Ultrastructure of the central subnucleus of the nucleus tractus solitarii and the esophageal afferent terminals in the rat

The central subnucleus of the nucleus tractus solitarii (ceNTS) receives afferent projections from the esophageal wall and projects to the nucleus ambiguus, thus serving as a relay nucleus for peristalsis of the esophagus. Here we examine the synaptic organization of the ceNTS, and its esophageal afferents by using transganglionic anterograde transport of cholera toxin-conjugated horseradish peroxidase (CT-HRP). When CT-HRP was injected into the subdiaphragmatic esophagus, many anterogradely labeled terminals were found only in the ceNTS. The ceNTS was composed of round or oval-shaped, small neurons (14.7x8.7 micro m) containing sparse organelles and an irregularly shaped nucleus. The average number of axosomatic terminals was only 1.3 per section cut through the nucleolus. Most of them (92%) contained round vesicles and formed asymmetric synaptic contacts (Gray's type I), and a few (8%) contained pleomorphic vesicles and formed symmetric synaptic contacts (Gray's type II). All anterogradely labeled terminals contacted dendrites but not the neuronal somata. The labeled terminals were large (2.55+/-0.07 micro m) and exclusively Gray's type I. More than half of them (60%) contacted small dendrites (less than 1 micro m in diameter), and contained dense-cored vesicles. More than 40% of the labeled terminals contacted two to four dendrites, thus forming a synaptic glomerulus. Sometimes a labeled terminal that contacted an unlabeled terminal by an adherent junction was found within the glomerulus. The large terminals and these complex synaptic relations appeared to characterize the esophageal afferent projections in the ceNTS.     

Monosynaptic inputs from the nucleus tractus solitarii to the laryngeal motoneurons in the nucleus ambiguus of the rat

The cricothyroid (CT) and the posterior cricoarytenoid (PCA) muscles in the larynx are activated by the laryngeal motoneurons located within the nucleus ambiguus; these motoneurons receive the laryngeal sensory information from the nucleus tractus solitarii (NTS) during respiration and swallowing. We investigated whether the neurons in the NTS projected directly to the laryngeal motoneurons, and what is the synaptic organization of their nerve terminals on the laryngeal motoneurons using the electron microscope. When wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) was injected into the NTS after cholera toxin subunit B-conjugated HRP (CT-HRP) was injected into the CT muscle or the PCA muscle, the anterogradely WGA-HRP-labeled terminals from the NTS were found to directly contact the retrogradely CT-HRP-labeled dendrites and soma of both the CT and the PCA motoneurons. The labeled NTS terminals comprised about 4% of the axosomatic terminals in a section through the CT motoneurons, and about 9% on both the small (PCA-A) and the large (PCA-B) PCA motoneurons. The number of labeled axosomatic terminals containing round vesicles and making asymmetric synaptic contacts (Gray’s type I) was almost equal to that of the labeled terminals containing pleomorphic vesicles and making symmetric synaptic contacts (Gray’s type II) on the CT motoneurons. The labeled axosomatic terminals were mostly Gray’s type II on the PCA-A motoneurons, while the majority of them were Gray’s type I on the PCA-B motoneurons. These results indicate that the laryngeal CT and PCA motoneurons receive a few direct excitatory and inhibitory inputs from the neurons in the NTS. Accepted: 2 June 2000     

Fine structural survey of tyrosine hydroxylase immunoreactive terminals in the myenteric ganglion of the rat duodenum

We have examined whether the noradrenergic neurons have direct synaptic projections to the myenteric ganglion neurons of the duodenum and the ultrastructure of their terminals by using immunogold–silver labeling for tyrosine hydroxylase. In the neuropil of the myenteric ganglia, about half of the axon terminals contained round clear vesicles and the rest of them contained pleomorphic clear vesicles. The sizes of axon terminals contacting the dendrites as a whole were 1.62 ± 0.07 μm. All axon terminals formed asymmetric synaptic contacts with dendrites or somata. Immunohistochemical study revealed that the tyrosine hydroxylase-immunoreactive nerve terminals were distributed throughout the ganglia and contained exclusively pleomorphic clear synaptic vesicles (about 20–80 nm long). The tyrosine hydroxylase-immunoreactive terminals were generally large (1.99 ± 0.07 μm). A considerable number of the tyrosine hydroxylase-immunoreactive terminals made asymmetric synaptic contacts with small dendrites, spines or somata of the myenteric ganglion neurons. Serial ultrathin sections through the myenteric neurons revealed that about 16% of the total number of axosomatic terminals showed tyrosine hydroxylase immunoreactivity. These results indicated that the myenteric ganglion neurons of the duodenum receive direct synaptic projection of sympathetic noradrenergic neurons and that their terminals contain pleomorphic vesicles and form asymmetric synaptic contacts.     

C-FOS expression in the subnucleus gelatinosus of the human nucleus tractus solitarii

The dorsal portion of the nucleus tractus solitarii (NTS) shows selective dendritic lesions in adults who died after an episode of acute heart failure, suggesting excitotoxic glutamate-induced neuronal death. Cerebral hypoxia and/or ischaemia also produce hyperexpression of specific genes (c-fos, c-jun) which may be involved, in vulnerable districts, in the mechanisms of excitotoxic neuronal death. In the present study, we examined NTS in 23 adults, who died shortly after an ischaemic and/or hypoxic event, on transverse serial sections of the medulla, stained with haematoxylineosin, Nissl, Klüver-Barrera and Luxol fast blue, and immunohistochemical staining by anti-tyrosine hydroxylase and anti-Fos. In 10 cases, at the level of the dorsal portion of the NTS, corresponding to the subnucleus gelatinosus, bilateral symmetrical hypereosinophilic areas and strong Fos-like immunoreactivity were detected. The hypoxic-ischaemic origin of these findings was supported by the strong hypereosinophilic appearance and shrinking of neurons, and by selective Fos-like immunoreactivity, the expression of Fos being mainly associated with cellular damage and subsequent death following hypoxic-ischaemic injury. In 7 other cases, Fos-like immunoreactivity was found at the level of the subnucleus gelatinosus, in the absence of hypereosinophilia or pyknosis in histological staining. The immediate-early gene expression induces to ascribe the absence of morphologically evident hypoxicischaemic lesions to the rapidity of death. The selective vulnerability of the subnucleus gelatinosus to hypoxic-ischaemic injury may not only be explained with reference to vascularization of the medullary tegmentum, but also to the structural and functional characteristics of the subnucleus itself.     

Synaptology of the hypoglossal nucleus in the rat

Summary The purpose of this study was to define the types and distribution of synaptic terminals in the hypoglossal nucleus (XII) of the rat. Based on differences in bouton and vesicle size and shape, synaptic specializations and association with postsynaptic organelles, five types of terminals were identified in XII. In order of decreasing frequency they were: 1) S-boutons (spherical vesicles with an asymmetrical synapse); 2) F-boutons (flattened vesicles with a symmetrical synapse); 3) P-boutons (pleomorphic admixture of flattened and spherical vesicles with a symmetrical synapse); 4) C-boutons (pleomorphic vesicles with a subsynaptic cistern); and 5) Tboutons (spherical vesicles with an asymmetrical synapse and subsynaptic dense bodies). S-boutons were the predominant type found on dendrites, while boutons containing flattened vesicles were more prevalent on motoneuron somata. C-boutons were restricted exclusively to cell bodies and large dendrites, and T-boutons were seen primarily on smaller dendritic profiles. These results are, in general, comparable to those previously described in the ventral horn and cranial nerve motor nuclei in several species. However, differences were noted. Specifically, large M-boutons and axo-axonic synapses were not observed in the present study. The functional significance of these findings are discussed in relation to oro-lingual behaviour.     

Fine structure of the semicompact formation of the nucleus ambiguus of the rat

 We investigated the fine structure of the semicompact formation of the nucleus ambiguus (AmS), which was identified by retrogradely labeled pharyngeal (PH) motoneurons. When cholera toxin subunit B-conjugated horseradish peroxidase was injected into the lower pharyngeal muscle, many retrogradely labeled PH neurons were found throughout the AmS. Besides the PH neurons, two types of neurons were recognized in the AmS: unlabeled medium-sized neurons and unlabeled small neurons. The PH neuron was large (27.6 × 44.1 μm) and polygonal, and contained many Nissl bodies and well-developed cell organelles with a prominent spherical nucleus. The medium-sized neuron was dark and oval (19.3 × 33.2 μm), and contained many free ribosomes and much swollen rough endoplasmic reticulum with a distorted oval nucleus. The small neuron was spindle-shaped (12.3 × 20.2 μm), and had poorly developed cell organelles with an irregularly shaped nucleus. The average number of axosomatic terminals in a sectional plane was largest in the PH neurons (32.8), smaller in the medium-sized neurons (23.1), and smallest in the small neurons (6.3). The number of axo-somatic terminals containing round vesicles (Gray’s type I) was almost equal to that of terminals containing pleomorphic vesicles (Gray’s type II) in the PH neuron, and slightly smaller in the small and the medium-sized neurons. About 60% of the axodendritic terminals were Gray’s type I, and 40% were type II. These results indicate that there are two different types of interneurons besides the PH motoneurons in the AmS. Accepted: 24 June 1997     

Observations on the fine structure of the lateral vestibular nucleus (Deiters' nucleus) in the cat

Summary A study has been made of the ultrastructure of the lateral vestibular nucleus of the normal cat. The study includes light microscopical observations made in Golgi material. The internal structure of the various types of cells is described. The soma of the larger nerve cells is surrounded by a protoplasmic layer, constituted by astroglial sheets, dendrites and boutons; glial cell bodies are usually located outside the layer. The smaller nerve cells display few axosomatic synapses and may be in direct contact with myelinated fibres and glial perikarya. Spines are present on the soma of large and small nerve cells and on all parts of the dendrites. The proximal dendrites are usually the part of the neurons which is most amply supplied with boutons.Various types of boutons and cell junctions are described and an attempt is made to correlate the findings in electron micrographs with those made in Golgi sections.The study serves as a basis for observations made in experimental material where afferent fibres to the nucleus have been damaged.This investigation has been supported in part by Grant NB 02215-07 from the National Institute of Neurological Diseases and Blindness, US-Public Health Service. This aid is gratefully acknowledged.     

Somatostatin immunoreactivity in axon terminals in rat nucleus tractus solitarii arising from central nucleus of amygdala: coexistence with GABA and postsynaptic expression of sst2A receptor

Axon terminals synapsing on neurones in the nucleus tractus solitarii (NTS) that originate from the central nucleus of the amygdala (CeA) have been shown to contain gamma-aminobutyric acid (GABA) immunoreactivity. Here we investigated whether such terminals also contain somatostatin (SOM), a neuropeptide found in axons distributed throughout the NTS and in somata in the CeA, and known to modulate cardiovascular reflexes when microinjected into the NTS. With fluorescence microscopy, SOM immunoreactivity was seen in the varicosities of some axons throughout the NTS that were anterogradely labelled with biotin dextran amine injected into the CeA. Such varicosities were frequently observed in close proximity to dendrites of NTS neurones that were immunoreactive for the SOM receptor sst(2A) subtype, and in many cases also for catecholamine synthesising enzymes. In the caudal, cardioregulatory zone of NTS, SOM immunoreactivity was localised by electron microscopic pre-embedding gold labelling to boutons containing dense-cored and clear pleomorphic vesicles and forming symmetrical synapses, mostly onto dendrites. Additional post-embedding gold labelling for GABA suggested that a subpopulation (29%) of GABAergic terminals sampled in this area of NTS contained SOM. Almost all boutons anterogradely labelled from the amygdala were GABA-immunoreactive (-IR) and 21% of these were SOM-IR. A similar proportion of these boutons (22%) formed synapses onto dendrites containing immunoreactivity for the SOM receptor sst(2A) subtype. These observations provide evidence that some of the GABAergic projection neurones in the CeA that inhibit baroreceptor reflex responses in the NTS in response to fear or emotional stimuli could release SOM, which might modulate the activity of NTS neurones via an action on sst(2A) receptors.     

Inhibition of swallowing reflex following phosphorylation of extracellular signal-regulated kinase in nucleus tractus solitarii neurons in rats with masseter muscle nociception

Pain is associated with swallowing abnormalities in dysphagic patients. Understanding neuronal mechanisms underlying the swallowing abnormalities associated with orofacial abnormal pain is crucial for developing new methods to treat dysphagic patients. However, how the orofacial abnormal pain is involved in the swallowing abnormalities is not known. In order to evaluate neuronal mechanisms of modulation of the swallows by masticatory muscle pain, here we first induced swallows by topical administration of distilled water to the pharyngolaryngeal region. The swallowing reflex was significantly inhibited after capsaicin (10, 30 mM) injection into the masseter muscle compared to vehicle injection. Moreover the number of phosphorylated extracellular signal-regulated kinase-like immunoreactive (pERK-LI) neurons in the nucleus tractus solitarii (NTS) was significantly increased in the rats with capsaicin injection into the masseter muscle compared to that with vehicle injection. Rostro-caudal distribution of pERK-LI neurons in the NTS was peaked at the obex level. The capsaicin-induced inhibitory effect on swallowing reflex was reversed after intrathecal administration of mitogen-activated protein kinase (MAPK) kinase (MEK) inhibitor, PD98059. The present findings suggest that phosphorylation of ERK in NTS neurons may be involved in capsaicin-induced inhibition of swallowing reflex.     

The reciprocal connections of endomorphin 1- and endomorphin 2-containing neurons between the hypothalamus and nucleus tractus solitarii in the rat

In the CNS, endomorphin 1- and endomorphin 2-immunoreactive neuronal cell bodies have been principally found both in the hypothalamus and nucleus tractus solitarii. Functionally, the hypothalamus and nucleus tractus solitarii are closely related in many aspects, especially in visceral functions. On the other hand, there are also many endomorphin-immunoreactive fibers and terminals in the two regions. In the present study, to investigate whether endomorphin 1-immunoreactive and endomorphin 2-immunoreactive neurons in the hypothalamus and nucleus tractus solitarii project reciprocally between these two regions, fluorescent retrograde labeling combined with immunofluorescence histochemical staining for endomorphin 1 and endomorphin 2 was used. After injection of Fluoro-Gold into the nucleus tractus solitarii of rats, endomorphin 1/Fluoro-Gold or endomorphin 2/Fluoro-Gold double-labeled neuronal cell bodies were predominantly observed in the arcuate nucleus of the hypothalamus, a few of which were also observed in the posterior hypothalamic area and periventricular hypothalamic nucleus. After injection of Fluoro-Gold into the medial zone of hypothalamic tuberal region and the lateral hypothalamic area, respectively, endomorphin 1/Fluoro-Gold or endomorphin 2/Fluoro-Gold double-labeled neuronal cell bodies were found chiefly in the medial, commissural, lateral and gelatinous parts of the nucleus tractus solitarii. These results provide morphological evidence that there exist reciprocal endomorphinergic connections between the hypothalamus and nucleus tractus solitarii.     

Immunohistochemical localization of putative neurotransmitters within the feline nucleus tractus solitarii

With the aid of immunohistochemical techniques the distribution of substance P, met-enkephalin, serotonin, somatostatin, alpha-melanocyte stimulating hormone, neurotensin and neurophysin immunoreactivities were mapped throughout the rostro-caudal extent of the cat's nucleus tractus solitarii. Three of the putative neurotransmitters (substance P, enkephalin and serotonin) were found to be widely distributed as varicose fibers and punctate structures. The densities of their immunoreactivities were plotted in a range from very dense, dense, moderate, occasional, to none, at different levels of the nucleus of the solitary tract. Substance P immunoreactivity was the most varied and dense of all the neurotransmitters studied. Its accumulations ranged from very dense in the lateral, dense in portions of the parvocellular and lateral, moderate in medial and commissural and occasional in ventrolateral and portions of the parvocellular subdivisions. Both the enkephalin and serotonin immunoreactivities had patterns similar to that of substance P immunoreactivity, although their amounts were not as great. Following colchicine treatment neurons containing substance P and enkephalin immunoreactivity were found in many subdivisions of the nucleus of the solitary tract. Somatostatin, alpha-melanocyte stimulating hormone, neurotensin and neurophysin immunoreactivities were present in the nucleus of the solitary tract as isolated varicose fibers scattered throughout the nucleus. Immunoreactive neurons were not found for these putative neurotransmitters after colchicine treatment. The presence of substance P immunoreactivity within subdivisions which receive visceral afferent input is discussed in relation to the role of substance P as a possible transmitter of the afferent limb of the vagus nerve. The distribution of enkephalin and serotonin immunoreactivities in the nucleus of the solitary tract reflect their involvement in the regulation or modulation of cardiovascular and respiratory functions. While the significance of somatostatin, alpha-melanocyte stimulating hormone, neurotensin and neurophysin immunoreactivities within the nucleus of the solitary tract is not understood at present, these substances might possibly play a role in visceral functions.     

Glutamatergic neurotransmission in the nucleus tractus solitarii: Structural and functional characteristics

Glutamate is the main excitatory transmitter in the central nervous system. As such, it plays a major role in transmitting and processing visceral sensory information within the nucleus tractus solitarii (NTS). Here, we review current knowledge on NTS glutamatergic transmission. We describe the main organizational features of NTS glutamatergic synapses as determined by work performed during the last decade using antibodies against glutamate receptors and transporters proteins. In light of these recent neuronatomical findings, we discuss some functional properties of developing and adult NTS glutamatergic synapses.     

CO2 decreases membrane conductance and depolarizes neurons in the nucleus tractus solitarii

Summary To identify central sites of potential CO₂/H⁺-chemoreceptive neurons, and the mechanism responsible for neuronal chemosensitivity, intracellular recordings were made in rat tissue slices in two cardiopulmonary-related regions (i.e., nucleus tractus solitarii, NTS; nucleus ambiguus, AMBc) during exposure to high CO₂. When the NTS was explored slices were bisected and the ventral half discarded. Utilizing such dorsal medullary slices removed any impinging synaptic input from putative chemoreceptors in the ventrolateral medulla. In the NTS, CO₂-induced changes in firing rate were associated with membrane depolarizations ranging from 2–25 mV (n = 15). In some cases increased e.p.s.p. activity was observed during CO₂ exposure. The CO₂-induced depolarization occurred concomitantly with an increased input resistance ranging from 19–23 M (n = 5). The lower membrane conductance during hypercapnia suggests that CO₂-induced depolarization is due to a decreased outward potassium conductance. Unlike neurons in the NTS, AMBc neurons were not spontaneously active and were rarely depolarized by hypercapnia. Eleven of 12 cells tested were either hyperpolarized by or insensitive to CO₂. Only 1 neuron in the AMBc was depolarized and it also showed an increased input resistance during CO₂ exposure. Our findings suggest that CO₂/H⁺-related stimuli decrease potassium conductance which depolarizes the cell and increases firing rate. Although our in vitro studies cannot guarantee the specific function of these cells, we believe they may be involved with brain pH homeostasis and cardiopulmonary regulation.     

Direct contacts between glossopharyngeal afferent terminals and hypoglossal motoneurons revealed by double labeling with cobaltic-lysine and horseradish peroxidase in the Japanese toad

Glossopharyngeal (IX) afferents and hypoglossal (XII) motoneurons of the Japanese toad were simultaneously labeled with cobaltic-lysine and horseradish peroxidase, respectively. Some of the terminal branches of the IX afferents had direct contacts with the dorsal dendrites, the lateral dendrites and the somata of the XII motoneurons, but not with the medial dendrites. Such direct contacts mainly occurred in the rostral region of the dorsomedial XII nucleus, where tongue-retractor motoneurons predominate, but not in the caudal region nor in the ventrolateral XII nucleus.     

Interaction of baroreceptor afferents from carotid sinus and aorta at the nucleus tractus solitarii

Summary In chloralose-urethane anaesthetized cats, low-threshold baroreceptor afferents of the carotid sinus and aortic nerves were stimulated electrically. Evoked responses were recorded within the nucleus tractus solitarii near the obex. At a certain electrode position in this area an evoked potential (E. P.) was elicited by stimulation of the homolateral carotid sinus or aortic nerve as well as the contralateral sinus or aortic nerve.At this site an interaction of these four baroreceptor nerves was demonstrated by testing the E. P. of one nerve after a conditioning stimulation of another nerve. Simultaneous E. P.'s did not show arithmetical summation. A strong reduction of the test-E.P. (mean value of reduction: 50%) occurred with a conditioning-testing interval of 10–20 msec. The test-E. P. came back to the control amplitude at an interval of 100–150 msec.Neither picrotoxin nor strychnine changed the time course or extent of these interactions.It was further observed that the most effective conditioning-testing interval for inhibition of test response corresponded closely to the difference between the arrival times of arotic and sinus nerve activities evoked by the cardiovascular pulse (aortic 16±5 msec before sinus nerve).A summary of these studies was presented at the 35th Meeting of the Deutsche Physiologische Gesellschaft [5].     

Depressor and bradycardic actions of L-proline injected into the nucleus tractus solitarii of anesthetized rats

L-Glutamate has been considered to be a neurotransmitter in the nucleus tractus solitarius (NTS) of the afferent baroreflex pathway, though this has not yet been decisively shown. A bolus injection of a neurotransmitter candidate amino acid L-proline into the cisterna magna and that of L-glutamate shows the same pressor action in the freely moving rat, but the actual nuclei responding L-proline remain undetermined. Besides L-glutamate, L-proline might be another candidate amino acid in the NTS. The present study was therefore performed to characterize the circulatory action of L-proline injected into the NTS where responses to glutamate in the anesthetized rat had already been shown. The NTS was first determined as a site on the dorsal surface of the medulla where a microinjection of L-glutamate decreased arterial pressure and heart rate. Microinjected L-proline (1.65 to 13.2 nmol, 33 nl) into the NTS decreased arterial pressure and heart rate in a dose-dependent manner. The injection of a mixed solution (66 nl) of kynurenate, an ionotropic excitatory amino acid receptors antagonist (1.32 nmol), and L-proline (6.6 nmol) into the NTS abolished the depressor and bradycardic actions with L-proline alone (6.6 nmol, 66 nl). However, a mixture of an increased concentration of kynurenate (6.6 nmol) with glutamate augmented the actions seen with glutamate alone (0.66 nmol, 66 nl). D-Proline (13.2 nmol, 66 nl), the optic isomer of L-proline, produced no change in arterial pressure or heart rate, suggesting that the actions of L-proline in the NTS were optically specific. The results indicate that L-proline but not D-proline induces its depressor and bradycardic actions through ionotropic excitatory amino acid receptors in the NTS of the anesthetized rat. L-Proline may become a candidate transmitter of baroreceptor information in the NTS.     

Substance P-like immunoreactive neurons in the nucleus tractus solitarii of the rat send their axons to the nucleus accumbens

By a double-labeling method combining the retrograde tracing of horseradish peroxidase with an immunocytochemical technique, substance P-like immunoreactive neurons in the medial and commissural subnuclei of the nucleus tractus solitarii (NTS) of the rat were found to send axons to the nucleus accumbens.     

Coexistence of NMDA and AMPA receptor subunits with nNOS in the nucleus tractus solitarii of rat

We previously showed that most neuronal nitric oxide synthase (nNOS)-containing neurons in the nucleus tractus solitarii (NTS) contain NMDAR1, the fundamental subunit for functional N-methyl-D-aspartate (NMDA) receptors. Likewise, we found that almost all nNOS-containing neurons in the NTS contain GluR1, the calcium permeable AMPA receptor subunit. These data suggest that AMPA and NMDA receptors may colocalize in NTS neurons that contain nNOS. However, other investigators have suggested that non-NMDA receptors are located primarily on second-order neurons and NMDA receptors are located predominantly on higher-order neurons in NTS. We now seek to test the hypothesis that NMDA receptors, AMPA receptors and nNOS are colocalized in NTS cells. We performed triple fluorescent immunohistochemical staining of nNOS, NMDAR1 and GluR1, and performed confocal laser scanning microscopic analysis of the NTS. The distributions of nNOS immunoreactivity (IR), NMDAR1-IR and GluR1-IR in the NTS were similar to those we reported earlier. Superimposed images revealed that almost all NMDAR1-IR cells contained GluR1-IR and almost all GluR1-IR cells contained NMDAR1-IR. Some double-labeled cells were additionally labeled for nNOS-IR. All nNOS-IR neurons contained both GluR1-IR and NMDAR1-IR. These studies support our hypothesis that NMDA and AMPA receptors are colocalized in NTS neurons and are consistent with a role of both types of ionotropic receptors in transmission of afferent signals in NTS. In addition, these data provide support for an anatomical link between ionotropic glutamate receptors and nitric oxide in the NTS.     

Cortical and tectal afferent terminals in the suprageniculate nucleus of the cat

The suprageniculate nucleus (Sg) of the cat was observed electron microscopically after wheat germ agglutinin-horseradish peroxidase (WGA-HRP) injection into the anterior ectosylvian visual cortical area (AEV) and superior colliculus (SC). Small axon terminals filled with round synaptic (RS) vesicles were labeled with HRP injected into the AEV and SC, whereas large axon terminals containing round synaptic (RL) vesicles were labeled after HRP injection in the SC. After producing a lesion in the AEV and adjoining orbito-insular cortex and injecting WGA-HRP into the SC, degenerated terminals and HRP-labeled RS terminals were occasionally found to make synaptic contacts with a single dendritic profile of Sg neurons.