Somatic Profiles Research Articles

Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice.

The phenotypic effect of the weaver mutation in the ventral midbrain of homozygous mutants is associated with the progressive loss of dopaminergic neurons. To discover whether the number of mesencephalic dopaminergic cells is altered in weaver heterozygotes (wv/+), we studied mice between 20 and 365 days of age. We counted tyrosine hydroxylase (TH)-immunopositive cells in the substantia nigra (SN), retrorubral nucleus (RRN), and ventral tegmental area (VTA), and measured cross-sectional areas of neuronal somata in the SN of wv/+ and age-matched wild-type controls (+/+). The number of TH-positive cells in the wv/+ ventral midbrain was on average 13% lower than normal. Cell loss was detected selectively in the SN (12%) and VTA (23%). The areas of somatic profiles in the wv/+ nigral neurons were on average reduced by 9.8%. The neuronal losses in the SN and VTA correlated with a 13.8% reduction in dopamine level in the ventral striatum in wv/+ mice at 14-16 months of age. Our findings imply that a single dose of the weaver gene in the mouse is associated with cellular damage leading to a chronic deficiency in the mesostriatal dopaminergic system.

Localization of mu-opioid receptor-like immunoreactivity in the central components of the vagus nerve: a light and electron microscope study in the rat.

mu-Opioid receptor, the opioid receptor that shows the highest affinity for morphine, appears to induce a variety of side-effects, at least partly, directly through the mu-opioid receptor on neurons constituting the autonomic part of the vagus nerve. Thus, in the present study, location of mu-opioid receptor-like immunoreactivity in the central components of the autonomic part of the vagus nerve was examined in the rat. The intense immunoreactivity was observed light microscopically in the neuropil of the commissural subnucleus and the dorsal part of the medial subnucleus of the nucleus of the solitary tract, and in the neuropil of the rostral half of the ambiguus nucleus. The immunoreactivity was moderate in the neuropil of the rostral and lateral subnuclei and ventral part of the medial subnucleus of the nucleus of the solitary tract, and weak in the neuropil of the dorsal motor nucleus of the vagus nerve. In the nodose ganglion, many neurons of various sizes (17-48 microns in soma diameter) showed moderate immunoreactivity. After unilateral vagotomy at a level proximal to the nodose ganglion, the immunoreactivity in the ipsilateral ambiguus nucleus was apparently reduced within 48 h of the operation, and completely disappeared by the seventh day after the operation. In the nucleus of the solitary tract and dorsal motor nucleus of the vagus nerve, the reduction of immunoreactivity after the ganglionectomy was detectable on the fourth day after the operation, and became readily apparent by the seventh day after the operation; the immunoreactivity, none the less, still remained on the 10th day after the operation. Electron microscopically, the immunoreactivity in the ambiguus nucleus was seen mainly on dendritic profiles and additionally on somatic ones; no immunoreactivity was detected in axonal profiles. The immunoreactivity in the dorsal motor nucleus of the vagus nerve was observed only on dendritic profiles. The immunoreactivity in the nucleus of the solitary tract was seen on axonal and dendritic profiles, but not on somatic profiles. The immunoreactive axon terminals in the nucleus of the solitary tract were filled with spherical synaptic vesicles and made asymmetric synapses with dendritic profiles. The results indicate that the mu-opioid receptor in the central components of the autonomic part of the vagus nerve is located on dendrites and cell bodies of efferent neurons in the ambiguus, on dendrites of efferent neurons in the dorsal motor nucleus, and on axons which arise from nodose ganglion neurons and terminate in the nucleus of the solitary tract. The receptors on these structures may constitute the targets of enkephalin-containing and beta-endorphin-containing afferent axons arising from brainstem neurons. The receptors on the axon terminals of nodose ganglion neurons may be involved in regulation of the release of neurotransmitters and/or neuromodulators.

Cytoskeletal protein immunoexpression in fetal neural grafts: distribution of phosphorylated and nonphosphorylated neurofilament protein and microtubule-associated protein 2 (MAP-2).

The present study examined the immunocytochemical expression of important cytoskeletal proteins within the neurons of an extended series of neocortical grafts and smaller group of ventral mesencephalic (nigral) grafts. Using antibodies that were directed at all three neurofilament (NF) epitopes, NF-L, NF-M, and NF-H, we attempted to determine whether these neurons would have an altered cytoskeletal profile following the stress of transplantation, because previous studies have shown such changes following ischemia or direct brain injury. We studied phosphorylated NF protein, which is found predominantly in axons, nonphosphorylated NF protein, which is found predominantly in the somata-dendritic compartment, and MAP-2, a specific microtubule marker that is localized exclusively in the somato-dendritic compartment. The results show that in all neocortical grafts examined, both phosphorylated and nonphosphorylated NF immunoexpression was significantly downregulated and appeared only in relatively few axons and somatic profiles, respectively, even though there were numerous Nissl-stained neuronal profiles in the grafts. There was no particular pattern to the immunopositive profiles. At later times occasional neuronal profiles were positive for phosphorylated NF protein, suggesting a reaction to cellular injury. In contrast to neocortical grafts, the cytoskeletal profiles of MAP-2 and phosphorylated NF protein in nigral grafts appeared very similar to age-matched control although the nonphosphorylated NF protein expression did appear somewhat lessened at 1-2 mo postoperative. Because cytoskeletal proteins play important roles in neuronal size, shape, and structural stability, they may subserve key cellular issues in neural grafting. These results show a significant loss of cytoskeletal protein expression in neocortical grafts that does not occur in nigral grafts. These results suggest that fetal neurons from different brain regions (i.e., graft source) may respond differently to the grafting procedure insofar as their cytoskeletal makeup is concerned. In addition, a potential lack of appropriate growth substrates or synaptic contacts may also produce cytoskeletal alterations. As such, the cytoskeletal protein profiles in central nervous system (CNS) grafts may be useful markers for functional performance, perhaps reflecting a degree of cellular injury.

Cytoskeletal protein immunoexpression in fetal neural grafts: Distribution of phosphorylated and nonphosphorylated neurofilament protein and microtubule-associated protein 2 (MAP-2)

The present study examined the immunocytochemical expression of important cytoskeletal proteins within the neurons of an extended series of neocortical grafts and smaller group of ventral mesencephalic (nigral) grafts. Using antibodies that were directed at all three neurofilament (NF) epitopes, NF-L, NF-M, and NF-H, we attempted to determine whether these neurons would have an altered cytoskeletal profile following the stress of transplantation, because previous studies have shown such changes following ischemia or direct brain injury. We studied phosphorylated NF protein, which is found predominantly in axons, nonphosphorylated NF protein, which is found predominantly in the somata-dendritic compartment, and MAP-2, a specific microtubule marker that is localized exclusively in the somato-dendritic compartment. The results show that in all neocortical grafts examined, both phosphorylated and nonphosphorylated NF immunoexpression was significantly downregulated and appeared only in relatively few axons and somatic profiles, respectively, even though there were numerous Nissl-stained neuronal profiles in the grafts. There was no particular pattern to the immunopositive profiles. At later times occasional neuronal profiles were positive for phosphorylated NF protein, suggesting a reaction to cellular injury. In contrast to neocortical grafts, the cytoskeletal profiles of MAP-2 and phosphorylated NF protein in nigral grafts appeared very similar to age-matched control although the nonphosphorylated NF protein expression did appear somewhat lessened at 1-2 mo postoperative. Because cytoskeletal proteins play important roles in neuronal size, shape, and structural stability, they may subserve key cellular issues in neural grafting. These results show a significant loss of cytoskeletal protein expression in neocortical grafts that does not occur in nigral grafts. These results suggest that fetal neurons from different brain regions (i.e., graft source) may respond differently to the grafting procedure insofar as their cytoskeletal makeup is concerned. In addition, a potential lack of appropriate growth substrates or synaptic contacts may also produce cytoskeletal alterations. As such, the cytoskeletal protein profiles in central nervous system (CNS) grafts may be useful markers for functional performance, perhaps reflecting a degree of cellular injury.

Ultrastructure and synaptology of the nucleus ambiguus in the rat: the compact formation.

The fine structure of the esophagomotor compact formation of the nucleus ambiguus was studied. Esophageal motoneurons are atypical in that they have extensive direct somato-somatic and somato-dendritic appositions without intervening glial processes. A unique feature is the presence of finger- and leaf-like somatic protrusions which partially wrap longitudinally oriented dendrites and, occasionally, small groups of dendrites and axons. The neuropil contains many longitudinally oriented, small-diameter dendrites of relatively uniform size (1.1 +/- 0.4 S.D. micrograms in diameter). Motoneuronal somatic profiles have 0-5 synapses per profile which represents a synaptic density of 10.6 synapses per soma. Axodendritic synapses measure 0.5 x 0.7 microgram in the transverse plane and are up to 3.0 micrograms long in the sagittal plane. Many axon terminals contact both a soma and dendrite in close apposition. Most axon terminals (> 90%) contain round vesicles and form asymmetric junctions with somata and dendrites. Axon terminal degeneration after electrolytic lesions and labelling after injection of wheat germ agglutinin-horseradish peroxidase in the nucleus of the tractus solitarius show that afferent connections to the compact formation form axodendritic synapses. The ultrastructure and synaptology of esophageal motoneurons is characterized by the close apposition of somata and dendrites (somatic-dendritic bundling), and the longitudinal orientation of dendrites (dendritic bundling), axons and axon terminals in the neuropil. These features may be important morphological substrates for synchronization and coordination of esophageal motoneuronal activity and esophageal peristalsis.

Presynaptic localization of μ-opioid receptor-like immunoreactivity in retinal axon terminals within the terminal nuclei of the accessory optic tract: a light and electron microscope study in the rat

Neurophil within the terminal nuclei of the accessory optic tract of the rat showed intense to moderate μ-opioid receptor-like immunoreactivity (MOR-LI). After unilateral enucleation, MOR-LI within the terminal nuclei almost disappeared or was markedly reduced on the side contralateral to the operation. Electron microscopy revealed that MOR-LI axon terminals within the terminal nuclei were filled with round synaptic vesicles and in asymmetric synaptic contact mainly with dendritic profiles, and occassionally with somatic profiles.

GABAergic regulation of noradrenergic spinal projection neurons of the A5 cell group in the rat: An electron microscopic analysis

Recent studies have demonstrated an important contribution of the A5 noradrenergic cell group of the rostral medulla in the regulation of nociceptive messages at the level of the spinal cord. These noradrenergic controls parallel those arising from the serotonin-containing neurons of the nucleus raphe magnus. In the present study, we used postembedding immunogold staining to identify GABA-immunoreactive terminals that synapse upon identified spinally projecting noradrenergic neurons of the A5 cell group in the rat. A5 projection neurons were identified by Fluoro-Gold transport from the spinal cord; sections containing retrogradely labelled cells were then immunoreacted for tyrosine hydroxylase (TH) to identify the catecholamine-containing, presumed noradrenergic, neurons. Double-labelled A5 cells were intracellularly filled with Lucifer Yellow (LY) and then the LY was photo-oxidized to an electron-dense product. Seven intracellularly filled TH-immunoreactive projection neurons were studied with postembedding immunocytochemistry. Each A5 neuron received a significant GABA-immunoreactive terminal input. Out of a pooled total of 151 terminal profiles found in apposition to intracellularly labelled somatic and dendritic profiles, 31 (20.5%) were GABA-immunoreactive. The proportion of GABA-immunoreactive terminals that contacted somatic profiles (12/72; 17%) was similar to the proportion that contacted TH-labelled dendritic profiles (19/79; 24%). There was a discernible synaptic specialization in about 50% of the labelled terminals that contacted the TH projection neuron. Both symmetric and asymmetric synaptic specializations were found. Labelled terminals contained round or pleiomorphic vesicles, but not flat vesicles; many also contained dense-core vesicles. Our results indicate that noradrenergic neurons of the A5 cell group, which contribute to both antinociceptive and cardiovascular controls through their projection to the spinal cord, are regulated by local GABAergic, presumably inhibitory, mechanisms. Whether the initiation of A5 neuron activity results from a lifting of tonic GABAergic inhibitory control, as has been proposed for the neurons of the nucleus raphe magnus, remains to be determined.

Ultrastructural characteristics of callosal neurons in deep layers of cat primary auditory cortex (AI)

An electron microscope study of retrogradely labelled nonpyramidal neurons has been carried out in layers V-VI of the primary auditory cortex (AI) after HRP injections into the contralateral AI of cats. From 2 to 9 synapses were usually revealed on somatic profiles of these callosal neurons. Synapses occupied 15.8 +/- 1.7% (on the average) of the somatic surface of these neurons. All of the revealed synapses on the somata of these callosal neurons had symmetric contacts and were formed by axon terminals with small elongated synaptic vesicles. An average length of these synaptic contacts in sections was 1.6 +/- 0.1 mm. HRP-labelled axon terminals of callosal fibres in layers V-VI contained round synaptic vesicles and formed asymmetric synapses on spines and dendrites. Possible functional significance of axo-somatic synapses in formation of impulsation patterns of the callosal neurons is discussed.

Visceral and Somatic Profiles of Needless Pain and Nonpainful Sensations in Idiopathic Headache

The syndromes commonly called idiopathic headaches (IH) are the most frequent painful pathologies. The term derives from the fact that the IH necessarily but not exclusively involve the head area. Having abandoned the etiopathogenetic criterion of classification (vascular and tension headaches) which was proposed many years ago, The International IH Society has introduced a phenomenonological/descriptive classification, which is logically sound considering the idiopathy and clinical multiformity of IH. This classification may be useful until it is possible to substitute it with a nosography based on sure etiological data. The distinction between "chronicized" migraine (migraine attacks with daily intercritical headache) and tension-type headaches perhaps represents the greatest diagnostic difficulty, since the two forms require different therapeutic tools even though they have clinical analogies. In our center we are developing a nosological method to differentiate tension-type headaches from chronicized migraines on the basis of a criterion that is theoretically sound because it draws on the anatomofunctional features of these IH, and practical because it is easy to apply. This method is founded on solid algological knowledge. In fact, the IH are simply the most common manifestations of the spontaneous activation of the sensory/pain transmitting afferences, decodified at the level of the integrative areas as "useless" painful and nonpainful sensations of either a visceral or a somatic type, according to the type of IH. The adjective "idiopathic," attributed to the IH, refers to the uselessness of the sensations which dominate these syndromes. They are useless because they are not induced by harmful, environmental, or endogenous stimuli, and do not culminate in a passive or active defensive reaction.(ABSTRACT TRUNCATED AT 250 WORDS)

Convergent vasopressinergic and hippocampal input onto somatospiny neurons of the rat lateral septal area

Electron microscopic immunocytochemistry was combined with acute anterograde axon degeneration, following transection of the fimbria-fornix, to describe the innervation of somatospiny neurons by vasopressin-immunoreactive and degenerated hippocamposeptal axon terminals in the rat lateral septal area. Vasopressin-immunopositive boutons characterized by symmetric synaptic membrane specializations, and the degenerated hippocamposeptal axon terminals which form asymmetric synaptic contacts, frequently terminate on the same dendritic and somatic profiles, and particularly on the somata of somatospiny neurons. Although hippocamposeptal fibers predominantly form axospinous synapses in the lateral septal area, they terminate mainly on the dendritic shafts and soma of the vasopressin-receptive neurons. Of 720 vasopressin-immunoreactive terminals in the mediolateral part of the lateral septal area, 80% form synaptic contacts with dendritic shafts: 50% on small (distal) dendritic profiles and 30% on large (proximal) dendrites. Synaptic contacts between vasopressin-immunoreactive terminals and dendritic spines were not observed. The remaining 20% of immunoreactive boutons formed axosomatic synaptic contacts with a total of 58 neurons; 31% of these neurons exhibited somatic spines in the plane of the section analysed. Previous studies have demonstrated that in the lateral septal area vasopressin modulates the action of the excitatory amino acid-containing hippocamposeptal fibers, and also plays a role in the maintenance of long term potentiation evoked by fimbria-fornix stimulation. The convergent vasopressinergic and hippocampal input onto the same somatospiny neurons of the lateral septal area suggests that these neurons are targets of these physiological actions.

Visceral and Somatic Profiles of Needless Pain and Nonpainful Sensations in Idiopathic Headache

Visceral and Somatic Profiles of Needless Pain and Nonpainful Sensations in Idiopathic Headache

Adrenergic fibers in the spinal cord of the monkey: light and electron microscopic study

The adrenergic innervation of the monkey ( Macaca fascicularis) thoracic spinal cord was examined by means of peroxidase-antiperoxidase immunohistochemical method using antisera directed phenylethanolamine N-methyl transferase (PNMT). At light microscopic level the PNMT-positive profiles are seen as brown granules, presumably axon terminals, or varicose fibers. They are localized in the intermediolateral nucleus, central gray and the intermediate gray which connects the two. Occasional fibers are seen in ventral and dorsal horns. The descending adrenergic fiber tract is found in the lateral margin of the lateral funiculus. At electron microscopic level, the PNMT-positive presynaptic profiles exhibit densely packed small clear vesicles, a few large dense core vesicles and numerous mitochondria. They make synaptic contact with dendritic profiles (97%) and somatic profiles (3%) and demonstrate either symmetric or asymmetric synaptic specialization. The descending adrenergic fiber tract consists mainly of unmyelinated fibers and is located in the ventral half of the lateral funiculus.

Ultrastructural localization of neuropeptide Y and galanin immunoreactivity in the paraventricular nucleus of the hypothalamus in the rat

Preembedding immunoperoxidase staining methods were used to allow ultrastructural localization of neuropeptide Y (NPY) and galanin immunoreactivity (IR) in the paraventricular nucleus (PVH) of the rat hypothalamus. NPY-IR was localized exclusively in axons and axon terminals which could be grouped into three types: (1) symmetric axo-somatic contacts predominantly with parvocellular neurons, many of which displayed neurosecretory specializations, (2) predominantly asymmetric contacts onto larger dendritic processes, including some of magnocellular neurosecretory neurons, and (3) predominantly symmetric contacts with small dendritic and spine-like profiles. Galanin-IR terminals displayed a more limited distribution and formed both symmetric and asymmetric contacts with parvocellular neurons, and primarily asymmetric contacts with larger dendritic shafts. Numerous dendritic and somatic profiles, including those of some magnocellular neurosecretory neurons, were lightly stained for galanin IR. These results establish that NPY and galanin IR afferents form a variety of conventional synaptic contacts in the PVH. The two peptidergic terminal types differed with respect to the frequency of their interaction with various postsynaptic targets and/or their distribution upon them. Both peptidergic inputs arise at least in part from brainstem catecholaminergic neurons, and the relationship of the present results to the fine structure of catecholaminergic terminals is discussed.

Morphology and distribution of serotoninergic and oculomotor internuclear neurons in the cat midbrain.

Serotoninergic fibers have been reported in both the abducens and facial nuclei of the cat. Furthermore, serotoninergic dorsal raphe and oculomotor internuclear neurons occupy similar locations in the periaqueductal gray overlying the oculomotor and trochlear motor nuclei. To resolve the issue of whether these two populations of neurons overlap, serotoninergic fibers were assayed in the abducens and facial nucleus; then the morphologies and distributions of identified serotoninergic neurons and oculomotor internuclear neurons were determined. Both the abducens and facial nuclei contained varicosities labelled with antibody to serotonin, but a much higher density of immunoreactive fibers was present in the latter, especially in its medial aspect. Distinct synaptic profiles labelled with antibodies to serotonin were observed in both nuclei. In both cases, terminal profiles contained numerous small, predominantly spheroidal, synaptic vesicles as well as a few, large, dense-core vesicles. These profiles made synaptic contacts onto dendritic and, in the facial nucleus, somatic profiles that occasionally displayed asymmetric, postsynaptic, membrane densifications. Following injection of horseradish peroxidase into either the abducens or facial nuclei, double-label immunohistochemical techniques demonstrated that the serotoninergic and oculomotor internuclear neurons form two distinct cell populations. The immunoreactive serotoninergic cells were distributed within the dorsal raphe nucleus, predominantly caudal to the retrogradely labelled oculomotor internuclear neurons. The latter were located in the oculomotor nucleus along its dorsal border and in the adjacent supraoculomotor area. Intracellular injection of horseradish peroxidase revealed that oculomotor internuclear neurons have multipolar somata with up to ten long, tapering dendrites that bifurcate approximately five times. Their dendritic fields were generally contained within the nucleus and adjacent supraoculomotor area. In contrast, putative serotoninergic neurons were often spindle-shaped and exhibited far fewer primary dendrites. Many of these long, narrow, sparsely branched dendrites crossed the midline and extended to the surface of the cerebral aqueduct. In the vicinity of the aqueduct they branched repeatedly to form a dendritic thicket. The axons of the intracellularly stained serotoninergic neurons emerged either from the somata or the end of a process with dendritic morphology, and in some cases they produced axon collaterals within the periaqueductal gray. Thus the oculomotor internuclear and serotoninergic populations differ in both distribution and morphology.(ABSTRACT TRUNCATED AT 400 WORDS)

Laminar distribution of GABA-immunoreactive neurons and processes in area 18 of the cat

Intracortical inhibition mediated by the neurotransmitter gamma-amino butyric acid (GABA) plays a crucial role in the formation of the physiological response properties of neurons in mammalian visual cortex. Using a potent antibody developed against the amino acid neurotransmitter, GABA (Immunoclear Co., USA), we have identified GABA-immunoreactive neuronal somata and processes in area 18 of the cat. The GABA-positive neurons included multipolar, bipolar and bitufted but not pyramidal cell types. The density of GABA-immunoreactive neurons was higher in Layers I–IV (range 182–205 cells/mm 2) than in Layers V–VI (range 78–92 cells/mm 2). The mean areal measurement of GABA-immunoreactive somatic profiles was 135 μm 2 ( s. d. = 66). We observed numerous GABA-immunoreactive fiber fragments predominantly in Layers I, III, IV and V. Most of the fibers were oriented with their long axis tangential to the cortical surface, but, vertically-oriented fibers were observed as well. Many of the fibers were axonal-like and appeared beaded in Layer I and occasionally in II, while most of the fibers in the other layers appeared myelinated. A dense GABA-immunoreactive neuropil was present in Layer V. Results from our studies provide immunohistochemical evidence for a system of GABA-immunoreactive neurons and axonal collaterals which presumably mediate inhibition in the visual cortex. Since many of the GABA-immunoreactive fibers were oriented tangential to the cortical surface, the structural elements required for inhibition between functional columns are present. GABA-mediated inhibition both within and between functional columns likely assists in the formation of receptive field properties in the visual cortex.

Sprouting of GABAergic synapses in the red nucleus after lesions of the nucleus interpositus in the cat

An immunocytochemical study using anti-GAD serum was performed to examine the plastic changes of GABAergic inhibitory synapses in the red nucleus (RN) after lesions of the nucleus interpositus (IP) of the cat. Light-microscopic analyses revealed that 20-175 d after the unilateral lesion of the IP, somatic profiles of large neurons in the magnocellular RN contralateral to the lesion were more densely covered with GAD-immunoreactive puncta than those in the ipsilateral RN. Electron-microscopic analyses demonstrated that the GAD-immunoreactive puncta observed with the light microscope were synaptic terminals and that the number of GAD-immunoreactive synaptic terminals per unit length of somatic membrane of RN neurons was increased on the deafferented side. The GAD-immunoreactive terminals on somata of RN neurons made symmetric synaptic contacts with somatic membranes on both the deafferented and control sides. The number of immunoreactive synapses on somata of RN neurons was markedly increased on the deafferented side following IP lesion, whereas that of the unlabeled asymmetric synapses was decreased. These observations indicate that new GABAergic synapses were formed on somata of RN neurons after deafferentation from the IP.

A quantitative study of synaptic reorganization in red nucleus neurons after lesion of the nucleus interpositus of the cat: an electron microscopic study involving intracellular injection of horseradish peroxidase

A quantitative electron microscopic analysis of the corticorubral projection was performed in the red nucleus (RN) of adult cats to determine morphological correlates of synaptic reorganization that occur following a lesion of the interpositus nucleus (IP). Corticorubral synaptic endings were identified by lesioning the sensorimotor cortex 2–6 days before electrophysiological experiments. Horseradish peroxidase (HRP) was injected into electrophysiologically identified RN neurons. Sagittal sections 100 μm thick were cut and reacted by diaminobenzidine. Sections containing HRP-positive neurons were selected and embedded in Epon. In normal cats, degenerating corticorubral terminals in the RN region frequently made contact with dendritic profiles, having small cross-sections, while a few made contact with somatic profiles. Similar results were obtained when degenerating terminals making contact with HRP-filled dendrites were analyzed. In the experimental animals, the cortical lesion was performed more than 8 weeks after lesion of the IP. In these animals, degenerating corticorubral terminals were frequently found on proximal dendrites and somata in RN region and HRP-positive neurons in contrast to the findings in normal cats. The results indicate that new corticorubral synapses were formed on proximal dendrites and somata of RN neurons as a consequence of IP lesions.

A quantitative electron microscope study of cerebellar axon terminals on the magnocellular red nucleus neurons in the cat

In the red nucleus (RN) of the cat, the bouton covering ratio (BCR: the ratio of whole somatic surface length and that covered with axon terminals) and the density of axon terminals in contact with somatic profiles (DAST: the number of axosomatic terminals per 100 μm of somatic surface membrane) were calculated in each neuronal somatic profile over 60 μm in diameter. The mean BCR was61.4±1.43 (S.E.M.) %. The mean DAST of axosomatic terminals filled with spherical synaptic vesicles (S-terminals) was27.7±0.95, and that of terminals with plemorphic and/or flattened vesicles (F-terminals) was 10.3±1.12. Subsequently, sequential changes of the BCR and DAST of intact terminals were examined in the RN deafferented from the cerebellorubral fibers. The mean BCR and DAST were decreased most markedly during the survival period of 4–7 days; thus decrease was chiefly due to degeneration of S-terminals (BCR:16.7±1.17%, DAST of S-terminals: 7.1±1.12, DAST of F-terminals: 5.8±1.22). In the RN 11–63 days after the operation, both the BCR and DAST tended to re-increase slightly and the majority of the re-increased terminals appeared to be F-terminals. Possible meanings of this re-increase of axosomatic terminals are discussed.

Somatic Profiles in Chronic Schizophrenia

Somatic Profiles in Chronic Schizophrenia

An electron microscope study of synaptic organization in the lateral reticular nucleus of the medulla oblongata in the cat

Synaptic organization in the lateral reticular nucleus (LRN) was investigated electron microscopically in the cat. The number of synaptic knobs encountered in a survey of 69 somatic profiles cut through the nucleolar plane varied from 0 to 20 per profile. In 5564 μm of cell perimeters analyzed the number of synaptic knobs per 100 μm was 5.2, ranging from 0 to 22 in each somatic profile. About 46% of the axosomatic synaptic knobs were filled with round vesicles, and 54% with pleomorphic ones. Out of 1424 axodendritic synaptic knobs, about 63% were filled with round vesicles, and 37% with pleomorphic ones. After placing lesions in the spinal cord, frontal cortices or red nuclear areas, electron-dense degenerated synaptic knobs were observed in the LRN. In the cats with spinal lesions degenerated knobs with the active zones of the synapses were found both on somatic and dendritic profiles. On the other hand, in the cats with cortical or rubral lesions degenerated knobs with the active zones were encountered only upon dendritic profiles. These degenerated knobs found in the present study never exceeded more than 3% of the total synaptic population in the areas examined. Thus, the axon terminals of fibers arising from the spinal cord, frontal cortices and red nuclear areas constituted only a small fraction of the total axonal endings in the LRN.