Thirumalai Vatsala, Cline Hollis T
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.
J Neurophysiol. 2008 Sep;100(3):1635-48. doi: 10.1152/jn.90568.2008. Epub 2008 Jun 18.
Dopamine is a key neuromodulator of locomotory circuits, yet the role that dopamine plays during development of these circuits is less well understood. Here, we describe a suppressive effect of dopamine on swim circuits in larval zebrafish. Zebrafish larvae exhibit marked changes in swimming behavior between 3 days postfertilization (dpf) and 5dpf. We found that swim episodes were fewer and of longer durations at 3 than at 5dpf. At 3dpf, application of dopamine as well as bupropion, a dopamine reuptake blocker, abolished spontaneous fictive swim episodes. Blocking D2 receptors increased frequency of occurrence of episodes and activation of adenylyl cyclase, a downstream target inhibited by D2-receptor signaling, blocked the inhibitory effect of dopamine. Dopamine had no effect on motor neuron firing properties, input impedance, resting membrane potential, or the amplitude of spike afterhyperpolarization. Application of dopamine either to the isolated spinal cord or locally within the cord does not decrease episode frequency, whereas dopamine application to the brain silences episodes, suggesting a supraspinal locus of dopaminergic action. Treating larvae with 10 microM MPTP reduced catecholaminergic innervation in the brain and increased episode frequency. These data indicate that dopamine inhibits the initiation of fictive swimming episodes at 3dpf. We found that at 5dpf, exogenously applied dopamine inhibits swim episodes, yet the dopamine reuptake blocker or the D2-receptor antagonist have no effect on episode frequency. These results led us to propose that endogenous dopamine release transiently suppresses swim circuits in developing zebrafish.
多巴胺是运动回路的关键神经调节剂,然而多巴胺在这些回路发育过程中所起的作用却鲜为人知。在此,我们描述了多巴胺对斑马鱼幼体游泳回路的抑制作用。斑马鱼幼体在受精后3天(dpf)至5 dpf之间的游泳行为会出现显著变化。我们发现,3 dpf时的游泳发作次数比5 dpf时少,且持续时间更长。在3 dpf时,应用多巴胺以及多巴胺再摄取阻滞剂安非他酮可消除自发的虚构游泳发作。阻断D2受体可增加发作的发生频率,而腺苷酸环化酶(一种受D2受体信号抑制下游靶点)的激活则可阻断多巴胺的抑制作用。多巴胺对运动神经元的放电特性、输入阻抗、静息膜电位或动作电位后超极化的幅度均无影响。将多巴胺应用于离体脊髓或脊髓局部均不会降低发作频率,而将多巴胺应用于脑部则会使发作停止,这表明多巴胺能作用的部位在脊髓以上。用10微摩尔的MPTP处理幼体可减少脑中的儿茶酚胺能神经支配,并增加发作频率。这些数据表明,多巴胺在3 dpf时会抑制虚构游泳发作的起始。我们发现,在5 dpf时,外源性应用多巴胺会抑制游泳发作,但多巴胺再摄取阻滞剂或D2受体拮抗剂对发作频率没有影响。这些结果使我们提出,内源性多巴胺释放会短暂抑制发育中的斑马鱼的游泳回路。