Opera Medica et Physiologica

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Full-length research paper
Printed March 03, 2025;
Published ahead of print March 03, 2025; Printed March 03, 2025; OM&P 2025 Volume 12 Issue 1, pages 66-71; doi:10.24412/2500-2295-2025-1-66-71
Abstract Full Text

Aim: the effect of cryopreservation and molecular hydrogen (Н2) on the sperm quality characteristics, metabolic, oxidative and antioxidant indices of spermatozoa. Sperm diluted with BioXcell diluent, sperm after cryopreservation and sperm after cryopreservation with Н2 were studied as comparison groups. Qualitative indices of spermatozoa, intensity of free-radical processes, activity of antioxidant enzymes and ATP concentration were measured in all groups. Lipoperoxidation was found to be reduced, and antioxidant activity was increased in sperm after cryopreservation with Н2. It was shown that the content of diene, triene conjugates, malonicdialdehyde decreased in spermatozoa and the activity of superoxidedismutase and catalase increased in sperm after cryopreservation with Н2. Reduction of oxidative processes under the action of Н2 was accompanied by an increase in the concentration of ATP in spermatozoa. After thawing, a significant preservation of spermatozoa motility was recorded under H2 action compared to the group without H2. Thus, H2 is effective in its ability to quench reactive oxygen species and thereby protect spermatozoa from the effects of oxidative stress during cryoconservation. These properties of H2 protect spermatozoa at low temperatures and determine the preservation of high functional activity of spermatozoa after thawing.

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07_66-71.pdf632.34 KB

Full-length research paper
Printed March 03, 2025;
Published ahead of print March 03, 2025; Printed March 03, 2025; OM&P 2025 Volume 12 Issue 1, pages 58-65; doi:10.24412/2500-2295-2025-1-58-65
Abstract Full Text

Helicobacter pylori (H. pylori) is a bacterium distributed worldwide and common in developing countries. In addition to its gastric manifestation, it has a potential role in the development of non-digestive tract disorders like cardiovascular diseases including dyslipidemia, diabetes, obesity, hypertension, chronic kidney disease, and liver disease. It is unclear whether diabetics are more liable for H. pylori infection or whether H. pylori infection raises the risk of diabetes. This study aims to evaluate the glycemic measures in patients having gastritis with and without H. pylori. A community-based cohort study was carried out on patients diagnosed with gastritis by gastroscopy examination. Our sample was divided into H. P-positive group (150 female & 155 male) and H. P-negative group (175 female & 68 male). Diagnosis of Helicobacter pylori infection was done by 13C urea breath test. A control group (60 female and 60 male) that had neither gastritis nor H.P infection were included in this study. Laboratory investigations were performed after a 10 h fast, including fasting blood glucose (mg/dl), fasting serum insulin (IU/ml), HbA1c and 2h postprandial plasma glucose. HOMA-IR index was used to study the relation between Helicobacter pylori and insulin resistance. Helicobacter pylori infection was significantly associated (p < 0.05) with glycemic measures in patients with gastritis. In gastritis with and without Helicobacter pylori, glycemic measures were significantly (p < 0.05) increased in females. It can be concluded that by causing insulin resistance, H. pylori contributes to diabetes and may be magnified to promote long-term diabetes.

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06_58-65.pdf837.43 KB

Full-length research paper
Printed March 03, 2025;
Published ahead of print March 03, 2025; Printed March 03, 2025; OM&P 2025 Volume 12 Issue 1, pages 48-57; doi:10.24412/2500-2295-2025-1-48-57
Abstract Full Text

Hexavalent chromium Cr (VI) causes reactive stress and inflammation in the heart; hence this study examines how oxidative stress from Cr (VI) affects the circulatory system and the inflammatory and oxidative processes that generate it. Fifty mice were split into five groups. One group was a control, while four received oral Cr (VI) (5 mg, 10 mg, 20 mg, and 50 mg) daily for 30 days. At the conclusion of the study, blood concentrations of ATP, troponin I, and CK-MB were assessed for cardiac injury. To assess oxidative stress, glutathione (GSH), superoxide dismutase (SOD), malondialdehyde (MDA), and catalase (CAT) were examined. Inflammatory biomarkers, including tumor necrosis factor-alpha (TNF-α) and interleukin-1 beta (IL-1β), were identified in a composite of cardiac tissue. Significant cardiac injury and reactive stress were evidenced by the substantial increases in CK-MB, troponin I, and MDA levels in relation to dosage. Antioxidant markers like CAT, SOD, and GSH went down a lot, which means the body's antioxidant defenses were not as strong as they used to be. Increased TNF-α and IL-1β levels, particularly with larger Cr (VI) doses, indicated an inflammatory response. Research demonstrates that Cr (VI) causes oxidative stress and inflammation in the heart, which worsens with greater doses. This study shows how important it's to find more safety drugs that can protect the heart from the damage that Cr (VI) does.

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05_48-57.pdf642.86 KB

Full-length research paper
Printed March 03, 2025;
Published ahead of print March 03, 2025; Printed March 03, 2025; OM&P 2025 Volume 12 Issue 1, pages 38-47; doi:10.24412/2500-2295-2025-1-38-47
Abstract Full Text

The Epstein-Barr virus (EBV) is an oncogenic virus that persists in a latent state within B-lymphocyte cells. This virus has been associated with numerous forms of haematologic malignancies, including leukaemia. The focus has been on the association between single nucleotide polymorphisms (SNPs), such as those in Interleukin-10, and leukaemia patients. The enzyme-linked immunosorbent assay (ELISA) was employed to identify Epstein-Barr virus EBNA-1-IgG, whereas the Sanger sequencing approach was utilised to detect Interleukin-10 SNPs. This study aimed to ascertain the presence of Epstein-Barr virus EBNA-1-IgG in patients with acute lymphocytic leukaemia and to investigate Interleukin-10 single nucleotide polymorphisms (SNPs) -819T˃C (rs1800871) and -592A˃C (rs1800872) in patients with acute lymphoblastic leukaemia. The statistical examination of the immunological assay indicated no significant difference between the proportion of patients positive for EBV EBNA-1-IgG and the positive controls. The statistical analysis reveals a substantial disparity in the proportion of CC genotype carriers at IL10 -819T˃C (rs1800871) between patients and controls within the molecular study framework. A notable difference was seen in the prevalence of TC genotype carriers at IL10 -819T˃C (rs1800871) between patients and controls. A significant difference was observed between healthy controls and patients with AC, AA, and CC genotype carriers at IL10 -592A>C (rs1800872). This study illustrates the notable prevalence of Epstein-Barr virus (EBV) in individuals with acute lymphoblastic leukaemia. This study demonstrates the association between acute lymphoblastic leukaemia and the CC and TC genotypes at IL10-819T˃C (rs1800871), along with the AC, CC, and AA genotypes at IL10 -592A˃C (rs1800872).

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Full-length research paper
Printed March 03, 2025;
Published ahead of print March 03, 2025; Printed March 03, 2025; OM&P 2025 Volume 12 Issue 1, pages 30-37; doi:10.24412/2500-2295-2025-1-30-37
Abstract Full Text

Background: acute myeloid leukemia (AML) is characterized as an aggressive blood cancer with rapid growth of immature leukemic cells. It appears that each subtype of AML displays a distinct miRNA profile. miRNAs play a role in regulating gene expression that is implicated in AML pathogenesis. This study was designed to assess the level of miRNA-155 gene expression in relation to chemotherapy resistance in various AML patient groups, with the hope of developing a novel marker for targeted therapy and early diagnosis and prognosis of cancer stem cells in AML patient. Methods: 120 AML cases were studied. Based on chemotherapy stage, 40 patients were assigned to each group (newly diagnosed, under treatment, and relapsed). Baghdad Teaching Hospital (Iraq) provided the cases and samples from February 2022 to April 2023. This study also included 40 healthy controls. The qRT-PCR method, which uses the ΔCt-value and fold change (2-ΔΔCt), was used to count the genes after they were standardized to the level of a housekeeping gene (U6). Results: in this study, significantly elevated levels of miRNA-155 were observed in AML patients compared to controls, with a higher fold change detected in the newly diagnosed group. Conclusions: upregulation of miRNA-155 is suggested to be linked to AML development and is strongly associated with the progression of leukemic stem cells. These results might serve as accurate predictors of AML and potential therapeutic targets for the elimination of LSCs.

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03_30-37.pdf790.82 KB

Full-length research paper
Printed March 03, 2025;
Published ahead of print March 03, 2025; Printed March 03, 2025; OM&P 2025 Volume 12 Issue 1, pages 20-29; doi:10.24412/2500-2295-2025-1-20-29
Abstract Full Text

Urinary bladder cancer (UBC) is the most common malignancy of urinary tract, ranking tenth worldwide. In Iraq, UBC is the seventh among 10 most prevalent cancers. This study is designed to assess the expression of CD276 in different bladder tissue specimens from Iraqi UBC patients using immunohistochemistry (IHC). A total of 70 paraffin-embedded tissue blocks of bladder cancer were collected from the archive of the Histopathology Unit of several public hospitals and private labs in Baghdad, following formal authorizations, in addition to ten biopsies of bladder tissues without significant pathology assembled from the forensic medicine department and used for comparison purposes. The results showed that the expression of CD276 was positive in 41.43% of malignant cases and negative in 100% of normal bladder tissues with significant differences of P = 0.011 between the studied groups. It can be concluded that the present investigation reported elevated expression of CD276 in Iraqi UBC patients, correlated negatively with clinical features including patients′ age, sex, tumor′s size, stage, grade, and histological type. This suggests that this marker may be considered a target molecule in diagnosis or therapy of UBC.

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02_20-29.pdf995.52 KB

Full-length research paper
Printed March 03, 2025;
Published ahead of print March 03, 2025; Printed March 03, 2025; OM&P 2025 Volume 12 Issue 1, pages 5-19; doi:10.24412/2500-2295-2025-1-5-19
Abstract Full Text

Uncontrolled cell proliferation is a hallmark of breast cancer (BC), a malignant disease that frequently results in the development of tumors. With distinct genetic profiles and clinical consequences, it has multiple molecular subtypes, such as triple-negative, HER2-positive, luminal A, and luminal B. This study investigated the relationship between the expression of the microRNAs miR-195 and miR-206 in a sample of female BC patients from Iraq and their illness features and demographic distribution. Most BC cases occur in women between the ages of 40 and 59. The study included 60 patients and 60 healthy women. There were no appreciable variations between the right and left breast placements, and the average age of BC patients was 49.27 ± 10.66. Luminal A was the most prevalent molecular subtype of invasive ductal carcinoma (IDC), which was the most prevalent kind overall. The highest rates of BC were found in stages II and III, at 40% and 36%, respectively. While there were no discernible changes between the luminal a, luminal B, and HER2 subtypes, RT-qPCR using miR-16 as an internal reference revealed that miR-195 was markedly increased in BC patients relative to controls. With no discernible variations between molecular subtypes, miR-206 was downregulated in BC patients; however, it was significantly downregulated in stages II, III, and IV in comparison to stage I. These results imply that miR-195 and miR-206 might be involved in the onset and development of BC.

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01_5-19.pdf1.75 MB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 166-198; doi:10.24412/2500-2295-2024-4-166-198
Abstract Full Text

The most complications of diabetes mellitus are associated with endothelial dysfunction, the nature of which is not fully understood. Oscillations of calcium (Ca2+) and nitric oxide (NO) concentrations may play a role in regulating endothelial functioning under normal and pathological conditions. We suHGested that changes of Ca2+ and NO oscillations characteristics in endothelial cells may play a role in the pathogenesis of diabetes mellitus complications. To test this hypothesis, we assessed the dependence on the glucose concentration (normo- and hyperglycemia) of the amplitude-frequency characteristics of Ca2+ and NO oscillations in endothelial cells from mouse skin microvessels at rest and during functional tests (heating), the effect of the vasodilator acetylcholine (ACh), insulin, as well as when blocking NOS and PI3K. Hyperglycemia changes the amplitude-frequency characteristics of Ca2+ and NO oscillations in endotheliocytes and the proportion of cells with oscillations. In addition, hyperglycemia changes the characteristics of Ca2+ and NO oscillations in endothelial cells in presence of ACh, L-NNA, wortmannin and insulin at rest (37 °C) and heating to 40 °C. It indicates the participation of TRPV-, NOS-, ACh- and PI3K-associated signaling pathways in the regulation of Ca2+ and NO oscillations in endoteliocytes in health and disease.

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17_Серов_166-198.pdf2.89 MB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 149-165; doi:10.24412/2500-2295-2024-4-149-165
Abstract Full Text

Despite the large volume of empirical data on the effects of magnetic fields on living organisms, there are almost no studies showing the possibility of the existence of magnetic effects in processes outside the cell or in vitro. The protein folding process in a cell can be sensitive to magnetic fields. We the first time experimentally demonstrated the possibility of biochemical effects of extremely low frequency magnetic fields and hypomagnetic fields on chemical renaturation using hen egg-white lysozyme as an example. The degree of lysozyme renaturation was estimated at different magnetic conditions by fluorescence intensity and enzymatic activity. The extremely low frequency magnetic field (50 Hz, 40 μT) accelerates the renaturation compared to the control and a hypomagnetic field (less than 40 nT). The effects of hypomagnetic and extremely low frequency magnetic field on the protein fluorescence spectrum were opposite. It confirms the participation of the recently described level mixing mechanism in the implementation of magnetobiological effects. The magnetic nanoparticles abolished the effects of extremely low frequency magnetic and hypomagnetic fields fluorescence and activity of lysozyme, which indicates their ability to modulate magnetobiological effects. The results obtained expand fundamental ideas about the mechanisms of action of magnetic fields on isolated protein molecules and can be useful in the practice of using magnetic nanoparticles in biomedicine.

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16_Саримов_149-165.pdf3.53 MB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 138-148; doi:10.24412/2500-2295-2024-4-138-148
Abstract Full Text

Infertility is a major public health problem worldwide and its prevalence is as high as 17, 5% depending on the population studied The research is aimed to study the possibility of using miR-20a, miR-135a, miR-34b, miR-449v, miR-449c as markers of male infertility and to evaluate the dependence of the effectiveness of ART programs on the level of expression of exosomal microRNAs. The experimental group included patients entering the program of ART (assisted reproductive technologies) with the diagnosis of idiopathic male infertility (n = 30), the control group included couples with female infertility of tubal origin (n = 19). The isolation of exosomal microRNA from ejaculate was performed using the exoRNeasy Midi regent kit. The miRCURY LNA miRNA SYBR® Green PCR System was used to evaluate the expression of the following exosomal microRNAs: miR-20a, miR-135a, miR-34b, miR-449c, miR-449c and control miR-16. The expression of exosomal miR-449c and miR-135a was significantly different in the experimental group (p = 0.03 and p = 0.04, respectively). There was also a tendency to decrease the expression for such microRNAs as: miR-20a, miR-34b and miR-449c. Moreover, the expression level of miR-34b, miR-449c, and miR-449c and miR-135a has a direct correlation with the effectiveness of ART programs (p < 0.05 for miR-135a). The strength of correlation relationship of the above relationships using Cheddock scale was moderate. MicroRNA molecules selected for the study not only demonstrated their potential ability to be used as a diagnostic marker of male infertility, but also showed the ability to reflect the efficiency of fertilization and embryo formation processes.

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15_Галимова_138-148.pdf640.07 KB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 130-137; doi:10.24412/2500-2295-2024-4-130-137
Abstract Full Text

This study examined female rats' physiological and histological responses to cadmium chloride and lead acetate. Histological lung tissue examinations included oxidative stress and antioxidant status. Six female rat groups were studied. A group that served as a control was provided with water that had been distilled. The dosage of cadmium chloride that was administered to the second group was 5 mg/kg, whereas the dosage that was administered to the third group was 10 mg/kg. The fourth group received a dosage of lead acetate that was 50 mg/kg, whereas the fifth group received 100 mg/kg. All of the standard concentrations of lead acetate and cadmium chloride were administered to the sixth group in accordance with their protocol. Following thirty days of treatment of cadmium chloride and lead acetate to rats, the levels of oxidative indicators like MDA and 8-OHDG showed a substantial increase (P < 0.05). On the other hand, the levels of antioxidants like GSH, SOD, and CAT showed a significant drop (P ≤ 0.05 following the administration of these substances. Histological research has shown that exposure to cadmium chloride and lead acetate is associated with an increased risk of blood clots in the lungs as well as a thickening of the pulmonary alveolar wall. This is in comparison to a control group. These results demonstrate that cadmium chloride and lead acetate treatment adversely affected lung tissue's physiological and histological properties. The researchers discovered that the detrimental effect was more pronounced when the two drugs were administered concurrently to rats.

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14_Razooqi_130-137.pdf1020.74 KB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 122-129 ; doi:10.24412/2500-2295-2024-4-122-129
Abstract Full Text

The present study was carried out to evaluate different estrus synchronization protocols in mice and follow up the proportion of delivery and gender of litters. Five protocols were tested with total number of 48 adult females that divided equally into six groups including control. Total number of 24 adult males were divided equally and introduced for mating for four days. Hormonal synchronization including intraperitoneal administration of single or double dose of 0.5 µg Cloprostenol (Prostaglandin F(PGF)) and 3 µg of Progesterone (P4), with or without 5 IU of equine Chorionic Gonadotropin (eCG) in five protocols. Results showed that estrus and mating rate increase significantly after administration of PGF (P<0.05). However, low delivery rate was evident in all groups. There were no differences in the average number and the proportion of gender of litters within groups. In conclusion, synchronization of estrus in mice was not fully achieved using the current protocols. However, administration of prostaglandin increases mating rate, but the pregnancy success might fundamentally depend on other factors such as managemental.

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13_Alhilfi_122-129.pdf888.54 KB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 111-121; doi:10.24412/2500-2295-2024-4-111-121
Abstract Full Text

This study aimed to evaluate the efficacy of High-Frequency Transcutaneous Electrical Nerve Stimulation (TENS) in combination with Complex Decongestive Physical Therapy (CDPT) on lower limb lymphedema. Every participant provided informed consent for the randomized controlled trial. The trial was conducted at Ahmed Maher Teaching Hospital and High-Top Clinic in Egypt. 60 patients with secondary lower limb lymphedema, ages 35 to 65, were involved in the trial and were split into two groups at random. Group A received CDPT and High-Frequency TENS, while Group B received CDPT only. Both interventions were administered thrice weekly for eight weeks. A non-flexible tape was used to assess the limb girth as the major result; the Lymphedema Quality of Life Questionnaire (LYMQOL) was used as a secondary outcome. ANOVA tests were used in the statistical analysis to compare the pre and post-treatment outcomes within and across groups. The findings revealed that both groups had significantly lower limb girth and improved LYMQOL scores, with Group A showing more improvements than Group B (p < 0.05). The results indicate that for patients with lower limb lymphedema, the combination of High-Frequency TENS and CDPT is superior to CDPT alone in terms of limb girth reduction and improved quality of life. This combination of therapies may be a useful strategy for treating lymphedema and enhancing patient outcomes.

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12_Albarakat_111-121.pdf935.92 KB

Invited review
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 104-110; doi:10.24412/2500-2295-2024-4-104-110
Abstract Full Text

Cognitive impairments are among the most common types of neurological disorders that require the creation of reliable diagnostic and correction tools. Along with the development of effective drugs, in recent years a line of research has been actively developing, in which various methods of non-invasive brain stimulation with feedback from the current physiological parameters of a person, and primarily from the rhythmic components of the electroencephalogram (EEG), are successfully used to diagnose and correct cognitive impairments. The purpose of the presented work is to analyze recent publications, consider the achievements of this line of research and highlight the most promising directions for its further development. Studies using transcranial magnetic and electrical stimulation, as well as sensory types of stimulation - acoustic, photic and audiovisual stimulations, in which non-invasive stimulation is carried out on the basis of feedback signals from the patient's own bioelectrical processes, are considered. The advantages of EEG-guided light-music stimulation, developed by the authors for the correction of various cognitive disorders, are demonstrated.

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11_Федотчев_104-110.pdf462.07 KB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 93-103; doi:10.24412/2500-2295-2024-4-93-103
Abstract Full Text

Asthma is a common chronic multifactorial respiratory disease. Genes involved in the metabolism of drugs used for asthma management play an important role in asthma development. The aim of the study was to analyze the methylation of the promoter regions of AOC1, GLCCI1 and ARG2 genes involved in the metabolism of drugs used for asthma treatment in asthma patients and controls from the Republic of Bashkortostan. DNA was extracted from peripheral blood samples of 157 asthma patients and 155 control subjects. Methylation-Sensitive High Resolution Melting analysis and sequencing of bisulfite-treated genomic DNA were applied to estimate the degree of methylation. Analysis of the methylation status of promoter region of the AOC1 gene revealed a higher frequency of full methylation (100%) of the studied region in patients with severe and moderate asthma than in controls (38.61%; p=0.002; OR=2.58; 95%CI 1.4-4.75). A significantly higher level of promoter methylation of the GLCCI1 gene was found in patients with severe and moderate asthma compared to control group (p=0.01; OR=3.1; 95%CI 1.22-7.88). A low level of promoter methylation of the ARG2 gene was determined in both analyzed groups of patients and controls. The results of MS-HRM analysis were confirmed by bisulfite sequencing of analyzed samples. Thus, this study revealed differences in the level of methylation of promoter regions of AOC1 and GLCCI1 genes between samples of asthma patients and controls. The results of the study expand general understanding of the possible contribution of DNA methylation to asthma development.

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10_Савельева_93-103 +.pdf1.06 MB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 80-92; doi:10.24412/2500-2295-2024-4-80-92
Abstract Full Text

Previous studies have demonstrated that administration of clobetasol at a concentration of 0.25 mg/kg stimulates the synthesis of neurotrophic growth factors, likely triggering the phosphatidylinositol-3-kinase (PI3K) and mitogen-activated protein kinase (MAPK) signaling pathways, resulting in increased levels of structural and axonal proteins necessary for the functional recovery of damaged somatic nerves. However, it has been shown that using higher concentrations of the drug (0.5 and 1.0 mg/kg) leads to a reduction in both structural and axonal proteins in both segments of the nerve conduit and exerts an inhibitory effect on the expression of neurotrophic factors responsible for cytoskeletal remodeling and axonal growth regulation.

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09_Ревин_80-92.pdf1.09 MB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 71-79; doi:10.24412/2500-2295-2024-4-71-79
Abstract Full Text

The liver is a vital organ involved in a wide range of processes such as detoxification, protein synthesis, metabolism, and hormone production. Liver diseases, both inherited and viral hepatitis, liver cancer and fatty degeneration are among the leading causes of death in the world. Recent advances in 3D cell culture technology include the use of pluripotent stem cells and adult stem cells that are cultured in vitro to form self-organizing systems. Organoids are self-organizing multicellular structures that reproduce the structure and function of organs and can be used to model the development, maintenance and repair of organs ex vivo. That is why the search for new methods for the formation of hepatic organoids seen as an urgent task. For the fabrication of 3D organoids we isolated hepatic duct cells from rat liver. The obtained cellular structures were analyzed using atomic force microscopy to estimate their mechanical properties and demonstrated increasing of Young Modulus in comparison with normal liver sections. Morphometric evaluation showed that extracellular matrix fibers occupy up to 60% of the organoid, while cell agglomerations up to 40% of it. We observed the spontaneously formed fibrotic liver tissue-like constructs within 21 days. So, obtained hepatic organoids characterized by a tissue-like structure with a predominance of extracellular matrix fibers in its composition similar to liver tissue affected by fibrosis. 

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08_Науменко_71-79.pdf404.16 KB

Invited review
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 60-70; doi:10.24412/2500-2295-2024-4-60-70
Abstract Full Text

Molecular genetic studies make it possible to determine associations of multifactorial diseases (MFDs) with many specific SNPs, which influence on MFDs etiopathogenesis is often difficult to explain. This is due to the one-sided focus of strategies in the search for mechanisms of these SNPs influence, which are mainly limited to determining the role of protein-coding genes, near or within which these polymorphisms are located. This article provides data on the mechanisms of SNP influence on MFDs etiopathogenesis due to changes in the transposable elements, which leads to their activation, dysfunction or susceptibility to exogenous viral infections. As a result, the relationship of transposable elements with specific proteins, non-coding RNA and epigenetic factors changes, which is a predisposing factor for MFDs development. Indeed, most disease-associated SNPs are located in intronic and regulatory regions of genes, and in intergenic regions. Transposable elements of the human genome are also localized in these places. Therefore, the association of specific SNPs with certain MFDs is due to the different activities of specific transposable elements. Determining the influence of SNPs on transposable elements is promising in bioinformatics studies with the construction of maps of the distribution of these elements in the genome within genes and in intergenic regions with the identification of changes in their structure under the influence of polymorphisms. Using neurodegenerative diseases as an example, it has been shown that pathological functioning and activation of retroelements due to SNPs in the regions of their location in the human genome leads to these MFDs development.

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07_Мустафин_60-70.pdf478.11 KB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 51-59; doi:10.24412/2500-2295-2024-4-51-59
Abstract Full Text

During cardiac surgery, as well as on-pump CABG, it is crucial to monitor arterial blood parameters in order to assess the condition of patients and risks that might occur in the operating room. In some cases, the cardiac activity of patients undergoing on-pump CABG cannot be self-restored and resuscitation measures are required. Thus, the aim of the study was to analyze the differences between the two groups of patients (self-restoration of cardiac activity vs additional resuscitation measures were required) and identify arterial blood parameters potentially indicating that the patient is at risk. The data of 21 patients were analyzed with Python packages. Statistically significant differences were found between the control group (self-restoration of cardiac activity) and the test group (additional resuscitation measures were required) in the following arterial blood parameters: the levels of sodium, chloride, glucose and blood osmolality. We believe that hyponatremia and blood hypoosmolality might be a reason for cell edema which creates a greater load on the heart and leads to inability of self-restoration of cardiac activity.

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06_Киселева_51-59.pdf1.33 MB

Full-length research paper
Printed December 02, 2024;
Published ahead of print December 01, 2024; Printed December 02, 2024; OM&P 2024 Volume 11 Issue 4, pages 40-50; doi:10.24412/2500-2295-2024-4-40-50
Abstract Full Text

Over the past three decades, the majority of norovirus outbreaks and sporadic cases have been caused by strains of the GII.4 genotype. Notably, this period has seen a periodic change in the norovirus variants within the GII.4 genotype, with some variants acquiring epidemic distribution. Currently, six polymerase gene variants classified as P-type GII.P4 (GII.P4US95, GII.P4FarmingtonHills, GII.P4Hunter, GII.P4Yerseke, GII.P4DenHaag, and GII.P4NewOrleans) are represented in public nucleotide sequence databases, corresponding to GII.4 genotype variants of the gene encoding the main capsid protein VP1 of norovirus. In this study, the nucleotide sequence of the complete RdRp gene was obtained for a strain from Nizhny Novgorod, identified as GII.4Sydney[P4NewOrleans]. According to the results of Bayesian phylogenetic analysis based on RdRp GII.P4 gene sequences available in the GenBank database divided the analyzed strains into clusters according to polymerase variant. Within these clusters, lineages of intervariant recombinants are formed in accordance with the affiliation of the capsid protein variants associated with this polymerase variant. Analysis of the deduced amino acid sequences revealed substitutions specific to different polymerase variants that have emerged and become established within the norovirus population. It appears that the emergence of new norovirus variants within the GII.4 genotype involves selection for strains in which the polymerase and major capsid protein genes have coevolved, conferring certain advantages that facilitate further dissemination. These findings are highly relevant for advancing therapeutic strategies targeting RdRp inhibition for norovirus treatment and for development of specific prophylactic agents.

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05_Епифанова_40-50.pdf1.5 MB

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