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首页> 外文期刊>Pharmacological reports: PR >Repeated administration of the dopaminergic agonist apomorphine: development of apomorphine aggressiveness and changes in the interaction between dopamine D2 receptors and G-protein
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Repeated administration of the dopaminergic agonist apomorphine: development of apomorphine aggressiveness and changes in the interaction between dopamine D2 receptors and G-protein

机译:多巴胺能激动剂阿扑吗啡的重复给药:阿扑吗啡的攻击性发展以及多巴胺D2受体与G蛋白之间相互作用的变化

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摘要

The repeated administration of dopamine receptor agonists produces a progressive increase in the acute behavioral effects of these drugs, known as behavioral sensitization. These includes the development of impulsive aggressive behavior after repeated small doses of apomorphine. The aim of this investigation was to study the behavioral specificity of the apomorphine-induced aggressiveness model and its possible relationship with changes in the D2 receptor-G-protein interaction. Apomorphine (1 mg/kg, sc) was administered daily for three weeks to two groups of maleWistar rats. One of the groups was repeatedly tested for the development of aggressiveness. Apomorphine aggressiveness developed stepwise with repeated behavioral testing. Neither apomorphine-treated group displayed any behavioral change in the open field test, forced swimming test, or quipazine-induced wet-dog shake response test. Three weeks of apomorphine administration in the home cage increased the GDP binding affinity and reduced the [35S]GTP S binding in striatal membranes, but this effect was not present in apomorphine-treated rats that had developed aggressiveness. In conclusion, sensitization to apomorphine, as measured by the expression of aggressiveness, developed only with accumulating apomorphine-induced fighting, was behaviorally specific, and appeared to be dependent on the D2 receptor-G-protein interaction. The absence of sensitization to the dopaminergic stimulation may be mediated by the downregulation of D2 receptor sensitivity via changes in the GDP affinity of G-proteins.
机译:多巴胺受体激动剂的重复给药使这些药物的急性行为作用逐渐增加,这被称为行为敏化。这些包括反复重复小剂量阿扑吗啡后的冲动攻击行为。这项研究的目的是研究阿扑吗啡诱导的侵略性模型的行为特异性及其与D2受体-G蛋白相互作用的变化的可能关系。每天向两组雄性Wistar大鼠施用阿扑吗啡(1 mg / kg,sc),持续三周。其中一组被反复测试了攻击性的发展。阿扑吗啡的攻击性通过反复的行为测试逐步发展。阿朴吗啡治疗组在野外试验,强迫游泳试验或奎巴嗪诱导的湿狗摇晃反应试验中均未表现出任何行为变化。在家笼中施用阿扑吗啡三周可增加GDP结合亲和力,并降低纹状体膜中[35S] GTP S的结合,但这种作用在具有阿扑吗啡治疗的大鼠中没有表现出来。总而言之,对阿扑吗啡的敏化作用(通过侵略性的表达来衡量)仅在阿扑吗啡诱导的战斗不断积累的情况下发展,在行为上具有特异性,并且似乎取决于D2受体-G蛋白相互作用。对D2受体敏感性的下调可能是由于对G蛋白的GDP亲和力的变化而引起的,对多巴胺能刺激不敏感。

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