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阿扑吗啡对小鼠新奇反应的损害及其被抗精神病药物的拮抗作用。

Impairment of responses to novelty by apomorphine and its antagonism by neuroleptics in mice.

作者信息

Misslin R, Ropartz P, Jung L

出版信息

Psychopharmacology (Berl). 1984;82(1-2):113-7. doi: 10.1007/BF00426392.

Abstract

The effects of several doses of apomorphine (AP: 0.062-8 mg/kg) on novelty preference (NP) in male Swiss mice were studied. AP induced a dose-dependent reduction of NP as well as of locomotor activity. The decrease in NP appeared to be related to the effect of the drug in reducing locomotion, and may be explained by a drug-induced increase in perseverance and stereotypy interfering with locomotion and NP by response incompatibility. These results contrast with those obtained with methamphetamine (MA) in a previous study (Misslin and Ropartz 1981) replicated here which also shows a reduction of NP. Furthermore, the neuroleptic thioridazine did not antagonize the effects of AP or MA on NP in mice, whereas the substituted benzamides tiapride and sulpiride did so. The substituted benzamides appear to act selectively on a restricted dopamine receptor population.

摘要

研究了几种剂量的阿扑吗啡(AP:0.062 - 8毫克/千克)对雄性瑞士小鼠新奇偏好(NP)的影响。阿扑吗啡诱导了NP以及运动活性的剂量依赖性降低。NP的降低似乎与药物减少运动的作用有关,并且可能是由于药物诱导的坚持性和刻板行为增加,通过反应不相容性干扰了运动和NP。这些结果与之前一项研究中使用甲基苯丙胺(MA)得到的结果形成对比(Misslin和Ropartz,1981年,此处重复该研究),该研究也显示NP降低。此外,抗精神病药物硫利达嗪并未拮抗阿扑吗啡或甲基苯丙胺对小鼠NP的影响,而取代苯甲酰胺替阿普明和舒必利则有此作用。取代苯甲酰胺似乎选择性地作用于有限的多巴胺受体群体。

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