McDougall Sanders A, Hernandez Rita M, Reichel Carmela M, Farley Cristal M
Department of Psychology, California State University, San Bernardino, CA, 92407, USA.
Psychopharmacology (Berl). 2005 Apr;178(4):431-9. doi: 10.1007/s00213-004-2033-1. Epub 2004 Nov 18.
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.
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.
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).
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.
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.
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。
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。
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。
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。
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。