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部分D2样多巴胺受体激动剂特古瑞得在多巴胺能张力高低状态下均表现为功能性拮抗剂:来自断奶前大鼠的证据。

The partial D2-like dopamine receptor agonist terguride acts as a functional antagonist in states of high and low dopaminergic tone: evidence from preweanling rats.

作者信息

McDougall Sanders A, Hernandez Rita M, Reichel Carmela M, Farley Cristal M

机构信息

Department of Psychology, California State University, San Bernardino, CA, 92407, USA.

出版信息

Psychopharmacology (Berl). 2005 Apr;178(4):431-9. doi: 10.1007/s00213-004-2033-1. Epub 2004 Nov 18.

Abstract

RATIONALE

In adult rats, the partial D(2)-like agonist terguride acts as an antagonist at normosensitive D(2)-like post-synaptic receptors, while it acts as an agonist at the same receptors during states of low dopaminergic tone.

OBJECTIVE

The purpose of the present study was to determine whether partial D(2)-like agonists exhibit both antagonistic and agonistic actions during the preweanling period.

METHODS

In experiments 1 and 2 (examining the agonistic actions of terguride), preweanling rats were either given an escalating regimen of amphetamine to induce a state of amphetamine withdrawal or pretreated with the tyrosine hydroxylase inhibitor AMPT. Distance traveled was measured after rats were injected with saline, terguride (0.4-1.6 mg/kg), or the full D(2)-like receptor agonist NPA (0.01 mg/kg). In experiment 3 (examining the antagonistic actions of terguride), preweanling rats were pretreated with terguride 30 min before they were tested with saline, NPA (0.05 mg/kg), or amphetamine (1.5 mg/kg).

RESULTS

NPA had an exaggerated locomotor activating effect when tested under conditions of amphetamine withdrawal, while the partial D(2)-like agonist did not enhance distance traveled under any circumstance. Similarly, NPA increased and terguride did not affect the distance-traveled scores of AMPT-pretreated rats. In experiment 3, terguride pretreatment significantly reduced the distance traveled of amphetamine-treated and NPA-treated rats.

CONCLUSIONS

The behavioral evidence indicates that, during the preweanling period, terguride antagonizes D(2)-like post-synaptic receptors in a state of high dopaminergic tone; however, there is no evidence that terguride is capable of stimulating D(2)-like post-synaptic receptors during states of low dopaminergic tone.

摘要

理论依据

在成年大鼠中,部分D₂样激动剂特古瑞得在正常敏感的D₂样突触后受体上起拮抗剂作用,而在多巴胺能张力较低的状态下,它在相同受体上起激动剂作用。

目的

本研究的目的是确定部分D₂样激动剂在断奶前阶段是否表现出拮抗和激动作用。

方法

在实验1和实验2(研究特古瑞得的激动作用)中,给断奶前的大鼠给予递增剂量的苯丙胺以诱导苯丙胺戒断状态,或用酪氨酸羟化酶抑制剂AMPT进行预处理。在大鼠注射生理盐水、特古瑞得(0.4 - 1.6毫克/千克)或完全D₂样受体激动剂NPA(0.01毫克/千克)后,测量其行进距离。在实验3(研究特古瑞得的拮抗作用)中,在断奶前的大鼠用生理盐水、NPA(0.05毫克/千克)或苯丙胺(1.5毫克/千克)进行测试前30分钟,用特古瑞得进行预处理。

结果

在苯丙胺戒断条件下进行测试时,NPA具有夸大的运动激活作用,而部分D₂样激动剂在任何情况下都不会增加行进距离。同样,NPA增加了AMPT预处理大鼠的行进距离得分,而特古瑞得没有影响。在实验3中,特古瑞得预处理显著降低了苯丙胺处理和NPA处理大鼠的行进距离。

结论

行为学证据表明,在断奶前阶段,特古瑞得在多巴胺能张力高的状态下拮抗D₂样突触后受体;然而,没有证据表明特古瑞得在多巴胺能张力低的状态下能够刺激D₂样突触后受体。

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