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Regulatory Mechanisms
in Biosystems
Regulatory Mechanisms
in Biosystems
ISSN 2519-8521 (Print) ISSN 2520-2588 (Online) Regul. Mech. Biosyst., 9(3), 379-383 doi: 10.15421/021856
Changes in erythrocytopoesis indices in dogs with babesiosis
V. I. Holovakha*, O. V. Piddubnyak*, T. I. Bakhur*, N. V. Vovkotrub*, A. A. Antipov*, M. V. Anfiorova**, B. V. Gutyj***, L. G. Slivinska***, O. P. Kurdeko****, A. O. Macynovich****
*Bila Tserkva National Agrarian University, Bila Tserkva, Ukraine **Odessa State Agrarian University, Odessa, Ukraine
***Stepan Gzhytskyi National University of Veterinary Medicine and Biotechnologies, Lviv, Ukraine ****Vitebsk Order of the Badge of Honor State Academy of Veterinary Medicine, Vitebsk, Belarus Republic
Holovakha, V. I., Piddubnyak, O. V., Bakhur, T. I., Vovkotrub, N. V., Antipov, A. A., Anfiorova, M. V., Gutyj, B. V., Slivinska, L. G., Kurdeko, O. P., & Macynovich, A. O. (2018). Changes in erythrocytopoesis indices in dogs with babesiosis. Regulatory Mechanisms in Biosystems, 9(3), 3 79-383. doi:10.15421/021856
Babesiosis is a common disease in dogs. Babesia canis (Piana & Galli-Valerio, 1895) (Sporozoa, Babesiidae) causes the destruction of erythrocytes, resulting in hypotensive shock and total tissue damage due to lack of oxygen. Because of babesiosis, anemia develops in dogs, and in the first hours of the disease it is normocytic, normochromic and nonregenerative, and on the 2-3rd day of the course, macrocytic, hypochromic anemia with reticulocytosis develops. Scientists have studied the most common indicators of evaluation of erythrocytopoesis during babesiosis (the number of red blood cells, hemoglobin, hematocrit index, indices of "red" blood MCH and MCV), but the age structure of erythrocytes, their acid resistance and the ferrum-transferrin complex for this parasitic pathology have not been sufficiently studied. We carried out research on dogs of service breeds, which were divided into two groups: the first (618 months old, n = 10) and the second (2-8 years, n = 15). According to the conducted studies, in dogs of different age groups with babesiosis revealed oligocythemia with anisocytosis and poikilocytosis, oligochromia, decreased hematocrit index and macrocytosis. Significant changes in the morpho-functional state of erythrocytes in dogs of both groups have been revealed, in particular, changes in the population (age) composition of red blood cells: the number of "old" erythrocytes increases (they are rapidly destroyed), the "young" forms of red blood cells decrease and the time for their hemolysis is reduced. As a result of the study of the ferrum-transferrin complex in dogs with babesiosis in both groups, an increase in the level of free ferrum (UIBC) and a decrease in the saturation of transferrin with the trace element was found, which makes it impossible to form a hemoglobin molecule in the bone marrow.
Keywords: erythrocytes; population composition of erythrocytes; acid resistance; hemoglobin; MCN; MCV; ferrum; transferring; ferrum-transferrin complex.
Article info
Received20.07.2018
Received in revised form 28.08.2018
Accepted 02.09.2018
Bila Tserkva National Agrarian University, PI. Soborna, 8/1, Bila Tserkva, 09117, Ukraine. Tel.: +38-067-693-17-73.
Odessa State Agrarian University, Krasnova st., 3a, Odessa, 65010, Ukraine. Tel.: +38-048-765-93-17. E-mail: odau_vetmed@ukr.net
Stepan Gzhytskyi National University ofVeterinary Medicine and Biotechnologies Lviv, Pekarska st., 50, Lviv, 79010, Ukraine. Tel.: +38-097-290-41-51. E-mail: maksymovych@lvet.edu.ua
Vitebsk Order of the Badge ofHonor State Academy ofVeterinary Medicine, 1stDovator st., 7/11, Vitebsk, 210026, Belarus Republic. E-mail: vsavm@vsavm.by
Introduction
One of the most common diseases in dogs is babesiosis. Areas of infection are found in the tropics (Jain et al., 2017; Ybanez et al., 2018), Mediterranean countries (Salem & Farag, 2014), Eastern (Davitkov et al., 2015; Bartnicki et al., 2017) and Western Europe (Eichenberger et al., 2016), Asia (Liu et al., 2016; Wang et al., 2018) and America (Di Cicco et al., 2012; Rojas et al., 2014). The analysis of recent public-cations proves that babesiosis in dogs occurs in almost all regions of Ukraine (in 18 of 24). The territory of six regions (mostly Southern and Steppe zones of Ukraine) remain free of this invasion. The infestation of dogs occurs during an attack of ixodid ticks (Arachnoidea, Ixodidae) and exposure of the pathogen with their saliva to a susceptible animal (Bajer et al., 2014).
Metabolites of Babesia canis (Piana & Galli-Valerio, 1895) (Sporo-zoa, Babesiidae), accumulating in erythrocytes, cause disorders of blood, nervous and cardiovascular systems, the gastrointestinal tract, liver, kidneys, etc. (Lobetti et al., 2012; Zygner et al., 2012; Tasaki et al., 2013). Parasites cause destruction of red blood cells, resulting in hypotensive shock and total tissue damage due to lack of oxygen (Goddard et al., 2015). Because of babesiosis in dogs, anemia appears, which is normo-cytic, normochromic and non-regenerative in the first hours of the
disease. On the 2-3rd days of the course of the disease, macrocytic, hypochromic anemia with reticulocytosis develops.
Sources from the literature usually describe the most common indicators of evaluation of erythrocytopoesis during babesiosis (the number of erythrocytes, hemoglobin, hematocrit index, indices of "red" blood - MCH and MCV).
However, data are absent on the changes in other indicators of evaluation of erythrocytopoesis in the course of this parasitic pathology: the red blood cells' age structure, their acid resistance and the ferrum-transferin complex (FTC). Therefore, the purpose of this article is to study the changes in age composition of erythrocytes, their acid resistance and indicators of FTC in dogs with babesiosis.
Materials and methods
The objects of the study were dogs of service breeds, which were divided into two groups: the first (age from 6 to 18 months, n = 10) and the second one (from 2 to 8 years old, n = 15). Blood samples were taken in vacuum tubes of 10 ml volume (Vacutest, Italy). An anticoagulant ethylendiaminetetraacetic acid (EDTA) was used for blood tests.
In the dogs' blood, the total number of erythrocytes, hemoglobin content, hematocrit, MCV (average volume of erythrocyte) was deter-
mined by an automatic hematological analyzer Mythic 18 (Orphee S.A., Switzerland) and reagents by PZ Coimay S.A. (Poland). MCH (hemoglobin content in erythrocyte) was calculated mathematically.
Acid resistance of erythrocytes was determined by the method of A. I. Terskov and I. I. Hitelzon. Blood for research was taken into centrifuge tubes, where heparin was pre-added at a rate of 10 IU per 10 ml of blood. The plasma was separated by centrifugation (1,500 rpm for 20 minutes). The erythrocyte suspension was thoroughly cleaned with 0.85% sodium chloride solution, cooled to 4 °C (to prevent oxidation of the lipoproteins), followed by centrifugation under the same conditions. The erythrocyte suspension was taken by capillary (0.02 ml) and transferred to a test tube where 10 ml of isotonic sodium chloride solution was pre-introduced The capillary was washed in the top layer ofthe solution and the contents of the test tube were thoroughly mixed. In this case 0.2% suspension of erythrocytes was obtained (Terskov & Hitelzon, 1967).
Measurement of optical density of the solutions was carried by a photometer at 540 nm wavelength (cuvettes with 10 mm process solute-on thickness). Before the study, both cuvettes were filled for 5-10 min with hemolytic solution with the abovementioned concentration. The control cuvette was filled with 4 ml of 0.85% sodium chloride, and the experimental one was filled with 2 ml of hemolytic solution and 2 ml of 0.2%o erythrocytes' suspension added. Hemolytic with erythrocytes' suspension was stirred by pipette tip. The sample extinction was determined immediately after mixing. Extinction changes were recorded every 30 seconds until a constant indicator is reached, during 30 seconds (Golovakha et al., 2017).
The difference between the initial and final (after hemolysis) optical density is seen as 100%o and the AE percentage was calculated (the next extinction index was subtracted from previous one and seen as "X"), which reflects the relative percentage of non-hemolyzed erythrocytes every 30 seconds. This calculation excludes dependence of the results on the number of erythrocytes and hemoglobin concentration. The obtained data was depicted graphically. The horizontal axis reflects time from 0 and every 30 seconds, the ordinate axis - the erythrocytes' hemolysis percentage. The left side of the diagram indicates hemolysis of "old" erythrocyte populations, the central part with the peak is formed by the destruction of "mature" and partially "young" cells, the right side is the hemolysis result of only "young" erythrocytes (Terskov & Hitelzon, 1967).
The population structure of the erythrocytes was determined by fractionation of sucrose density gradient by the I. Sizova method (Sizo-va et al., 1980). Blood samples were put into centrifuge tubes, with previously added heparin at 10 IU per 10 ml of blood. Plasma was separated by centrifugation (1,500 rpm for 20 minutes). The erythro-cytes' suspension was washed three times by cooled to 4 0C (to prevent oxidation of lipoproteins) 0.85%o sodium chloride solution followed by centrifugation under the same conditions.
The erythrocytes' suspension was taken by a 0.1 ml pipette and moved to Florinski test tubes, previously filled with 0.9 ml of isotonic sodium chloride solution. The pipette was washed in the upper layer of the solution and the tube content was thoroughly mixed (thus obtaining 10% erythrocytes suspension). 0.5 ml of erythrocytes' suspension was introduced into the 450 tilted column, and sucrose solution was put layer over layer on the column wall (the first layer - with the highest concentration, the last - with the lowest). It is provides the distribution of eryth-rocytes in different concentrations of sucrose, depending on the eryth-rocytes' age.
The column was carefully leveled at 900 to avoid mixing of the sucrose layers, and every last layer was carefully separated into a separate graded tube (7 in total). Isotonic sodium chloride solution was added into each tube, totaling volume to 10 ml. All 7 tubes were thoroughly mixed and checked for the optical density.
Measurement of the solutions' optical density was carried by the photometer at 520 nm wavelength (cuvettes with 10 mm working layer thickness). A 0.85% sodium chloride solution was a control one. The received extinction amount was seen as 100%), and each tube index was seen as "X" and thus calculating the percentage of a particular fraction. The indicators of the first three tests (in sucrose solutions of 30%, 26% and 22% concentrations) were added. The obtained result was a percentage indicator of the "old" erythrocytes' number. The same was done
with the fourth and fifth indicators (18% and 14% solutions), by calculating the concentration of "mature" cells, while adding percentage of the sixth and the seventh results (10% and 6% sucrose solutions) and a relative indicator of the "young" population's content was obtained (Sizova et al., 1980; Wijk & Solinge, 2005).
In the blood serum the following were determined: the content of the ferrum, the total and unsaturated ferrum-binding ability of the serum (TIBS, UIBS), the level of transferrin and the saturation of it by ferrum (ferrosine method).
Mathematical analysis of the study results was conducted in Statis-tica 6.0 (StatSoft Inc., USA). Differences between average values were considered statistically significant at P < 0.05 (ANOVA).
Results
Clinically, babesiosis in dogs was manifested by hyperthermia (up to 41.2 0C), drowsiness, shaky stroke, anemia in the mucous membranes of the eyes and oral cavity, dull hair, thirst, vomiting. In sick animals there were: tachycardia, tachypnea, oliguria, yellow-brown urine. In dogs of first group (age up to 18 months), the number of erythrocytes was reduced and averaged 3.8 ± 0.33 T/L, which is 57.6%o less than in clinically healthy animals. Oligocythemia was found in all animals. In dogs of the second group, too, oligocythemia was established - 4.7 ± 0.36 T/L (minimal norm is 5.0 T/L). Along with oligocythemia in animals, anisocytosis and poikilocytosis have been observed, indicated dystrophic changes in the structural elements ofthe bone marrow.
We also found changes in the population composition of erythrocytes. In particular, the number of "old" erythrocytes in dogs of the first group on average was 15.4 ± 2.46%, which is almost three times more than in the clinically healthy animals (P < 0.05). However, the most "old" populations of erythrocytes were found in older dogs (second group). In them, the number of "old" in the group on average was 27.9 ± 4.98%, which is 5.2 times more than in the clinically healthy animals (P < 0.01). Such a number of "old" erythrocytes, obviously, is evidence of an increase in aging processes of "red" cells.
Unlike "old" populations, the number of "mature" red cells in patients of both groups did not differ from the number in clinically healthy animals (P < 0.5, Table 1). The number of "young" forms of erythrocy-tes, compared with clinically healthy, in dogs with babesiosis, especially the second group, was reduced and averaged 35.0 ± 5.80%, which is 17.7% less than in clinically healthy animals. Reduction of "young" red blood cells is evidence of depletion of the "red" bone marrow and inhibition of adaptive processes for hemic hypoxia.
Table 1
Indices of the total number of erythrocytes and their population structure in dogs
Animal Erythrocytes, population structure of erythrocytes, %
groups T/l "old" "mature" "young"
Clinically healthy 5.7-7.67 1.6-11.3 33.0-58.0 35.2-62.3
(n = 10) 6.6 ± 0.25 5.4 ± 1.12 41.9 ± 3.25 52.7 ± 2.59
Infected, age up to 2.57-4.96 6.2-25.5 27.7-41.6 35.1-56.2
1.5 years (n = 10) 3.8 ± 0.33 15.4 ± 2.46 36.8 ± 1.38 47.8 ± 2.26
P < 0.001 0.05 0.5 0.5
Infected, age 2.52-7.75 3.8-66.2 19.7-56.0 12.4-61.3
2-8 years (n = 15) 4.7 ± 0.36 27.9 ± 4.98 37.1 ± 2.57 35.0 ± 5.80
P < 0.01 0.01 0.5 0.05
Changes in the population composition of erythrocytes also affect their osmotic (acid) resistance, since the time of hemolysis depends on their age, leads to the destruction of intracellular structures and lowering the resistance of the membrane to increased pressure inside the cell.
The analysis ofthe erythrograms (acid erythrocytes hemolysis) shows that the time of the main peak in dogs of the first group was 3.7 min; its height was 20% (Fig. 1). The whole hemolysis of erythrocytes was completed in 6.5 min. The time of hemolysis of "old" and "mature" erythrocytes in dogs of the first group was 3.5 min, which is 2 min less, compared to clinically healthy dogs of the same age. It testifies to the rapid destruction of these populations as a result of the depletion of the structural and functional state of membranes of red blood cells. Regar-
ding the hemolysis of the "young" red blood cells (right side of the graph), its duration in both patients and healthy dogs was 3 min, but in animals with babesiosis invasion there was an additional peak indicating the unstable resistance of the membranes of "young" red blood cells to the action of hemolysis due to toxic effects products of microscopic parasites' catabolism.
Fig. 1. Acid resistance of erythrocytes in dogs with babesiosis aged up to 1.5 years (n = 10)
Analyzing the erythrograms of dogs of the second group (Fig. 2), it should be noted that the left side of the graph (hemolysis of the "old" and "mature" populations) was more acute and expired for 3 min, while in healthy dogs, it was 2 min longer. It may indicate the blocking effect of invasive agents on the elements of the erythroid bone marrow sprout, inhibition of erythrocyte maturation processes and increased aging. The complete hemolysis time was 5.5 min, which is 1.5 min less, compared to healthy dogs, indicating a change in the functional state of the membranes ofthe "young" populations.
^ The time of hemolysis, min.
Fig. 2. Acid resistance of erythrocytes in dogs with babesiosis aged 2-8 years (n = 15)
The content of the respiratory blood enzyme (hemoglobin) in dogs with babesiosis was reduced. In particular, in young dogs (first group), its average number was 98.0 ± 6.59 g/l, which is 38.0% less than in clinically healthy (P < 0.001). Similar values of this chromoprotein were also found in dogs ofthe second group (P < 0.001, Table 2). It should be noted that oligochromemia was established in 90.0 and 80.0%) of dogs of the first and second groups, which testifies to the increased destruction of red blood cells. If the number of erythrocytes and hemoglobin content in dogs with babesiosis are reduced, then the indices of "red" blood, in particular, the MCH, did not differ from the values in clinically healthy animals (Table 2).
One of the commonly used indicators of erythrocytopoesis is the hematocrit index, which determines the total volume of erythrocytes, characterizing certain types of anemia (Gutyj et al., 2017; Slivinska et al., 2018). In dogs with babesiosis, this indicator was lower than normal (P < 0.01). It should be noted that low values of hematocrit were detected in 90.0% and 73.3%o of dogs from the first and second groups, respectively.
Different forms of anemia can be diagnosed using an average volume of red blood cells (MCV). MCV in dogs should not exceed 80 pm3. However, in some of the sick dogs of both the first and the second groups, the MCV was within the range of 80.2-101.3 pm3. That is, in
such cases there is an increased inflow into the peripheral blood of immature erythrocytes.
But, it is impossible to evaluate erythrocytopoesis without indicators of the fenum-transferin complex, the basis of which is the ferrum. It is the element that plays an important role in the transfusion of oxygen and carboxylic acid in the cells of the body. The content of ferrum in blood serum of dogs with babesiosis on average did not differ from the values in clinically healthy animals (P < 0.5, Table 3). However, a detailed analysis of the obtained values shows that some dogs (60.0% and 66.7% respectively) exhibit hyposideremia, which indicates a low intake of ferrum into the body.
Table 2
Changes in erythrocytopoesis in dogs with babesiosis
Animal groups Hemoglobin, g/l Hematocrit index, % MCH, fmol MCV, ^m3
Clinically healthy 145.0-168.0 46.0-57.0 20.4-28.2 64.6-82.5
(n = 10) 158.0 ± 2.84 50.0 ± 1.46 24.0 ± 0.94 74.8 ± 2.29
Infected, age up to 52,0-142.0 19.0-35.0 19.6-33.3 58.1-101.2
1.5 years (n = 10) 98.0 ± 6.59 28.1 ± 1.21 26.4 ± 1.86 76.6 ± 4.72
P < 0.001 0.001 0.5 0.5
Infected, age 72.0-148.0 17.0-46.0 18.2-30.8 57.6-101.3
2-8 years (n = 15) 100.0 ± 5.95 30.8 ± 2.33 21.7 ± 1.06 65.9 ± 2.44
P < 0.001 0.01 0.2 0.05
Table 3
Indicators of the ferrum-transferrin complex in dogs
Animal Biometric Ferrum, TIBC, UIBC,
groups indicator ^mol/l ^mol/l ^mol/l
Clinically healthy (n = 10) Lim M ± m 22.4-36.7 28.3 ± 1.38 62.5-83.2 70.8 ± 2.63 34.6-48.7 42.5 ± 1.64
Infected, aged up to 1.5 years (n = 10) Lim M ± m 16.8-40.3 23.6 ± 2.70 60.6-91.7 80.2 ± 2.96 41.3-72.8 56.6 ± 4.09
P < 0.2 0.05 0.05
Infected, aged 2-8 years (n = 15) Lim M ± m 17.8-39.6 26.6 ± 2.52 76.3-111.4 89.5 ± 3.45 43.1-89.4 62.9 ± 2.90
P < 0.5 0.01 0.001
In the rest of the animals (30.0%) and 26.7%), respectively), hyper-sideremia was found (> 35 pmol/l), which obviously indicates an increased accumulation of ferrum in the blood for the destruction of red blood cells. But it is important that the value of the content of the ferrum cannot on its own reflect the state of its exchange. Therefore, it is important to determine other indicators of its metabolism, in particular, TIBC (indicating the content of a non-protein-transferrin-bound ferrum) and UIBC (toxic level indicator of the ferrum).
TIBC in dogs with babesiosis was elevated in the first and second group by 13.3%) and 26.6%) respectively (P < 0.01). High values of TIBC indicate dystrophic changes in the transferrin receptor apparatus, which leads to a reduced transport of the ferrum from the depot to the bone marrow, enhanced erythrocyte hemolysis, and the accumulation of free ferrum. An indicator of the last one is the UIBC, which indicates the non-transferring pool of the ferrum. In dogs with babesiosis, UIBC averaged 56.6 ± 4.09 and 62.9 ± 2.90 pmol/l in the first and second groups, respectively, which is by 33.2% and 48.0% more than in clinically healthy animals (P < 0.05 and P < 0.001). This value indicates the accumulation of toxic (free) ferrum and reduced binding of the protein transferrin to the trace element.
It is not advisable to evaluate the exchange of a ferrum without determining the content of transferrin in serum and its saturation with ferrum. The content of transferrin in dogs with babesiosis was elevated and was in the first and second group 3.6 ± 0.13 and 4.0 ± 0.13 g/l, respectively.
In contrast to the amount of transferrin, the coefficient of its saturation with ferrum was lower, compared with healthy animals, and was in young dogs (first group) - 29.5 ± 3.17%, in older (the second group) -29.8 ± 2.66% (P < 0.05, Table 4). Reduced saturation (less than 30%) of transferrin with ferrum was detected in 30.0% and 33.3% of animals, respectively, indicating a low synthesis of the structure of the protein molecule of transferrin in the liver and slow transport of the trace element to the depot and bone marrow.
Table 4
Indicators of the ferrum-transferrin complex in dogs
Animal Biometric Transferrin Coefficient of transferrin's
groups indicator content, g/l saturation with ferrum, %
Clinically healthy Lim M ± m 2.79-3.72 33.30-44.60
(n = 10) 3.20 ± 0.12 39.90 ± 1.41
Infected, age up to Lim M ± m 2.71-4.10 19.80-48.70
1.5 years (n = 10) 3.60 ± 0.13 29.50 ± 3.17
P < 0,05 0,05
Infected, age Lim M ± m 3.41-4.98 17.60-43.50
2-8 years (n = 15) 4.0 ± 0.13 29.80 ± 2.66
P < 0.01 0.05
Discussion
The development of babesiosis in dogs is a complex process which is determined by a number of biological, natural-climatic and socioeconomic factors (Iguchi et al., 2014). The pathogenesis of this disease is determined by the specific type of pathogen and the corresponding reactions occurring in the organism of the affected animal, which, in turn, depend on the biology and life cycle of the Babesia canis and the conditions in which the interaction of the macro- and microorganism occurs (Al Izzi et al., 2013; Bajer et al., 2016; Piane et al., 2016). The peculiarity of the pathogenesis of the disease is the reproduction of the causative agent of babesiosis in the organism of a susceptible animal inside the erythrocytes of the capillaries in the internal organs, and then in the erythrocytes of the blood stream. Parasites are feeding in red blood cells through osmosis. The metabolites of parasites that have been excreted during this, cause a violation of the function of the organs of the hematopoesis of the host, disturbed blood circulation, etc. That is why the leading role in pathogenesis is given to the destruction of erythro-cytes and as a consequence - the development of anemia. The destruct-tion of red blood cells occurs in the spleen, which leads to the appearance of blood in the free hemoglobin, which is excreted in the urine in the unchanged form or in the form of urobilinogen. Thus, for babesiosis, changes in the functions of the circulatory system, especially the morphological composition of blood, are adaptive (Di Mauro & Schoeffler, 2016).
As a result of hemoglobin destruction, endogenous siderosis develops, as indicated by the increased content of ferrum in serum. This can cause the trapping of the trace element in the liver and kidneys and the development of hemochromatosis. Thus, in dogs with babesiosis, rege-nerative-macrocytic anemia develops, which is accompanied by oligo-cythemia, oligochromia, macrocytosis, reticulocytosis, thrombocytopenia, and elevated erythrocyte sedimentation rate (ESR). At the same time, the decrease in the number of erythrocytes prevailed over the decrease in the content of hemoglobin, which gives grounds to consider such a process as hemolytic (Sunaga et al., 2013).
In dogs with babesiosis at the first stages of the disease, poikilocy-tosis with the presence of echinocytes and acanthocytes (spherical stellate cells), and stomatocytes (pelori in the form of a slit) were detected. The third stage of the disease was characterized by schizocytes (fractures of red blood cells) and basophilic granularity of erythrocytes.
Hypoxia and intoxication caused by metabolites of babesia lead to dystrophic changes in hepatocytes and disturbance of their bilirubin and protein-synthesizing functions (Crnogaj et al., 2017). It is known from literary sources that merozoites of the pathogen bind to the receptors of the caudal-lateral surface in the hepatocytes due to the presence of a protein in them, which is homologous to the connecting portion of the thrombospondin in hepatocytes. Inside the liver cell, the parasite rapidly breeds and merozoites, formed in large numbers, break the hepatocyte. Bloodparasites have a destructive effect on the vessels, including the vessels of the portal system. Violation of blood circulation in the liver leads to increased portal pressure accordingly the slowing of blood flow (Zygner et al., 2012; Sunaga et al., 2013).
Pathomorphological changes in the liver are characterized by a dis-complexation of the liver beams, granular dystrophy, hepatocyte necrosis. Due to babesiosis, a mixed - hemolytic-parenchymal jaundice with a sign of cholestasis develops. The severity of the disease is determined by the presence and intensity ofjaundice. The most informative indicator
of the early stages of the development of liver disease is hyperferment-emia; the more severe degree of damage to hepatocytes is shown by hypo- and dysproteinemia.
Conclusions
In dogs of service breeds from different age groups with babesiosis we found oligocytemia with anisocytosis and poikilocytosis, oligochromemia, decreased hematocrit index and macrocytosis. We detected significant changes in the morpho-functional state of erythrocytes in dogs of both age groups due to the catabolic effect of ultramicroscopic invasion on their membranes and the processes of erythrocytopoesis. In dogs with babesiosis, the population (age) composition of erythrocytes varies: the number of "old" erythrocytes increases (they are rapidly destroyed) and the "young" forms of red blood cells (which do not completely provide tissue with oxygen) are reduced. It is, in turn, reflected in the acid resistance of the "red" cells and reduction in the time of hemolysis. The undeniable proof of the work of erythron and processes of transfusion of gases in the body is the ferrum-transferrin complex. As a result of its study in dogs with babesiosis from both age groups, an increase in the level of free ferrum (UIBC) was found and a reduction in the saturation of transferrin with this trace element, which makes it impossible to form hemoglobin molecules in the bone marrow.
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