Surmann A, Havemann-Reinecke U
Psychiatric Hospital, University of Göttingen, Federal Republic of Germany.
J Neural Transm Suppl. 1995;45:143-55.
Male rats, treated with apomorphine (APO: 2mg/kg s.c.) in an Animex-Motility-Meter, showed individually different motility patterns, each expressed by oral stereotyped behaviour and enhanced locomotor activation reproducible in a second test 4 days later. One group of the rats showed stereotyped sniffing with an increased locomotor activation, S(L,G)-rats, being predominantly "mesolimbic active" rats. The other groups could be classified as mainly licking or gnawing rats, L(S,G)-rats or G(L,S)-rats, with less increase of locomotor activation, resembling predominantly "nigrostriatal active" rats. The G(L,S)-rats seemed to be mostly "nigrostriatal active". In this study the different types of rats were treated with neuroleptic drugs in presence of APO. Haloperidol (HAL; 0.2 and 0.4 mg/kg i.p.) had a clear dose dependent antagonizing effect on APO-induced stereotypies and locomotor activity: a pronounced effect on the L(S,G)- and G(L,S)-rats and less on S(L,G)-rats. In contrast, clozapine (CLO; 10 and 15 mg/kg i.p.) did not antagonize the stereotyped behaviour in the rats tested but showed a characteristic shift in the S(L,G)- and G(L,S)-rats: the predominant stereotypy of these rats, quantified by scoring, changed to licking. In the L(S,G)-rats the predominant licking stereotypy was not changed and the locomotor activity, which was completely antagonized in the S(L,G)- and G(L,S)-rats at both CLO-doses, was affected by 15 mg/kg, only. Furthermore, after the combined treatment with APO and HAL or APO and CLO these rat-types also differed in their amount of ACTH and corticosterone release. DA-1/DA2 and/or DA-1/DA3 receptor mechanisms may be involved in these individually different motility patterns and endocrine reactions. In summary, pretesting of rats with APO and measuring the motility and endocrine parameters may give us information on a preexisting different sensitivity of individuals to react to DAergic stimulation.
在Animex运动测量仪中,用阿扑吗啡(APO:2mg/kg皮下注射)处理的雄性大鼠表现出个体不同的运动模式,每种模式都通过口部刻板行为和增强的运动激活来表达,4天后在第二次测试中可重现。一组大鼠表现出刻板的嗅探行为,运动激活增加,即S(L,G)大鼠,主要是“中脑边缘活跃”大鼠。其他组可主要分为舔舐或啃咬大鼠,即L(S,G)大鼠或G(L,S)大鼠,运动激活增加较少,主要类似于“黑质纹状体活跃”大鼠。G(L,S)大鼠似乎大多是“黑质纹状体活跃”。在本研究中,在APO存在的情况下,用抗精神病药物处理不同类型的大鼠。氟哌啶醇(HAL;0.2和0.4mg/kg腹腔注射)对APO诱导的刻板行为和运动活动具有明显的剂量依赖性拮抗作用:对L(S,G)和G(L,S)大鼠有显著作用,对S(L,G)大鼠作用较小。相比之下,氯氮平(CLO;10和15mg/kg腹腔注射)在受试大鼠中并未拮抗刻板行为,但在S(L,G)和G(L,S)大鼠中表现出特征性变化:通过评分量化,这些大鼠的主要刻板行为转变为舔舐。在L(S,G)大鼠中,主要的舔舐刻板行为没有改变,而在两种CLO剂量下,S(L,G)和G(L,S)大鼠中完全被拮抗的运动活动仅在15mg/kg时受到影响。此外,在APO与HAL或APO与CLO联合治疗后,这些大鼠类型在促肾上腺皮质激素和皮质酮释放量上也有所不同。DA-1/DA2和/或DA-1/DA3受体机制可能参与了这些个体不同的运动模式和内分泌反应。总之,用APO对大鼠进行预测试并测量运动和内分泌参数,可能会让我们了解个体对多巴胺能刺激反应的预先存在的不同敏感性。