Fusiform Neurons Research Articles

Evidence for calcitonin gene-related peptide contacts on a population of lamina I projection neurons

Using double-labeling techniques, we evaluated small diameter primary afferent input, as indicated by calcitonin gene-related peptide-immunoreactive varicosities, to a population of lamina I projection neurons in the rat lumbar spinal cord. About one third of the lamina I neurons labeled after injections of a retrograde tracer into the region surrounding the brachium conjunctivum received contacts from immunoreactive varicosities. Significantly fewer immunoreactive varicosities were in apposition to fusiform neurons than pyramidal or flattened neurons. A positive correlation was found between the size of the retrogradely labeled neuron and the number of contacts received. This study demonstrates that a known population of nociceptive lamina I neurons received direct input from presumed nociceptive primary afferents.

The reticular thalamic nucleus (RTN) of the rat: Cytoarchitectural, Golgi, immunocytochemical, and horseradish peroxidase study

Experiments have been performed on adult albino rats in order to study the cellular organization of the thalamic reticular nucleus. For this purpose four approaches have been used: Nissl stain, Golgi impregnation, retrograde transport of horseradish peroxidase after injection in different thalamic nuclei, and immunocytochemistry with antibodies against GABA and glutamic acid decarboxylase. In sections through the horizontal plane, three morphologically different neurons have been observed. Cells with round perikarya and with multipolar dendrites were found predominantly in the rostral pole of the nucleus. Neurons with large fusiform cell body and with dendrites arborizing mainly on the horizontal plane were detected through the whole extent of the nucleus. Small fusiform neurons were observed almost exclusively in the medial third of the dorso-ventral extent of the nucleus. The Golgi impregnation method demonstrated that dendrites of small fusiform neurons develop in the vertical plane perpendicular to the dendritic arborization of large fusiform neurons. In coronal sections neurons with round perikarya and with large fusiform cell bodies are detectable while small fusiform neurons are only rarely visible. These data have been confirmed by statistical form factor analysis. Moreover, by means of the horseradish peroxidase and the immunocytochemical study, it has been confirmed that all three groups of neurons project within the thalamus and that they are GABAergic. The data concerning the distribution within the nucleus of the three morphologically different neurons are discussed in relation to the topographic distribution of cortical sensory afferents and to the topographic maps within different sectors of the reticular nucleus.

Distribution and morphology of area 17 neurons that project to the cat's extrastriate cortex

We used intracellular dye injections in lightly fixed cortical slices to examine the distribution and morphology of area 17 neurons that project to extrastriate cortex. Both the projection to the medial bank of the posterior lateral suprasylvian sulcus (PMLS) and the projection to area 18 arise from a number of different morphological types distributed throughout layers 2-6. The majority are found in the superficial layers and include large, medium, and small pyramidal neurons. Some are also found in the deep layers and they include very large, pyramidal neurons as well as some heretofore undescribed, fusiform neurons. The projection to area 18 contains two types not found in the projection to PMLS: spinous stellate neurons in layer 4 and inverted pyramidal neurons in layer 3. Finding that a variety of morphological types contribute projections to a single cortical area raises the possibility that corticocortical projections, like retinogeniculate and geniculocortical projections, comprise multiple parallel pathways with different physiological properties and patterns of termination. Finding that the projection to area 18 contains morphological types that do not project to PMLS indicates that the projections from area 17 are likely to contribute to the functional specialization of extrastriate visual areas.

Identification and electrophysiology of isolated pars compacta neurons from guinea-pig substantia nigra

Single nuerons from the substantia nigra of the adult guinea-pig were dissociated. Two morphological types of neurons were identified: (i) large multipolar neurons (20–40 μm greatest diameter) and (ii) small fusiform neurons ( <20 μm diameter). Neurons of both types showed catecholamine fluorescence and were retrogradely labelled by rhodamine-conjugated microspheres injected into the striatum. Two types of neuron (Type A and Type B) were also identified electrophysiologically in perforated patch recordings of membrane potential and whole-cell current. Type A neurons had a low spontaneous firing frequency (5 Hz) broad action potentials (4 ms) and a threshold of ∼−45 mV. They were inhibited by the dopamine D 2 receptor agonist, quinpirole. Type B neurons were characterized by a faster firing frequency (25 Hz), shorter action potential duration (1.5 ms) and a threshold of ∼−50 mV. These cells were unaffected by quinpirole. Large multipolar neurons were usually found to be of the A type and small fusiform, neurons of the B type. The properties of the large multipolar, Type A neurons suggest that they form part of the nigrostriatal, dopaminergic population of the pars compacta.

Evidence for separate morphological classes of Renshaw cells in the cat's spinal cord

Although some functions of Renshaw cells are well defined, pharmacological evidence suggests that there may be more than one type of Renshaw cell involved in recurrent inhibition of motoneurons, or one type employing more than one inhibitory amino acid neurotransmitter. Identified Renshaw cells were intracellularly stained with horseradish peroxidase (HRP), revealing the existence of a distinctive group of fusiform neurons as well as the more common multipolar cells. The fusiform neurons may represent a subgroup of Renshaw cells having separate functions and/or synaptic mediators.

Somatodendritic morphology of on‐ and off‐cells in the rostral ventromedial medulla

The rostral ventromedial medulla (RVM) contains two classes of physiologically defined neurons, on-cells and off-cells, that are implicated in nociceptive modulation. In a continuing effort to detail the neural circuitry that underlies the activity of these two distinct neuronal types, the somatodendritic morphology of on- and off-cells was studied in the cat, rat, and ferret. In lightly anesthetized animals, on-cells increased and off-cells decreased their discharge rate during a withdrawal reflex evoked by noxious stimuli. Following their physiological characterization by using intracellular recording, on- and off-cells were injected with either horseradish peroxidase or biocytin and their somatodendritic arborizations were examined. Labeled on- and off-cells included fusiform and stellate cells of all sizes as well as large multipolar neurons. Although the somatic shape of both on- and off-cells in RVM was heterogeneous, off-cells tended to be fusiform neurons whose long axis was oriented mediolaterally. The dendritic domains of both on- and off-cells extended bilaterally past the lateral edge of the trapezoid body or pyramid and ventrally to, and sometimes including, the trapezoid body or pyramid. In contrast to their extensive mediolateral spread, the dendritic domains of both cell types were limited to the ventral half of the reticular formation and were compressed along the rostrocaudal axis. The dendritic arbor of individual on- and off-cells extended well beyond the cytoarchitectonic boundaries of any single nuclear region, within the domain delineated as the RVM. The spatial domains of the dendritic arbors of on- and off-cells are further evidence that the on- and off-cells throughout the RVM constitute an integrated unit in the modulation of nociceptive transmission.

Intraneuronal accumulations of lysosomes in the cerebellum of rats and dogs after dosing with MDL-832

1, 2, 9, 10-tetramethoxyaporphine phosphate (MDL-832) was once considered a potential human antitussive. MDL-832 was administered orally in the diets of Sprague-Dawley rats at dose levels of 0, 5, 10, 20, 40, 80 and 160 mg/kg/day for 3 and 6 months and in gelatin capsules to Beagle dogs at 0, 5, 10, 15, 30 and 60 mg/kg/day for 3, 6 and 12 months. Histopathologic examinations of hematoxylin and eosin-stained cerebellar sections revealed intracytoplasmic brown pigment accumulations in large fusiform neurons (presumably the motor type) of the pons. The pigment granules were found to be PAS-positive, non-acid fast, iron-free, Sudan B-positive and fuchsinophilic. Intraneuronal pigment accumulations were seen in rats after 3 months of treatment at 80 mg but not at 40 mg and after 6 months at 20 mg but not at 10 mg. For dogs the effect was observed after 3 months at 60 mg but not at 30 mg and after 12 months at 10 mg but not at 5 mg.

Vasoactive intestinal polypeptide (VIP) containing cells in the developing rat occipital hemisphere

Numerous cells were observed to show intense vasoactive intestinal polypeptide (VIP) immunoreactivity from birth to postnatal day 8 in the subventricular zone of the rat occipital hemisphere. This cell population was markedly reduced by postnatal day 8, but isolated clusters of VIP cells persisted into adulthood. In addition, long, L-shaped VIP fibers were seen in the hemispheric wall up to postnatal day 16, but not in the adult. Parallel to the reduction in number of the subventricular VIP cells an increasing number of VIP cells appeared in the neo- and allocortex, developing by postnatal day 12 all the features of the mature cortical bipolar fusiform neurons. As possible alternatives, the migration of subventricular VIP cells into the cortex, the transient character of the subventricular VIP population or the expression of VIP by radial glia are discussed.

Neuronal typology of the thalamic area triangularis of Gallotia galloti (reptilia, sauria).

In a Golgi study of the area triangularis (AT), a rostral nucleus of the ventral thalamus of Gallotia galloti, we have identified four major neuronal types on the basis of their morphological characteristics: medium-sized fusiforms with two processes, medium-sized fusiforms with three or four processes, small bipolars, and small and medium-sized multipolars. These neurons are characterized by a simple morphology and radial arrangement. Cell size varies from small to medium, and all axons project laterally. These characteristics distinguish AT neurons from those of neighboring nuclei. In addition, we found some evidence of differential topographic distribution of each neuronal type within the nucleus. Medium-sized fusiform neurons with two processes are located in the most ventral part, where they constitute the ventral nuclear limit. Small multipolar neurons prevail in the dorsal and ventromedial parts, and in the rest of the nucleus medium-sized neurons, including both fusiform with three or four processes and multipolar types, are normally found. Finally, we discuss a putative homology of the reptilian AT with a part of the mammalian zona incerta.

Intermediate and deep layers of the macaque superior colliculus: A golgi study

We studied the intermediate and deep layers of the macaque superior colliculus by means of the Golgi technique in an attempt to better understand the structural features of this important oculomotor center. For this study, we examined the optic (stratum opticum, SO), intermediate gray (stratum griseum intermedium, SGI), intermediate white (stratum album intermedium, SAI), and deep gray (stratum griseum profundum, SGP) layers. These are the four layers in which neurons having saccade-related activity are localized. We identified eight neuronal types on the basis of differences in somatic and dendritic morphologies: large multipolar neurons (Type I); large pyramidal neurons (Type II); large fusiform neurons (Type III); medium fusiform neurons with spiny, radially oriented dendrites (Type IV); medium round neurons with fan-shaped dendritic trees (Type V); medium stellate neurons with varicose dendrites (Type VI); medium multipolar neurons with robust, spiny dendrites (Type VII); and local interneurons (Type VIII). Most neuronal types possessed features that are homologous to presynaptic dendritic features in other brain centers. With the exception of the medium stellate neurons (Type VI), which are aspinous, and the local interneurons (Type VIII), which are sparsely spinous, all other types had a moderate number of spines on their dendrites. Dendrites that terminated in the optic layer had specializations not observed elsewhere, suggesting that these tips may sample a tectal afferent that is not present in the more ventral layers. These eight types comprise all the neuronal morphologies observed in a large number of Golgi-impregnated macaque brains (n = 50). We suggest that they represent the full range of neuron types in the saccade-related layers of the macaque tectum.

Golgi Morphology of the Neurons in Frontal Sections of Human Interthalamic Adhesion

The Golgi morphology of the neurons in the human interthalamic adhesion (IA, which is not present in every human brain) is very variable. Four types of Golgi-impregnated neurons were found in the adult human IA: (1) fusiform neurons (most characteristic of the human IA); (2) neurons with an oval perikaryon; (3) triangular neurons (rarely found), and (4) multipolar neurons (polygonal perikaryon and at least 4 primary dendrites). Fusiform neurons, as well as triangular and multipolar ones, belong to the isodendritic type, but the neurons with oval perikarya do not.

GABA and glycine immunoreactivity in the guinea pig superior olivary complex

Immunoperoxidase immunocytochemistry was employed to examine the distribution of γ-aminobutyric acid (GABA)- and glycine (GLY)-immunoreactive cells, fibers, and terminals in the guinea pig superior olivary complex. The nuclei studied were the lateral superior olive (LSO), medial superior olive (MSO), superior paraolivary nucleus (SPN), and the medial, ventral, and lateral nuclei of the trapezoid body (MNTB, VNTB, and LNTB, respectively). The majority of LSO neurons exhibited GABA-immunoreactive (+) labeling. These same neurons were also lightly GLY+. Extensive perisomatic punctate GLY+ labeling was ovserved on most LSO neurons; these puncta most likely correspond to synaptic terminals. A very small number of MSO fusiform neurons were GABA+, and none were GLY+. The GLY positive perisomatic punctate labeling around most MSO neurons, although abundant, was not as profuse as that observed in the LSO. The MNTB neurons corresponding to the principal and elongate types were intensely GLY+ and were contacted by small numbers of GLY+ puncta. There was extensive GLY+ punctate labeling in the SPN that surrounded the cell bodies of most of its large, radiate neurons and many of the smaller, fusiform neurons. The few large, radiate neurons that were lightly GLY+ possessed far fewer GLY+ puncta on their perikarya. The distribution of GABA+ puncta was generally diffuse and scattered throughout the nuclei described above. In the VNTB and LNTB, several large neurons of various shapes were GLY+ as were the small, oval neurons. The extent of GLY+ punctate labeling was quite variable in both nuclei. The majority of perikarya in the VNTB and LNTB were GABA+. A light distribution of GABA+ puncta was observed on most cell bodies in both nuclei. Peridendritic GABA+ punctate labeling was dense in the VNTB neuropil. Two small populations of GLY+ neurons were observed outside of the named nuclei of the SOC; one was located dorsal to the LSO, near its dorsal hilus, and the other was identified near the medial pole of the LSO. The somata of both populations possessed extremely sparse GLY+ punctate labeling. In general, these results agree with and expand on findings in rodents from previous studies. There appears, however, to be differences between the guinea pig and cat with regard to the proportions of GABA+ neurons in the LSO and GLY+ punctate labeling in the MSO.

Morphology and electrophysiological properties of immunocytochemically identified rat dopamine neurons recorded in vitro

In vitro intracellular recordings were made from neurons in the rat midbrain slice. Two neuronal types could be distinguished in dopamine-containing (DA) midbrain regions based on electrophysiological criteria. One neuron type exhibited short duration action potentials (less than 1.5 msec), could fire at high frequencies (greater than 10 Hz), and exhibited either phasic or burst firing patterns. This neuron did not exhibit tyrosine hydroxylase immunoreactivity. A second neuronal type exhibited a unique set of electrophysiological properties, which included (1) a spontaneous pacemaker-like depolarizing potential, (2) a highly regular firing pattern, (3) long duration (greater than 2 msec) action potentials, and (4) a high (i.e., depolarized) spike threshold. This neuron was consistently double labeled using intracellular staining and immunocytochemical localization of the catecholamine-specific enzyme tyrosine hydroxylase, and thus represented the DA neuronal type. Midbrain DA neurons stained with Lucifer yellow could be separated into 3 classes based on their location and morphology: (1) fusiform neurons with laterally projecting dendrites in the dorsal substantia nigra zona compacta region, (2) multipolar cells with laterally and ventrally projecting dendrites in the ventral substantia nigra zona compacta, and (3) neurons with fusiform and multipolar somata and radially projecting dendrites in the ventral tegmental area. The dendrites also exhibited spine-like protrusions and ended with specialized forked processes. Spontaneously firing DA cells recorded in vitro had a number of distinguishing electrophysiological characteristics in common with those of DA neurons recorded in vivo, such as the presence of a slow depolarizing potential driving spike activity and a characteristic depolarized spike threshold (approximately-36 mV). However, in contrast to that found in vivo, the DA cells characterized here exhibited substantially higher input resistances and fired spontaneously in a very regular pacemaker pattern. Burst firing was not observed. Spike activity was apparently dependent on 4 depolarizing events: (1) a voltage-dependent TTX-sensitive slow depolarization, (2) a cobalt-sensitive low threshold depolarization that was activated during the rebound from brief membrane hyperpolarizations, (3) high threshold dendritic calcium spikes which gave rise to the spike afterhyperpolarization, and (4) a high threshold initial segment sodium spike. These depolarizations were modulated by several processes, including a 4-aminopyridine-insensitive delayed repolarization, an instantaneous and time-dependent anomalous rectifier, and an afterhyperpolarization. Although low threshold depolarizations and rebound action potentials could be triggered by the membrane repolarization following small membrane hyperpolarizations, comparatively larger hyperpolarizations attenuated this rebound activation, thereby suppressing anodal break excitation.(ABSTRACT TRUNCATED AT 400 WORDS)

Organization of the septal region in the rat brain: A Golgi/EM study of lateral septal neurons

The combined Golgi/electron microscope (EM) technique was used to analyze the fine structure and synaptic organization of the various types of neurons in the rat lateral septum (LS), i.e., in the dorsolateral (LSd), intermediolateral (LSi), and ventrolateral (LSv) nuclei of the septal complex. Two characteristic cell types were observed in the LSd: type I with thick, short dendrites densely covered with short spines, and type II with longer and thinner dendrites exhibiting fewer but longer spines. This latter type was by far the most frequently impregnated cell type in the LSd and was also present in the LSi. Synaptic contacts on spines of either cell type were asymmetric; the majority of the presynaptic boutons contained clear round synaptic vesicles. Occasionally terminals were found that contained both clear and dense-core vesicles. Typical fusiform neurons with a low number of spines and rather long dendrites, sometimes invading other LS nuclei, were found in the LSi. The LSv contained numerous small neurons with small dendritic fields. A relatively large number of terminals with dense-core vesicles were found to establish synaptic contacts with identified LSv neurons. The morphological heterogeneity of LS neurons is discussed with regard to other studies on afferent and efferent fiber systems as well as immunohistochemical studies of this particular region of the septal complex.

Projections from the medial cortex in the brain of lizards: Correlation of anterograde and retrograde transport of horseradish peroxidase with timm staining

Efferent projections of the medial cortex of the lizards Podarcis hispanica and Gallotia stehlinii were studied by examining the transport of horseradish peroxidase; results were correlated with those from Timm-stained sections. Two efferent systems were found. The first reaches the distal part of the outer plexiform layer in the medial, dorsomedial, and dorsal cortices, i.e., zones that are negative to Timm staining, and possibly originates from horizontal fusiform neurons. The second reaches the Timm-positive zones in the cortex and septum and is topographically arranged: the vertical portion of the intermediate and caudal medial cortex and the entire rostral medial cortex project to the inner two-thirds of the outer plexiform layer of the dorsomedial cortex and of the medial subfield of the dorsal cortex; to the paraventricular zone of the inner plexiform layer of the medial cortex; and bilaterally to the dorsal part of the dorsal precommissural septum. The dorsal part of the intermediate and caudal medial cortex and the ventralmost folded part of its caudal edge project rostrally to the juxtasomatic zone of the outer plexiform layer and the entire inner plexiform layer of the intermediate and lateral subfields of the dorsal cortex and to the ventral part of the dorsal septum. In its intense Timm reaction and its ultrastructural properties, as reported in earlier studies, the Timm-positive fiber system of the lizard brain shows a close resemblance to the mossy fiber system of the mammalian hippocampus.

Neurons with galanin innervate cholinergic cells in the human basal forebrain and galanin and acetylcholine coexist

Immunocytochemistry with antibodies against cholinacetyltransferase (ChAT) and the novel peptide galanin (GA) were conducted as a single label or as double label experiments on the basal forebrain nuclei of brains from eleven human subjects without prior history of neurological disease. ChAT positive or cholinergic neurons form the major population of cells in the basal nucleus of Meynert. A minor portion of these ChAT positive neurons demonstrate a coexistence with GA positive immunoreactivity suggesting that they are cholinergic/GA neurons. Small fusiform neurons with long dendrites and complex local axonal networks are GA immunoreactive and are local circuit interneurons. The cholinergic cells in the basal nucleus are innervated by a fine network of GA immunoreactive axons and terminals which enwrap their perikarya and dendrites. It is suggested that GA in local circuit interneurons may provide a significant control or modulation of the cholinergic neurons and of cholinergic functions within the basal nucleus. In human diseases which feature a destruction of the basal forebrain cholinergic neurons, surviving GA neurons may inhibit most remaining cholinergic neurons and their function, with severe consequences.

Postnatal development of the parabrachial gustatory zone in rat: Dendritic morphology and mitochondrial enzyme activity

Previous studies have shown that behavioral and neurophysiological responses to tastes develop during rat's postnatal life. The present experiments evaluated morphological and metabolic development of neurons in the gustatory zone of the caudal parabrachial nucleus (PBNc) of rat. Histological reconstruction studies were conducted to establish coordinate systems for PBNc gustatory zones in developing rats. Reliability of coordinate systems were evaluated in separate experiments following infusions of horse-radish peroxidase in the thalamic taste area. Morphological and Golgi impregnation studies were performed to characterize neuronal and dendritic architecture in PBNc gustatory zones defined by coordinates. Conventional histochemical studies were performed for the mitochondrial respiratory enzymes cytochrome C oxidase (CO, EC 1.9.3.1) succinate dehydrogenase (SDH, EC 1.3.99.1), and NADH-dehydrogenase (NADH-DH, EC 1.6.99.3). Results show that two somatic morphologies can be statistically characterized in PBNc gustatory zones: Multipolar somatic types and fusiform somatic types. Multipolar and fusiform neurons of neonatal and adult rats project axons to the thalamic taste area, and dendrites of these neurons grow extensively between approximately 16 days after birth to approximately 35 days after birth. Activity of CO, SDH, and NADH-DH increases in the PBNc gustatory zones during the period of dendritic growth, and continues to increase slightly to approximately 45 days. These results provide the first demonstration of postnatal morphological and metabolic developmental in a central gustatory relay. Postnatal development of gustatory system therefore appears similar to that reported for other sensory systems, to the extent that morphological and metabolic development accompanies the ontogeny of taste responses.

A Golgi‐electron microscopic study of fusiform neurons in the hilar region of the dentate gyrus

The fusiform cells of the dentate gyrus are located in a portion of the hilus within 100 micron of the granule cell layer. They have ovoid somata and bipolar dendrites that generally run parallel to the granule cell layer. The dendrites of these cells are either spiny or sparsely spiny. The spiny fusiform cell has numerous spines along its dendrites, which are contacted by terminals with the features of granule cell axon collaterals. This cell type also displays somal spines that are contacted by similar terminals. In contrast, the sparsely spiny fusiform cell displays only a few spines, which are contacted by multiple small axon terminals that synapse with both the stalk and end bulb of the spine. Most synaptic input for this cell type is made with the smooth surfaces of the soma and dendrites. A variety of terminals form synapses with the sparsely spiny fusiform cell, including terminals that resemble the fine axon collaterals of mossy fibers. The somata of these two cell types also display differences in the amount of Nissl bodies and the degree of nuclear infolding. The results indicate that spiny fusiform cells are similar to mossy cells, another hilar cell type that receives its major synaptic input from axon collaterals of mossy fibers from granule cells. The distribution of the dendrites of spiny fusiform cells and the pattern of granule cell axon collaterals suggest a high degree of convergence from granule cells. In contrast, the variety of axodendritic synapses for sparsely spiny fusiform cells suggests that more diverse inputs affect this cell's activity. Therefore, the structure and circuitry of these two hilar cell types are probably different. This study adds further evidence to indicate that the hilus contains a large variety of cell types with different neuronal connections.

Superior colliculus efferents to five subcortical visual system structures in the ground squirrel

We compared the laminar location and morphology of superior colliculus cells projecting to the dorsal and ventral lateral geniculate nuclei (LGd, LGv), the pretectum (PT), the parabigeminal nucleus (Pb), and nucleus lateralis posterior (LP) in the ground squirrel Spermophilus tridecemlineatus. Horseradish peroxidase was iontophoretically injected into LGd, LGv, PT, Pb and each of the 3 subdivisions of the LP. After survival periods of 24-72 h the animals were perfused intracardially and brain sections processed histochemically. A Zeiss ZIDAS image analysis system was used to determine the soma size of labeled neurons and to prepare histograms showing the relation between cell size and frequency. After injections in the LGd, LGv, Pb and PT, labeled neurons were present throughout the stratum griseum superficiale and the upper portion of the stratum opticum. They were mainly fusiform neurons whose long axes ranged from 12 to 44 microns. There were also some multipolar cells 9-22 microns in diameter with the highest frequencies found in the 12-14 and 16-17 microns ranges. Differences were found in the exact location and/or soma size of the neurons projecting to the 4 nuclei. After injections in rostrolateral and caudal LP the labeled cells were always large multipolar neurons specifically located in the lower half of the stratum griseum superficiale. Their somata measured 9-22 microns in diameter but the highest frequencies were found in the 16-17 and 19-20 microns ranges. Our findings suggest that there are different populations of superior colliculus cells projecting to different visual system structures.

Distribution and morphology of abducens motoneurons innervating the lateral rectus and retractor bulbi muscles in the frog Rana ridibunda

The distribution and morphology of the neurons innervating the lateral rectus and retractor bulbi muscles of the frog Rana ridibunda were studied by means of retrograde axonal transport of horseradish peroxidase (HRP). The neurons are located in the rhombencephalon in two distinct groups which lie dorsolateral and lateral to the fasciculus longitudinalis medialis and represent the main and accessory abducens nuclei, respectively. From HRP injections into the two muscles, it can be concluded that multipolar neurons located rostrally in the main abducens nucleus innervate the lateral rectus muscle. The retractor bulbi muscle receives its innervation from bipolar, fusiform neurons located in the caudal portion of the main abducens nucleus and throughout the rostrocaudal extent of the accessory abducens nucleus.