Lukacova Kristina, Pavukova Eva, Kostal Lubor, Bilcik Boris, Kubikova Lubica
Department of Physiology and Ethology, Institute of Animal Biochemistry and Genetics, Slovakia.
Department of Physiology and Ethology, Institute of Animal Biochemistry and Genetics, Slovakia.
Neuroscience. 2016 Sep 7;331:158-68. doi: 10.1016/j.neuroscience.2016.06.032. Epub 2016 Jun 23.
Songbirds, like humans, learn vocalizations and their striatum recruits new neurons in adulthood. Injury in striatal vocal nucleus Area X, involved in song learning and production in songbirds, is followed by massive regeneration. The newborn neurons arise from the subventricular zone (SVZ) rich in dopamine D3 receptors (D3Rs). The aim of this study was to investigate whether the D3Rs affect the rate of neuronal recovery in Area X. Male zebra finches (Taeniopygia guttata) received bilateral neurotoxic lesion of Area X and were implanted with osmotic minipumps containing D3R agonist 7-OH-DPAT, antagonist U99194, or saline. Treatment with 7-OH-DPAT but not U99194 led to significant reduction of lesion size and increased numbers of migrating neuroblasts and newborn cells in the Area X. These cells were detected in the lesion border as well as the lesion center. Lesion also led to increased mRNA expression of the D3Rs in the neurogenic SVZ and in the nucleus robustus arcopallialis (RA) involved in song production. Moreover, lesion alone prolonged the song duration and this may be facilitated by D3Rs in RA. Parallel lesion and stimulation of D3Rs prolonged it even more, while blocking of D3Rs abolished the lesion-induced effect. These data suggest that D3R stimulation after striatal injury accelerates the striatal recovery and can cause behavioral alterations.
鸣禽和人类一样,会学习发声,并且其纹状体在成年后会招募新的神经元。参与鸣禽歌曲学习和发声的纹状体发声核X区受损后会大量再生。新生神经元源自富含多巴胺D3受体(D3R)的脑室下区(SVZ)。本研究的目的是调查D3R是否影响X区神经元的恢复速度。雄性斑胸草雀(Taeniopygia guttata)接受X区双侧神经毒性损伤,并植入含有D3R激动剂7-OH-DPAT、拮抗剂U99194或生理盐水的渗透微型泵。用7-OH-DPAT而非U99194进行治疗可显著减小损伤大小,并增加X区迁移的神经母细胞和新生细胞的数量。这些细胞在损伤边界以及损伤中心均被检测到。损伤还导致神经源性SVZ以及参与发声的巨细胞核(RA)中D3R的mRNA表达增加。此外,单独损伤会延长鸣叫持续时间,而RA中的D3R可能会促进这一现象。并行损伤和刺激D3R会使其延长得更多,而阻断D3R则会消除损伤诱导的效应。这些数据表明,纹状体损伤后刺激D3R可加速纹状体恢复,并可导致行为改变。