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正常敏感和D1超敏大鼠对D1和D2多巴胺激动剂联合给药的行为反应变化。

Changes in behavioural responses to the combined administration of D1 and D2 dopamine agonists in normosensitive and D1 supersensitive rats.

作者信息

Dall'Olio R, Gandolfi O, Vaccheri A, Roncada P, Montanaro N

机构信息

Institute of Pharmacology, University of Bologna, Italy.

出版信息

Psychopharmacology (Berl). 1988;95(3):381-5. doi: 10.1007/BF00181952.

DOI:10.1007/BF00181952
PMID:2901128
Abstract

The selective D1 receptor stimulant SKF 38393 dose-dependently increased grooming time in rats without affecting locomotor activity or eliciting stereotyped behaviour. The selective D2 receptor agonist LY 171555 induced a dose-dependent increase in rat motility, a marked decrease in grooming time and a low occurrence of stereotyped behaviour. Concurrent administration of the two selective agonists induced high-degree stereotyped responses and reductions in locomotor and grooming behaviours. Rats withdrawn from repeated treatment with the selective D1 receptor blocker SCH 23390 (0.05 mg/kg twice daily for 21 days; 7 days of washout) did not exhibit any change of locomotor and grooming responses to threshold doses of LY 171555 and SKF 38393 given alone or in combination. On the contrary, a significantly greater occurrence of high-degree stereotyped responses to the combination of the two selective agonists was observed. The data support the view that D1 and D2 receptors have a cooperative role in the generation of stereotypies and suggest that D1 receptor supersensitivity needs D2 stimulation to be revealed.

摘要

选择性D1受体激动剂SKF 38393可使大鼠理毛时间呈剂量依赖性增加,而不影响其运动活性或引发刻板行为。选择性D2受体激动剂LY 171555可使大鼠运动性呈剂量依赖性增加,理毛时间显著减少,且刻板行为发生率较低。同时给予这两种选择性激动剂会引发高度刻板反应,并减少运动和理毛行为。用选择性D1受体阻滞剂SCH 23390重复治疗(0.05毫克/千克,每日两次,共21天;洗脱7天)后停药的大鼠,对单独或联合给予的阈剂量LY 171555和SKF 38393的运动和理毛反应均未表现出任何变化。相反,观察到对两种选择性激动剂组合出现高度刻板反应的发生率显著更高。这些数据支持了D1和D2受体在刻板行为产生中具有协同作用的观点,并表明D1受体超敏反应需要D2刺激才能显现出来。

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本文引用的文献

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Dopaminergic behaviour stereospecific promoted by the D1 agonist R-SK & F 38393 and selectively blocked by the D1 antagonist SCH 23390.D1激动剂R-SK & F 38393可立体特异性地促进多巴胺能行为,并被D1拮抗剂SCH 23390选择性阻断。
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Mode of action of apomorphine and dexamphetamine on gnawing compulsion in rats.阿扑吗啡和右旋苯丙胺对大鼠啃咬强迫行为的作用机制
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在D1和/或D2受体不可逆拮抗后,选择性和非选择性多巴胺激动剂对幼鼠的行为影响。
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The differential behavioural effects of benzazepine D1 dopamine agonists with varying efficacies, co-administered with quinpirole in primate and rodent models of Parkinson's disease.在帕金森病的灵长类和啮齿类动物模型中,将不同效能的苯并氮杂卓D1多巴胺激动剂与喹吡罗联合使用时的差异行为效应。
Psychopharmacology (Berl). 1995 Feb;117(3):287-97. doi: 10.1007/BF02246103.
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The competitive NMDA antagonists CGP 43487 and APV potentiate dopaminergic function.
Psychopharmacology (Berl). 1995 Apr;118(3):310-5. doi: 10.1007/BF02245960.
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Interaction between accumbens D1 and D2 receptors regulating rat locomotor activity.伏隔核D1和D2受体之间的相互作用调节大鼠的运动活动。
Psychopharmacology (Berl). 1989;99(4):558-62. doi: 10.1007/BF00589908.
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Synergistic blockade of some dopamine-mediated behaviours by (-)-sulpiride and SCH 23390 in the rat.(-)-舒必利与SCH 23390对大鼠某些多巴胺介导行为的协同性阻断作用
Psychopharmacology (Berl). 1989;98(3):342-6. doi: 10.1007/BF00451685.
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Motor activity following the administration of selective D-1 and D-2 dopaminergic drugs to normal common marmosets.对正常普通狨猴施用选择性 D-1 和 D-2 多巴胺能药物后的运动活动
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Psychopharmacological responsiveness to the dopamine agonist quinpirole in normal weanlings and in weanling offspring exposed gestationally to cocaine.正常断奶幼崽以及孕期暴露于可卡因的断奶幼崽后代对多巴胺激动剂喹吡罗的精神药理学反应。
Psychopharmacology (Berl). 1992;108(3):256-62. doi: 10.1007/BF02245109.
10
Effects of acute dopamine depletion on responsiveness to D1 and D2 receptor agonists in infant and weanling rat pups.急性多巴胺耗竭对幼龄和断奶期大鼠幼崽对D1和D2受体激动剂反应性的影响。
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多巴胺激动剂相关行为产生中D-1/D-2受体的强制性相互作用。
Eur J Pharmacol. 1986 Nov 19;131(2-3):301-6. doi: 10.1016/0014-2999(86)90588-1.
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Stereotyped behaviour in response to the selective D-2 dopamine receptor agonist RU 24213 is enhanced by pretreatment with the selective D-1 agonist SK&F 38393.选择性D-1激动剂SK&F 38393预处理可增强对选择性D-2多巴胺受体激动剂RU 24213的刻板行为反应。
Neuropharmacology. 1986 Aug;25(8):947-9. doi: 10.1016/0028-3908(86)90027-4.
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Responses to selective D-1 and D-2 agonists after repeated treatment with selective D-1 and D-2 antagonists.在用选择性 D-1 和 D-2 拮抗剂反复治疗后对选择性 D-1 和 D-2 激动剂的反应。
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Dopamine D-1 receptor agonists combined with the selective D-2 agonist quinpirole facilitate the expression of oral stereotyped behaviour in rats.多巴胺 D-1 受体激动剂与选择性 D-2 激动剂喹吡罗联合使用可促进大鼠口腔刻板行为的表达。
Eur J Pharmacol. 1987 Jan 13;133(2):137-45. doi: 10.1016/0014-2999(87)90144-0.
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Enhanced stereotyped response to apomorphine after chronic D-1 blockade with SCH 23390.在用SCH 23390进行慢性D-1受体阻断后,对阿扑吗啡的刻板反应增强。
Psychopharmacology (Berl). 1987;91(3):394-6. doi: 10.1007/BF00518199.
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Dopaminergic mechanisms and motor function: characterization of D-1 and D-2 dopamine receptor interactions.多巴胺能机制与运动功能:D-1和D-2多巴胺受体相互作用的特征
Eur J Pharmacol. 1986 Apr 9;123(1):109-14. doi: 10.1016/0014-2999(86)90694-1.
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SCH-23390 antagonism of a D-2 dopamine agonist depends upon catecholaminergic neurons.SCH-23390对D-2多巴胺激动剂的拮抗作用取决于儿茶酚胺能神经元。
Eur J Pharmacol. 1985 Jul 11;113(1):109-14. doi: 10.1016/0014-2999(85)90349-8.
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Selective D-1 dopamine receptor increase following chronic treatment with SCH 23390.长期使用 SCH 23390 治疗后,选择性 D-1 多巴胺受体增加。
Eur J Pharmacol. 1985 Feb 12;109(1):127-8. doi: 10.1016/0014-2999(85)90549-7.