Felix W. Moll, Ylva Kersten, Saskia Erdle, Andreas Nieder
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引用次数: 0
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.
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.