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Contemporary Pharmacotherapeutics and the Management of Aggressive Behavior in an Adolescent Animal Model of Maladaptive Aggression

机译:当代药物治疗和侵袭性侵害青少年动物模型中的侵略性行为管理

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Objective Antipsychotic and anticonvulsant medications are increasingly being used as pharmacotherapeutic treatments for maladaptive aggression in youth, yet no information is available regarding whether these drugs exhibit aggression- specific suppression in preclinical studies employing adolescent animal models of maladaptive aggression. This study examined whether the commonly used antipsychotics medications haloperidol and risperidone and the anticonvulsant medication valproate exert selective aggression-suppressing effects using a validated adolescent animal model of maladaptive aggression. Methods Twenty-seven-day old Syrian hamsters ( Mesocricetus auratus ) were administered testosterone for 30 consecutive days during the first 4 weeks of adolescent development. The following day (during late adolescence), experimental animals received a single dose of haloperidol (0.00, 0.025, 0.50, 1.0 mg/kg), risperidone (0.00, 0.01, 0.03, 1.0 mg/kg), or valproate (0.00, 1.0, 5.0, 10.0 mg/kg) and tested for offensive aggression using the Resident/Intruder Paradigm. As a baseline, non-aggressive behavioral control, a separate set of pubertal hamsters was treated with sesame oil vehicle during the first 4 weeks of adolescence and then tested for aggression during late adolescence in parallel with the haloperidol, risperidone or valproate-treated experimental animals. Results Risperidone and valproate selectively reduced the highly impulsive and intense maladaptive aggressive phenotype in a dose-dependent fashion. While haloperidol marginally reduced aggressive responding, its effects were non-specific as the decrease in aggression was concurrent with reductions in a several ancillary (non-aggressive) behaviors. Conclusion These studies provide pre-clinical evidence that the contemporary pharmacotherapeutics risperidone and valproate exert specific aggression-suppressing effects in an adolescent animal model of maladaptive aggression.
机译:目的抗精神病药和抗惊厥药物越来越多地被用作青年中存在的不良侵略性药物治疗方法,但这些药物是否在采用白炽动动物模型的临床前抑制的临床前的侵略性的临床前抑制没有任何信息。本研究检测了常用的抗精神病药药物氟哌啶醇和立培酮以及抗惊厥药物药物丙戊糖使用验证的青少年动物模型对不良侵略性的抗癌性动物模型产生了选择性侵略抑制效果。方法在青少年发育的前4周连续30天持续27天的叙利亚仓鼠(Mesocricetus auratus)睾酮持续30天。第二天(在晚期青春期期间),实验动物接受单剂量的氟哌啶醇(0.00,0.025,0.50,1.0mg / kg),立酮(0.00,0.01,0.03,1.0mg / kg)或戊酸酯(0.00,1.0 ,5.0,1.0 mg / kg)并使用居民/入侵者范式进行进攻性侵略。作为基线,非侵略性行为控制,在青春期的前4周内用芝麻油载体对一套单独的青春期仓鼠进行处理,然后在与氟哌啶醇,立妥酮或丙丙酮处理的实验动物平行的晚期青春期期间进行攻击。结果利培酮和丙普洛特选择性地以剂量依赖的方式减少了高冲动和强烈的不良侵袭性表型。虽然Haloperidol积极降低侵略性的响应,但其影响是非特异性,因为侵略性的减少并发在于减少几个辅助(非侵略性)行为。结论这些研究提供了临床前证据,即当代药物治疗率立酮和丙酮醛酸盐在适应性侵略性的青少年动物模型中发挥特异性侵略性抑制作用。

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