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Z Dabrowski

Publications and source records attributed to Z Dabrowski.

At least 37 records · Page 2Linked to original sources

The effect of aluminium on the heam biosynthesis (in vitro) in bone marrow cells in rats.

The study has been carried out on male Wistar rats. The aim of the present study was to trace the effect of aluminium chloride and aluminium nitrate at concentration 10 microM and 20 microM on haem biosynthesis in vitro in bone marrow cell culture. The ability of haem biosynthesis in bone marrow cell culture after 48 h of experiments with aluminium chloride and aluminium nitrate significantly decreased in relation with the control value.

Aluminum↗

The effect of aluminium upon the activity of selected bone marrow enzymes in rats.

This study was carried out on male Wistar rats. The bone marrow activities of acetylcholinesterase (AchE-EC.3.1.1.7.), glutathione reductase (GR-EC.1.6.4.2.) and glucose-6-phosphate dehydrogenase (G6PD-EC.1.1.1.49.) were determined as affected by aluminium. The present experiments have revealed that within the first days there will be an increase in enzyme activity in the bone marrow. Simultaneously a decline in the activity of bone marrow could be observed which occurred later in the first course of the experiment.

Acetylcholinesterase↗

Effects of aluminum on erythroidal cells in bone marrow in rats.

The study has been carried out on Wistar rats. The aim of the present study was to trace the effect of aluminum on erythroidal cells in bone marrow in rats. The number of proerythroblast after 10 days of experiment with aluminum slowly decreased up to 80 days of experiments. However, the number of basophilic erythroblasts after 10 days insignificantly increased but after 20 days gradually decreased up to 80 days of experiments. The bone marrow polichromatic erythroblasts after 10 days of experiment slightly decreased, however after 20, 40 and 80 days of experiments the values decreased significantly. The quality of orthochromatic erythroblasts after 10 days of experiments dropped and after 20, 40 and 80 days of experiments significantly decreased compared to the control value. Aluminum also brings about histological changes in the bone marrow. The statistical significant reductions of hemoglobin and hematocrit levels were found in the aluminum exposed rats.

Aluminum↗

Effect of mercury and combined effect of mercury and dimethylsulphoxide (DMSO) on the activity of acetylcholinesterase (AchE-E.C. 3.1.1.7) of rat lymphocytes during in vitro incubation.

The effect of mercury and combined effect of mercury and DMSO on the activity of acetylcholinesterase of rat lymphocytes was studied during in vitro incubation. It was found that mercury is a very strong inhibitor of AchE. Dimethylsulphoxide performs a protective role for this enzyme. The activity of AchE in the lymphocytes treated with mercury and DMSO regardless of mercury concentration was similar to that in control series.

Animals↗

In vitro patterns of enzymic tetrahydrofolate dehydrogenase (EC 1.5.1.3) expression in bone marrow stromal cells.

The toxicity of antifolate drug therapy on microenvironmental function of hemopoietic marrow stromal cells may be critical enough to justify the development of a simple cell culture model to appraise the dihydrofolate reductase (DHFR)/tetrahydrofolate dehydrogenase (EC 1.5.1.3) (4HFDH) enzymic system in individual stromal cells. The localization and pattern of expression of 4HFDH/DHFR in cultured bone marrow stromal cells were studied in situ in morphologically identifiable cells. The 4HFDH/DHFR expression varies quantitatively and qualitatively according to cell types and thus constitutes specific phenotypic patterns for fibroblastic stromal cells, endothelial cells, monocyte-macrophages, and osteoclast-like cells. Data indicate a good correlation between the labeling of the enzymic expression and the resistance of cells to methotrexate treatment. This conclusion is also supported by similar features shown by cell sublines bearing multiple DHFR gene copies. Levels of 4HFDH/DHFR expression in marrow stromal cells should provide useful markers underlining the effects of cytostatic drugs used in chemotherapy (for example, methotrexate injuries or resistance). The method can be applied to isolated cells, stromal colonies (fibroblast CFU), or whole adherent layers from marrow cultures. Moreover, with this method, enzymic reactions can be carried out in situ and visual correlations between a supportive microenvironment (hemopoietic foci) and the 4HFDH/DHFR levels on the stromal adherent layer are possible.

Animals↗

The effect of intrarenal nickel subsulfide injections upon the activity of selected erythrocyte and bone marrow enzymes in rats.

The experiments were carried out on Wistar rats. The animals were divided into five groups: Group 1: control group; Group 2: the animals received a single intrarenal dose of nickel subsulfide (Ni3S2) in saline; Group 3: the animals receiving a single intrarenal dose of saline; Group 4: the animals receiving a single intrarenal dose of Ag2S in saline; Group 5: the animals receiving a single intrarenal dose of activated charcoal in saline. Prior to the procedure peripheral blood indices were determined. The experiments included animals manifesting polycythemia. Samples of blood and bone marrow were collected and the activities of AchE, GR and G6PD were determined. An increase in the activity of the three studied enzymes was detected in Groups no. 2 and 5.

Acetylcholinesterase↗

Post-exercise anaemia as a result of exercise overloading of the organism.

The aim of the present study was to determine the relation between the exercise load used in training and the changes in the basic parameters of the erythrocytic system. The experiments were carried out on 33 Wistar rats (females and males). The animals were forced to run at a velocity of 1.47 km/h inside an electrically-driven rotating drum. The experiments were performed for 35 days. In the 1st - (females) and 2nd - (males) group the exercise period was prolonged by 1 min per day on successive days, and by 2 min per day in the 3rd - (females) and 4th - (males) group. Prior to and after the training period the haemoglobin concentration, haematocrit, erythrocyte and reticulocyte counts were determined in the venous blood. Reticulocytes were divided into four age groups and the percentage each particular age group was calculated. All the trained groups manifested a decrease in haemoglobin concentration, hematocrit values and erythrocyte count and a concomitant elevation of the reticulocyte count with a shift towards youngest forms was found. Rats of the 3rd and 4th groups developed post-exercise anaemia.

Anemia↗

The activity of erythrocyte enzymes in rats subjected to running exercises.

The studies were carried out on male Wistar rats subjected to running within an electric rotating drum. The animals were divided into four experimental groups, differing one from another as to the duration of training. Each training session lasted 30 days. In the first group the daily run lasted 3 min, in the second group 5 min; in the third group, a 1 min run on the first day, and one min longer on each successive day; in the fourth group a 2 min run on the first day and for two min longer on each successive day. The determinations made prior to and after training included the peripheral blood erythrocyte (Er) and reticulocyte (Ret.) count, the hemoglobin concentration (Hb) and packed cell volume (PCV) and, determined by spectrophotometric methods, the activity of pyruvate kinase (PK), glucose-6-phosphate dehydrogenase (G6PD) and glutathione reductase (GR). Training induced an improvement of all enzymatic activities. The heavier the physical exertion, the more intensive was the enzymatic activity of red blood cells, due to the intensification of bone marrow erythropoetic activity under physical exertion and the appearance of young red cells in peripheral blood. All the experimental groups revealed a drop in erythrocyte count (Er), hemoglobin concentration (Hb), and hematocrit values (PCV), as well as an increase in the reticulocytes count (Ret) and in the activity of all the enzymes investigated. In the fourth group anemia was detected: prolonged endurance training decreased the RBC by 24.2%, Hb by 31.1%, PCV by 26.2% and increased the reticulocyte count by 881.6%.(ABSTRACT TRUNCATED AT 250 WORDS)

Age Factors↗

Bone marrow cyclic nucleotides (cAMP, cGMP) in phenylhydrazine-induced anemia.

The studies were carried out on male Wistar rats. The animals were divided into two groups: control and experimental. The hematocrit value and reticulocyte count were determined in blood samples collected from control and experimental rats. The experimental rats received subcutaneous injections of phenylhydrazine manufactured by Sigma for the duration of 3 days. On the 5th day blood samples were collected from all the control and experimental animals and determinations of hematocrit and reticulocyte count were repeated. cAMP levels were determined in bone marrow extracts by means of a radiocompetitive method. The cGMP level was determined by a radioimmunological assay. A significant elevation of cAMP level was detected in experimental rats, whereas the cGMP level changed only slightly.

Anemia↗

Cytochemical localization of adenylate cyclase activity in rat bone marrow.

The localization of adenylate cyclase (AC) in rat bone marrow was studied at the ultrastructural level using a cytochemical technique with adenosine triphosphate (ATP) as substrate. The strongest precipitate occurred around cytoplasmic membranes of cells of granulocytic lineage. Around cells of erythrocytic lineage, as well as megakaryocytes, lymphocytes and the plasma cells, the granules resulting from the cytochemical reaction revealed various degrees of density. The region within the bone marrow tissue where the cells manifested an increased reaction product was called 'reaction fields'. Most often the 'reaction fields' were formed by maturing cells of the granulocytic and erythrocytic lineages, surrounding the reticular cells. The reaction precipitate was also apparent around the advential and endothelial cells of the sinuses. Mature cells migrating from the bone marrow space to the sinus lumen also showed an intensified reaction product. The causes of such localization of AC were discussed.

Adenosine Triphosphate↗

Experimental model of chronic pancreatic fistula in dogs.

The authors performed a chronic pancreatic fistula in the dog by a modified method of Herrera et al. in which one of the arms of a metal cannula is introduced into the stomach instead of the duodenum. This technique protects the duodenum, the main source of hormones acting on the pancreas in the digestive tract, from surgical trauma and its consequences. The duodenum is anastomosed end-to-end and the continuity of the digestive tract is restored. The model can next be used to study the action of drugs on the exocrine function of the pancreas.

Animals↗

The effect of molybdenum upon blood serum enzymatic ceruloplasmin activity in rats.

Experiments were carried out on 61 male and female Wistar rats. Following 21-day intraperitoneal administration of molybdenum (Na2MoO4 X 2H2O), significant differences in the level of blood serum ceruloplasmin were noted in female rats depending upon the applied dose of molybdenum. In analogous groups of male rats no statistically significant differences were observed, which might indicate that the effect of molybdenum upon enzymatic ceruloplasmin activity is sex-related. The rats on an increased dietary level of 14 ppm molybdenum, of 10.8 ppm copper content and 507 ppm inorganic sulphur, showed decreased blood serum ceruloplasmin activity irrespective of their sex.

Animals↗

Histochemical and quantitative determination of the mercury content in the spleen and bone marrow of mice.

The experiments were carried out on "Swiss" mice which received injections of mercuric chloride. The organs examined included the spleen and bone marrow. The detection of mercury in the cells of the above organs was performed according to the histochemical method developed by Timm[13]. In both cases Timm's Ioethod failed, proving to be invalid for determination of the lowest mercuric concentrations. By use of the hXE technique, it was found that the minimum concentration of mercury in the tissue detectable by cyto-chemical methods amounts to 0.65-1.0 ppm.

Animals↗