Neurochemical Characterization of Dopaminoceptive Cells in Song Control Nuclei of Canaries and Their Activation During Song Production: A Multiplex Fluorescent In Situ Hybridization Study

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Chelsea M. Haakenson, Jacques Balthazart, Jonathan W. VanRyzin, Ashley E. Marquardt, Sydney E. Ashton, Margaret M. McCarthy, Gregory F. Ball
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Abstract

Highly sensitive in situ hybridization procedures (RNAScope) were used to quantify the expression of three dopamine receptors (Drd1, Drd2, and Drd3) in two song control nuclei (HVC and the Area X of the basal ganglia) that are known to receive dopaminergic inputs and in the periaqueductal gray (PAG) of male and female canaries. Both sexes were treated with testosterone to ensure they would sing actively. We also determined the excitatory versus inhibitory phenotype of the cells expressing these receptors as well as their activation following a period of song production. The three receptor types were identified in each brain area, with the exception of Drd3 in Area X. The density of cells expressing each receptor varied as a function of receptor type and brain area. Surprisingly few sex differences were detected; they do not seem to explain the sex differences in testosterone-induced song. Overall, the density of Drd-positive cells was much lower in PAG than in the two song control nuclei. In HVC, the majority of cells expressing the three receptor subtypes were VGlut2-positive, whereas colocalization with Vglut2 occurred in few cells in Area X and in an intermediate proportion of cells in PAG. The number of inhibitory cells expressing dopamine receptors was limited. Most dopaminoceptive cells in Area X did not express either excitatory or inhibitory markers. Finally, cellular activation during singing behavior, as measured by the expression of Egr1, was observed in cells expressing each of the three dopamine receptor subtypes, except Drd3 in the PAG.

Abstract Image

金丝雀鸣唱控制核中多巴胺感受细胞的神经化学特征及其在鸣唱过程中的激活:多重荧光原位杂交研究
我们使用高灵敏度的原位杂交程序(RNAScope)来量化三种多巴胺受体(Drd1、Drd2和Drd3)在已知接受多巴胺能输入的两个鸣唱控制核团(HVC和基底节X区)以及雌雄金丝雀的uctal灰质周围(PAG)中的表达。雌雄金丝雀都接受了睾酮治疗,以确保它们能积极歌唱。我们还测定了表达这些受体的细胞的兴奋与抑制表型,以及它们在歌唱后的激活情况。除了 X 区的 Drd3 外,我们在每个脑区都发现了三种受体类型。表达每种受体的细胞密度随受体类型和脑区的不同而变化。令人惊讶的是,检测到的性别差异很小;它们似乎无法解释睾酮诱导鸣唱的性别差异。总体而言,PAG 中 Drd 阳性细胞的密度远低于两个鸣唱控制核。在 HVC 中,大多数表达三种受体亚型的细胞都是 VGlut2 阳性,而在 X 区很少有细胞与 Vglut2 共定位,在 PAG 中也只有中等比例的细胞与 Vglut2 共定位。表达多巴胺受体的抑制性细胞数量有限。X 区的大多数多巴胺感受性细胞既不表达兴奋性标记,也不表达抑制性标记。最后,除了PAG中的Drd3外,在表达三种多巴胺受体亚型的细胞中都观察到了歌唱行为过程中的细胞活化(通过Egr1的表达来测量)。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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