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1694及其他多巴胺能药物对转圈行为的影响。

Effects of 1694 and other dopaminergic agents on circling behavior.

作者信息

Dankova J, Boucher R, Poirier L J

出版信息

Eur J Pharmacol. 1977 Mar 21;42(2):113-21. doi: 10.1016/0014-2999(77)90350-8.

Abstract

One hour after the administration of 40 mg/kg of amineptine chlorydrate (1694) the HVA concentration in the striatum was increased but the concentrations of DA, NA, 5HT and 5-HIAA in the striatum, cortex, thalamus-hypothalamus and pons-midbrain of rats were not significantly altered. Unilateral lesioning at the level of the entopeduncular nucleus in cats and rats resulted in spontaneously occurring ipsiversive circling behavior in the two species. However circling was more sustained in cats than in rats. Apomorphine, d-amphetamine, methamphetamine, L-dopa and piribedil (ET-495) exaggerated the ipsiversive circling. 1694 (amineptine chlorydrate), a new agent, was comparatively more active than L-dopa and ET-495 and less active than apomorphine, d-amphetamine and methamphetamine. Although in higher doses (30--40 mg/kg), 1694 caused increased exploratory activity it was not associated with any stereotypy. Its biochemical and pharmacological effects are comparable to those of d-amphetamine and methamphetamine. Removal of the contralateral (with respect to the side of the entopeduncular lesion) motor cortex in the lesioned cat abolished spontaneous and drug-induced circling movements. The results of this and of previous studies support the idea that these dopaminergic agents act on the striopallidal system of the intact side which is no longer properly counterbalanced by the corresponding system of the lesioned side. Although this experimental model is useful to determine the degree of dopaminergic activity of various chemical agents it does not duplicate the motor disorders encountered in parkinsonism which are associated with a decreased concentration of dopamine.

摘要

给予大鼠40mg/kg盐酸阿密曲替林(1694)1小时后,纹状体中高香草酸(HVA)浓度升高,但纹状体、皮质、丘脑 - 下丘脑以及脑桥 - 中脑中多巴胺(DA)、去甲肾上腺素(NA)、5 - 羟色胺(5HT)和5 - 羟吲哚乙酸(5 - HIAA)的浓度未发生显著变化。猫和大鼠在内侧缰核水平进行单侧损伤后,两种动物均出现了自发的同侧旋转行为。然而,猫的旋转行为比大鼠持续时间更长。阿扑吗啡、右旋苯丙胺、甲基苯丙胺、左旋多巴和匹立地尔(ET - 495)会加剧同侧旋转。新型药物1694(盐酸阿密曲替林)的活性相对高于左旋多巴和ET - 495,但低于阿扑吗啡、右旋苯丙胺和甲基苯丙胺。虽然高剂量(30 - 40mg/kg)的1694会增加探索活动,但未引发任何刻板行为。其生化和药理作用与右旋苯丙胺和甲基苯丙胺相当。对损伤的猫切除对侧(相对于内侧缰核损伤侧)运动皮层后,自发和药物诱导的旋转运动均消失。本研究及先前研究的结果支持这样一种观点,即这些多巴胺能药物作用于完整侧的纹状体苍白球系统,而该系统不再能被损伤侧的相应系统适当平衡。尽管这个实验模型有助于确定各种化学药物的多巴胺能活性程度,但它无法复制帕金森病中出现的与多巴胺浓度降低相关的运动障碍。

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