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The main findings of this study are that we determined that there are Trypanosoma cruzi strains adapted to transplacental transmission and completely different from the commonly used laboratory reference strains. This implies a specific strategy for the vertical transmission of Chagas disease.

We examined the cerebellum and cerebrum of 4 vaccinated dogs, 3–60-mo-old, that displayed clinical signs of canine distemper virus (CDV) infection, and died 7–40 d after developing neurologic signs. The main histologic lesions were demyelination, gliosis, meningitis, perivascular lymphocytic cuffing, and inclusion bodies. These lesions were similar in all 4 cases regardless of the time since vaccination, except that meningoencephalitis and gliosis were subacute in 3 dogs and chronic in 1 dog. However, these differences did not appear to be related to their vaccination status. Immunohistologically, a CDV-positive immunoreaction was seen mainly in astrocytes, neurons and their axons, lymphocytes around and in the blood vessels of the pia mater and choroid plexus, ependymal cells of each ventricle, and the cells of the choroid plexus. The histologic and immunohistologic changes were similar in the cerebellum and cerebrum. The genetic characterization of the virus strains in 2 of these naturally occurring canine distemper cases confirmed that they were South American wild-type strains (Kiki and Uy251) belonging to the EU1/SA1 lineage. These strains are not included in the commercial CDV vaccines available in Uruguay.

Toxic honeydew produced by Flatidae Epormenis cestri in Uruguay has been shown to cause among honeybees (Apis mellifera) colonies a massive larva death called “River disease”, but the intrinsic mechanisms are still unknown. Because fat body cells, oenocytes and trophocytes, are known to regulated larvae metabolism, and to be affected by xenobiotics, we tested whether apoptosis of these cells can be an underlying cause of larvae death. Ten colonies were divided into two groups and fed with common honey or toxic honeydew obtained from colonies affected by “River disease”. Five-dayold larvae were collected and processed for histology and immunohistochemistry for caspase-3. The area, diameter, and immunostaining area in oenocytes and trophocytes were measured. The oenocyte and trophocyte cellular area decreased in the treated group (p=0.002; pA. mellifera larvae.

SummaryChagas disease is mainly transmitted by vertical transmission (VT) in non-endemic areas and in endemic areas where vector control programs have been successful. For the present study, we isolated natural strains vertically transmitted through three generations and proceeded to study their molecular mechanism of VT. No parasitemia was detected in immunocompetent mice, but they were able to induce an immune response and colonize different organs. VT experiments revealed that infection with the different strains did not affect mating, pregnancy or resorptions, but despiting low parasitemia, VT strains reached the placenta and resulted in higher vertical transmission rates than strains of either moderate or high virulence. While the virulent strain modulated more than 2500 placental genes, VT strains modulated 150, and none of the modulated genes is shared between them. VT strains downregulate genes associated with cell division and replication and upregulate immunomodulatory genes leading to anti-inflammatory responses and tolerance. The virulent strain stimulates a strong pro-inflammatory immune response, and this molecular footprint correlated with histopathological analyses. We herein describe a unique placental response regarding the passage of T cruzi VT isolates across the maternal-fetal interphase, challenging the current knowledge derived mainly from studies of laboratory-adapted or highly virulent strains.

We examined in the present study main epidemiological features of canine mast cell tumors in Uruguay, principal breeds of occurrence, age, gender, anatomical distributions, and associated differences of pathological grading. During a three-year period, eighty four out of 405 skin specimens of dogs mainly received at the Veterinary Faculty of Montevideo from private clinics were mast cell tumors. Mix-breed dogs were mostly affected, followed by Labrador Retrievers, Boxers, Pit bulls and Golden Retrievers. Age of patients ranged from 3 to 15 years (median 7.9), and the incidence in females was slightly higher than in males. Tumors were more frequent in the trunk, followed by extremities, scrotum and neck. The majority of specimens were of high malignancy.

espanolLa aversion condicionada con Cloruro de Litio (LiCl) ha demostrado ser una herramienta util para modelar la dieta en rumiantes. En este ensayo estudiamos el uso del LiCl para controlar el consumo de olivos en ovinos. Se usaron 22 ovejas, todas fueron sometidas a un periodo de pre-condicionamiento donde se las acostumbro a una rutina de consumo. Luego, se paso al periodo de condicionamiento, donde se usaron hojas frescas de olivos, cuando se logro que todos los animales consumieran la planta se dosifico con LiCl (200 mg/kg PV) a la mitad de animales. Se monitoreo el efecto del LiCl durante 6 dias consecutivos, y luego mensualmente durante 6 meses. El LiCl genero una disminucion significativa en el consumo de hojas de olivos. En el presente trabajo, proponemos que la aversion condicionada inducida por el uso de LiCl es una herramienta util para controlar que los ovinos consuman los olivos. EnglishConditioned aversion with Lithium Chloride (LiCl) has shown to be a useful tool for modeling diet in ruminants. In this paper, we studied the LiCl use to control olive trees consumption by ewes. For this purpose, 22 crossbred ewes were exposed to a preconditioning period where they were trained in a specific consumption routine. Once the conditioning period began, fresh olive leaves were given to eat, half were dosed with LiCl aqueous solution (200 mg/kg BW), while the other half were dosed with water. The effect of LiCl was monitored during 6 consecutive days after administration, and every month for 6 months. The LiCl generated a significant decrease consumption of olive leaves. We propose that the conditioned aversion induced by LiCl is a useful tool to control olive trees consumption.

SARS-CoV2 is a single strand RNA virus member of the type 2 coronavirus family, responsible for causing COVID-19 disease in humans. The objective of this study was to test the ivermectin drug in a murine model of coronavirus infection using a type 2 family RNA coronavirus similar to SARS-CoV2, the mouse hepatitis virus (MHV). BALB/cJ female mice were infected with 6,000 PFU of MHV-A59 (Group Infected; n=20) and immediately treated with one single dose of 500 μg/kg of ivermectin (Group Infected + IVM; n=20), or were not infected and treated with PBS (Control group; n=16). Five days after infection/treatment, mice were euthanized to obtain different tissues to check general health status and infection levels. Overall results demonstrated that viral infection induces the typical MHV disease in infected animals, with livers showing severe hepatocellular necrosis surrounded by a severe lymphoplasmacytic inflammatory infiltration associated with a high hepatic viral load (52,158 AU), while ivermectin administration showed a better health status with lower viral load (23,192 AU; p

SARS-CoV2 is a single strand RNA virus member of the type 2 coronavirus family, responsible for causing COVID-19 disease in humans. The objective of this study was to test the ivermectin drug in a murine model of coronavirus infection using a type 2 family RNA coronavirus similar to SARS-CoV2, the mouse hepatitis virus (MHV). BALB/cJ female mice were infected with 6,000 PFU of MHV-A59 (Group Infected; n=20) and immediately treated with one single dose of 500 μg/kg of ivermectin (Group Infected + IVM; n=20), or were not infected and treated with PBS (Control group; n=16). Five days after infection/treatment, mice were euthanized to obtain different tissues to check general health status and infection levels. Overall results demonstrated that viral infection induces the typical MHV disease in infected animals, with livers showing severe hepatocellular necrosis surrounded by a severe lymphoplasmacytic inflammatory infiltration associated with a high hepatic viral load (52,158 AU), while ivermectin administration showed a better health status with lower viral load (23,192 AU; p

Este artículo se encuentra disponible en la siguiente URL: https://journals.sagepub.com/doi/pdf/10.1177/0300985818817071 This is the pre-peer reviewed version of the following article: Ortega, J., Verdes, J. M., Morrell, E. L., Finnie, J. W., Manavis, J., & Uzal, F. A. (2019). Intramural vascular edema in the brain of goats with "Clostridium perfringens" Type D enterotoxemia. Veterinary Pathology, vol. 56, n. 3 (01 may.), pp. 452?459, which has been published in final form at https://doi.org/10.1177/0300985818817071 Este es el pre-print del siguiente artículo: Ortega, J., Verdes, J. M., Morrell, E. L., Finnie, J. W., Manavis, J., & Uzal, F. A. (2019). Intramural vascular edema in the brain of goats with "Clostridium perfringens" Type D enterotoxemia. Veterinary Pathology, vol. 56, n. 3 (01 may.), pp. 452?459, que se ha publicado de forma definitiva en https://doi.org/10.1177/0300985818817071 Enterotoxemia caused by Clostridium perfringens type D is an important disease of sheep and goats with a worldwide distribution. Cerebral microangiopathy is considered pathognomonic for ovine enterotoxemia and is seen in most cases of the disorder in this species. These lesions are, however, rare and poorly described in goats. In this paper, we describe the vasculocentric brain lesions observed in 44 cases of caprine spontaneous C. perfringens type D enterotoxemia. Only one goat had gross changes in the brain, which consisted of mild cerebellar coning. However, 8/44 (18%) of the cases showed microscopic brain lesions, characterized mainly by intramural vascular proteinaceous edema, a novel and diagnostically significant finding. The precise location of the edema was better observed with PAS and Gomori’s stains. The areas of the brain most frequently affected were cerebral cortex, corpus striatum (basal ganglia) and cerebellar peduncles and both arterioles and venules were involved. Most of the goats of this study showed lesions in the intestinal tract (enteritis, colitis and typhlitis), although pulmonary congestion and edema, hydrothorax, hydropericardium and ascites were also described. This is the largest study to date of neuropathological changes in naturally-occurring cases of caprine type D enterotoxemia, and it describes the main features of the cerebral microangiopathy in this species. Although the intramural edema found, for the first time, in these caprine cases is useful for the diagnosis of enterotoxemia when observed, its absence cannot exclude the disease because, in goats, it is only present in a small number of cases.

Histology is often underappreciated for the detection of the amphibian pathogenic fungus Batrachochytrium dendrobatidis, the cause of the potentially lethal skin disease chytridiomycosis. We evaluated the sensitivity of histology to detect chytrids in 20 wild specimens of 2 frog species from Uruguay that were clinically normal, but confirmed by PCR to be infected by B. dendrobatidis. We detected maturing and sporulated sporangia in 15 of 20 (75%) frogs, which is more sensitive than previously reported for histology. The effort needed to identify chytrids in histologic skin sections of Physalaemus henselii and Pleurodema bibroni required examination of 3.2 and 8.7 mm of skin sections for each frog species, respectively.

We communicate the finding of a subcutaneous neoplasia in a female specimen of the toad Melanophryniscus montevidensis (Bufonidae) from Uruguay. The lesion extended from the cephalic to the abdominal region, and both gross and microscopic features were typical of lipomas. This is to our knowledge the fourth case reported in amphibians.

Amphibian parasites of the Order Dermocystida (Ichthyosporea) are widespread pathogens known mainly from Europe and North America, which cause primarily a disease of skin and subcutaneous tissue in their hosts. The taxonomy of these organisms has been problematic given their conserved morphology, similar clinical disease and pathology. Currently recognized taxa belong to the three closely related genera, Amphibiocystidium, Amphibiothecum, and Rhinosporidium, whereas species of Dermocystidium and Sphaerothecum destruens include fish parasites. Here, we review the taxonomy of Dermocystida based on a molecular phylogenetic analysis, principally of amphibian parasites, including DNA sequences obtained from amphibian hosts collected in the central-eastern region of South America. A new taxonomic arrangement is proposed, which includes the designation of type material for Dermocystidium pusula, synonymization of Amphibiothecum with Dermocystidium, and the restriction of Amphibiocystidium to its type species A. ranae. We also review the taxonomic status of Dermosporidium hylarum until the present work included in the synonymy of the human and animal pathogen R. seeberi, and considered herein as a valid taxon, however. In addition, a new species of Sphaerothecum parasitic to amphibians is described, being the first record of this genus in the southern hemisphere and in an amphibian host. Fil: Borteiro, Claudio. Universidad de la República; Uruguay. Museo Nacional de Historia Natural; Uruguay Fil: Baldo, Juan Diego. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Biología Subtropical. Universidad Nacional de Misiones. Instituto de Biología Subtropical; Argentina Fil: Maronna, Maximiliano M.. Universidade de Sao Paulo; Brasil Fil: Pontes Baêta Da Costa, Délio. Universidade Estadual Paulista Julio de Mesquita Filho; Brasil Fil: Sabbag, Ariadne Fares. Universidade Estadual Paulista Julio de Mesquita Filho; Brasil Fil: Kolenc, Francisco. Museo Nacional de Historia Natural; Uruguay Fil: Debat, Claudio Martínez. Universidad de la República; Uruguay Fil: Haddad, Célio F. B.. Universidade Estadual Paulista Julio de Mesquita Filho; Brasil Fil: Cruz, Juan Carlos. Universidad de la República; Uruguay Fil: Verdes, José Manuel. Universidad de la República; Uruguay Fil: Ubilla, Martín. Universidad de la República; Uruguay

Intoxication with Solanum bonariense in cattle causes cerebellar cortical degeneration with perikaryal vacuolation, axonal swelling, and death primarily of Purkinje cells, with accumulation of electron-dense residual storage bodies in membrane-bound vesicles. The pathogenesis of this disease is not fully understood. Previously, we proposed that inhibition of protein synthesis in Purkinje cells among other altered metabolic pathways could lead to cytoskeletal alterations, subsequently altering cell-specific axonal transport. In the present study, immunohistochemical and histochemical methods were used to identify neuronal cytoskeletal alterations and axonal loss, demyelination, and astrogliosis in the cerebellum of intoxicated bovines. Samples of cerebellum from 3 natural and 4 experimental cases and 2 control bovines were studied. Immunoreactivity against neurofilament (NF)-200KDa confirmed marked loss of Purkinje neurons, and phospho-NF protein, β-tubulin, and affinity reaction against phalloidin revealed an altered perikaryal distribution of neuronal cytoskeletal proteins in the remaining Purkinje cells in intoxicated cattle. Reactive astrogliosis in every layer of the cerebellar cortex was also observed with anti–glial fibrillary acidic protein immunohistochemistry. In affected cattle, demyelination and axonal loss in the cerebellar white matter, as well as basket cell loss were demonstrated with Klüver–Barrera and Bielschowsky stains, respectively. Based on these results, we propose that neuronal cytoskeletal alterations with subsequent interference of the axonal transport in Purkinje cells may play a relevant role in the pathogenesis of this neurodegenerative disorder, and also that demyelination and axonal loss in the cerebellar white matter, as well as astrogliosis in the gray matter, likely occur secondarily to Purkinje cell degeneration and death., Facultad de Ciencias Veterinarias

We report infection by Ichthyophonus sp. in a South American amphibian, the hylid frog Hypsiboas pulchellus in Uruguay. This frog had a large subcutaneous mass over the urostyle and dorsal musculature comprised of parasitic cysts with mild granulomatous inflammation but otherwise appeared healthy.

The presence of Cryptosporidium spp. was detected in broiler chickens of 32-40 days of age, colonizing the bursa of Fabricius. The histologic study with haematoxylin and eosin staining was done on specimens of trachea, complete intestinal tract and bursa. Samples of intestinal content were also studied using Kinyoun staining technique. All birds with signs of illness were positive to the presence of parasite, showing a hypertrophic bursa of Fabricius, filled with caseous content. The bursal epithelial cells were full of different developmental stages of Cryptosporidium spp. This note describing the presence of Cryptosporidium spp. in industrial flocks of broiler chickens, is the first report of this parasite in Uruguay

We present gross and histologic evidence of coinfection in amphibians by fungal-like parasites of the order Dermocystida (Amphibiocystidium sp.) and the fungus Batrachochytrium dendrobatidis. The condition was observed in frogs Hypsiboas pulchellus (Hylidae) from Uruguay in 2009 to 2012. This report is the first of dermocystids in Neotropical amphibians since 1940.

Rabies has been an enigmatic disease because microscopic findings in central nervous system tissues do not always correlate well with the severity of the clinical illness. Immunohistochemical staining of the calcium-binding protein calbindin (specifically CbD28k) seems to be the technique most used to identify Purkinje neurons under normal and pathological conditions. In the present work, we evaluated CbD28k immunoreactivity in the cerebellar cortex of normal and natural Rabies virus (RABV)-infected cattle. We examined brains from 3 normal cows and from 6 crossbreed cattle with a histologic diagnosis of rabies. Samples were taken from the cerebral cortex, cerebellum, hippocampus, and brainstem. Immunohistochemistry was carried out using the following primary antibodies: anti-RABV, anti-GFAP, and anti-CbD28k. In the cerebellar cortex, RABV infection caused the loss of CbD28k immunostaining in Purkinje cells; some large interneurons in the granular layer maintained their positive CbD28k immunoreaction. The identification of this loss of CbD28k reactivity in cerebellar Purkinje cells of RABV-infected cattle presents a potentially valuable tool to explore the impairment of Ca2+homeostasis. In addition, this may become a useful method to identify specific molecular alterations associated with the higher prevalence of Negri bodies in Purkinje cells of cattle. Furthermore, we detected the presence of rabies viral antigens in different regions of the central nervous system, accompanied by microglial proliferation and mild reactive astrogliosis.

Solanum bonariense intoxication is characterized by cerebellar neuronal vacuolation, degeneration, and necrosis. Cerebellar Purkinje cells seem especially susceptible, but more research is needed to determine the pathogenesis of neuronal necrosis and the mechanism of Purkinje cell susceptibility. Calbindin D28k (CbD28k) is highly expressed in Purkinje cells and has been used as a marker for normal and degenerative Purkinje cells. The goal of this study was to describe S bonariense-induced disease by ascertaining Purkinje cell-specific degenerative changes using CbD28k expression and to correlate this with apoptosis in Purkinje cells, as determined using TUNEL (transferase-mediated dUTP-biotin nick end-labeling) and ultrastructural changes. In all cases, an increase in both dose and duration of S bonariense intoxication resulted in a decrease in the number of Purkinje cells. CbD28k immunohistochemistry was an excellent marker for Purkinje cells because immunoreactivity did not change in normal or degenerative tissues. This finding suggests that excessive calcium excitatory stimulation does not induce rapid neuronal degeneration and death. As found in previous studies, TUNEL tests and electron microscopy suggest that Purkinje cell degeneration and death are not occurring via an apoptotic process. These findings suggest that S bonariense poisoning induces progressive Purkinje cell death that is not mediated by excitotoxicity or apoptotic activation., Facultad de Ciencias Veterinarias

Solanum bonariense is a perennial poisonous shrub that induces cerebellar cortical degeneration when eaten by cattle. The aim of this research was to outline a protocol to induce a conditioned aversion to this plant. During the pre-conditioning period ten calves (126±12kg BW) were maintained at half of their normal energy intake with lucerne hay and water ad libitum, to stimulate consumption of S. bonariense. Every two days they were offered 100g ofS. bonariense leaves for 5 minutes. Calves began eating the target plant on day 10 and consumed all the plant material on day 12. The conditioning period began after each calf consumed the entire amount of S. bonariense for three consecutive sessions. Five animals were randomly selected for conditioning, and after ingestion ofS. bonariense they were dosed by oral gavage with lithium chloride (LiCl) at 200mg kg-1 BW (treated group), while the other five received a similar volume of water by oral gavage (control group). After 2 doses of LiCl the treated group ate no S. bonariense while the control group consumed the entire 100g. We confirmed that LiCl is a powerful tool to induce conditioned aversions against S. bonariense in calves, which persists for at least 3 months. RESUMO: Solanum bonariense é uma planta tóxica, arbustiva e perene que induz a degeneração cortical cerebelar quando ingerida por bovinos. O presente trabalho objetiva criar um protocolo para induzir aversão condicionada para essa planta em bovinos. Durante o período de adaptação às condições experimentais, dez bezerros (126±12kg) foram mantidos com metade de seu fornecimento alimentar energético normal que incluiu feno de alfafa e água ad libitum, para estimular o consumo de S. bonariense. A cada dois dias, foram fornecidas oralmente 100g de folhas de S. bonariense por cinco minutos. Os bezerros começaram a ingerir a planta no 10o dia de experimento e consumiram toda a planta no 12o dia. O período condicionado começou após cada bezerro ter consumido a quantidade total de S. bonariense por três sessões consecutivas. Cinco animais foram aleatoriamente selecionados para aversão condicionada e, após ingestão da planta, receberam solução oral de 200mg kg-1 de peso vivo de cloreto de lítio (LiCl) (grupo tratado), enquanto que os outros cinco bovinos receberam dosagem oral com volume similar de solução fisiológica (grupo controle). Após duas doses of LiCl, o grupo tratado não comeu folhas de S. bonariense, enquanto que o grupo controle consumiu toda a quantidade fornecida. Os resultados do presente trabalho demonstram que LiCl é uma ferramenta útil para induzir aversão condicionada contra S. bonariense em bezerros, que persiste por pelo menos 3 meses.

Cattle in western Uruguay that were eating Solanum bonariense developed periodic episodes of ataxia, hypermetria, hyperesthesia, head and thoracic limb extension, opisthotonus, nystagmus, and falling to the side or backward. Similar clinical signs were experimentally reproduced in cattle by administration of S. bonariense via rumen cannula at a dose of 1,024 g/kg body mass. No significant gross lesions were observed in field cases or experimentally induced cases. Spontaneous and induced histologic lesions were similar and included vacuolation, degeneration, and loss of Purkinje cells. Axonal spheroids, microcavitations, and other changes of wallerian-type degeneration in cerebellar white matter were also observed. Ultrastructural changes included increased number of electron-dense residual storage bodies in membrane-bound vesicles in affected Purkinje cells, and similar vesicles and mitochondria in axonal spheroids. No histologic lesions were detected in the other examined tissues. The Purkinje-cell swelling and vacuolation with subsequent cerebellar degeneration are suggestive of Purkinje-cell specific toxin that produces abnormal lysosome function and cell specific axonal transport. This is the first report of S. bonariense toxicity.

Dorsal root ganglion neurons from streptozotocin (STZ)-induced diabetic, genetic diabetic and normal mice were cultured in serum-containing media with or without nerve growth factor (NGF). The immunocytochemical analysis carried out after 1 week in culture revealed that the ratios of neurons immunoreactive to calcitonin gene-related peptide (CGRP) in NGF-free medium in the STZ-diabetic mice (average 23.2%) were significantly lower than those in the normal mice (45.1%). The ratios of neurons immunoreactive to CGRP and substance P (SP) in the NGF-free medium were also lower in the genetic diabetic mice (23.6% and 21.8%) than those in the normal ones (40.7% and 34.2%). However, treatment with NGF restored these reduced immunoreactivities in the diabetic groups in a dose-dependent manner. These results show that NGF can be effective for the diabetes-induced depletion of CGRP and SP in sensory neurons, and suggest its possible role in the prevention and improvement of diabetic sensory neuropathy.

Neurons are an extreme example of a cell type whose architecture must have an influence on its local metabolism. Their extremely long projections, specially when axons are considered, together with ultrastructural characteristics such as the absence of concluding evidences for the presence of ribosomes inside axons, induced neurobiologists to propose different maintenance paradigms for the different parts of the neuron. Three neuronal territories will be discussed here, a) the axon; b) the soma and dendrites; and c) the synapse. The characteristics of the axonal territory will be described first. In accordance to the widespread dogma of the absence of ribosomes in axons, axonal proteins (structural ones or those functionally destinated to membranes or nerve endings) should be synthesized in the somatic territory and conveyed after towards the axon via two different velocity transport mechanisms [0.5 to 5 mm/day and 420 mm/day, respectively (for review see Ochs, 1982)]. The possibility that the axonal territory could synthesize some of its proteins has not been generally accepted. Thus, the half-life of each cytoskeletal axonal protein should be estimated to be several times longer than the duration of their transport to the nerve endings. For instance, if we consider neurofilament proteins (Nf)—which normally are transported at a rate of lmm/day—in a 1 meter length nerve, they will arrive to the nerve endings 1000 days after their synthesis. This could mean that if the half-life of Nf is 1000 days, 50% of the Nf transported to the nerve endings will be degraded before the original bulk arrives to its destination. Even with a half life of 4000 days (about 11 years), a 1/16 of the Nf transported to the nerve endings will not arrive given that they will be degraded. The above mentioned problem have been extensively discussed by Alvarez and Torrez (1985), whom proposed that under these conditions the most peripheral portions of axons should always be partially deprived of cytoskeletal proteins. Furthermore, it is well known from Cajal’s studies (1928) that the total volume of the axonal territory in the longest axons is more than three order of magnitude greater than the somatic territory. On the other hand, the branching of axons at their ends will increase instead of diminish their total volume, increasing even more their possible hindrance. However, axons have been generally found to be homogeneously healthy throughout their length (see Alvarez and Torrez, 1985). Consequently, a local system of protein synthesis should be considered to maintain the homogeneity of axons; otherwise, some special mechanisms for protecting axonal cytoskeletal proteins from degradation must be found in axons. Thus, whether the axonal territory may synthesize at least a part of its own proteins or not, should be a main question, the answer of which—if positive—would change the point of view of a lot of normal or pathological neuronal functions which are related to protein synthesis.

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