Emilia Sas

An atlas of the brain of the electric fish Apteronotus leptorhynchus

This atlas consists of a set of six macrophotographs illustrating the important external landmarks of the apteronotid brain, as well as 54 transverse levels through the brain stained with cresyl violet. There are 150 microns between levels and the scales have 1 mm divisions (100 microns small divisions). In general the neuroanatomy of this brain is similar to that of other teleosts except that all parts known to be concerned with electroreception are greatly hypertrophied (electrosensory lateral line lobe, nucleus praeminentialis, caudal lobe of the cerebellum, torus semicircularis dorsalis, optic tectum and nucleus electrosensorius). There are other regions of this brain which are hypertrophied or which have not been described in other teleosts, but which are not known to be directly linked to the electrosensory/electromotor system; these regions are mentioned in the accompanying text.

The organization of afferent input to the caudal lobe of the cerebellum of the gymnotid fish Apteronotus leptorhynchus

SummaryThe caudal lobe of the cerebellum of the high frequency gymnotid fish Apteronotus leptorhynchus is that region of the cerebellum lying lateral to the posterolateral sulcus. It consists of three granular masses-the eminentia granularis posterior pars lateralis, a transitional zone T, and the eminentia granularis posterior pars medialis-with their associated molecular layers.We have used the retrograde transport of wheat germ agglutinin conjugated horseradish peroxidase to study the afferent input to the various subdivisions of the caudal lobe. Each granular mass receives different types of input. Eminentia granularis posterior pars lateralis receives a massive bilateral input from an isthmic nucleus, nucleus praeeminentialis, concerned with descending control of the electrosensory system and from a rhombencephalic nucleus, the lateral reticular nucleus, which itself receives a major spinal input. In addition eminentia granularis posterior receives lesser input from other pretectal, (N. at base of dorsomedial optic tract, pretectal complex “B”) mesencephalic (dorsal tegmental N., nucleus raphe dorsalis), isthmic (bed N. of praeeminentialis-cerebellaris tract, locus coeruleus) and rhombencephalic nuclei (lateral tegmental N., eurydendroid cells, octaval N., perihypoglossal N., paramedian reticular N., medullary reticular formation, medullary raphe, efferent octavolateralis N., inferior olive, and funicular N.). The input from nucleus praeeminentialis dorsalis is mapped topographically onto eminentia granularis posterior with respect to their rostro-caudal location. We could not define any topography in the mapping of the dorso-ventral body axis upon eminentia granularis posterior; small injections of WGA-HRP produced several small clusters of labeled cells within nucleus praeeminentialis dorsalis which does suggest a more complex organization of this projection.Zone T receives most of its input from the ipsilateral WIIIth nerve ganglion cells and certain pretectal nuclei, but it also receives a small input from nucleus praeeminentialis dorsalis. Eminentia granularis posterior pars medialis receives minor input from a small pretectal nucleus and a small ventral diencephalic nucleus, this region appears to receive its major input from eurydendroid cells of eminentia granularis posterior. The molecular layer associated with each granular mass receives contralateral input from separate clusters of inferior olivary cells. In addition the eurydendroid cells (cerebellar output neurons) of eminentia granularis posterior pars lateralis receive a substantial direct input from cells located in the medial aspect of nucleus praeeminentialis dorsalis.

Somatostatin-like immunoreactivity in the brain of an electric fish (Ateronotus leptorhynchus) identified with monoclonal antibodies

The immunohistochemical localization of somatostatin-like immunoreactive (SSir) cells and fibers in the brain of the gymnotiform teleost (Apteronotus leptorhynchus) was investigated using well-characterized monoclonal antibodies directed against somatostatin-14 and -28. Large populations of SSir neurons occur in the basal forebrain, diencephalon and rhombencephalon and a dense distribution of fibers and terminal fields is found in the ventral, dorsomedial and dorsolateral telencephalon, hypothalamus, centralis posterior thalamus, subtrigeminal nucleus, the motor nucleus of vagus and in the ventrolateral medulla. Immunoreactive neurons in the forebrain are concentrated mainly in the ventral telencephalic areas, the region of the anterior commissure and entopeduncular nucleus. In a fashion similar to the large basal telencephalic cells of other species, the cells of the rostral nucleus entopeduncularis have a significant projection to the dorsal telencephalon. The preoptic region and the peri- and paraventricular hypothalamic nuclei are richly endowed with SSir cells; some of these cells contribute fibres to the pituitary stalk and gland. In the thalamus, only the n. centralis posterior stands out for the density of SSir cells and terminals; these cells appear to project to the prepacemaker nucleus, thus suggesting an SS influence on electrocommunication. In the mesencephalon most SSir cells occur in the optic tectum, torus semicircularis and interpeduncular nucleus. The rhombencephalic SSir cells have a wider distribution (central gray, raphe, sensory nuclei, reticular formation, electrosensory lateral line lobe and surrounding the central canal). The results of this study show the presence of SS in various sensory systems, electromotor system and specific hypothalamic nuclei, suggesting a modulatory role in the processing of sensory information, electrocommunication, endocrine and motor activities.

Identification of a Nucleus isthmi in the Weakly Electric Fish Apteronotus leptorhynchus (Gymnotiformes)

The nucleus isthmi of teleost fish, amphibians, reptiles and birds, and its probable homologue, the nucleus parabigeminalis of mammals, share in common certain features such as location in the dorsal tegmentum and reciprocal connectivity with the optic tectum. In gymnotid fish the nucleus isthmi is located dorsolaterally in the brainstem tegmentum, ventral to the torus semicircularis and the lateral mesencephalic reticular area and dorsal to the rostral nucleus praeeminentialis. The nucleus isthmi has an ovoid shape, with a compact cellular part on its dorsal, medial and ventral aspects surrounding a hilar region with a sparse population of larger cells. Following wheat germ agglutinin-conjugated horseradish peroxidase injections into the optic tectum, anterogradely labeled fine terminals were observed leaving the tectobulbar tract and entering the ipsilateral nucleus isthmi via its laterally facing hilar region. Retrogradely labeled cells were present in the nucleus isthmi on both sides, indicating the presence of a bilateral isthmotectal projection similar to that reported in amphibians. The putative isthmal nucleus stains densely for acetylcholinesterase. Based on the similarity of its location, shape, cholinesterase histochemistry and reciprocal connectivity with the optic tectum, we identified this structure as the nucleus isthmi of gymnotids. An interesting observation of this study was that the nucleus isthmi, in addition to receiving fine terminals from the optic tectum, is also the recipient of a sparser population of thicker-caliber afferent fibers which terminate not only in the large-celled hilar region but also within the smaller-celled component of the nucleus; this projection appears to emanate from the torus semicircularis dorsalis.