Synaptic dimorphism in Onychophoran cephalic ganglia

The taxonomic location of the Onychophora has been controversial because of their phenotypic and genotypic characteristics, related to both annelids and arthropods. We analyzed the ultrastructure of the neurons and their synapses in the cephalic ganglion of a poorly known invertebrate, the velvet worm Peripatus sedgwicki, from the mountainous region of El Valle, Mérida, Venezuela. Cephalic ganglia were dissected, fixed and processed for transmission electron microscopy. The animal has a high degree of neurobiological development, as evidenced by the presence of asymmetric (excitatory) and symmetric (inhibitory) synapses, as well as the existence of glial cell processes in a wide neuropile zone. The postsynaptic terminals were seen to contain subsynaptic cisterns formed by membranes of smooth endoplasmic reticulum beneath the postsynaptic density, whereas the presynaptic terminal showed numerous electron transparent synaptic vesicles. From the neurophylogenetic perspectives, the ultrastructural characteristics of the central nervous tissue of the Onychophora show important evolutionary acquirements, such as the presence of both excitatory and inhibitory synapses, indicating functional synaptic transmission, and the appearance of mature glial cells.

Synaptic dimorphism in Onychophoran cephalic ganglia.

The taxonomic location of the Onychophora has been controversial because of their phenotypic and genotypic characteristics, related to both annelids and arthropods. We analyzed the ultrastructure of the neurons and their synapses in the cephalic ganglion of a poorly known invertebrate, the velvet worm Peripatus sedgwicki, from the mountainous region of El Valle, Mérida, Venezuela. Cephalic ganglia were dissected, fixed and processed for transmission electron microscopy. The animal has a high degree of neurobiological development, as evidenced by the presence of asymmetric (excitatory) and symmetric (inhibitory) synapses, as well as the existence of glial cell processes in a wide neuropile zone. The postsynaptic terminals were seen to contain subsynaptic cisterns formed by membranes of smooth endoplasmic reticulum beneath the postsynaptic density, whereas the presynaptic terminal showed numerous electron transparent synaptic vesicles. From the neurophylogenetic perspectives, the ultrastructural characteristics of the central nervous tissue of the Onychophora show important evolutionary acquirements, such as the presence of both excitatory and inhibitory synapses, indicating functional synaptic transmission, and the appearance of mature glial cells.

Levels of amino acid neurotransmitters during mouse olfactory bulb neurogenesis and in histotypic olfactory bulb cultures.

The developmental changes in the levels of amino acid neurotransmitters were analyzed by high pressure liquid chromatography during mouse olfactory bulb neurogenesis, from embryonic day (E)13 until the young adult age, between postnatal days (P)30 and P40. During the embryonic period, high levels of glutamate, aspartate and GABA were observed, with the values of GABA about 2-fold higher than those of glutamate and aspartate. At P0, the production of these neurotransmitters experienced birth stress as shown by a significant 2-fold reduction in their levels. During the first two postnatal weeks, a progressive increase in the glutamate content was detected diminishing slightly in the adult stage. The aspartate concentrations showed a maximal value at P3 and then decreased gradually until the second postnatal week; in the young adult age, its concentration was comparable with that of glutamate. The postnatal GABA contents increased progressively from birth to maturity, showing maximal levels at P3, P11 and in the adult. Throughout the studied developmental period, the concentration of glycine remained relatively low. With regard to taurine, very low concentrations were detected during the prenatal period but after birth, the taurine content gradually increased with age, and in the adult animal, its concentration was comparable with those of GABA and glutamate. Our data demonstrate the predominance of GABA and glutamate during olfactory bulb synaptogenesis, however, in the adult animal, both glutamate and aspartate exert the same influence in the excitatory synaptic transmission; in the adult inhibitory synaptic transmission, taurine appears to play an important neuromodulatory or neurotransmitter role as that of GABA. To determine the intrinsic neurotransmitter production, primary histotypic olfactory bulb cultures were prepared from mice at P10. The comparative analysis of in vitro neurotransmitter contents with those in in situ adult animal showed higher levels of endogenously produced glutamate, glycine and GABA in the olfactory bulb than the extrinsic ones coming from olfactory nerve axons and higher olfactory brain centers. On the other hand, most of aspartate and taurine neurotransmitters apparently come from extrinsically located neurons.

Levels of amino acid neurotransmitters during mouse cerebellar neurogenesis and in histotypic cerebellar cultures.

The variation in the levels of excitatory (glutamate and aspartate) and inhibitory (GABA, glycine and taurine) neurotransmitters during neurogenesis in mouse cerebellum, from embryonic day (E) 15 until the young adult stage, was analyzed by high-pressure liquid chromatography. Between E15 and E21, high contents of GABA, glutamate and aspartate were detected, with the GABA levels approximately 2- to 3-fold higher than those of glutamate and aspartate. After birth, the levels of GABA remained high during the first 2 postnatal weeks and then reached a plateau comparable to adult values by the third week. The levels of glutamate and aspartate increased gradually from birth to the young adult stage, showing peak values at postnatal days (P) 3 and P11. Glycine and taurine were present at relatively low concentrations during the prenatal period, then rose significantly by about 4-fold after birth; their levels decreased by the end of the first postnatal week but increased gradually thereafter until reaching adult values by the third week. To determine the endogenous neurotransmitter production in the cerebellar cortex, primary histotypic cerebellar cultures prepared at P10 were analyzed and the in vitro transmitter contents were compared with the adult in situ values. The cultures showed about the same levels of glutamate and aspartate; however, their concentrations were lower by half than in vivo, suggesting that both play an equally important role in the excitatory neurotransmission of the cerebellar cortex internal circuitry pathways and that in mature cerebellum, about 50% of the excitatory synaptic inputs derive from the afferent climbing and mossy fibers. The in vitro GABA and glycine contents were comparable with the in vivo levels, whereas the taurine concentrations were about 5-fold lower in vitro than in vivo. These findings indicate that most of the GABA and glycine transmitters are produced intrinsically while a high proportion of taurine in the cerebellum comes from extracerebellar afferents. This study provides data on the changing levels of the amino acid neurotransmitters in developing mouse cerebellum and the relative proportions of neurotransmitter contents that are produced by intrinsic neurons in contrast to those derived from extrinsic afferent fibers.

Levels of monoamine and amino acid neurotransmitters in the developing male mouse hypothalamus and in histotypic hypothalamic cultures.

The variation in the levels of the monoamine and amino acid neurotransmitters was studied during the period of neurogenesis in male mouse hypothalamus, from embryonic day 15 until the age of young adult. The results shown in this study demonstrate that the monoamines appear early in the fetal brain and that the maximum expression of the catecholaminergic system, particularly that of dopamine, occurs during the late neonatal period or mouse infancy, when the role played by the catecholamines on the maturation of the neurosecretory systems is more significant. In relation to the amino acid neurotransmitters, glutamate and taurine seem to be the principal transmitters of the hypothalamus since their concentrations were about five-tenfold higher than the levels of glycine and GABA. Both amino acids had the same pattern of variation during development, showing elevated values during the prenatal, late neonatal and early pubertal period. Increased concentrations of the inhibitory neurotransmitter GABA were observed on the day before birth, at the end of the neonatal period and throughout the prepubertal period, suggesting that the influence of GABA on hypothalamic neurogenesis increases by the time when the hypothalamic nuclei have reached maturity and the local circuits have been established. To determine the intrinsic neurotransmitter production, primary hypothalamic histotypic cultures prepared from mice at postnatal days 8-10 were analyzed for their content of neurotransmitters. The in vitro analysis revealed that the hypothalamic neurons intrinsically produce dopamine, glutamate, taurine and glycine in homologable amounts with those of young adult animals. The comparative analysis also showed that about 50% of the GABA content and less than 5% of the hypothalamic epinephrine level are locally produced, while serotonin comes mainly from extrinsically located neurons.

The prevalence of antibiotic-resistant faecal Escherichia coli in healthy volunteers in Venezuela.

Faecal samples were collected from healthy volunteers in two regions in Venezuela, the village of Grulla (n = 195) and the city of Mérida (n = 181), and analysed for the prevalence of antibiotic resistant faecal Escherichia coli as well as the antibiotic susceptibility of the strains isolated. The highest prevalences of resistance were observed for amoxicillin, oxytetracycline, sulfamethoxazole and trimethoprim. The percentages found for Grulla were 46, 38, 44 and 30%, respectively; for Mérida 39, 65, 56 and 36%, respectively. In Mérida, a significantly higher prevalence of resistance for oxytetracycline was found (P < 0.05). Significant differences in the distribution of the MIC values between Grulla and Mérida were observed for amoxicillin, chloramphenicol and oxytetracycline (P < 0.05). In Grulla, the most frequent pattern was resistance to amoxicillin only and in Mérida to oxytetracycline only. Amoxicillin resistance was due to production of TEM1 beta-lactamase.

Hypothalamic synaptogenesis and its relationship with the maturation of hormonal secretion.

1. Information obtained during the last decade has demonstrated that hypothalamic neurons release a wide variety of neuroactive substances, such as neurotransmitters, mostly monoamines and amino acids, and neuromodulators such as the peptides vasopressin (AVP) and oxytocin (OXT) and hypophysial releasing hormones. 2. Synapse formation between hypothalamic neurons was followed at different times within a given nucleus and among different nuclei during development of the mouse hypothalamus. 3. The amounts of various neurotransmitters and hormones were determined at various stages of development. 4. A correlation is presented of the biochemical and ultrastructural features and their functional implications during maturation.

[Protein-energy malnutrition and hypobaric stress effects on ultrastructure of the heart muscle in rats]. / Efecto de la desnutrición calórico-proteica y del estrés hipóxico sobre la ultraestructura del músculo cardíaco de rata.

A model that simulated nutritional and hypoxic stress is discussed. Wistar male adult rats were used in four groups: A1, A2, B1 and B2. A1 and A2 groups were fed with a diet whose composition was: 16% protein, 43% carbohydrate, and 6% lipids. Group B1 and B2 received the same type of diet but was restricted to 70% the amount consumed by groups A1 and A2. All groups were fed for 15 days. After these 15 days, the half of both groups were introduced into an hypobaric chamber simulating an altitude of 3,500 m for two hours. Pieces of the rats hearts were used for biochemical and ultrastructural studies. In group B a dear decrease in the body and the heart weight was observed. Also a decrement of the heart proteins concentration was noticed. On the contrary the mitochondrial proteins increased. These biochemical changes correlate with the ultrastructural changes observed in the same group in which a decrease of the myofibrilles and abnormal configurations of the mitochondria were found. The undemourishment and the hypobaric stress produced an evident alteration in the ultrastructure of the heart.

[Ultrastructural analysis of anastomosis group 9 of Rhizoctonia solani]. / Análisis ultraestructural del AG-9 de Rhizoctonia solani.

The ultrastructure of R. solani AG-9 (S-21, ATCC 62804) was investigated with transmission electron microscopy (TEM). The most important characteristics were those related with cell wall thickness, cytoplasmic matrix composition, number of nuclei and nucleoli and secretory material production. The majority of examined hyphae showed lateral cell walls thinner than those recorded before. The cytoplasmic matrix consistently appeared differentiated into two classes, one formed by a highly electron dense granular fine material and the other one showing a coloidal substance of very low density which give these cells a 'tiger-like' aspect. The grannular dense matrix always had abundant free ribosomes and usually surrounded the cytoplasmic organelles and the septal pore apparatus. The somatic cells showed up to 5 nuclei, some of which with three nucleoli. Masses of secretory material surrounded by membrane were regularly seen in the cytoplasm, with sizes similar to those of nuclei.

Existence of a putative specific postsynaptic density protein produced during Purkinje cell spine maturation.

This study identified a 140 kDa polypeptide as a putative specific component of Purkinje cell spines' postsynaptic densities and which began to appear during the critical period of cerebellar cortex synaptogenesis. Mouse cerebellar cortices at postnatal days 5, 7, 9, 11, 15 and young adult, between days 30 and 40, were used to purify subcellular fractions of synaptosomes, synaptic membranes and postsynaptic densities. The purity of the subcellular fractions was assessed by electron microscopy and the protein composition of the different fractions was characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Polypeptides of apparent molecular weights of 25, 26, 27, 30, 33, 37, 43, 45, 52, 64, 74, 85, 94, 110, 125, 130, 165 and 174 kDa were found in the synaptosomal fractions of all the ages studied, even before the critical period of synaptogenesis, at postnatal day 7, when the postsynaptic densities were still nonexistent, indicating that the polypeptides are nonspecific constituents of these structures. On the other hand, a 140 kDa polypeptide was detected in the postsynaptic density fractions at postnatal day 11, immediately after postsynaptic structures began to appear, suggesting the possibility that this protein is a specific component of the cerebellar cortex postsynaptic densities. The 140 kDa polypeptide was electroeluted from the gel and analysed for its amino acid composition by reverse-phase high-pressure liquid chromatography. The analysis showed that this protein has a high content of nonpolar amino acid residues, such as leucine, isoleucine, glycine, phenylalanine and valine. A hypothetical model relative to the participation of the 140 kDa protein in the molecular organization of the postsynaptic density is suggested which may contribute to the understanding of the role played by this structure in synaptic function.

Development of the neurogliohemal complex in the mouse neurohypophysis.

The mouse neurohypophysis was studied at different ages of development in order to analyse the ultrastructural changes that lead to the maturation of the neurogliohemal complex and to determine the existence of permeability between the blood capillaries and the neurohypophysial channels. In all the studies ages, two groups of 5 animals each were intravenously injected with different tracer solutions: to one group, 10 microliters of cationized ferritin were used and to the other, 10 microliters of ferrous fumarate were applied. For the ultrastructural studies the tissue samples were processed using the conventional techniques for electron microscopy. At day 17 of prenatal age, some hypothalamic axons (10 axonic profiles/20 microns2) were already seen within the neurohypophysis, increasing threefold (26 to 30 axonic profiles/20 microns2) at prenatal day 19. In these axons terminals, the first neurosecretory vesicles began to appear. At this early age, the glial cells formed few prolongations. Between postnatal days 1 and 9, numerous axon terminals containing dense neurosecretory vesicles composed the neuropile areas. After day 9, there was a broadening of the intercellular space, which we have termed as neurohypophysial channels; these were actually expansions of the existing extracellular space in the neurohypophysis. Between days 9 and 21, the population of axon terminals showing a higher density of neurosecretory vesicles continued to increase in number. Some of these axon terminals were separated by irregular neurohypophysial channels. The glial cells showed scarce cytoplasm and formed numerous lamellar prolongations, which became increasingly finer surrounding bundles of individual axons.(ABSTRACT TRUNCATED AT 250 WORDS)

Intradermal implants of histotypic adrenal gland rotary cultures.

The implantation of histotypic adrenal gland cultures is described in the present study. The cultures were prepared from mice at birth and were rotary incubated for 10 days. When the cells reached phenotypic maturation, they were implanted in the dermal bed of the auricular pavilion of young adult mice. This location was ideal for implantation because transillumination enabled daily inspection of the progress of implant survival. Twenty days after implantation, the implants and associated tissues were removed to study the degree of maturation and the viability of the implants. Some cultures showed a moderate percentage of steroidal cells, while others demonstrated a high predominance of the chromaffin cells. All the implanted cultures successfully survived a postoperative period of 20 days. Both adrenergic and noradrenergic cells reached their maximum grade of cytological differentiation and neither inflammatory reactions nor adverse immunological effects were observed. On the contrary, the implants were profusely vascularized by the host tissue, particularly in those implants with a higher content of chromaffin cells.

Ultrastructure of the heart muscle in rats under hypobaric stress and under high NaCl intake.

Cellular metabolic alterations in the heart have been widely investigated under a variety of experimental conditions in which the oxygen supply was diminished. However, there is relatively scarce information about the effect of the reduced food intake and saline loading on the ultrastructural changes occurring in myocardial cells exposed to hypobaric stress during short periods of time. The purpose of the present study was to analyze the effects of hypobaric stress, NaCl intake and undernourishment on the body and heart weights and the ultrastructural changes produced in the rat myocardial cells under these conditions. The body and heart weights in all the experimental groups were determined as well as the total and mitochondrial protein concentrations. A significant decrease in body and cardiac weights was observed in both groups of undernourished animals submitted to hypobaric stress or not. On the other hand, a slight increase in the mitochondrial protein concentration was obtained in the same groups. Cardiac muscle samples were processed for light- and electron-microscopic observations. Few ultrastructural alterations were seen in the experimental groups fed with a standard diet; however, an increase in the mitochondrial size was shown in the rats that received 0.9 and 1.3% NaCl solutions. In the groups of animals with one third of the normal protein-calorie intake, more intense changes were noted; disappearance of the contractile structures, with almost complete extinction of the Z bands, was commonly observed in the rats submitted to hypobaric stress. The ultrastructural alterations seen in the undernourished animals were even more evident, showing generalized damage to the intracellular components.

Cerebral implants of histotypic hypothalamic cultures.

In the present report, the implantation of hypothalamic histotypic cultures within the cerebral hemisphere is described. The cultures were prepared from 10-day-old mice and rotary incubated during 6 or 10 days. When the cells reached their phenotypic characteristics at the end of the incubation period, the cultures were implanted in the posterior area of the lateral ventricle. 30 days postoperatively, the whole implanted area was removed and processed for light and electron microscopy observations. The implanted cultures completed maturation in the host tissue and no rejection signs were noticed; on the contrary, we were able to observe a favorable reaction from the host tissue, such as the formation of secondary blood vessels which penetrated the mass of the implanted culture. Well-developed magno- and parvocellular neurons were seen to contain neurosecretory vesicles in their terminals, and the neuroglial relationships established within these implants were homologable to those normally found.

[A leiomyosarcoma of vascular origin. A case report]. / Leiomiosarcoma de origen vascular. Informe de un caso.

Leiomyosarcomas arising from the wall of the blood vessels, are highly malignant tumours. Although 75% of the cases have been reported in the inferior vena cava, nevertheless scanty mention is made in the literature of an analogous tumor originating from smaller blood vessels. This paper deals with a 53-year-old man with a tumor in the right axilla. Surgery consisted in wide local excision. Histopathology revealed a mesenchymal tumor in an axillary blood vessel. Electron microscopy revealed tumor cell with all the characteristics of a leiomyosarcoma. The patient refused adjuvant therapy and died 10 months later with local recurrence and lung metastases.

Release of neurotransmitters and neurosecretory substances during in vitro maturation of mouse hypothalamic cultures.

The maturation of the neurosecretory activity of a hypothalamic nerve cell population grown in vitro, prepared from 10-day-old mice and cultured for 6 days, has been demonstrated in the present report. A low-molecular weight polypeptide of 30-kD was found to be released into the culture media during the 6-day period of incubation, as analyzed by SDS-polyacrylamide gel electrophoresis. Comparative electrophoresis of the in situ hypothalamic, neurohypophysis and cerebral cortex homogenates revealed the presence of a 30-kD protein component in both the hypothalamus and neurohypophysis but not in the cerebral cortex. The release of the 30-kD polypeptide into the incubation media indicates an expression of the neurosecretory activity of the peptidergic neurons of the hypothalamus during in vitro maturation. On the other hand, high pressure liquid chromatography with electrochemical detection showed appreciable quantities of released dopamine (DA), epinephrine and serotonin (5-HT) in the incubation media in which the neurons were allowed to differentiate. There was a steady release of DA during the 6-day incubation period, varying from 0.21 +/- 0.02 to 0.49 +/- 0.05 ng/mg protein. The epinephrine level increased progressively from day 1 to 6 of culture, from 3.73 +/- 0.57 to 12.08 +/- 1.81 ng/mg protein, respectively. The measured 5-HT level was 0.07 +/- 0.001 on day 2 and increased to 0.38 +/- 0.05 ng/mg protein on day 6 of culture. These data demonstrate the functional maturation of catecholaminergic, serotoninergic and peptidergic neurons in these rotary histotypic cultures of the mouse hypothalamus.

In vitro hypothalamic neurogenesis: morphological maturation of mouse hypothalamic cultures and in vitro versus in situ biochemical analysis.

The morphological and biochemical changes that occur during in vitro neurogenesis of the mouse hypothalamus were studied in rotary cultures prepared from mice between 4 and 16 days of postnatal age. After 6 days of in vitro growth, histotypic cultures with a high degree of morphological differentiation were obtained in cultures prepared from 8- to 10-day-old mice. Before day 8, the cultures showed immature neurons, while after day 12 most of them exhibited an undesired number of degenerated cells. Light-microscopic, Golgi and ultrastructural studies clearly showed the stages of development of the neurosecretory cells in culture. The particular organization of the hypothalamic cells in these cultures can be homologized to its equivalent region in vivo, as demonstrated by their morphological similarities as well as by the fact that the majority of the neurons orient their axons toward the external part of the culture in order to release the neurosecretory material outside the in vitro grown neuronal population, as is the case in situ since hypothalamic neurons release their neurosecretory products at the vascular system. Biochemical parameters such as DNA, RNA and protein contents were determined during the period of in situ development used for the preparation of histotypic cultures and compared to the biochemical changes that occurred during in vitro maturation. The changes in the in vitro DNA and protein contents showed the same variation pattern as in situ. The DNA/protein and RNA/protein ratios also had comparable characteristics, having peak values at days 10 and 16 in situ and in the histotypic cultures prepared from 10-day-old mice. These studies have demonstrated the correlation between the in vitro biochemical and morphological development and the significance of the critical period during hypothalamic neurogenesis for successful organotypic preparations.

Ultrastructural characteristics of different stages of human chagasic myocarditis.

Myocardial damage was analyzed in the different stages of Chagas' disease. Myocardial biopsies from chagasic patients, whose clinical histories were initially unknown to the examiner, were examined and evaluated by electron microscopy using a table in which 244 characteristics were considered. When the ultrastructural results were associated with their respective clinical reports, it was found that Chagas' disease stages showed significant myocardium damage between stages IA and II: IA (normal EKG and cineventriculogram), 13.0%; IB (early left ventricular damage with normal EKG), 14.5%; II (advanced left ventricular damage, abnormal EKG), 25.5%; stage III (congestive heart failure) showed a decrement to 22.5% if compared with stage II. The acute stage of the illness was characterized by the presence of the parasites within the myocytes which were surrounded by inflammatory cell infiltrate. During Chagas' disease evolution the most affected organelle was the sarcoplasmic reticulum.

Ultrastructural reversible changes in fish neuromuscular junctions after chronic exercise.

Neuromuscular junctions (NJs) of fin muscles of teleostean fishes, Lebistes reticulatus, were ultrastructurally analyzed during 60 min of chronic exercise and a subsequent period of 90 min of induced recovery. NJs from 30-min-exercised fishes showed an almost complete depletion of synaptic vesicles (SVs), corresponding to 83% of SV consumption; 76% of axon terminals were branched at the end of this period. During the recovery period, it was possible to observe the reversibility of the changes induced by the exercise and the transitory events that lead to the reacquirement of the normal NJ morphology. After 15 min of rest, SV population increased to a value of 54.6 SVs/micron2 and the percentage of branched axons was 66.5%. At 60 min of recovery the number of SVs reached a value of 84.6 SVs/micron2. The SV population was fully reestablished at 80 min of rest, while the percentage of branched axons was found within normal ranges after 90 min of recovery. These results demonstrate that chronic exercise induced physiological depletion of NJ SVs and other axon terminal morphological changes, as well as that postexercise rest induces the reestablishment of the normal NJ morphology.

Dendritic RNA and postsynaptic density formation in chick cerebellar synaptogenesis.

In order to investigate the ribosomal origin of the postsynaptic densities during chick cerebellar maturation, a new procedure for synaptosomal preparation was implemented. Samples from embryonic chick cerebellar cortex, from 14 to 20 days of development and young adult chicks, were initially mechanically dissociated after treatment with 1.25% trypsin for 10 min; with this procedure we were able to obtain a dendritic suspension from which an enriched synaptosomal fraction was prepared in a discontinuous Ficoll sucrose gradient. RNA and protein values determined from the synaptosomal fractions showed the following variations: from 46.3 ng RNA/mg of wet weight at day 14 to 616.7 ng RNA/mg of wet weight at day 18; in young adult chicks, the average was 242 ng RNA/mg of wet weight. RNA/protein ratio varied from 78.9 micrograms RNA/mg protein at day 16 to 329.8 micrograms RNA/mg protein at day 18; in the young adult chick, this ratio decreased to 68.4 micrograms RNA/mg protein. The highest value of RNA was obtained at day 18 of chick embryo development coinciding with the maximum period of synaptic formation and consequently of the PSDs. These results seem to reinforce the hypothesis of the ribosomal origin of the PSDs.