Exploring Anatomical Links Between the Crow's Nidopallium Caudolaterale and Its Song System

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Felix W. Moll, Ylva Kersten, Saskia Erdle, Andreas Nieder
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Abstract

Crows are corvid songbirds that exhibit remarkable cognitive control, including their ability to vocalize on command. The activity of single neurons from the crow's associative telencephalic structure nidopallium caudolaterale (NCL) is correlated with the execution of this vocal and many non-vocal behaviors. However, whether anatomical connections directly link the crow NCL to its “song system” remains unclear. To address this, we used fluorescent tracers along with histological staining methods to characterize the connectivity of the crow's NCL in relation to its song system. Consistent with previous findings in other songbirds, we found that the NCL sends dense projections into the dorsal intermediate arcopallium (AID) directly adjacent to the song system's telencephalic motor output, the robust nucleus of the arcopallium (RA). Similarly, we demonstrate dense NCL projections into the striatum engulfing the basal ganglia song nucleus “area X.” Both of these descending projections mirror the projections of the nidopallial song nucleus HVC (proper name) into RA and area X, with extremely sparse NCL fibers extending into area X. Furthermore, we characterized the distribution of cells projecting from the lateral part of the magnocellular nucleus of the anterior nidopallium (MAN) to NCL. Notably, a separate medial population of MAN cells projects to HVC. These two sets of connections—MAN to NCL and MAN to HVC—run in parallel but do not overlap. Taken together, our findings support the hypothesis that the NCL is part of a “general motor system” that parallels the song system but exhibits only minimal monosynaptic interconnections with it.

Abstract Image

探讨乌鸦喙部与鸣叫系统的解剖学联系
乌鸦是鸦科鸣禽,表现出非凡的认知控制能力,包括根据命令发出声音的能力。鸦尾侧联合端脑结构(nidopallium caudolaterale, NCL)单个神经元的活动与这种发声行为和许多非发声行为的执行有关。然而,解剖学上的联系是否将乌鸦的NCL与其“鸣叫系统”直接联系起来仍不清楚。为了解决这个问题,我们使用荧光示踪剂和组织学染色方法来表征乌鸦的NCL与其鸣叫系统的连通性。与之前在其他鸣禽中发现的结果一致,我们发现NCL将密集的投影发送到与鸣禽系统的端脑运动输出(arcopallium的强大核)直接相邻的背侧中间弓鞘(AID)。同样,我们发现密集的NCL投射到纹状体中,吞没基底节区歌核“X区”。这两种下降的投射都反映了乳头状歌核HVC(专有名称)在RA和X区的投射,极其稀疏的NCL纤维延伸到X区。此外,我们表征了从乳头状前(MAN)大细胞核外侧部分投射到NCL的细胞分布。值得注意的是,一个单独的MAN细胞群向HVC转移。这两组连接- MAN到NCL和MAN到hvc -并行运行,但不重叠。综上所述,我们的发现支持了一种假设,即NCL是“一般运动系统”的一部分,与歌曲系统相似,但只表现出最小的单突触相互联系。
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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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