Crocker A D, Russell R W
Department of Clinical Pharmacology, School of Medicine, Flinders University of South Australia, Bedford Park.
Pharmacol Biochem Behav. 1990 Mar;35(3):511-6. doi: 10.1016/0091-3057(90)90281-l.
The main aim of the present study was to investigate if responses to the direct dopamine agonist, apomorphine, could be modified by changes in the activity of cholinergic neurones. A novel approach was adopted in which these responses were assessed following reduction of muscarinic receptor concentration (mAChR) in the brain (assessed from [3H] QNB binding) by the alkylating derivative of oxotremorine, N-[4-(2-chloroethylmethylamino)]-2-pyrrolidone (BM 123). Stereotyped responses elicited by apomorphine were significantly reduced when QNB binding was 12% and 50% of control values. No changes in [3H] spiperone binding were found. There was significant hypothermia in the group with 12% QNB binding sites which was significantly increased by apomorphine. Body temperature returned to normal when QNB binding was 50% of control values. There was a significant decrease in activity when QNB sites were reduced to 12% of normal and vertical activity was still significantly reduced at 50% QNB binding, though horizontal activity was not then different from controls. These data are consistent with the hypothesis that changes in the function of mAChR modify responses elicited by dopamine receptor stimulation in both the striatum and other brain regions.
本研究的主要目的是调查对直接多巴胺激动剂阿扑吗啡的反应是否会因胆碱能神经元活性的变化而改变。采用了一种新方法,即通过氧化震颤素的烷基化衍生物N-[4-(2-氯乙基甲基氨基)]-2-吡咯烷酮(BM 123)降低大脑中毒蕈碱受体浓度(通过[³H]QNB结合评估)后评估这些反应。当QNB结合为对照值的12%和50%时,阿扑吗啡引发的刻板反应显著降低。未发现[³H]螺哌隆结合有变化。QNB结合位点为12%的组出现显著体温过低,阿扑吗啡使其显著升高。当QNB结合为对照值的50%时,体温恢复正常。当QNB位点降至正常的12%时,活动显著减少,当QNB结合为50%时,垂直活动仍显著减少,尽管水平活动此时与对照无差异。这些数据与以下假设一致,即毒蕈碱受体功能的变化会改变纹状体和其他脑区中多巴胺受体刺激引发的反应。