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镇静性药物依托拉嗪的行为药理学

Behavioural pharmacology of the serenic, eltoprazine.

作者信息

Olivier B, Mos J, Rasmussen D

机构信息

Department of Pharmacology, Duphar B.V., Weesp, The Netherlands.

出版信息

Drug Metabol Drug Interact. 1990;8(1-2):31-83. doi: 10.1515/dmdi.1990.8.1-2.31.

Abstract

In this paper the effects of serenics (eltoprazine and fluprazine) are described in several animal models for offensive agonistic, defensive agonistic and predatory behaviour. They are compared with the effects of a number of other putative anti-aggressive compounds or drugs used clinically in order to ameliorate aggressive behaviour of psychiatric patients. In isolation-induced offensive aggression in mice, eltoprazine has a marked and potent anti-aggressive activity, although numerous other psychoactive drugs also exert anti-aggressive effects. The behavioural specificity of this anti-aggressive profile was investigated using an ethologically derived animal model, social interaction in male mice. In this model, eltoprazine has a very specific anti-aggressive (serenic) profile, inhibiting aggression while social interaction and exploration are not decreased but even enhanced; inactivity, a measure for sedation, is not affected. Such a profile contrasts sharply with that of neuroleptics (chlorpromazine, haloperidol), psychostimulants (d-amphetamine) or benzodiazepines (chlordiazepoxide), which exert severe sedation (neuroleptics) or even aggression-enhancing effects (BDZ). After subchronic treatment no tolerance for the anti-aggressive effects of eltoprazine occurred. The specific anti-aggressive effects of eltoprazine were also found in rat models of offensive agonistic behaviour. In one such model - resident-intruder aggression - eltoprazine reduced offensive behaviour specifically, leaving social interactions and exploration intact, and did not induce sedation or other unwanted side-effects. The neuroleptic haloperidol was very sedative in this model, as was the 5-HT1A-agonist buspirone. Benzodiazepines (chlordiazepoxide) have a biphasic effect in this paradigm, enhancing offence at low doses and decreasing it at higher doses, due to muscle relaxation. In another offensive model, colony-aggression, in which a dominant and subordinate male in a colony are confronted with a male intruder, eltoprazine reduced offensive behaviour of both the dominant and the subordinate against the intruder. In contrast, chlordiazepoxide enhanced aggression, at least at lower doses, whereas alcohol had, up to very high doses, no effect on the offensive behaviour. In a brain-stimulation induced offensive model--hypothalamically-induced aggression in rats--eltoprazine specifically reduces offence. Locomotion, a measure for sedation, was either unaffected or even somewhat enhanced, indicating the absence of any sedatory activity of this serenic compound. In contrast, haloperidol heavily sedated animals, making them incapable of aggression.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本文描述了安定药(依托哌嗪和氟哌嗪)在几种动物模型中对攻击性争斗行为、防御性争斗行为和捕食行为的影响。将它们与其他一些公认的抗攻击化合物或临床上用于改善精神病患者攻击行为的药物的效果进行了比较。在隔离诱导的小鼠攻击性攻击行为中,依托哌嗪具有显著且强效的抗攻击活性,尽管许多其他精神活性药物也具有抗攻击作用。使用一种从行为学衍生而来的动物模型——雄性小鼠的社会互动,研究了这种抗攻击特征的行为特异性。在这个模型中,依托哌嗪具有非常特异的抗攻击(安定)特征,抑制攻击行为的同时,社会互动和探索行为并未减少,反而有所增强;作为镇静指标的静止行为未受影响。这种特征与抗精神病药物(氯丙嗪、氟哌啶醇)、精神兴奋剂(右旋苯丙胺)或苯二氮䓬类药物(氯氮卓)形成鲜明对比,这些药物会产生严重的镇静作用(抗精神病药物)甚至增强攻击行为(苯二氮䓬类药物)。亚慢性治疗后,未出现对依托哌嗪抗攻击作用的耐受性。依托哌嗪的特异性抗攻击作用在大鼠攻击性争斗行为模型中也得到了证实。在其中一个这样的模型——定居者 - 入侵者攻击模型中,依托哌嗪特异性地减少了攻击行为,同时保持社会互动和探索行为完好无损,并且不会诱导镇静或其他不良副作用。抗精神病药物氟哌啶醇在这个模型中具有很强的镇静作用,5 - HT1A激动剂丁螺环酮也是如此。苯二氮䓬类药物(氯氮卓)在这个范式中具有双相作用,低剂量时增强攻击行为,高剂量时则减少攻击行为,这是由于肌肉松弛作用。在另一个攻击性模型——群体攻击模型中,群体中的优势雄性和从属雄性面对雄性入侵者,依托哌嗪减少了优势雄性和从属雄性对入侵者的攻击行为。相比之下,氯氮卓至少在低剂量时增强了攻击行为,而酒精直到非常高的剂量对攻击行为都没有影响。在一个脑刺激诱导的攻击性模型——大鼠下丘脑诱导的攻击行为中,依托哌嗪特异性地减少了攻击行为。作为镇静指标的运动行为要么未受影响,甚至有所增强,这表明这种安定化合物没有任何镇静活性。相比之下,氟哌啶醇使动物深度镇静,使其无法进行攻击行为。(摘要截断于400字)

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