The tertiary gustatory center in sunfishes is not nucleus glomerulosus

Injection of horseradish peroxidase into the secondary gustatory nucleus of the green sunfish, Lepomis cyanellus, resulted in retrogradely filled neurons bilaterally in the viscerosensory column of the brainstem and in anterograde transport revealing ipsilateral terminal fields in the preglomerular tertiary gustatory nucleus, the nucleus of the torus lateralis and the central and periventricular nucleus of the inferior lobe. Thus, the glomerular nucleus of percomorph teleosts is not a tertiary gustatory center. It is proposed that the term ‘nucleus glomerulosus’ be reserved for the nucleus involved with vision and that the preglomerular subdivision involved in gustation be termed ‘nucleus gustatorius tertius’

An Evolutionary Interpretation of Teleostean Forebrain Anatomy

During the past few years, our investigations of the forebrain in the zebrafish (a teleost fish) have shown that its molecular anatomy and expression patterns of genes involved in the regulation of neuronal transmitter phenotypes, such as gamma-aminobutyric acid- (GABA-)ergic neurons, are very similar to those seen in mammalian model organisms such as mouse and rat. For example, we have been able to identify previously undiscovered homologies, such as subpallial regions in the zebrafish that are homologous to the medial and lateral ganglionic eminences in mammals, as well as regions homologous to the larval eminentia thalami and its adult derivative, the bed nucleus of the stria medullaris. Furthermore, in what we term the partial eversion model of the telencephalon in teleosts, we propose homologies to all four mammalian pallial areas and conclude that the posterior zone of the dorsal telencephalic area in teleosts is homologous to the piriform cortex and is formed by a migratory stream of cells originating in a dorsomedial zone of the pallium (the primordial medial zone of area dorsalis telencephali). In this review we critically discuss and justify these findings in the context of forebrain evolution in fishes. Copyright (C) 2009 S. Karger AG, Base

Connections of the corpus cerebelli in the green sunfish and the common goldfish

Examination of the connections of the corpus cerebelli in one perciform (Lepomis cyanellus) and one cypriniform teleost (Carassius auratus) reveal that ipsilateral afferent connections in both species arise from an anterior group of nuclei in the diencephalon and mesencephalon, and a posterior group of nuclei in the rhombencephalon. Some nuclei of the anterior group and all those of the posterior group have in addition a weaker, and the medial octavolateralis nucleus a stronger, contralateral component. The inferior olivary nucleus in both species projects solely contralaterally. Nucleus paracommissuralis, the ventral accessory optic nucleus and nucleus isthmi are minute in Carassius compared to Lepomis. The latter species has in addition a bilateral corpopetal projection (ipsilaterally stronger) from the lateral cuneate nucleus. Efferent fibers in both species reach the contralateral nucleus ruber, oculomotor nucleus, nucleus of the medial longitudinal fasciculus, torus semicircularis, ventromedial and ventrolateral thalamic nuclei, optic tectum and superior and inferior reticular formation. An additional weaker ipsilateral terminal field could be observed in all nuclei except in the ventrolateral and ventromedial thalamic nuclei, the dorsal periventricular pretectal nucleus and the optic tectum. Lepomis in addition has a bilateral terminal field in the ventral accessory optic nucleus (contralaterally stronger). In both species, stronger ipsilateral and weaker contralateral terminal fields were present in the torus Iongitudinalis and the valvula cerebelli. The two patterns of corpopetal connections in Lepomis and Carassius were used as models for perciforms and cypriniforms in the analysis of the existing information in the literature on teleosts. While most discrepancies in the literature on percomorphs and ostariophysines could be interpreted consistently, the available information on mormyrids revealed a very different pattern of corpopetal organization: presence of additional connections (from a division of the nucleus preglomerulosus) and absence of otherwise well-established corpopetal connections in teleosts. In a second step, a phyletic analysis of teleostean corpopetal organization revealed that while teleosts share with all other vertebrates a group of corpopetal connections from the rhombencephalon, they evolved many new, more anteriorly located afferent inputs to the corpus cerebelli. Furthermore, electroreceptive mormyrids in addition evolved newly at least one corpopetal connection and lost many others

Possible multiple evolution of indirect telencephalo-cerebellar pathways in teleosts: studies in Carassius auratus and Pantodon buchholzi

Among vertebrates, telencephalo-pontine systems exist only in birds and mammals. However, three nuclei in the diencephalon and mesencephalon of teleost fishes have been indicated — analogous to the pons — to represent relay stations between telencephalon and cerebellum. Since two of these nuclei (dorsal preglomerular nucleus, dorsal tegmental nucleus) have only been described in the highly derived, electrosensory mormyrids, we investigated telencephalic connections in two nonelectrosensory teleosts, the goldfish Carassius auratus and the freshwater butterflyfish Pantodon buchholzi, and cerebellar connections only in the latter species, since for C. auratus these connections are already established. Horseradish peroxidase tracing reveals that C. auratus has a dorsal tegmental nucleus and a paracommissural nucleus both of which are telencephalo-recipient and project to the cerebellum, and that P. buchholzi has a dorsal preglomerular nucleus with such connections. These results extend our knowlegde of the distribution and, therefore, the phylogeny of telencephalo-cerebellar systems in teleosts. Similar to tetrapods, teleosts appear to have developed telencephalo-cerebellar systems several times independently