Maj J, Przewlocka B, Kukulka L
Pol J Pharmacol Pharm. 1977 Jan-Feb;29(1):11-21.
The activity of rats receiving low doses of dopaminergic agonists and neuroleptics was tested in the "open-field" test. Apomorphine, piribedil, L-DOPA, and nomifensine given at low doses (1-500 mug/ig) depressed the activity of animals. Spiperone and chlorpromazine given at low doses increased the activity, particularly in respect of one of the parameters investigated: the time of walking. Low doses of pimozide, haloperidol, and fluphenazine did not affect measurably the animal behavior. Spiperone counteracted the sedation induced by low doses of apomorphine, piribedil, and nomifensine. Chlorpromazine prevented the sedation produced by apomorphine. In the rats with a lesion of the substantia nigra only nomifensine retained its sedative action, while apomorphine and piribedil ceased to produce it. The reported results further support the hypothesis about the existence and the role of dopaminergic autoreceptors.
在“旷场”试验中测试了接受低剂量多巴胺能激动剂和抗精神病药物的大鼠的活动情况。低剂量(1 - 500微克/千克)给予的阿扑吗啡、匹罗卡品、左旋多巴和诺米芬辛会抑制动物的活动。低剂量给予的螺哌隆和氯丙嗪会增加活动,特别是在所研究的参数之一:行走时间方面。低剂量的匹莫齐特、氟哌啶醇和氟奋乃静对动物行为没有明显影响。螺哌隆可抵消低剂量阿扑吗啡、匹罗卡品和诺米芬辛引起的镇静作用。氯丙嗪可防止阿扑吗啡产生的镇静作用。在黑质受损的大鼠中,只有诺米芬辛保留其镇静作用,而阿扑吗啡和匹罗卡品不再产生这种作用。所报道的结果进一步支持了关于多巴胺能自身受体的存在及其作用的假说。