Replacement of synaptic terminals in lamina II and Clarke's nucleus after unilateral lumbosacral dorsal rhizotomy in adult cats

Evidence from previous light-microscopic studies suggested that lumbosacral dorsal rhizotomy in cats elicits sprouting of converging undamaged systems into partially deafferented Clarke's nucleus and lamina II. We therefore applied quantitative electron-microscopic methods to determine whether this sprouting is associated with replacement of synaptic terminals (reactive reinnervation). We used stereological and morphometric methods to estimate terminal number per cross section in right and left lamina II and Clarke's nucleus in adult cats after acute and chronic unilateral (right-sided) lumbosacral deafferentation. Planimetric measurements of area indicated no significant shrinkage of either region as a result of the deafferentation; an increase in area occupied by glial cytoplasm (gliosis) equaled the decrease occupied by axonal components. The gliosis appears to persist indefinitely, although the degenerative debris stainable with conventional light-microscopic methods does not persist. Analysis of the synaptic population of lamina II reveals that the large central or "scalloped" terminals comprise a substantial fraction (greater than 40%) of the total area occupied by terminals in control material and that this population is largely lost upon deafferentation, leaving a large population of small terminals with spherical vesicles. Nevertheless, estimates of total terminal number indicate no difference between control and deafferented lamina II, suggesting a rapid and virtually complete replacement of lost dorsal root terminals by small terminals containing spherical vesicles. Terminal number in Clarke's nucleus also remains constant despite the loss of the dorsal root input. We conclude that there is also a virtually complete and rapid replacement of lost terminals in Clarke's nucleus by terminals containing spherical vesicles. These data provide an example of a case in which axonal sprouting demonstrated with light-microscopic methods is associated with electron-microscopic evidence of reactive reinnervation.     

Synaptic displacement in intracentral neurons of Clarke's nucleus following axotomy in the cat

The dorsal spinocerebellar tract was severed unilaterally in 12 cats which were killed at 4, 15, 35, and 90 days. Clarke's neurons of L3 segment were studied by electron microscopy for chromatolytic, synaptic, and glial changes. Some large neurons of Clarke's nucleus were chromatolyzed by 4 days, and all large cells by 15 days. Small cells of Clarke's nucleus remained unchanged. At 35 and 90 days chromatolytic cells were all reduced in size. These atrophic cells were characterized by pale Nissl bodies, dark dendrites, synapses with pale matrix, and giant synaptic terminals. Synaptic changes were noted on chromatolyzed neurons by 4 days. The first signs of synaptic changes were reductions in the number of synaptic complexes, widening of synaptic clefts, and the appearance of cisternae under postsynaptic membrane of giant synapses. Occasional boutons with pale matrix and decreased numbers of synaptic vesicles were noted. There was a moderate increase in the astrocytic processes on the neuronal surface membrane. Some of these processes were inserted into the widened synaptic clefts. Some synapses remained unchanged. At 15 days the synaptic changes were similar but now occurred on all large cells. The synaptic matrix was less dense and the number of vesicles was less in the separated boutons. At 90 days all boutons, except giant synapses on the base of proximal dendrites, were small and some were arranged in dense patches. Some synapses were pale, and others were unchanged. The patchy distribution of numerous small boutons on the atrophic Clarke's neurons is considered to be due to collateral sprouting and formations of new terminals. These findings have implications in relation to spinal shock and recovery from it.     

Fine structure of inclusion body in the nucleus of Alzheimer glia type II in the brain of hepatocerebral degeneration

Summary Best's carmine positive inclusion bodies in the nuclei of Alzheimer glia type II were observed diffusely in the brain with a special type of hepatocerebral degeneration. These inclusion bodies were examined with an electron microscope. The results showed that a body consisted of -glycogen particles, amylopectin-like substances, and capsules enveloping glycogen particles.It was speculated that the inclusion body is produced and accumulated in the nucleus by the disturbance of glycogen metabolism in the nucleus itself.     

Ultrastructural quantitative analysis of glutamatergic and GABAergic synaptic terminals in the phrenic nucleus after spinal cord injury

Quantitative analysis of electron microscopic postembedding immunochemically stained material indicates that 48% of all terminals in the rat phrenic nucleus are glutamatergic and 33% are γ-aminobutyric acid (GABA) ergic. Three distinct types of glutamatergic terminals were observed in the rat phrenic nucleus: terminals characterized by large, loosely arranged spherical synaptic vesicles (SI) or small, compact spherical synaptic vesicles (Ss) and elongated terminals containing spherical synaptic vesicles with neurofilaments (NFs). All three types of glutamatergic terminals display asymmetrical synaptic membrane densities with postsynaptic dense bodies being present in some of the S-type terminals. The GABAergic immunoreactive terminals in the phrenic nucleus most closely resemble F-type terminals. They are characterized by flattened or pleomorphic synaptic vesicles and symmetric synaptic membrane densities. Among the 48% glutamatergic terminals, 27% are SI, 65% are Ss, and 8% are NFs, respectively. Significantly fewer glutamate, GABA, and unlabeled terminals per unit area are present in the phrenic nucleus 30 days after a C2 spinal cord hemisection as compared to nonhemisected controls. The average number of active zones per terminal, however, is greater in the hemisection group (1.45 ± 0.03) than in the control group (1.34 ± 0.03), with the active zones in the glutamate terminals mainly accounting for this difference. Moreover, the length of the active zones in the glutamate terminals was significantly longer in the hemisection group (0.37 ± 0.013 μm) as compared to the controls (0.24 ± 0.008 μm). In addition, the mean length of synaptic active zones in GABAergic terminals was also found to be longer in the hemisection group (0.36 ± 0.022 μm) as compared to controls (0.28 ± 0.014 μm). Finally, there is also a significantly higher ratio of synaptic active zones to the total number of glutamate-labeled terminals after injury (1.73 ± 0.08) as compared to controls (1.41 ± 0.04). The number of double/multiple synapses, the percentages of Sl, Ss, and NFs-type terminals, and the percentages of synaptic active zones contacting either distal dendrites or proximal dendrites/somata do not change significantly 30 days after injury. These results are important for a more complete understanding of the synaptic plasticity that occurs in the phrenic nucleus after spinal cord injury and to show how the plasticity may relate to the unmasking of latent bulbospinal respiratory connections which restore function to the hemidiaphragm paralyzed by an ipsilateral spinal cord hemisection. © 1996 Wiley-Liss, Inc.     

Glycogen accumulation in spinal cord motor neurons due to partial ischemia

Summary Partial ischemia of the spinal cord in adult cats was induced by abdominal aortic ligation. The most striking abnormality was an accumulation of glycogen in large motor neurons and astroglia in the peripheral anterior horns. Little or no histological and ultrastructural abnormalities were present in these regions. The first glycogen deposits appeared after 1/2 h in glial cells, whereas glycogen accumulation in neurons was first noticeable 1 h after ligation reaching a maximum in 24 h. A gradual decrease occurred with disappearance of glycogen at 10 days. Increase in UDPG-transferase was found preceeding glycogen appearance, and increase in glycogen-phosphorylase activity occurred later concurrent with glycogen accumulation. This unique neuronal glycogen deposition may be due to the UDPG-transferase normally present in -motor neurons of the anterior horns. Other possible mechanisms are also considered.     

Electron microscopic analysis of the synaptic organization of the globus pallidus in the cat

The synaptic organization of the feline globus pallidus (GP) was studied electron microscopically. The axon terminals were classified into five types on the basis of the size and shape of synaptic vesicles and the type of postsynaptic differentiations. Type I and II axon terminals were characterized by large, pleomorphic vesicles and by a symmetric and an asymmetric synaptic contact, respectively. Type III and IV axon terminals were characterized by small, pleomorphic vesicles and by a symmetric and an asymmetric synaptic contact, respectively. Type V axon terminals were characterized by elongated and large round vesicles and by a symmetric synaptic contact. The origins of these terminals were determined by a combined degeneration and HRP tracing technique. Following injections of HRP into the caudate nucleus or electrolytic lesions in this nucleus, type I terminals were anterogradely labeled with HRP or degenerated, respectively. Although type III, IV, and V terminals were labeled with HRP after HRP injections into the subthalamic nuclear region, only type IV and V terminals degenerated after lesions in that area. Type II terminals did not show any alterations following such treatment. These results suggest that type I terminals originate from the caudate nucleus, that type IV and V terminals come from the subthalamic nucleus or caudal to it, and that type III terminals are the terminals of intrinsic axon collaterals of GP neurons which send axons to the subthalamic nucleus. Occasionally convergence of different kinds of axon terminals on the same GP neuron was also observed. These terminals originated from the caudate nucleus and the subthalamic nucleus or caudal to it.(ABSTRACT TRUNCATED AT 250 WORDS)     

Projections from auditory cortex to the cochlear nucleus in rats: Synapses on granule cell dendrites

Previous work has demonstrated that layer V pyramidal cells of primary auditory cortex project directly to the cochlear nucleus. The postsynaptic targets of these centrifugal projections, however, are not known. For the present study, biotinylated dextran amine, an anterograde tracer, was injected into the auditory cortex of rats, and labeled terminals were examined with light and electron microscopy. Labeled corticobulbar axons and terminals in the cochlear nucleus are found almost exclusively in the granule cell domain, and the terminals appear as boutons (1–2 μm in diameter) or as small mossy fiber endings (2–5 μm in diameter). These cortical endings contain round synaptic vesicles and form asymmetric synapses on hairy dendritic profiles, from which thin (0.1 μm in diameter), nonsynaptic “hairs” protrude deep into the labeled endings. These postsynaptic dendrites, which are typical of granule cells, surround and receive synapses from large, unlabeled mossy fiber endings containing round synaptic vesicles and are also postsynaptic to unlabeled axon terminals containing pleomorphic synaptic vesicles. No labeled fibers were observed synapsing on profiles that did not fit the characteristics of granule cell dendrites. We describe a circuit in the auditory system by which ascending information in the cochlear nucleus can be modified directly by descending cortical influences. © 1996 Wiley-Liss, Inc.     

The fine structure of the perigeniculate nucleus in the cat

The fine structure of the cat's perigeniculate nucleus has been analyzed and compared to that of dorsal thalamic relay nuclei. Golgi preparations and electron micrographs of perigeniculate cells commonly show somatic spines. The most common presynaptic elements for these spines and for the adjacent perikaryal surfaces are relatively large axon terminals containing round synaptic vesicles and making multiple asymmetric contacts. These "RLD" terminals (so termed for their round vesicles, large average size of the terminals, and dark mitochondria) are also presynaptic to dendritic spines and shafts of proximal and secondary dendrites. Comparisons with adjacent parts of the dorsal lateral geniculate nucleus show that these RLD terminals are cytologically distinct from retinogeniculate terminals and that small numbers of RLD terminals also occur in the geniculate A laminae. Three other major classes of perigeniculate synaptic terminals, resemble major classes of terminals in the dorsal lateral geniculate nucleus. These include two types of terminal with flat or ovoid synaptic vesicles and dark mitochondria, "FD1" and "FD2" terminals, and a class of small terminal with densely clustered round vesicles and dark mitochondria, "RSD" terminals. RSD terminals, which resemble corticogeniculate axon terminals, represent the only class of perigeniculate terminal that does not contact perikarya. FD2 terminals resemble lateral geniculate presynaptic dendrites and participate in serial and triadic synaptic contacts, being both pre- and postsynaptic; however, in contrast to the arrangement characteristic of thalamic relay nuclei, these contacts do not occur within synaptic glomeruli. A fifth major class of perigeniculate presynaptic terminal has large flat or polymorphic synaptic vesicles and pale mitochondria. These "FP" terminals are seen infrequently in the lateral geniculate A laminae. Similarities between perigeniculate and lateral geniculate fine structure may relate in part to common sources of afferent input to the two nuclei.     

A fine structural study of degenerative-regenerative pathology in the surgically deafferentated lateral vestibular nucleus of the rat

Summary An experiment was designed to examine the course of degeneration, phagocytosis, and regeneration in the central nervous system following surgical deafferentation. The anterior cerebellar vermis was ablated in young male rats. The animals were sacrificed by perfusion at postoperative times ranging from 24 hrs to 6 months. The lateral vestibular nuclei, to which the anterior cerebellar vermis projects, were processed for electron microscopy. Degenerating synaptic terminals, of the dark variety, were seen from 24 hrs to five days postoperatively. Phagocytosis of degenerating terminals occurred during this time. Degenerating axons persisted through 6 months survival, and phagocytosis of these degenerating axons was observed. Astrocyte scar formation began at 1 month postoperatively. The relative number of axosomatic synaptic terminals containing flattened vesicles (F terminals; presumed inhibitory in function) increased in operated animals. The highest F scores were found from 24 hrs to two weeks postoperatively, and then the F scores declined through six months. The significance of these sprouting activities is discussed in relation to the abortive sprouting phenomenon described by Ramón y Cajal.This research was supported by NASA Task No. 970-21-11-11 at Ames Research Center and NIH Training Grant No. 5T01 GM00793-11 at Tulane University.     

Glycogen distribution in mouse hippocampus

The hippocampus is a limbic structure involved in the consolidation of episodic memory. In the recent decade, glycogenolysis in the rodent hippocampus has been shown critical for synaptic plasticity and memory formation. Astrocytes are the primary cells that store glycogen which is subject to degradation in hypoglycemic conditions. Focused microwave application to the brain halts metabolic activities, and therefore preserves brain glycogen. Immunohistochemistry against glycogen on focused microwave-assisted brain samples is suitable for both macroscopic and microscopic investigation of glycogen distribution. Glycogen immunohistochemistry in the hippocampus showed a characteristic punctate signal pattern that depended on hippocampal layers. In particular, the hilus is the most glycogen-rich subregion of the hippocampus. Moreover, large glycogen puncta (>0.5 µm in diameter) observed in neuropil areas are organized in a patchy pattern consisting of puncta-rich and -poor astrocytes. These observations are discussed with respect to distinct hippocampal neural activity states observed in live animals.     

The accessory optic system in the frog, Rana pipiens: An electron microscopic study of the retinal afferents utilizing the anterograde tracer biocytin

The retinal afferents to the basal optic nucleus in the frog, Rana Pipiens, were labeled anterogradely with biocytin and subsequently studied at the electron microscopic level. Labeled synaptic terminals in the nucleus varied in size from 0.5 μm to 2.0 μm and made symmetric synaptic contacts with large and small dendrites, although very rare axospinous and axosomatic contacts were also demonstrated.     

Organization and synaptic connections of cholinergic fibers in the cat superior colliculus

The cat superior colliculus (SC) receives a dense cholinergic input from three brainstem nuclei, the pedunculopontine tegmental nucleus, the lateral dorsal tegmental nucleus, and the parabigeminal nucleus (PBG). The tegmental inputs project densely to the intermediate gray layer (IGL) and sparsely to the superficial layers. The PBG input probably projects only to the superficial layers. In the present study, the morphology of choline acetyltransferase (ChAT)-immunoreactive axons and synaptic endings in the superficial and deep layers of the SC was examined by light and electron microscopy to determine whether these cholinergic afferents form different types of synapses in the superifical and deep layers. Two types of fibers were found within the zonal (ZL) and upper superficial gray layers (SGL): small diameter fibers with few varicosities and larger diameter fibers with numerous varicosities. Quantitative analysis demonstrated a bimodal distribution of axon diameters, with one peak at approximately 0.3–0.5 μm and the other at 0.9–1.0 μm. On the other hand, ChAT-immunoreactive fibers in the IGL were almost all small and formed discrete patches within the IGL. Two types of ChAT-immunoreactive synaptic profiles were observed within the ZL and upper SGL using the electron microscope. The first type consisted of small terminals containing predominantly round synaptic vesicles and forming asymmetric synaptic contacts, mostly on dendrites. The second type was comprised of varicose profiles that also contained round synaptic vesicles. Their synaptic contacts were always symmetric in profile. ChAT-immunoreactive terminals in the IGL patches contained round or pleomorphic synaptic vescles, and the postsynaptic densities varied from symmetric to asymmetric, including intermediate forms. However, no large varicose profiles were observed. This study suggests that cholinergic fibers include at least two differnt synaptic morphologies: small terminals with asymmetric thickenings and large varicose profiles with symmetric terminals. The large varicose profile in the superficial layers is absent in the IGL. This result suggests that the cholinergic inputs that innervate the superficial layers and the patches in the IGL of the cat SC differ in their synaptic organization and possibly also in their physiological actions. © 1993 Wiley-Liss, Inc.     

The organization of the pulvinar in the grey squirrel (Sciurus carolinensis). II. Synaptic organization and comparisons with the dorsal lateral geniculate nucleus

The purpose of these experiments was to compare the synaptic organization of the subdivisions of the pulvinar defined in the preceding paper (Robson and Hall, '77) with each other and with the organization present in the dorsal lateral geniculate nucleus. The electron microscope was used to analyze normal synaptic arrangements and degenerating axonal terminals resulting from lesions. The dorsal lateral geniculate nucleus in the grey squirrel contains synaptic clusters similar to those described previously for other species. These clusters are characterized by large optic tract terminals which form multiple contacts onto large dendritic processes and other processes containing flat or pleomorphic vesicles. The geniculate lamina adjacent to the optic tract receives projections from the superior colliculus as well are from the retina. The terminals of the superior colliculus axons are small and medium sized and lie outside of the synaptic clusters. The retinal terminals are in the clusters. In the pulvinar, the rostro-medial subdivision contains synaptic clusters which resemble those in the lateral geniculate nucleus. These clusters contain large axon terminals which make multiple contacts onto large dendrites. However, these terminals are not contributed by an ascending sensory pathway but by axons from strait cortex. The rostro-lateral and caudal subdivisions of the pulvinar also contain synaptic clusters, but these clusters consist of a segment of a large dendrite which is ensheathed by medium-sized terminals. Since only a few of these medium sized terminals in any one cluster degenerate after tectal lesions, and none degenerate after cortical lesions, it is suggested that the morphological arrangement of these clusters may permit the convergence of axons from several sources, some of which are unidentified, onto the same dendritic segment.     

Electron microscopic identification of lamina I axon terminations in the nucleus submedius of the cat thalamus

Ascending lamina I axons were labeled with Phaseolus vulgaris leucoagglutinin and the synaptic connections of their terminals in nucleus submedius (Sm) were studied in the electron microscope. The terminals were large, contained rounded synaptic vesicles, and were involved in complex synaptic aggregations with pre- and postsynaptic dendrites. It was observed that clustered large boutons from a single axon could contact a single dendritic shaft. These observations support a sensory role for lamina I input to Sm.     

Barbiturate-induced glycogen accumulation in brain. An electron microscopic study

Glycogen accumulation in the mouse brain during prolonged barbiturate anesthesia (6 h with sodium phenobarbital, 250 mg/kg) was studied with the electron microscope. Areas examined included hypothalamus, hippocampus (area dentata), midbrain reticular formation, cerebellar cortex and frontal cerebral cortex. Large increases of particulate glycogen were noted in astrocytes of the area dentata and the frontal cortex. Smaller increases were sometimes seen in astrocytes of the cerebellar cortex. No changes were noted in the hypothalamus or midbrain reticular formation and glycogen was never seen in neurons, oligodendroglia or microglia. The greatest accumulation of astrocytic glycogen occured in areas of high synaptic density and near neuronal perikarya.     

Patterns of glutamate decarboxylase immunostaining in the feline cochlear nuclear complex studied with silver enhancement and electron microscopy

The cochlear nuclear complex of the cat was immunostained with an antiserum to glutamate decarboxylase (GAD), the biosynthetic enzyme for the inhibitory neurotransmitter GABA, and studied with different procedures, including silver intensification, topical colchicine injections, semithin sections, and immunoelectron microscopy. Immunostaining was found in all portions of the nucleus. Relatively few immunostained cell bodies were observed: most of these were in the dorsal cochlear nucleus and included stellate cells, cartwheel cells, Golgi cells, and unidentified cells in the deep layers. An accumulation of immunoreactive cells was also found within the small cell cap and along the medial border of the ventral cochlear nucleus. Immunostained cells were sparse in magnocellular portions of the ventral nucleus. Most staining within the nucleus was of nerve terminals. These included small boutons that were prominent in the neuropil of the dorsal cochlear nucleus, the granule cell domain, in a region beneath the superficial granule cell layer within the small cell cap region, and along the medial border of the ventral nucleus. Octopus cells showed small, GAD-positive terminals distributed at moderate density on both cell bodies and dendrites. Larger, more distinctive terminals were identified on the large cells in the ventral nucleus, in particular on spherical cells and globular cells. There was a striking positive correlation of the size, location, and complexity of GAD-positive terminals with the size, location, and complexity of primary fiber endings on the same cells. This correlation did not hold in the dorsal nucleus, where pyramidal cells receive many large GAD-positive somatic terminals despite the paucity of primary endings on their cell bodies. The GAD-positive terminals contained pleomorphic synaptic vesicles and formed symmetric synaptic junctions that occupied a substantial portion of the appositional surface to cell bodies, dendrites, axon hillocks, and the beginning portion of the initial axon segments. Thus, the cells provided with large terminals can be subjected to considerable inhibition that may be activated indirectly through primary fibers and interneurons or by descending inputs from the auditory brainstem.     

Four types of neuron in layer IVab of cat cortical area 17 accumulate 3H-GABA

Roughly 10% of the neurons in layer, IVah.of cat area 17 accumulate exogenous ³H-gamma-aminobutyric acid (GABA) but how many types of neuron comprise this population was unknown. We characterized these neurons by partial reconstruction of their somas from serial electron microscope autoradiograms and distinguished four types. GABA 1 was large (> 16.5 μm) and dark with a dense distribution of synaptic terminals, substantial geniculate input to the soma, and a moderate accumulation of GABA. GABA 2 was small (< 13 μm) and pale, also with a dense distribution of terminals but without evidence of somatic geniculate input, and a moderate accumulation of GABA. GABA 3 was radially fusiform (20μm × 8 μm) with varicose dendrites, a sparse distribution of synaptic terminals, and a heavy accumulation of GAB A. GAB A 4 was medium in size (15 μm) with a moderate distribution of synaptic terminals and a heavy accumulation of GABA. Reasons are presented for believing that each of these four categories of GABA-accumulating neuron represents a fundamental cell type.     

Leucine-enkephalin-containing neuron system in the facial nucleus of the rat with special reference to its fine structure

The light and electron microscopic localization of leucine-enkephalin-containing terminals in the facial nucleus of the rat were investigated by means of the peroxidase-antiperoxidase (PAP) immunocytochemical technique. By light microscopy, leucine-enkephalin-like immunoreactive (LEI) terminals were unevenly distributed in the facial nucleus. The greatest accumulation of the terminals was seen in the medial part of the nucleus. Electron microscopic examination of LEI-terminals in the medial part of the nucleus revealed that the predominant type of synaptic contacts of LEI-terminals in this area were axo-dendritic contacts (about 75%). These dendrites which made synapses with LEI-terminals were relatively large and rich in cytoplasmic organella, suggesting that they belonged to the proximal segment of the dendrite. A small number of LEI-terminals was found to make synaptic contact with neuronal perikarya (5%). These perikarya were very large and had nuclei with less chromatin particles. These findings suggest that LEI-terminals make contact with neurons which exist in the facial nucleus. The rest of the LEI-terminals (20%) were in apposition to the non-labelled axon terminals which contain small, clear and round vesicles.     

Synaptic organization of projections from basal forebrain structures to the mediodorsal thalamic nucleus of the rat.

The synaptic organization of the mediodorsal thalamic nucleus (MD) in the rat was studied with the electron microscope, and correlated with the termination of afferent fibers labeled with wheat germ agglutinin conjugated to horseradish peroxidase (WGA-HRP). Presynaptic axon terminals were classified into four categories in MD on the basis of the size, synaptic vesicle morphology, and synaptic membrane specializations: 1) small axon terminals with round synaptic vesicles (SR), which made asymmetrical synaptic contacts predominantly with small dendritic shafts; 2) large axon terminals with round vesicles (LR), which established asymmetrical synaptic junctions mainly with large dendritic shafts; 3) small to medium axon terminals with pleomorphic vesicles (SMP), which formed symmetrical synaptic contacts with somata and small-diameter dendrites; 4) large axon terminals with pleomorphic vesicles (LP), which made symmetrical synaptic contacts with large dendritic shafts. Synaptic glomeruli were also identified in MD that contained either LR or LP terminals as the central presynaptic components. No presynaptic dendrites were identified. In order to identify terminals arising from different sources, injections of WGA-HRP were made into cortical and subcortical structures known to project to MD, including the prefrontal cortex, piriform cortex, amygdala, ventral pallidum and thalamic reticular nucleus. Axons from the amygdala formed LR terminals, while those from the prefrontal and insular cortex ended exclusively in SR terminals. Fibers labeled from the piriform cortex formed both LR and SR endings. Based on their morphology, all of these are presumed to be excitatory. In contrast, the axons from the ventral pallidum ended as LP terminals, and those from the thalamic reticular nucleus formed SMP terminals. Both are presumed to be inhibitory. At least some terminals from these sources have also been identified as GABAergic, based on double labeling with anterogradely transported WGA-HRP and glutamic acid decarboxylase (GAD) immunocytochemistry.     

Retinal synapses of the cat medial interlaminar nucleus and ventral lateral geniculate nucleus differ in size and synaptic organization

The retinal terminals of the medial interlaminar nucleus (MIN) and ventral lateral geniculate nucleus (VLG) have been examined quantitatively to determine if there are morphological differences in their synaptic ultrastructure which reflect their distinctive physiologies. The cross-sectional area and density (number per unit area) of synaptic contact zones with conventional and presynaptic dendrites (F2 profiles) were measured for each retinal terminal. The densities of F2 presynaptic dendrites and F1 flattened vesicle axon terminals were also measured. Retinal terminals in MIN were often large (mean size= 2.7 μm² area) and had a high density of synaptic contacts (0.14 per μm surface area) with conventional dendrites, presynaptic dendrites, and dendritic spines. A high density of F2 presynaptic dendrites (0.08 per μm² area) was found in MIN. F1 axon terminals were also found frequently (0.04 per μm²). MIN retinal terminals were often organized in glomeruli like those of the dorsal lateral geniculate nucleus. The retinal terminals in VLG were almost always small (mean size= 0.94 μm² area), although they also had a high density of synaptic contacts (0.17 per μm surface area). They frequently synapsed on small dendrites and dendritic spines and less frequently on large dendrites. Unlike MIN, retinal terminals in VLG rarely contacted F2 presynaptic dendrites which were much less frequent in VLG (0.01 per μm² area). Like MIN, VLG contained numerous F1 axon terminals (0.06 per μm² area). No typical retinal glomeruli were found in VLG. These results show that MIN, which contains many Y cells, has a population of large retinal terminals and many F2 presynaptic dendrites. VLG, which apparently has only W cells, contains only small retinal terminals and has fewer F2 presynaptic dendrites. Both have a high density of F1 flat vesicle axon terminals.