Lane Scott D, Gowin Joshua L, Green Charles E, Steinberg Joel L, Moeller F Gerard, Cherek Don R
Department of Psychiatry & Behavioral Sciences, Graduate School of Biomedical Sciences, University of Texas Health Science Center-Houston, Houston, TX 77030, United States.
Pharmacol Biochem Behav. 2009 Apr;92(2):357-62. doi: 10.1016/j.pbb.2009.01.002.
Anticonvulsant drugs have demonstrated efficacy in the management of irritability and aggression in a variety of psychiatric populations. We examined the acute effects of topiramate on aggression using a laboratory model of human aggression (PSAP) in individuals at high risk for aggressive and violent behavior.Twelve subjects, on parole/probation and with an Axis-II personality disorder and/or a substance use disorder, received 100, 200, 300, and 400 mg in an ascending sequence, with intervening placebo doses.Subjects participated 2-3 days per week over 4-6 weeks. Due to cognitive side effects at 300 mg, two subjects only completed through the 200 mg dose. Topiramate produced an inverted U-shaped dose response curve, with increases in aggression peaking at 200 mg and a modest decrease at 400 mg. Statistical analysis revealed a polynomial trend for dose (p=0.001). The observed inverted U-shaped function in aggressive responding is consistent with non-human aggression studies of GABA-A modulators. Acute topiramate doses >400 mg may have anti-aggressive effects, but dose levels in the 200-300 mg range may produce increases in aggression and side effects.
抗惊厥药物已在多种精神疾病人群中显示出对易怒和攻击行为的治疗效果。我们使用人类攻击行为的实验室模型(PSAP),对有攻击和暴力行为高风险的个体研究了托吡酯对攻击行为的急性影响。12名处于假释/缓刑期、患有轴II型人格障碍和/或物质使用障碍的受试者,按递增顺序接受100、200、300和400毫克剂量,中间穿插安慰剂剂量。受试者在4至6周内每周参加2至3天的实验。由于300毫克剂量出现认知副作用,两名受试者仅完成了200毫克剂量的实验。托吡酯产生了倒U形剂量反应曲线,攻击行为增加在200毫克时达到峰值,400毫克时略有下降。统计分析显示剂量呈多项式趋势(p = 0.001)。观察到的攻击反应中的倒U形函数与GABA-A调节剂的非人类攻击研究一致。托吡酯急性剂量>400毫克可能具有抗攻击作用,但200 - 300毫克范围内的剂量水平可能会导致攻击行为增加和副作用。