The Organization of Central Retinal Projections in Anna's Hummingbirds (Calypte anna) and Zebra Finches (Taeniopygia castanotis)

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Cristián Gutiérrez-Ibáñez, Julia A. Bowen, Andrea H. Gaede, Douglas L. Altshuler, Douglas R. Wylie
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引用次数: 0

Abstract

Hummingbirds (family Trochilidae) are easily recognized due to their unique ability to hover. Critical to hovering flight is head and body stabilization. In birds, stabilization during flight is mediated, among other things, by the detection of optic flow, the motion that occurs across the entire retina during self-motion. Given this increased requirement for stabilization, it is not surprising that previous studies have shown that hummingbirds have neural specializations in the visual pathways involved in the detection of optic flow. Particularly, previous studies have found some structural and functional differences in the hummingbird brain, in the pretectal nucleus lentiformis mesencephali (LM): compared to other avian species, LM shows a massive hypertrophy, and LM neurons have unique response properties to optic flow stimuli. Here, we used intraocular injections of a neural tracer, cholera toxin subunit B (CTB) conjugated with a fluorescent molecule, to study the retinal projections in Anna's hummingbirds (Calypte anna) and compare them to those of a similarly sized non-hovering species, the zebra finch (Taeniopygia castanotis). Retinal targets in both birds were similar and correspond closely to those reported in other birds from a variety of avian clades. Importantly, we found differences in the projections to LM between hummingbirds and zebra finches. Consistent with previous reports of specialization of LM, it was more intensely labelled compared to other retinal-recipient nuclei in hummingbirds. Moreover, this increase in intensity was most apparent in the lateral subnucleus. This study reinforces previous evidence that the LM of hummingbirds is adapted to sustain the unique flight abilities of this clade.

Abstract Image

安娜蜂鸟(Calypte Anna)和斑胸草雀(Taeniopygia castanotis)视网膜中央突起的组织
蜂鸟(蜂鸟科)由于其独特的悬停能力很容易识别。悬停飞行的关键是头部和身体的稳定。在鸟类中,飞行过程中的稳定是通过检测光流来调节的,光流是在自我运动时发生在整个视网膜上的运动。考虑到这种对稳定的需求增加,以前的研究表明蜂鸟在检测光流的视觉通路中具有神经专门化就不足为奇了。特别是,前人的研究发现,蜂鸟的中脑叶前叶状体核(LM)在结构和功能上存在一些差异:与其他鸟类相比,LM表现出大量的肥大,LM神经元对光流刺激具有独特的反应特性。在这里,我们使用眼内注射一种神经示踪剂,霍乱毒素亚基B (CTB)与荧光分子结合,来研究安娜蜂鸟(Calypte Anna)的视网膜投影,并将它们与类似大小的非悬停物种斑马雀(Taeniopygia castanotis)的视网膜投影进行比较。这两种鸟类的视网膜靶点是相似的,并且与来自各种鸟类分支的其他鸟类的报道密切对应。重要的是,我们发现蜂鸟和斑胸草雀对LM的预测存在差异。与先前关于LM特化的报道一致,与蜂鸟的其他视网膜受体细胞核相比,它被标记得更强烈。此外,这种强度的增加在外侧亚核中最为明显。这项研究强化了先前的证据,即蜂鸟的LM适应于维持这一分支的独特飞行能力。
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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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