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与老年大鼠相比,年轻大鼠对选择性D1-多巴胺受体激动剂R-SK&F 38393和选择性D2-激动剂RU 24213的行为反应。

Behavioural responses to the selective D1-dopamine receptor agonist R-SK&F 38393 and the selective D2-agonist RU 24213 in young compared with aged rats.

作者信息

Molloy A G, Waddington J L

机构信息

Department of Clinical Pharmacology, Royal College of Surgeons, Dublin, Ireland.

出版信息

Br J Pharmacol. 1988 Oct;95(2):335-42. doi: 10.1111/j.1476-5381.1988.tb11651.x.

Abstract
  1. In aged male Sprague-Dawley rats (22 months) with a selective loss of D2- but not of D1-dopamine receptors, stereotyped behaviour induced by 0.5 mg kg-1 apomorphine was increased and prolonged in comparison with young (4 month) counterparts. This suggested a pharmacokinetic effect rather than a pharmacodynamic change. 2. The syndrome of non-stereotyped behavioural responses to the selective D1-agonist R-SK&F 38393, 1.25-20.0 mg kg-1, was unchanged in aged vs young animals, but the topography of individual behaviours constituting this overall syndrome was altered with aging. 3. Neither the overall syndrome of low intensity stereotyped behaviour nor the topography of individual behaviours induced by the selective D2-agonist RU 24213, 1.25-20.0 mg kg-1, were altered in aged vs young animals. 4. Loss of D2- but not D1-receptors with aging was therefore found to be associated with no change in responsivity to a D2-receptor agonist. The decreased intense grooming and increased vacuous chewing responses to the D1-agonist with aging parallel the previously demonstrated effects of selective D2-antagonists on these D1-stimulated behaviours. 5. It is suggested that age-related decline in D2-receptor activity may have greater functional consequences in relation to D1-:D2-interactions than in simply influencing responsivity to a D2-agonist. Such interactive effects should be taken into account when considering the pathophysiology and treatment of age-related extrapyramidal movement disorders.
摘要
  1. 在选择性丧失D2多巴胺受体而非D1多巴胺受体的老年雄性Sprague-Dawley大鼠(22个月)中,与年轻(4个月)大鼠相比,0.5 mg/kg阿扑吗啡诱导的刻板行为增加且持续时间延长。这表明是药代动力学效应而非药效学变化。2. 对于选择性D1激动剂R-SK&F 38393(1.25 - 20.0 mg/kg)的非刻板行为反应综合征,老年动物与年轻动物相比没有变化,但构成该总体综合征的个体行为的表现形式随年龄增长而改变。3. 对于选择性D2激动剂RU 24213(1.25 - 20.0 mg/kg)诱导的低强度刻板行为总体综合征及其个体行为的表现形式,老年动物与年轻动物相比均未改变。4. 因此发现,随着年龄增长D2受体而非D1受体的丧失与对D2受体激动剂的反应性无变化有关。随着年龄增长对D1激动剂的强烈梳理行为减少和空嚼反应增加,与先前证明的选择性D2拮抗剂对这些D1刺激行为的影响相似。5. 有人提出,与年龄相关的D2受体活性下降在D1:D2相互作用方面可能比单纯影响对D2激动剂的反应性具有更大的功能后果。在考虑与年龄相关的锥体外系运动障碍的病理生理学和治疗时,应考虑这种相互作用效应。

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