首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Behavioural responses to the selective D1-dopamine receptor agonist R-SKF 38393 and the selective D2-agonist RU 24213 in young compared with aged rats.
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Behavioural responses to the selective D1-dopamine receptor agonist R-SKF 38393 and the selective D2-agonist RU 24213 in young compared with aged rats.

机译:与年龄较大的大鼠相比年轻时对选择性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。

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摘要

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.
机译:1.在选择性丧失D2-但没有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)相比,由0.5 mg kg-1阿朴吗啡引起的刻板行为增加和延长同行。这表明药代动力学作用而不是药效学改变。 2.在老年和年幼动物中,对选择性D1激动剂R-SK&F 38393的非定型行为反应综合征1.25-20.0 mg kg-1不变,但构成该综合症的个体行为的地形因老化。 3.在老年和幼年动物中,由选择性D2激动剂RU 24213诱导的低强度刻板行为的综合症和个体行为的拓扑结构(1.25-20.0 mg kg-1)都没有改变。 4.因此,发现衰老的D2受体丢失,而不是D1受体丢失,与D2受体激动剂的反应性没有变化有关。随着年龄的增长,对D1激动剂的强烈梳理减少和液泡咀嚼反应增加,这与先前证明的选择性D2拮抗剂对这些D1刺激的行为的影响相似。 5.建议与年龄相关的D2-受体活性下降可能对D1-:D2-相互作用产生更大的功能性后果,而不是简单地影响对D2-激动剂的反应性。在考虑年龄相关的锥体束外运动障碍的病理生理和治疗时,应考虑到这种相互作用的影响。

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