首页> 外文期刊>Psychopharmacology >Hyperlocomotion and increased dopamine efflux in the rat nucleus accumbens evoked by electrical stimulation of the ventral subiculum: role of ionotropic glutamate and dopamine D1 receptors.
【24h】

Hyperlocomotion and increased dopamine efflux in the rat nucleus accumbens evoked by electrical stimulation of the ventral subiculum: role of ionotropic glutamate and dopamine D1 receptors.

机译:电刺激腹侧下丘引起的大鼠伏隔核中的过度运动和多巴胺外排增加:离子型谷氨酸和多巴胺D1受体的作用。

获取原文
获取原文并翻译 | 示例
           

摘要

RATIONALE AND OBJECTIVES: The role of glutamatergic afferents from the hippocampus in the modulation of dopamine (DA) efflux in the nucleus accumbens (NAcc) and concomitant increases in locomotor activity was examined following brief high-frequency electrical stimulation of the ventral subiculum (vSub). Reverse dialysis of ionotropic glutamate receptor (iGluR) antagonists into the NAcc identified the relative contributions of N-methyl-D-aspartate (NMDA) and non-NMDA glutamate receptors in the modulation of DA efflux, whereas microinjection of these compounds or selective DA D1 or D2 receptor antagonists were used to analyze the roles of glutamatergic and DA receptors in the stimulation-induced hyperlocomotion. METHODS AND RESULTS: Electrical stimulation of the vSub at 20 Hz (10 s, 300 microA) induced a significant increase in (1) DA levels in the NAcc (approximately 30% from pre-stimulation DA levels) and (2) locomotor activity (approximately 400%). The evoked DA release was completely blocked by reverse dialysis of a selective non-NMDA antagonist DNQX (10 microM and 100 microM), whereas only a high dose of the NMDA antagonist AP-V (100 microM) was effective. The increased motor activity, however, was only slightly attenuated by reverse dialysis of these drugs. Bilateral intra-NAcc injection of DNQX (1 microg/0.5 microl) blocked the increased motor activity induced by vSub stimulation relative to saline treatment. In contrast, bilateral intra-NAcc injection of AP-V (1 microg/0.5 microl) alone caused a significant increase in locomotor activity. The increased motor activity induced by vSub stimulation appears to be mediated through the DA D1 receptor, as systemic administration of the D1 antagonist SCH 23390 (0.25 mg/kg and 1 mg/kg), but not the D2 antagonist sulpiride (2 mg/kg and 10 mg/kg) blocked these effects. CONCLUSIONS: These data indicate an important role for hippocampal glutamatergic afferents in modulating the release of DA through iGluR on DA-receptive neurons in the NAcc and possibly on output neurons to the ventral tegmental area, which subsequently elicits a prolonged increase in locomotor behavior. The role of this circuit in mediating context-dependent behavioral sensitization to repeated administration of psychostimulants is discussed.
机译:理由和目的:在短暂高频电刺激腹侧下丘脑(vSub)后,检查了海马谷氨酸能传入分子对伏隔核(NAcc)多巴胺(DA)外排的调节和运动能力增加的作用。 。将离子型谷氨酸受体拮抗剂(iGluR)反向透析至NAcc中,可以确定N-甲基-D-天冬氨酸(NMDA)和非NMDA谷氨酸受体在调节DA外排中的相对作用,而这些化合物或选择性DA D1的微注射或D2受体拮抗剂用于分析谷氨酸能和DA受体在刺激诱发的超运动中的作用。方法和结果:在20 Hz(10 s,300 microA)下对vSub进行电刺激导致(1)NAcc中的DA水平显着增加(比刺激前DA水平约高30%)和(2)运动活动(约400%)。选择性非NMDA拮抗剂DNQX(10 microM和100 microM)的反向透析完全阻止了诱发的DA释放,而仅高剂量的NMDA拮抗剂AP-V(100 microM)有效。然而,通过反向透析这些药物,运动活动的增加仅被轻微减弱。相对于盐水治疗,双侧NAcc内DNQX注射(1微克/0.5微升)可阻止vSub刺激引起的运动活动增加。相反,单独的AP-V双侧NAcc内注射(1微克/0.5微升)引起运动活性的显着增加。 vSub刺激诱导的运动活动增加似乎是通过D1拮抗剂SCH 23390(0.25 mg / kg和1 mg / kg)的全身性给药而通过DA D1受体介导的,而不是D2拮抗剂舒必利(2 mg / kg)的全身性给药和10 mg / kg)可以阻止这些作用。结论:这些数据表明海马谷氨酸能传入分子在通过iGluR调节NAcc的DA受体神经元以及腹侧被盖区的输出神经元上DA的释放中起重要作用,随后引起运动行为延长。讨论了该电路在调解情境依赖性行为敏感性对重复给予精神刺激药的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号