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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Locomotor activity and accumbens Fos expression driven by ventral hippocampal stimulation require D1 and D2 receptors.
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Locomotor activity and accumbens Fos expression driven by ventral hippocampal stimulation require D1 and D2 receptors.

机译:运动运动和由腹侧海马刺激驱动的Fos表达需要D1和D2受体。

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Numerous studies have suggested that excitatory projections from the ventral hippocampus to the nucleus accumbens modulate locomotor activity in rats. Furthermore, the ability of ventral hippocampal neurons to alter locomotor activity may involve the dense dopaminergic innervation found in the nucleus accumbens. The purpose of this study was to: (i) more fully characterize the locomotor effects of acute alterations in ventral hippocampal activity; (ii) ascertain the influence of dopamine agonists and antagonists on locomotor changes produced by altered ventral hippocampal activity; and (iii) use immediate early gene induction to determine whether dopamine antagonists alter the response of nucleus accumbens neurons to ventral hippocampal stimulation. By comparing a variety of excitatory amino acid agonists, it was found that ventral hippocampal infusion of N-methyl-D-aspartate elevated locomotor activity in a subconvulsive manner, while other excitatory amino acid receptor agonists did not. Inactivation of the ventral hippocampus achieved by lidocaine infusion did not suppress ongoing locomotor activity, nor did it affect amphetamine-induced increases in locomotor activity. Increases in locomotor activity induced by ventral hippocampal N-methyl-D-aspartate infusion were blocked by systemic administration of haloperidol (a D2 receptor antagonist), SCH-23390 (a D1 receptor antagonist) or reserpine. Cellular expression of the protein product of the immediate early gene, c-fos, was dramatically increased in the nucleus accumbens shell after ventral hippocampal N-methyl-D-aspartate infusion, and haloperidol, SCH-23390 and reserpine attenuated this effect. These results suggest that the increases, but not decreases, in ventral hippocampal activity have a measurable effect on ongoing rates of locomotion, and that this effect requires both D1 and D2 receptors. Moreover, the studies of Fos expression suggest that dopamine receptor antagonists attenuate neuronal responses to ventral hippocampal stimulation within the nucleus accumbens, a brain region important in the generation and maintenance of locomotor activity.
机译:大量研究表明,从腹侧海马到伏隔核的兴奋性投射可调节大鼠的自发活动。此外,腹侧海马神经元改变运动能力的能力可能涉及伏伏核中密集的多巴胺能神经支配。这项研究的目的是:(i)更全面地表征急性改变腹侧海马活动的运动作用; (ii)确定多巴胺激动剂和拮抗剂对腹侧海马活动改变引起的运动变化的影响; (iii)使用立即早期基因诱导来确定多巴胺拮抗剂是否改变伏伏核神经元对腹侧海马刺激的反应。通过比较各种兴奋性氨基酸激动剂,发现腹侧海马输注N-甲基-D-天冬氨酸以惊厥的方式提高了运动活性,而其他兴奋性氨基酸受体激动剂则没有。通过利多卡因输注实现的腹侧海马失活不会抑制正在进行的运动活动,也不会影响苯丙胺诱导的运动活动增加。全身注射氟哌啶醇(一种D2受体拮抗剂),SCH-23390(一种D1受体拮抗剂)或利血平可阻止腹侧海马N-甲基-D-天冬氨酸输注引起的运动活动的增加。腹侧海马N-甲基-D-天门冬氨酸输注后,伏隔核壳中立即早期基因的蛋白产物c-fos的细胞表达急剧增加,氟哌啶醇,SCH-23390和利血平使这种作用减弱。这些结果表明,腹侧海马活动的增加而不是减少,对正在进行的运动速度具有可测量的影响,并且这种影响需要D1和D2受体。此外,Fos表达的研究表明,多巴胺受体拮抗剂减弱伏伏核内对腹侧海马刺激的神经元反应,伏伏核是在运动产生和维持中重要的大脑区域。

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