Opera Medica et Physiologica

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Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 174-188; doi:10.24412/2500-2295-2024-3-174-188
Abstract Full Text

Introduction. Acute limb ischemia is a critical condition requiring immediate revascularization. The risk of complications is affected by age, coronary heart disease, chronic kidney disease, respiratory failure, diabetes mellitus, thrombosis etiology, urgency and duration of surgery. The aim of the study was to evaluate the influence of the presented risk factors on the results of open revascularization for acute thrombosis in patients with acute COVID-19. Materials and methods. The results of open surgical treatment of acute limb ischemia of Rutherford class II in patients with acute COVID-19 (86 patients, group I) and 50 patients without COVID-19 (group II) were analyzed. Results. In-hospital mortality was 73.2% in group I and 12% in group II. Most deaths in group I were due to early rethrombosis. Risk factors - coronary heart disease, chronic kidney disease, diabetes mellitus, age >75 years had a greater negative impact in group I against the background of coronavirus infection. Conclusion. In patients in the acute stage of COVID-19, open revascularization is associated with a higher risk of complications and mortality in the early postoperative period relative to patients who underwent surgery without coronavirus infection. The impact of all the identified risk factors increases against the background of COVID-19, a statistically significant increase in the odds ratio of developing postoperative complications was found for such perioperative risk factors as: coronary heart disease, respiratory failure, polyvalent etiology of thrombosis and age over 75 years, among the intraoperative factors, the emergency nature of the operation and the duration of the surgical intervention are significant.

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15_Nikolsky_174-188.pdf746.49 KB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 158-173; doi:10.24412/2500-2295-2024-3-158-173
Abstract Full Text

The transition of the ion channel between the open and closed states is traditionally considered random. Current experimental data indicated the presence of oscillatory modes of regulation of open/closed states, and possible connections between these modes. The canonical methods Fourier or wavelet transforms, fractal analysis and mathematical modelling can evaluate open/closed states oscillatory modes, but cannot describe their relationship to each other. We first applied the method of bispectral analysis to solve this problem. The well-described potassium channels potential-dependent Kv, calcium-dependent KCa and the modelled potassium channel KcsA were studied. The relationship between fluctuations open/closed lifetimes at frequencies ~0.1, ~1 and ~10 Hz was shown. These frequencies correspond to rhythmic processes in cardiovascular and nervous systems functioning, including those regulated by potassium channels. The normalised integrated bispectrum index was chosen to quantitatively evaluate the interrelation of ion channel opening/closing states. The normalised bispectrum index notable increased upon alteration of the membrane potential from 0 to 20 mV. The obtained data expand our understanding of ion channel functioning principles and can be used in the search for new approaches to the pathological states (channelopathies) therapy.

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14_Astashev_158-173.pdf2.01 MB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 152-157; doi:10.24412/2500-2295-2024-3-152-157
Abstract Full Text

Сholelithiasis is a multifactorial process that is influenced by both environmental and genetic factors. Some evidence suggests that total plasma homocysteine correlates with the presence of gallstones, suggesting that hyperhomocysteinemia is a risk factor for cholelithiasis. The aim of this work was to analyze the association of polymorphic variants of the methylenetetrahydrofolate reductase MTHFR (rs1801133 (677C > T), rs1801131 (1298A > C)) and methionine synthase reductase MTRR (rs1801394 (66A > G)) genes with the development of gallstone disease in individuals from the Republic of Bashkortostan. DNA samples from 196 patients with cholelithiasis and 274 healthy individuals aged 23-87 years living in the Republic of Bashkortostan were used as research material. Genotyping was performed using the real-time PCR method. It has been established that the rs1801133*T allele and the rs1801133*TT genotype of the MTHFR gene are markers of an increased risk of developing cholelithiasis. An association was established between the rs1801133*TT genotype of the rs1801133 polymorphic variant of the MTHFR gene and the moderate severity of cholelithiasis and hereditary burden in patients with cholelithiasis. A study of the polymorphic variant of the MTRR gene revealed that the rs1801394*G allele increases the risk of cholelithiasis. Analysis of associations of the polymorphism rs1801131 of the MTHFR gene with the development of cholelithiasis did not reveal statistically significant differences between the compared groups of patients and controls. Determination of homocysteine levels and genetic testing of MTHFR and MTRR polymorphisms in patients with cholelithiasis may be useful in clinical practice.

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13_Fedorova_152-157.pdf560.97 KB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 136-151; doi:10.24412/2500-2295-2024-3-136-151
Abstract Full Text

This work is devoted to the study of mRNA expression patterns and the relative content of selenoproteins in mice with TAA-induced liver fibrosis and TAA-induced HCC. The main objective of this study is to evaluate the activation or suppression of selenoprotein synthesis during HCC progression and directly in the tumor in one TAA-treated mouse model, which is a pilot study and allows us to closely approximate the situation observed during HCC progression in vivo. It was found that as HCC progresses, there is an increase in the mRNA expression of thioredoxin reductases TXNRD1 and TXNRD2, deiodinase DIO3, glutathione peroxidases GPX1, GPX2, GPX4, and an inverse correlation in the expression of mRNA was characteristic of GPX3. In addition, the mRNA expression of endoplasmic reticulum resident selenoproteins: SELENOM, SELENON, SELENOT and SELENOS changed significantly. Also, in tumor liver samples and directly in the tumor itself, an increase in the expression of the selenoprotein SELENOP was recorded. The information obtained from the results of this work will significantly complement the existing data on the role of mammalian selenoproteins in various liver pathologies and in oncogenesis in general.

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12_Turovsky_136-151.pdf988.72 KB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 118-135; doi:10.24412/2500-2295-2024-3-118-135
Abstract Full Text

The study of the severity and consequences of infectious diseases is a relevant subject of research throughout the world, which was directly demonstrated by the situation with the 2020-2023 coronavirus pandemic. In our study, we analyzed a distribution of genotypes and alleles frequency of polymorphic variants of the IL6 rs1800795, TNFA rs1800629 and LZTFL1 rs10490770 gene polymorphisms, which were previously linked to the pathogenesis of COVID-19, in populations of Burzyan Bashkirs, Sterlibashevsky Bashkirs, Permsky Bashkirs, Kazan Tatars, Chuvash, Udmurts, Mari, Komi and Mordvins. Statistically significant differences were identified in the IL6 rs1800795 between the populations of the Burzyan Bashkirs and the Mari and Komi (p < 0.05). The Sterlibashevsky Bashkirs, Permsky Bashkirs and Udmurts also statistically significantly differed from the Komi population (p < 0.05). When studying the TNFA rs1800629, statistically significant differences were identified between the populations of Sterlibashevsky and Permsky Bashkirs and the Udmurts population (p < 0.05). Analysis of the LZTFL1 rs10490770 revealed statistically significant differences only between the Udmurt and Mari populations (p < 0.05). The data indicate that despite the geographic proximity of the examined populations of the Volga-Ural region, they were able to preserve the uniqueness of their gene pool.

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11_Sufyanova_118-135.pdf1.14 MB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 108-117; doi:10.24412/2500-2295-2024-3-108-117
Abstract Full Text

The aim: determination of correlation dependence of adaptogenic defense reactions in rats in the acute phase of pain stress on laser-puncture exposure to low-intensity IR radiation. Material and methods. Four groups of rats were used in the work: "experimental", which received after the injury a 10-day course of PPBM, and three comparison groups ("intact", "no exposure" and "placebo"). The intensity of lipid peroxidation, specific activity of antioxidant enzymes, protein concentration, malonic dialdehyde content in blood plasma and erythrocytes were determined by spectrophotometric method. Microcirculation indices were evaluated according to the previous series of our studies. Emotional and behavioral reactions were studied in the "open field" test. Results. Normalization of metabolic, microcirculatory and behavioral indices was registered in the experimental group. The correlation coefficients between the microcirculation index and the data of behavioral activity under pain stress were significantly less than the correlation coefficients between oxidative stress and cognitive functions, which confirms the determining role of oxidative metabolism disturbance in the formation of cognitive disorders. Conclusion: the registered adaptation and stress-limiting effect of PPBM in conditions of experimental pain stress allows us to recommend the technology of laser acupuncture for use in complex rehabilitation of patients with pain syndrome.

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10_Peretyagin_108-117.pdf582.99 KB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 93-107; doi:10.24412/2500-2295-2024-3-93-107
Abstract Full Text

A hypothesis is proposed about the role of evolutionary relationship of retroelements with transfer RNAs (tRNAs) on their processing to form small non-coding RNAs. This is evidenced by the use of tRNA as primers for reverse transcriptase, origin of SINE2 from tRNA, use of LINE1 enzymes by tRNA for pseudogenes formation. Under the influence of RISC enzymes, tRFs are formed from tRNA, that control gene expression at the epigenetic level. Non-coding RNAs formed from transcripts of retroelements are characterized by similar properties. An assumption has been made about the functioning of a species-specific epigenetic network between such non-coding RNAs formed from retroelements and tRNAs. Decoding such a network may open up the possibility of creating new epigenetic agents for the treatment of human diseases, and will also allow us to determine mechanisms of genetic code emergence in evolution. One of the bases for this network formation may be the distribution and composition of tRNAs and retroelements in the genome. I have provided data on this network mechanisms formation, describing the similar functional properties of tRNAs and retroelements, their influence on the same targets and pathways in the human organism. I suppose that the relationship between tRNAs and retroelements arose as an integral property of living things when life arose in RNA world, where tRNAs were originally used to perform many regulatory catalytic functions, one of which was later transformed into the transfer of amino acids for protein synthesis.

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09_Mustafin_93-107.pdf462.45 KB

Invited review
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 67-92; doi:10.24412/2500-2295-2024-3-67-92
Abstract Full Text

The paper presents an analysis of literature data on the characteristics of microbiocenoses across a wide range of infectious and somatic pathologies, as well as the results of our research on changes in the composition of the gastrointestinal tract microbiota in patients with various diseases. It is demonstrated that the microbiota responds consistently to any pathological changes occurring in the host organism, primarily manifested as a disruption in the balance between anaerobic (bifidobacteria, lactobacilli, bacteroids, clostridia, etc.) and aerobic components of the microbiocenosis. The predominance or suppression of specific types of microorganisms is primarily influenced by the composition of the individual's indigenous microbiota, rather than the specific pathology associated with dysbiosis.

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08_Belova_67-92.pdf821.01 KB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 58-66; doi:10.24412/2500-2295-2024-3-58-66
Abstract Full Text

Background: previous studies have implicated the INSIG2 rs6726538 single nucleotide polymorphism (SNP) as a potential risk factor for cervical cancer. Our objective was to examine the correlation between this genetic variation and the vulnerability of Iraqi women to cervical cancer. Methods: this case-control study analyzed rs6726538 genotypes and allele frequencies in 109 cervical cancer cases and 109 healthy controls. Logistic regression calculated odds ratios (OR) and 95% confidence intervals (CI). The rs6726538 SNP was genotyped using tetra-primer ARMS-PCR. Results: the AT genotype occurred more frequently in cases than controls (52.2% vs 34%, OR 0.783, 95% CI 0.38-1.25, p = 0.0391). The TT genotype was less common but showed a non-significant decreased cancer risk versus AA (OR 0.336, 95% CI 0.17-0.96, p = 0.0707). The T allele was significantly higher in cases (36.3% vs 20.6% in controls, p = 0.0023), while the A allele was higher in controls (79.4% vs 63.7% in cases, p = 0.05). Conclusion: this preliminary data indicates that the rs6726538 T allele and TT genotype may be associated with increased cervical cancer risk, while the A allele and AA genotype could have a protective effect. However, larger studies are required to validate these initial findings on how this SNP may impact cervical cancer susceptibility.

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07_Tahreer_58-66.pdf640.34 KB

Full-length research paper
Printed September 20, 2024;
Published ahead of print September 20, 2024; Printed September 20, 2024; OM&P 2024 Volume 11 Issue 3, pages 49-57; doi:10.24412/2500-2295-2024-3-49-57
Abstract Full Text

In the present study, we investigated the effect of α1-adrenergic receptor stimulation on the electrical activity of the right atrium cardiomyocytes with imposed rhythm in rats of different ages using methoxamine and methoxamine against the background of selective blockade of phospholipase C inhibitor (U-73122). Methoxamine increased the duration of the repolarization phase of the action potential. However, there were no changes in the other electrophysiological parameters studied. U-73122 markedly blocked all effects of α1-adrenoreceptor stimulation on the parameters of the electrical activity of working cardiomyocytes in 7-, 21-, and 100-day-old rats.

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06_Mansour_49-57.pdf661.18 KB

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