 和酒精在人类攻击性行为中存在相互作用。