Striatal hyperkinesis and neuron specific protein S100B

2021 ◽  
Vol 429 ◽  
pp. 119525
Author(s):  
Olim Naimov ◽  
Rustambek Matmurodov ◽  
Khanifa Khalimova
2018 ◽  
Vol 9 (4) ◽  
pp. 529-534
Author(s):  
D. V. Muraviova ◽  
M. R. Buniatov ◽  
G. A. Ushakovа

Acute and chronic stress are two of the most challenging issues faced by men situated in warzones. According to the main concept of G. Selye, stress response is the most important link during the adaptation of an organism to environmental factors. However, excessively intense or prolonged exposure to stress creates the threat of sustained homeostasis disorder. At present, the primary indicators in clinical studies are the general biochemical parameters of blood alanine aminotransferase, aspartate aminotransferase, bilirubin, creatine, urea, total protein, and glucose levels. But these indicators are not classical markers for determining the state of the nervous system itself and cannot reflect a patient's mental state. In this regard, we tested for a different biomarker; we made an attempt to determine the neurospecific S100b protein in the blood serum by analyzing the correlation between classical and specific methods for diagnosing the state of the nervous system. For this study, blood was collected from 20 patients aged 25 to 45 years old. Participants were divided into two groups: one group of provisionally healthy men and another group of patients who were admitted to the Department of Neurology of the I. Mechnikov Regional Clinical Hospital after military operations (from the territory of the ATU). The standard test kits of PrAT Reagent Company (Dnipro) were used to assess biochemical indicators in accordance with the given instruction in the supplier’s protocol. The activity of each of alanine aminotransferase, aspartate aminotransferase, direct and total bilirubin content, creatine, urea, total protein levels, and astrocyte-specific protein S100b was examined. The level of alanine aminotransferase in the men from the warzone was 23.9 ± 3.9 μmol/l, compared with the healthy men 31.2 ± 0.7 μmol/l. The level of aspartate aminotransferase in the group of men at the neurological department was similar to that in the healthy group. The content of direct bilirubin in the patients at the neurological department increased by 28.0%, compared with the healthy men. The concentration of creatinine, total protein, urea, and glucose levels did not significantly change, compared with healthy volunteers and were in the range of the standard reference data. The content of astrocyte-specific protein, S100b, in the blood of the patients was 0.011 μg/ml, 36.0% more than in the conditionally healthy men 0.007 μg/ml. Prolonged stress could, therefore, induce profound changes in blood brain barrier and registration of neurospecific protein in the blood of men in warzones. These changes could become chronic if or when these men develop other social and economic problems that can be monitored with the specific marker for S100b.


Author(s):  
John A. Trotter

Hemoglobin is the specific protein of red blood cells. Those cells in which hemoglobin synthesis is initiated are the earliest cells that can presently be considered to be committed to erythropoiesis. In order to identify such early cells electron microscopically, we have made use of the peroxidatic activity of hemoglobin by reacting the marrow of erythropoietically stimulated guinea pigs with diaminobenzidine (DAB). The reaction product appeared as a diffuse and amorphous electron opacity throughout the cytoplasm of reactive cells. The detection of small density increases of such a diffuse nature required an analytical method more sensitive and reliable than the visual examination of micrographs. A procedure was therefore devised for the evaluation of micrographs (negatives) with a densitometer (Weston Photographic Analyzer).


Author(s):  
U. Aebi ◽  
L.E. Buhle ◽  
W.E. Fowler

Many important supramolecular structures such as filaments, microtubules, virus capsids and certain membrane proteins and bacterial cell walls exist as ordered polymers or two-dimensional crystalline arrays in vivo. In several instances it has been possible to induce soluble proteins to form ordered polymers or two-dimensional crystalline arrays in vitro. In both cases a combination of electron microscopy of negatively stained specimens with analog or digital image processing techniques has proven extremely useful for elucidating the molecular and supramolecular organization of the constituent proteins. However from the reconstructed stain exclusion patterns it is often difficult to identify distinct stain excluding regions with specific protein subunits. To this end it has been demonstrated that in some cases this ambiguity can be resolved by a combination of stoichiometric labeling of the ordered structures with subunit-specific antibody fragments (e.g. Fab) and image processing of the electron micrographs recorded from labeled and unlabeled structures.


Author(s):  
Richard W. Burry ◽  
Diane M. Hayes

Electron microscopic (EM) immunocytochemistry localization of the neuron specific protein p65 could show which organelles contain this antigen. Antibodies (Ab) labeled with horseradish peroxidase (HRP) followed by chromogen development show a broad diffuse label distribution within cells and restricting identification of organelles. Particulate label (e.g. 10 nm colloidal gold) is highly desirable but not practical because penetration into cells requires destroying the plasma membrane. We report pre-embedding immunocytochemistry with a particulate marker, 1 nm gold, that will pass through membranes treated with saponin, a mild detergent.Cell cultures of the rat cerebellum were fixed in buffered 4% paraformaldehyde and 0.1% glutaraldehyde (Glut.). The buffer for all incubations and rinses was phosphate buffered saline with: 1% calf serum, 0.2% saponin, 0.1% gelatin, 50 mM glycine 1 mg/ml bovine serum albumin, and (not in the HRP labeled cultures) 0.02% sodium azide. The monoclonal #48 to p65 was used with three label systems: HRP, 1 nm avidin gold with IntenSE M development, and 1 nm avidin gold with Danscher development.


1994 ◽  
Vol 72 (05) ◽  
pp. 762-769 ◽  
Author(s):  
Toshiro Takafuta ◽  
Kingo Fujirmura ◽  
Hironori Kawano ◽  
Masaaki Noda ◽  
Tetsuro Fujimoto ◽  
...  

SummaryGlycoprotein V (GPV) is a platelet membrane protein with a molecular weight of 82 kD, and one of the leucine rich glycoproteins (LRG). By reverse transcription-polymerase chain reaction (RT-PCR), GPV cDNA was amplified from mRNA of platelets and megakaryocytic cell lines. However, since there are few reports indicating whether GPV protein is expressed in megakaryocytes as a lineage and maturation specific protein, we studied the GPV expression at the protein level by using a novel monoclonal antibody (1D9) recognizing GPV. Flow cytometric and immunohistochemical analysis indicated that GPV was detected on the surface and in the cytoplasm of only the megakaryocytes in bone marrow aspirates. In a megakaryocytic cell line UT-7, GPV antigen increased after treatment with phorbol-12-myri-state-13-acetate (PMA). These data indicate that only megakaryocytes specifically express the GPV protein among hematopoietic cells and that the expression of GPV increases with differentiation of the megakaryocyte as GPIb-IX complex.


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