Introduction. Hypofibrinogenemia is a rare coagulation disorder characterized by reduced plasma fibrinogen levels and an increased risk of hemorrhagic complications. Inherited forms, caused by mutations in the FGA, FGB, or FGG genes, have an estimated prevalence of 1:500,000 and often remain undiagnosed due to an asymptomatic course.Aim. To present a rare clinical case of hereditary hypofibrinogenemia with a paucisymptomatic course in a child, in order to address challenges in diagnosis, long-term follow-up, and determining indications for prophylactic therapy to prevent hemorrhagic complications.Materials and Methods. We report a clinical case of hereditary hypofibrinogenemia in an 8-year-old child. The diagnosis was suspected incidentally during a routine pediatric examination. The diagnosis was subsequently confirmed by a hematologist based on persistently low fibrinogen levels, a positive family history (maternal hereditary hypofibrinogenemia), and genetic testing. Differential diagnosis with acquired forms of hypofibrinogenemia was performed based on clinical and laboratory evaluation, including complete blood count, coagulogram, aggregatogram, biochemical parameters, and instrumental studies.Results. The key feature of this case was the mild clinical presentation, which included a neonatal cephalohematoma, a single episode of blood in stool, and rare epistaxis. This aligns with literature data on the highly variable phenotypic expressivity of hypofibrinogenemia. The importance of a detailed family history and genetic testing in diagnosing inherited coagulopathies, even in the absence of overt bleeding, is emphasized.Conclusion. This case highlights the need for physician vigilance regarding inherited coagulation disorders in patients with abnormal coagulation test results, even in the absence of significant clinical symptoms. The development and implementation of strategies for long-term patient monitoring and the prevention of potential hemostasis-related risks are of paramount importance.
Background. Hereditary Tyrosinemia Type 1 (HT1) is an orphan disease belonging to the group of amino acid metabolism disorders, with an autosomal recessive pattern of inheritance. It is caused by a mutation in the FAH gene, which encodes the enzyme fumarylacetoacetate hydrolase. The clinical presentation is polymorphic. Diagnosis is based on the detection of specific metabolites in biological samples and molecular genetic testing. Early diagnosis determines the effectiveness of therapy and the prognosis of the disease.Clinical case description. We present a clinical case of early detection of HT1 in a female newborn through expanded neonatal screening. The clinical picture was characterized by hepatomegaly, coagulopathy, and specific biomarkers, including elevated levels of succinylacetone in the blood. This finding served as the basis for immediate initiation of nitisinone therapy and an individually calculated low protein diet supplemented with a specialized amino acid mixture. Molecular genetic testing confirmed the diagnosis: a previously described pathogenic nucleotide sequence variant, chr15:80181069G>C in the FAH gene in a homo/hemizygous state, was identified. This variant leads to a missense substitution c.1090G>C, p.(Glu364Gln). During the follow up period, the patient has shown a favorable course of the disease.Conclusion. Early diagnosis of HT1 based on specific succinylacetone screening and timely initiation of pathogenetic therapy combined with dietary management ensure a favorable prognosis for the disease.
Background. One of the key factors in triggering the hyperinflammation cascade in patients with bronchial asthma and COVID-19 is the activation of NLRP3 cytosolic complexes and the GSDMD proteins by SARS-CoV-2, which are effector molecules for the lytic and inflammatory forms of pyroptosis.Aim. To determine prognostic criteria for worsening of mild bronchial asthma following an infectious disease caused by SARS-CoV-2.Materials and Methods. In patients with mild, partially controlled bronchial asthma (n = 86), who were divided into 2 groups: asthma without COVID-19 (n = 34) and asthma following mild COVID-19 (n = 52), peripheral blood inflammatory markers were evaluated. The patients were examined immediately after recovery and confirmation of a negative SARS-COV-2 test result, and six months post-infection. The control group included conditionally healthy volunteers (n = 15) with no history of COVID-19. Pulmonary function was monitored by measuring FVCL, OFV1, and OFV1/FVCL. NLRP3 and gasdermin D inflammasomes were measured by enzyme-linked immunosorbent assay.Results. The study revealed that in a number of patients with mild asthma, who had post-COVID conditions 6 months after COVID 19, there were elevated levels of NLRP3 inflammasome and gasdermin D (GSDMD), as well as a decreased pulmonary function, indicating a hyperinflammatory process. A predictive model for worsening of mild asthma after COVID-19 was developed: concurrent elevation of NLRP3 > 0.04 ng/ml and GSDMD > 0.38 ng/ml levels during the convalescence period serves as a marker of a high risk of post-COVID complications.Conclusion. The role of NLRP3 and GSDMD in exacerbating the course of asthma after COVID-19 has been established, and predictive threshold values of biomarkers in this patient population have been identified.
Background. The paper describes a method of low intensity photodynamic therapy (LIPDT) for the treatment of superficial basal cell skin cancer (SBCSC) stage I using topical application of the photosensitizer Photoditazine gel® or intravenous Photoditazine® solution. LIPDT is the treatment of choice in medical organizations lacking laser equipment, specialized facilities, or for remote use (in distant areas). It can also be used as an adjunct to other treatment methods.Aim. To provide a theoretical rationale for the use of a LIPDT device with Photoditazine® and Photoditazine gel® for the treatment of SBCSC.Materials and methods. The developed device consists of the following elements: a battery, a control board, a DC-DC voltage converter, a microcontroller, a driver, and an LED matrix. The mechanism of the device is based on the classical PDT method but has several key differences: automatic mode (eliminating the need for manual adjustment), low output radiation power (which prevents oxygen depletion in tumor tissue), and the ability to function under conditions unsuitable for standard PDT.Conclusion. The proposed LIPDT method for treating stage I SBCSC will reduce treatment costs while maintaining the effectiveness of the existing standard PDT method.
Background. In more than 30 % of cases, infertility is attributed to male factors. The diagnosis of male infertility is based on semen analysis. The assessed semen parameters include sperm concentration, motility, and morphology. Laboratory animal models enable the study of various biological processes, including the effects of external and internal factors on reproduction processes. However, to date, there is no simple, safe, non-terminal method for sperm collection in animals.Aim. To develop a non-terminal sperm collection technique using optimal electrical stimulation parameters in Wistar rats to study the influence of environmental factors on the reproductive function.Materials and methods. The study was performed on 30 male Wistar rats weighing 280–300 g. For sperm collection, a rectal electrical stimulator was used to obtain ejaculate. A hemocytometer and two types of microscopes were used for sperm analysis and counting: a Micromed P-1 LED (Russia) and a Levenhuk D90L LCD digital microscope (China).Results. All animals were divided into 6 groups of five individuals each, according to the electrical stimulation protocol. All stimulation protocols resulted in erection in all groups of animals. However, the safest and most cell-saving method was found to be rectal electrical stimulation of the seminal colliculus of rats at settings of 60 Hz and 4 V.Conclusion. A method for sperm collection in Wistar rats with an optimized electrical stimulation protocol has been developed, enabling the study of various factors affecting male fertility.
Background. Avian paramyxoviruses (subfamily Avulavirinae) are widespread avian pathogens that constantly circulate in wild and domestic animal populations. The subfamily Avulavirinae is divided into 3 genera, comprising 22 species. Epizootic surveillance of avulaviruses is conducted worldwide and is of critical importance due to their rapid spread via bird migrations. Avian viruses can cause significant economic damage to the poultry industry both in developing countries and in regions with sustainable economic development. Their infectious potential is of great interest and remains poorly understood.The majority of intercontinental flyways of migratory birds pass through the territory of continental Eurasia, where large numbers of migratory birds congregate in confined areas during stopovers, nesting and wintering. This creates favorable conditions for virus transmission and the emergence of new genetic variants.Aim. To analyze the species distribution of paramyxoviruses in wild birds across continental Eurasia.Materials and Methods. As a result of long-term studies of viruses in wild bird populations across continental Eurasia, avian avulavirus isolates were obtained.Results. Avian avulavirus isolates of APMV -1, -3, -4, -6, -8, -9, -11, -12, -13, -16, -20, and -21 were obtained. APMV-1 and APMV-4 were detected throughout Eurasia, most frequently in Anseriformes. APMV-3, -6, -9, -11, and -12 were recorded in the European part of Eurasia, APMV-8, -13, and -20 in its central part, and APMV-6, -16, and -21 in the Asian part, in Anseriformes, Passeriformes, Charadriiformes, Ciconiiformes, and Psittaciformes.
Background. Currently, the main groups of anti-inflammatory drugs used in medical practice are steroidal (glucocorticoids) and non-steroidal agents. However, despite their widespread use, these groups of anti-inflammatory drugs have a fairly wide range of negative side effects, which makes the search for low-toxic substances with anti-inflammatory effects currently relevant.The aim. To study anti-inflammatory, antinociceptive activity and acute toxicity of individual representatives of indenopyrroles and indenopyridazines.Methods. The acute toxicity of the studied compounds was studied using the method of Prozorovsky VB. Anti-inflammatory activity was assessed in a carrageenan-induced rat paw edema model. The production of active oxygen radicals by leukocytes was evaluated using luminol-dependent chemiluminescence. The antinociceptive activity of the compounds was assessed using the “writhing” and “hot plate” tests in mice.Results. The obtained results allowed the studied compounds to be classified as “practically nontoxic” (LD50 > 1000 mg/kg). Compounds 1в of the indenopyrrole series and indenopyridazines 2а-в were found to exhibit anti-inflammatory activity, reducing the severity of exudative inflammation. Compound 2a exhibited the greatest antiexudative activity, reducing edema by more than 60 % (p < 0.01). Compounds 2a-в and compound 1в reduced the production of reactive oxygen species by more than 40 % (p < 0.05) compared to the control. In the “hot plate” test, the studied compounds 1a, 1в, 2a-в exhibited an antinociceptive effect comparable to nimesulide; in the “acetic acid-induced writhing” test, the effect of compounds 1a, 2б, 2в was comparable to nimesulide, and the effect of compound 2a exceeded the comparison drug by 32.96 % (p < 0.05).Conclusion. The studied compounds of the indenopyrrole series and their indenopyridazine derivatives are virtually non-toxic compounds, exhibit an anti-inflammatory effect and reduce the severity of pain associated with inflammation.
Background. Maturation of the intestinal epithelial barrier in early life is accompanied by variability in biomarkers of enterocyte injury and permeability. However, longitudinal serum profiles of I-FABP and claudin-2 in seemingly healthy children, including those born preterm, remain insufficiently studied.Aim. To assess the dynamics of serum I-FABP and claudin-2 concentrations in children born at 34–41 weeks’ gestation during the first 24 months of life, with consideration of gestational age.Methods. This prospective observational cohort study included three time points: up to 7 days; 1–1.5 months/postmenstrual age (PMA) 40–41 weeks; and 18–24 months. At time points 1–2, 98 newborns were enrolled; by time point 3, follow-up was completed in 88 children: preterm (34–36 weeks, n = 30) and term (37–41 weeks, n = 58). Loss to follow-up was 10.2 % (n = 10). I-FABP and claudin-2 were measured by ELISA.Results. I-FABP remained stable during the first 1–1.5 months and increased by the second year of life: in preterm children 1.12 [1.07; 1.30] – 1.30 [0.97; 1.87] – 6.09 [3.18; 6.65] ng/mL (p < 0.001), and in term children 1.10 [0.80; 1.95] – 1.21 [0.92; 1.73] – 3.89 [2.33; 6.10] ng/mL (p < 0.001); no between-group differences were observed at the respective time points (p = 0.738; 0.610; 0.131). In preterm children, claudin-2 did not change significantly: 6.76 [3.00; 9.14] – 7.59 [5.20; 10.96] – 7.77 [6.33; 9.20] ng/mL (p = 0.497).In term children, claudin-2 increased: 1.85 [1.02; 5.22] – 5.10 [3.47; 8.31] – 7.95 [6.32; 11.28] ng/mL (p < 0.001). At time points 1–2, claudin-2 values were higher in preterm than in term children (p = 0.006; p = 0.009), whereas at time point 3 they were comparable (p = 0.326).Conclusions. Within the 34–41-week gestational range, gestational age does not determine I-FABP levels, whereas claudin-2 is gestational age-dependent. Interpretation of these biomarkers requires consideration of both chronological age and gestational age.
Restless legs syndrome (RLS) is a common sensorimotor neurological disorder that significantly disrupts sleep and is associated with an increased risk of chronic noncommunicable diseases. RLS is considered a common movement disorder, occurring approximately 50 % more frequently in women and in individuals of European descent. The etiology of the disease remains unknown. The pathophysiology of RLS is also not fully understood. Dopaminergic dysfunction is a key feature of RLS. Since its discovery, the role of iron deficiency has been emphasized, not iron levels in the peripheral blood, but rather its concentration in the central nervous system. The hyperdopaminergic state in RLS can lead to decreased endogenous opioid levels, which may contribute to impaired sensory processing. Overexpression of the estrogen signaling pathway has been confirmed in patients with RLS. RLS is characterized by an uncontrollable and distressing urge to move the legs and other body parts, often accompanied by unpleasant and irritating sensations. Symptoms often appear or worsen in the evening and at night and are relieved by voluntary movement. Currently, the diagnosis of RLS is based on the clinical picture, and therefore criteria have been developed for a more objective diagnosis. Non-pharmacological treatments include sleep hygiene, moderate-intensity exercise, yoga, leg massage, progressive compression devices for the lower extremity muscles, and avoiding factors that aggravate RLS. The development of new medications for the treatment of RLS has been somewhat delayed due to a limited understanding of its pathophysiology. Dopaminergic agonists, α2δ calcium channel ligands, and opioids are used in the treatment of RLS. The disorder is under-recognized by physicians and often remains undiagnosed. RLS is a treatable disease, but the risk of augmentation during drug therapy makes it necessary to develop effective non-drug treatment methods.
Background. Maintaining cognitive health and preventing dementia are priorities in modern medicine and science. Nootropics play an important role in neuroprotection. Multicomponent herbal remedies containing medicinal plant extracts hold promise as phytopharmacological regulatory systems for maintaining and restoring cognitive health.Aim. To analyze the psychophysiological characteristics of cognitive functions in middle-aged and older adults and to assess the effect of a phytoconstituent with nootropic properties on these characteristics.Materials and methods. Before and after a course of treatment with the phytoconstituent, participants underwent a comprehensive examination that included electrocardiography with heart rate variability assessment; evaluation of short-term and longterm memory using the “10-Word Memorization” test by A.R. Luria; and assessment of logical thinking using the “Complex Analogies” test.Results. The study identified two groups of participants: those with moderate and those with high levels of working memory and logical thinking. Group 1 was characterized by low parasympathetic nervous system markers and reduced heart rate variability. Group 2 demonstrated higher heart rate variability and elevated parasympathetic markers. After administration of the phytoconstituent, parasympathetic activity markers (RMSSD, HFmc2, HF%) increased in Cluster 1 and decreased in Cluster 2. Following the course of the phytoconstituent, Group 1 exhibited a more pronounced improvement in memory indices and logical reasoning abilities.Conclusion. An association was found between high levels of working memory and logical thinking and a predominance of parasympathetic influences on heart rhythm. Administration of the herbal preparation with nootropic properties resulted in improved cognitive function and a balanced autonomic nervous system.
Background. The accurate determination of human coronary artery (HCA) diameters plays a pivotal role in the diagnosis, risk assessment, and treatment planning of ischemic heart disease. Given that vascular networks possess a fractal structure and consist of arterial bifurcations (AB), a critical task is the prediction of the diameters of daughter (distal) arterial segments (AS) based on the known diameter of the mother (proximal) AS. Existing numerical modeling methods (ENMM) for predicting arterial diameters rely on approximate analytical dependencies derived empirically.Aim. To conduct a comparative analysis of the results of predicting diameters of daughter segments (bifurcation components) obtained using Graph Neural Networks and known numerical modeling methods based on morphometric data of real healthy human coronary arteries.Methods. To achieve this objective, various GNN architectures were implemented and tested: GCN, GraphSAGE, GAT, and TransformerConv. Additionally, ENMM and a Multilayer Perceptron (MLP) were evaluated. A comparative statistical analysis of the results was conducted. The study utilized previously obtained morphometric data on the internal diameters of AS comprising 30 corrosion cast graphs of healthy HCAs. Results. This study proposes the use of GNNs for this specific task for the first time. Comparative analysis demonstrated that all GNN models surpassed both ENMM and the Multilayer Perceptron in accuracy when predicting the diameters of smaller-caliber daughter AS. The TransformerConv architecture demonstrated the best performance, achieving a coefficient of determination R2 = 0.96 and RMSE = 0.199 for predicting the larger daughter segment diameter, and R2 = 0.76 and RMSE = 0.221 for the smaller segment.Conclusion. The developed models may serve as the foundation for creating clinical decision support systems, enabling more precise assessments of the structural status of human coronary arteries.
Background. The COVID-19 pandemic and the associated non-pharmaceutical interventions (NPIs) significantly altered the global epidemiology of various infectious diseases. Studying the dynamics of hospitalizations for acute intestinal infections in a specific region during different periods of the pandemic allows for assessment of the effect of these measures and identification of patterns in the recovery of the epidemic process. Aim. To evaluate the impact of the COVID-19 pandemic on the dynamics and structure of hospitalizations of children with acute intestinal infections (AII), including rotavirus infection (RVI), in Chita over the period 2014–2023.Materials and Methods. A retrospective analysis of statistical reporting data from the Regional Clinical Infectious Diseases Hospital in Chita was conducted. A total of 11,520 hospitalization cases of children aged 0–17 years with AII over a 10-year period were analyzed. Descriptive and non-parametric statistical methods were used, including time series analysis, the χ2 test, the φ-coefficient, and Spearman’s correlation analysis. Data processing was performed using IBM SPSS Statistics 26.Results. During the peak pandemic period (2020–2021), the number of hospitalizations for AII decreased 1.6-fold (χ2 = 9.680; p = 0.002), and for RVI – 1.4-fold (χ2 = 23.955; p < 0.001) compared to the pre-pandemic period. The etiological structure of AII did not change significantly: the proportion of RVI among all cases was 24.48 % (pre-pandemic), 23.68 % (peak pandemic), and 22.87 % (post-pandemic) (p > 0.05). A strong positive correlation was found between the total number of AII hospitalizations and RVI cases (r = 0.789; p = 0.008). In the post-restriction period (2022–2023), an increase in hospitalizations was observed.Conclusions. The anti-epidemic measures during the COVID-19 pandemic led to a significant reduction in hospitalizations for AII and RVI without affecting their etiological structure. The subsequent increase in incidence following the lifting of restrictions confirms the restoration of the epidemic process, which underscores the need for ongoing epidemiological surveillance and the expansion of vaccination programs.
Background. Despite the increasing prevalence of emotional overeating and obesity, the specific neurohormonal mechanisms involved in the pathogenesis of these pathological processes remain poorly understood. The incretin system may serve as an important therapeutic target for the correction of these eating disorders.Aim. To study the effects of the dual GIP/GLP-1 receptor agonist tirzepatide on feeding behavior parameters in a rat model of emotional overeating induced by intracranial self-stimulation (ICSS).Methods. Experiments were performed on male Wistar rats with electrodes implanted in the ventral tegmental area. Tirzepatide was administered subcutaneously at doses of 0.05, 0.10, and 0.30 mg/kg for 7 days. Food intake (number of seeds consumed) was assessed at 1 minute, 30 minutes, and on days 3 and 7 after administration.Results. No statistically significant changes in feeding activity were observed 30 minutes after tirzepatide administration. On the third day, a decrease in food intake was observed only at the maximum dose (0.30 mg/kg). On the seventh day, a significant anorexigenic effect was observed at doses of 0.10 and 0.30 mg/kg, indicating a doseand time-dependent effect.Conclusion. Tirzepatide does not exert a significant acute effect on feeding activity in the emotional overeating model at 30 minutes after administration. Repeated administration of the drug revealed a doseand time-dependent anorexigenic effect, manifested by a decrease in food intake on days 3 and 7 of the experiment. The most pronounced decrease in feeding activity was observed at doses of 0.10 and 0.30 mg/kg on day 7.
Background. Ongoing research is investigating the interaction between mycobacteria and macrophages. Upon infection with mycobacteria, macrophages release cytokines. These include IFNy, TNF, IL-1, IL-6, and IL-12p40, among others. These substances play a critical role in the host response to tuberculosis and other mycobacterial infections. Aim. To investigate and compare the cytokine patterns produced by human macrophages in response to interaction with antigens from both pathogenic and conditionally pathogenic mycobacterial strains in vitro.Methods. Blood monocytes were cultured for five days in the presence of 10 % active human serum. The resulting macrophages were then cultured with mycobacterial antigens from Mycobacterium tuberculosis, Mycobacterium avium, and Mycobacterium kansasii for 24 hours. Changes in macrophage gene expression profiles and the production of pro-inflammatory and anti-inflammatory cytokines were then assessed. A control group of “naive” macrophages cultured without any mycobacterial antigen was also used.Results. Stimulation of human macrophages with antigens from different mycobacterial species resulted in the formation of distinct cell phenotypes: protective (M. tuberculosis), characterized by the expression of IL6, IFNG, and TNF; pro-inflammatory (M. kansasii), with active expression of IL6, IL1B, and TNF; and pro-inflammatory (M. avium), expressing IL6 and IL12. The cytokine production findings were fully consistent with the gene expression data.Conclusion. These findings on macrophage-mycobacterial antigen interactions provide insight into the mechanisms by which both tuberculous and nontuberculous mycobacterial infections establish chronic macrophage infection.
Background. The challenges of organizing tuberculosis detection in sparsely populated areas are primarily associated with poor transportation access and a shortage of medical personnel. Under these conditions, the implementation of modern information technologies in clinical and radiological screening for the disease becomes highly relevant.Aim. To optimize methods for the detection and diagnosis of pulmonary tuberculosis using information technologies in the sparsely populated territory of the Republic of Sakha (Yakutia).Methods. A pilot study was conducted in seven medical organizations of the Republic of Sakha (Yakutia) to test a two-component organizational model for clinical and radiological tuberculosis screening utilizing information technologies: a central medical image archive and telemedicine for remote diagnosis, as well as artificial intelligence for double reading of fluorograms. Effectiveness was assessed by monthly monitoring of population coverage with fluorographic examinations, measuring the time spent on double reading of fluorograms, and assessing the time to tuberculosis diagnosis.Results. The pilot implementation of the two-component organizational model for clinical and radiological tuberculosis screening, employing information technologies and artificial intelligence in medical organizations, led to increased fluorographic examination coverage of the general population and individuals at risk for tuberculosis. This implementation also reduced the time required for double reading of fluorograms and shortened tuberculosis diagnostic timelines, both in the general medical network and at the specialized tuberculosis service level. Considering the specific characteristics of tuberculosis detection organization across different socio-territorial zones of the Far North, a model for clinical and radiological screening of pulmonary tuberculosis was developed. This model comprises two organizational variants tailored for use in the Arctic and industrial zones. The model consists of three stages (radiological, clinical, and specialized) implemented at the level of the central district hospital departments.Conclusion. The proposed model for tuberculosis screening using information technologies is recommended for implementation in sparsely populated districts of the Far North.
Background. Restrictions on the use of gadolinium-containing radiocontrast agents due to the risk of acute and long-term complications drive the search for new, safer, and more effective gadolinium-based nanoparticle formulations.Aim. Comparative assessment of the magnetocontrast properties of a gadolinium nanocomposite and a gadolinium-based contrast agent.Methods. The dynamics of organ accumulation and visual MRI patterns were studied in 5 healthy female Wistar rats using a Siemens Avanto device with a magnetic field of 1.5 T. Anesthetized animals were placed in a ventral position within the head coil, after which a preliminary MRI scan was performed. A gadolinium nanocomposite solution and a reference agent (Omniscan®) were injected at equivalent gadolinium doses into the lateral tail vein or into the abdominal cavity, followed by repeat MRI scans with image acquisition every 2–3 minutes. The primary imaging areas were the abdominal cavity and retroperitoneal space, including the thoracic cavity.Results. Comparative analysis showed that gadolinium nanoparticles stabilized with arabinogalactan exhibit magnetocontrast properties, as evidenced by T1-weighted image enhancement of the liver parenchyma after intravenous administration and of the abdominal cavity after intraperitoneal administration. The magnetocontrast image of the kidneys and bladder was higher after Omniscan® administration than after gadolinium nanocomposite administration. However, the maximum contrast coefficient of the gadolinium nanocomposite in the liver parenchyma increased by 20 % compared to baseline. Omniscan® administration resulted in a 13 % increase in T1-weighted image intensity of the liver parenchyma.
Men over the age of 45 are a socially significant group, most of whom have reached professional maturity and make a significant contribution to the country’s economy and their families. In the Arkhangelsk Region, the health status of 40–45-year-old men (57 %) is characterized by cardiovascular pathology, 14.7 % – by gastrointestinal pathology, 47.4 % – by bronchopulmonary pathology, and 17.0 % – by musculoskeletal disorders. Male specialists from the Hydrographic Service in Arkhangelsk carry out planned and special hydrographic works during the navigation period on a rotational basis, making short-term frequent trips of 16 days in the Northern Seas.The aim. To analyze the features of leukocyte content and phagocytosis in hydrographers of the Arkhangelsk region of the Hydrographic Service of the Russian Federation, taking into account their age and work experience in the northern seas.Materials and methods. Thirty-six men working in the hydrographic service of the Federation Council of the Russian Federation were examined with short 16-day shifts: 15 men aged 30–40 with 10 years of work experience and 21 men aged 50–65 with 20 years of work experience. The leukocytes count and phagocytosis in peripheral venous blood were determined, taking into account age and work experience. For statistical processing, Microsoft Excel 2010 and SPSS 20.0 for Windows were used as software packages.Results. It has been established that hydrographers of the younger age group with 10 years of work experience have a 1.5–2 times higher incidence of leukocyte, lymphocyte, and monocyte deficiency, which is associated with low phagocytosis activity. In the older age group of individuals with 20 years of work experience, leukocytosis, lymphocytosis, and monocytosis are recorded 1.5 times more frequently against the background of increased phagocytosis activity.Conclusion. The phagocytic activity of neutrophils is higher in the older age group with 20 years of experience in extreme conditions.
Background. Ischemic stroke (IS) remains one of the leading causes of death and disability worldwide. Due to the limitations of oral and parenteral routes of neuroprotectant administration in post-stroke patients, the use of rectal suppositories with melatonin (MT) is a promising direction for neuroprotective therapy.Aim. To evaluate the effect of rectal suppositories containing MT on the dynamics of neurological status and products of oxidative protein modification in experimental acute cerebral ischemia (EACI).Materials and methods. Male Wistar rats (n = 30) were divided into 3 groups: I – sham-operated animals; II – animals with EACI according to the method of Chen S.T. et al.; III – animals with EACI that received rectal suppositories weighing 100 mg, containing 2.5 mg of MT. Neurological status was assessed on days 3 and 7 using the Garcia J.N. scale, the paw placement test, and the Bederson test. In the ischemic focus of the brain (IFB), the content of early and late products of protein oxidative modification (POM) was evaluated.Results. In rats with EACI, neurological deficits developed on the corresponding day (decreased scores on the Garcia J.N. scale and the paw placement test, increased scores on the Bederson test) and an increase in the content of POM products in the IFB. Administration of MT suppositories contributed to the regression of these disorders: by day 7, there was an improvement in all neurological tests, and a decrease in POM products in the IFB.Conclusions. The results obtained suggest that the neuroprotective effect of MT in the form of rectal suppositories in EACI is mediated through an antioxidant mechanism of action.
