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Biomedical subjects

V A Otellin

Publications and source records attributed to V A Otellin.

At least 19 recordsLinked to original sources

Intracerebroventricular administration of creatine protects against damage by global cerebral ischemia in rat.

Although a large body of evidence shows that pretreatment of brain tissue with creatine protects against anoxic injury in vitro, only a couple of papers have investigated creatine protection in vivo, and they yielded conflicting results. We attempted to clarify how creatine may be protective in an in vivo model of global cerebral ischemia (GCI). We administered creatine either before of after GCI. We decided to administer it by intracerebroventricular infusion, to maximize its bioavailability to the brain. Our findings show that creatine is clearly protective in vivo when administered before ischemia. In that case, histological evaluation of damage was consistently improved in all regions examined, and neurological score was better in creatine-treated rats than in controls. When administered after ischemia, histology was improved in the hippocampus, while only a not significant trend toward improvement was observed in the cerebral cortex and in the caudo-putamen. Neurological score was not improved by creatine administration after GCI. Our findings show that creatine administration is protective in vivo. Such protection was clear in the case of pretreatment, and was present, to a lesser degree, when treatment was started after ischemia. Our results should encourage further research in the possible role of creatine therapy in neuroprotection.

Animals↗

Suppression of glial fibrillary acidic protein expression in astrocytes of the superficial glial delimiting membrane in traumatic subarachnoid hemorrhage.

Astrocyte reactions to brain damage are usually accompanied by increases in glial fibrillary acidic protein (GFAP) expression, though it remains unclear whether this reaction is universal. The aim of the present work was to study the reactions of astrocytes in the superficial glial delimiting membrane of the human brain to traumatic subarachnoid hemorrhage. Light microscopy and immunocytochemical studies showed that GFAP expression is suppressed in astrocytes in the superficial glial delimiting membrane for periods of up to three days from the moment of craniocerebral trauma accompanied by subarachnoid hemorrhage. These data provide evidence for the existence of regional characteristics in the reactions of astrocytes.

Adolescent↗

Formation of the neocortex in mice developing in conditions of prenatal serotonin deficiency.

We report here detailed studies of structural changes occurring in the mouse neocortex formed and stratified in conditions of prenatal experimental blockade of serotonin synthesis. Studies were performed using F1(C57BL/CBA) hybrid mice. Endogenous serotonin levels were decreased by exposure of the mice to parachlorophenylalanine, which inhibits the key serotonin synthesis enzyme tryptophan hydroxylase. Offspring brains were studied at 1, 5 and 10 days (n = 10-15 for each time point) of postnatal development. Controls consisted of intact animals at the same periods of development. These experiments showed that prenatal blockade of serotonin synthesis leads to impaired formation of all neocortical layers, impaired growth, development, and differentiation of neurons, and alterations in neuron shape and size. As postnatal development proceeded, significant numbers of neurons died in the brain structures of these animals.

Animals↗

Modification of histogenetic processes in rat nervous tissue after administration of dexamethasone during prenatal development.

Experiments on rats using confocal microscopy and immunocytochemistry showed that single doses of the synthetic corticosteroid hormone dexamethasone to pregnant females during the period of elevated sensitivity of the developing fetal nervous system (day 13 of intrauterine development) led to modification of histogenetic processes in the brain, reflected as changes in its structural-functional characteristics during postnatal ontogenesis.

Animals↗

Immunocytochemical detection of brain neurons using the selective marker NeuN.

The aim of the present work was to develop optimal protocols for immunocytochemical reactions for nuclear protein NeuN for light and laser confocal microscopy which avoid the thermal antigen demasking procedure, which degrades the state of the tissue and requires use of expensive adhesive-coated slices. Maximal antigen retention was obtained after fixation in zinc-formalin and Bouin's fluid (maximum one day). Two protocols are proposed allowing the thermal demasking procedure to be avoided during detection of neuron marker NeuN on paraffin sections examined by light and confocal microscopy.

Animals↗

[Organization and cytochemical features of barrier structures in human placenta].

The aim of the present study was to investigate structural pattern of human placental barrier elements using light and electron microscopy and immunocytochemistry. Some important peculiarities of organization of the placental barrier were detected: difference in structure and amount of collagen IV in the basal lamina of endothelium and trophoblast, occurrence of smooth muscle actin in the capillary wall forming syncytiocapillary membranes. In the intercapillary stroma of terminal villi, both fibroblasts and macrophages but not myofibroblasts were found. Since smooth muscle cells and myofibroblasts are absent, pericytes are most likely cells to contain smooth muscle actin in the area of syncytiocapillary membranes.

Actins↗

[Use of zinc-containing dehydrating fixatives for neurohistological studies].

The suitability of zinc-containing dehydrating fixatives for neurohistological study of paraffin sections using Nissl staining and immunocytochemical techniques was examined. It was found that zinc-containing dehydrating fixatives (zinc-ethanol-formaldehyde and zinc-acetone-isopropanol-formaldehyde) had a capacity for good preservation of both structure and antigenic properties of the nervous tissue and could be recommended for application in neurohistological studies.

2-Propanol↗

Expression of early gene proteins, structural changes in brain neurons in hypobaric hypoxia, and the correcting effects of preconditioning.

The Nissl method and immunocytochemistry were used to study the effects of severe hypobaric hypoxia and its actions in combination with the preconditioning actions of moderate hypoxia on the expression of the early gene proteins c-Fos and NGFI-A as well as structural changes in hippocampal and neocortical neurons in the rat brain. Severe hypoxia was found to suppress c-Fos and NGFI-A synthesis (3-24 h after exposure) and to induce delayed (days 3-7) structural damage to neurons, of the "light" and predominantly the "dark" types, which appear to reflect the development of necrotic and apoptotic processes respectively. Preconditioning with the regime used here corrected these derangements, resulting in increases in the expression of early gene proteins and significant reductions in structural damage to neurons after severe hypoxia.

Animals↗

Structural organization of astrocytes in the rat hippocampus in the post-ischemic period.

The aim of the present work was to study the location and structural organization of astrocytes in the rat hippocampus, which contain immunoreactive glial fibrillary acid protein (GFAP) after ischemic damage to the brain after intracerebroventricular administration of the neuroprotective agent creatine and without treatment. Light microscopy and immunocytochemical methods were used to study the brains of 26 adult male Sprague-Dawley (Koltushi) rats, some of which were subjected to total cerebral ischemia (12 min) under anesthesia with subsequent reperfusion (seven days). Creatine was given to 11 animals intracerebroventricularly using an osmotic pump (Alzet Osmotic Mini-Pump). The results showed that GFAP-immunoreactive hippocampal astrocytes were concentrated in two main zones (the stratum lacunosum-moleculare of field CA1 and the stratum polymorphae of the dentate fascia). The neuroprotective effect of creatine had the result that moderate ischemic damage to the hippocampus did not lead to changes in the zones containing activated astrocytes. The redistribution of GFAP-positive astrocytes in the post-ischemic period was associated with loss of pyramidal neurons in cytoarchitectonic field CA1. Complete loss of pyramidal neurons in this area of the hippocampus leads to a qualitatively new level of astrocyte activation--proliferation.

Animals↗

Immunocytochemical detection of astrocytes in brain slices in combination with Nissl staining.

The present study was performed to develop a simple and reliable method for the combined staining of specimens to allow the advantages of immunocytochemical detection of astrocytes and assessment of the functional state of neurons by the Nissl method to be assessed simultaneously. The protocol suggested for processing paraffin sections allows preservation of tissue structure at high quality and allows the selective identification of astrocytes with counterstaining of neurons by the Nissl method. The protocol can be used without modification for processing brain specimens from humans and various mammals--except mice and rabbits.

Animals↗

Glial fibrillary acidic protein in astrocytes in the human neocortex.

Glial fibrillary acidic protein (GFAP), expressed in the brain by astrocytes, is one of the major immunocytochemical markers of these cells. The aim of the present work was to study the structure of GFAP-positive astrocytes in the human neocortex. Immunocytochemical confocal laser microscopy was used to characterize the main types of GFAP-immunoreactive astrocytes in the human neocortex. These were astrocytes of layer I, forming the superficial glial delimiting membrane, along with transmembrane astrocytes of layer I, with very long processes penetrating several layers of the cortex, astrocytes of the middle layers of the neocortex, mostly of the protoplasmic type and involved in forming perivascular delimiting membranes, and typical white matter fibrous astrocytes. These data may help unify assessments of histopathological processes seen in various types of gliosis in the CNS.

Adolescent↗

[Suppression of glial fibrillary acidic protein expression in astrocytes of the superficial glial limiting membrane after traumatic subarachnoid hemorrhage].

Although typical astrocytic reaction to brain injury is accompanied by an increase of glial fibrillary acidic protein (GFAP) expression, to what degree this reaction is universal remains to be elucidated. The aim of the present study was to investigate the reaction of superficial glial limiting membrane of human brain to traumatic subarachnoid hemorrhage. Using light microscopy and immunocytochemistry, it was found that a suppresion of GFAP expression in astrocytes of superficial glial limiting membrane occurred up to 3 days following the brain trauma. The data obtained suggest the existence of regional peculiarities of astrocytic reaction.

Adolescent↗

[Immunocytochemical demonstration of catecholaminergic structures in paraffin sections of the rat brain using various methods of fixation].

The study was undertaken to investigate the effect of various methods of fixation of the brain upon the demonstrability of catecholaminergic structures using tyrosine hydroxylase (TH) immunocytochemical reaction. It was established that most complete demonstration of TH-containing structures was achieved after perfusion fixation with 4% paraformaldehyde followed by post-fixation in the Carnois fluid and after immersion fixation in the IHC zinc fixative (BD Pharmingen, U.S.A.). Immersion fixation in 4% paraformaldehyde, ethanol-formaldehyde, Carnois and Bouin fixatives can be used for demonstration of perikarya of catecholaminergic neurons.

Animals↗

[Neocortex formation in mice developing after prenatal serotonin depletion].

The objective of this study was a detailed investigation of structural changes taking place in murine neocortex during its formation and stratification after prenatal serotonin depletion. The study was carried out in murine embryos of F1 (C58BL/CBA) hybrid strain. For depletion of endogenous serotonin in mice, pchlorophenylalanin, an inhibitor of tryptophan hydroxylase - a key enzyme of serotonin synthesis, was used. Brain of the offspring was studied on postnatal days 1, 5 and 10 (n = 10-15 for each time point). Intact animals of respective developmental stages were used as a control. The study demonstrated that prenatal inhibition of serotonin synthesis resulted in malformation of all neocortical layers, disorders of neuronal growth, development and differentiation, changes in their shape and dimensions. During postnatal development, the loss of a significant numbers of cells was observed in the brain structures studied of serotonin-depleted animals.

Animals↗

[Modification of histogenetic processes in rat nervous tissue after dexamethasone administration during prenatal development].

In experiments performed on rats, using the methods of confocal microscopy and immunohistochemistry, it was detected that administration of a single dose of synthetic corticosteroid dexamethasone during the period of increased sensitivity of developing nervous system (embryonic day 13) resulted in modification of histogenetic processes in the brain, resulting in the changes of its structural and functional characteristics during postnatal period of ontogenesis.

Animals↗

[Immunocytochemical demonstration of brain neurons using NeuN as a selective marker].

The aim of the present study was to find optimal protocol of immunocytochemical reaction to NeuN nuclear protein for light and laser confocal microscopy, which would exclude the antigen heat unmasking procedure that results in deteriorating the state of the tissue and requires expensive adhesive-coated slides. Best preservation of the antigen was found to be provided by fixation in zinc-formalin and Bouin's fixative (for a period of less than 24 hrs). Two protocols allowing to avoid antigen heat unmasking procedure during demonstration of the NeuN neuronal label in paraffin sections by the light and confocal microscopy are presented.

Animals↗

[Structural organization of macrophages in forming human placenta].

Placental macrophages (Kashchenko-Hofbauer cells) belong to a special population of tissue macrophages of human fetal provisional organs. The aim of the present study was to investigate the structure of Kashchenko-Hofbauer cells at the stage of placenta formation using the methods of light and electron microscopy and immunocytochemistry. Cytological and cytochemical peculiarities of Kashchenko-Hofbauer cells revealed in this study, leave no doubt that they belong to the tissue macrophages group. Their cytoplasm is strongly reactive with antibodies against CD68 lysosomal antigen suggesting potentially high phagocytic activity of these cells. Weak nuclear labeling with proliferation marker PCNA was found in placental macrophages.

Antigens, CD↗