Background: Plants of the genus Achillea are widely used in both traditional and modern medicine and are known to be rich in biologically active secondary metabolites. Numerous phytochemical and histochemical studies have been con ducted on Achillea millefolium L.; however, Achillea asiatica Serg., which is widely distributed in Mongolia, remains comparatively underexplored. Therefore, investigating the distribution of biologically active compounds, the content of polyphenolic compounds, and the optimal extraction conditions of this species is of significant scientific and practical importance. Aim: The aim of this study was to identify biologically active compounds in Achillea asiatica Serg. using histochemical methods, to determine the content of polyphenolic compounds and optimal extraction conditions, and to evaluate the total and internal absorption coefficients of the plant raw material. Materials and Methods: The aerial parts of Achillea asiatica Serg. were collected in August 2025 from Erdene soum, Tuv province, Mongolia. Histochemical analysis was performed on transverse stem sections and flower petals using potassium dichromate, ferric chloride (III), methylene blue, Lugol’s iodine, and Dragendorff’s reagent, followed by ob servation under a light microscope. The total polyphenolic content was determined using the Folin–Ciocalteu method and expressed as gallic acid equivalents. Extraction experiments were conducted using powdered plant material sieved to par ticle sizes of 1, 2, and 3 mm and extracted with 20–80% ethanol. In addition, the total and internal absorption coefficients of the plant material were determined according to standard procedures. Results: Histochemical analysis revealed the presence of essential oils, polyphenolic compounds (tannins and flavo noids), and starch, while alkaloids were not detected. Polyphenolic compounds were observed in both stems and flow ers, with more pronounced accumulation in the vascular tissues. The highest total polyphenolic content (0.421%) was obtained from the 1 mm particle-size fraction extracted with 70–80% ethanol. Using 60% ethanol, the total absorption coefficient of the plant material was determined to be 5.74, and the internal absorption coefficient was 1.885. Conclution Achillea asiatica Serg. is rich in polyphenolic compounds, and their anatomical distribution is closely as sociated with the plant’s protective and biological functions. The use of 1 mm particle-size material and 70–80% ethanol was identified as the most suitable condition for extracting polyphenolic compounds. These findings provide a scientific basis for the standardization of Achillea asiatica Serg. as a medicinal and phytopharmaceutical raw material and support its further pharmacognostic and phytochemical investigation.

Background: Globally, research on identifying bioactive compounds from medicinal plants and characterizing their in vitro and in vivo pharmacological activities is progressing rapidly. Plants native to Mongolia have adapted to unique, extreme continental climatic conditions, accumulating distinct phytochemicals, and have historically been utilized in traditional medicine and dietary practices. Establishing the non-cytotoxic safety threshold of these wild and cultivated plant extracts in RBL-2H3 mast cells a universally accepted model for type I hypersensitivity and inflammation is a vital prerequisite. Determining these baseline non-toxic dose ranges provides the essential scientific foundation for subsequent cellular allergy models, animal studies, and the elucidation of molecular mechanisms underlying their therapeutic efficacy. Aim: To determine the cytotoxicity profile and establish the non-cytotoxic dose ranges of extracts from four selected Mongolian plant species (wild and cultivated) in RBL-2H3 cells. Materials and Methods: Plant samples including lingonberry (Vaccinium vitis-idaea), strawberry (Fragaria orientalis), black radish (Raphanus sativus), and blue-berried honeysuckle (Lonicera caerulea L.) were standardly collected, authenticated, and cataloged as herbarium specimens at the Botanic Garden and Research Institute, Mongolian Academy of Sciences. A total of 12 distinct extracts were prepared from plant leaves, stems, and fruits using water and ethanol extraction, followed by concentration via rotary evaporation and freeze-drying. Rat basophilic leukemia (RBL-2H3) cells were maintained in EMEM growth medium and utilized during the exponential growth phase. Cell viability and non-cytotoxic concentration thresholds were evaluated using the MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay. Result: Ethanolic extracts of strawberry leaves, black radish, and honeysuckle leaves (≥6.25 µg/mL), as well as aqueous extracts of honeysuckle fruits (≥6.25 µg/mL) and stems (≥25 µg/mL), exhibited dose-dependent cytotoxicity. Conversely, aqueous extracts of lingonberry leaves (≤200 µg/mL), strawberry leaves (≥100 µg/mL), and black radish (≤200 µg/mL), alongside ethanolic extracts of lingonberry leaves (≥50 µg/mL), demonstrated non-cytotoxic profiles. Furthermore, ethanolic extracts of honeysuckle stems (≤300 µg/mL) and fruits (≥12.5 µg/mL), as well as the aqueous extract of honeysuckle leaves (≤50 µg/mL), significantly enhanced RBL-2H3 cell viability. Conclusion The tested plant extracts influenced RBL-2H3 cell viability in a solvent polarity and plant organ dependent manner. Ethanolic extracts of strawberry leaves, black radish, and honeysuckle leaves, along with aqueous extracts of honeysuckle fruits and stems, demonstrated relatively high cytotoxicity, reducing cell viability by >40% starting at concentrations of 12.5, 25, and 50 µg/mL. In contrast, aqueous extracts of strawberry leaves and black radish, as well as both aqueous and ethanolic extracts of lingonberry leaves, maintained low cytotoxicity at concentrations below 200 µg/mL. Notably, ethanolic extracts of honeysuckle stems and fruits (>12.5 µg/mL) and its aqueous leaf extract (<100 µg/mL) enhanced cell viability, exhibiting significant cell proliferation promoting activity.

Background: Dental caries remains a major public health concern among children and adolescents in Mongolia. The mineral composition of drinking water-particularly fluoride and other essential minerals plays a crucial role in enamel mineralization and caries prevention. Fluoride directly influences the demineralization–remineralization balance of dental enamel and forms a temporary layer of fluid fluorapatite on the enamel surface when exposed to acids, thereby reducing the critical pH for dissolution and increasing acid resistance. In addition, fluoride inhibits the acid-producing metabolism of bacteria such as s.mutans within the biofilm and lowers biofilm acidity, thus slowing the rate of demineralization. Therefore, determining the relationship between population groups and water mineralization is essential for developing effective preventive strategies. Aim: To determine the severity and prevalence of dental caries among 5-, 12-, and 15-year-old children living in the 21 provinces of Mongolia and to evaluate the effects of selected minerals in drinking water (Ca, Mg, Cl, F) on dental caries. Materials and Methods: The study utilized oral examination data from a total of 421,970 children aged 0-17 years across 21 provinces and 321 soums in Mongolia. Sampling was conducted in Ulaanbaatar city (48.1%) and in all 21 rural provinces. Dental caries was assessed according to WHO criteria, and the effects of minerals in drinking water were analyzed using linear regression. Result: The average caries severity of primary teeth in 5-year-old children was 3.0-3.1 dft, which was higher than the caries severity of permanent teeth in 12- and 15-year-olds (1.54DMFdft–1.93 DMFT). Among 5-year-olds, boys had a slightly higher caries severity (3.17±3.52) compared to girls (2.92±3.40), while in the 12- and 15-yearold groups, girls showed higher caries severity than boys. Overall, 5566% of children had at least one carious tooth, and the prevalence among 5-year-olds was 63.5-66.2%. Linear regression analysis showed that fluoride (beta=–0.449, p<0.001) and magnesium (beta=–0.031, p<0.001) in drinking water had a statistically significant protective effect in reducing dental caries in both primary and permanent teeth. Conclusion The findings indicate that fluoride (F) and magnesium (Mg) in drinking water are important protective elements against dental caries, whereas calcium (Ca) and chloride (Cl) show no consistent association with caries experience.

Background: Staphylococcus aureus (S. aureus) is a leading cause of skin and soft tissue infections. The prevalence of methicillin-resistant (MRSA) and multidrug-resistant (MDR) strains has been increasing globally in recent years. In Mongolia, data on MRSA prevalence and antimicrobial susceptibility in purulent skin infections remain limited. Aim: To assess the prevalence of MRSA and MDR S. aureus and their antimicrobial susceptibility patterns in purulent skin infections. Materials and Methods: This laboratory-based retrospective study analyzed 22,753 samples collected between 2015−2025 at the National Dermatology Center of Mongolia, in which S. aureus was identified. MDR was defined according to the Magiorakos criteria as resistance to three or more antibiotic classes. Prevalence was expressed with 95% confidence intervals (CI). Group differences were assessed using the chi-square (χ²) test; and age- and sex-related risks were estimated using odds ratios (OR) with 95% CI. A p-value <0.05 was considered statistically significant. Results: MRSA was detected in 18.8% (n=4,278) and MDR in 40.7% (n=9,258) of cases. The prevalence of MRSA increased significantly from 0–1.6% during 2015–2019 to 15–34.2% during 2020–2025 (p<0.001). MDR prevalence peaked at 53.9% (n=1,682) in 2022. No statistically significant sex differences were observed for MRSA (female: 2,331; male: 1,947) or MDR (female: 4,958; male: 4,300) (p>0.05). MRSA prevalence was highest in children under 1 year (47.4%) and lowest in those aged 15–24 years (14.8%), while MDR prevalence increased significantly with age and was highest among individuals aged ≥81 years (p<0.001). The presence of MRSA was associated with a 16.76-fold higher likelihood of MDR S. aureus (p<0.001). Antibiotic resistance was highest for penicillin-class antibiotics (ampicillin 91.5%, amoxicillin 75.4%), whereas susceptibility remained high for vancomycin (4.4% resistance), nitrofurantoin (4.6%), and amikacin (10.1%). Conclusion Over the past decade, the prevalence of MRSA and MDR S. aureus in purulent skin infections has increased markedly. Although resistance to penicillin-class antibiotics remains high, susceptibility to vancomycin and nitrofurantoin is largely preserved. The higher prevalence observed in younger and older age groups highlights the need to strengthen infection control measures and promote the rational use of antibiotics.

Background: A child’s physical growth is fundamentally dependent on hormonal regulation, metabolism, and oxygen supply, within which bone mineralization specifically calcium (Ca²⁺) levels acts as a primary factor determining bone mineral density (BMD), muscle function, and hormonal activity. In cardiovascular disease (CVD), multiple physiological processes are disrupted at various levels, including decreased blood circulation and oxygen supply, increased energy expenditure, and reduced absorption of nutrients and micronutrients. In this context, research linking calcium levels in 6–7-year-old children with electrocardiographic (ECG) changes to physical growth has been scarce, which provided the rationale for conducting this study. Aim: To investigate the association between calcium levels and physical growth among 6–7-year-old children with electrocardiographic (ECG) abnormalities detected through early screening. Materials and Methods: This study was conducted using a case-control design. The case group included 143 children aged 6–7 with ECG changes, and the control group included 153 children without ECG changes, totaling 296 voluntary participants. Serum total calcium and albumin levels in both groups were measured using a fully automated biochemical analyzer. Statistical analysis was performed using SPSSv27, applying independent samples t-tests, ANOVA, and correlation analysis to compare means between the two groups. Results: The control group’s serum total calcium was 2.65±0.15 mmol/L, corrected calcium was 2.58±0.13 mmol/L, and the case group’s serum total calcium was 2.64±0.18 mmol/L, corrected calcium was 2.59±0.17 mmol/L, with no statistically significant difference observed between the study groups (p>0.05). When comparing total calcium in case-group children with normal height (2.66±0.20) versus those with stunted growth (2.61±0.13), a statistically significant difference was found (p<0.05). Correlation analysis between total and corrected calcium levels and physical growth indicators across study groups showed no statistically significant association. When height measurements were divided into four quartiles (Q1–Q4) and compared against total and corrected serum calcium, no statistically significant differences were found between the groups. Conclusions Comparison of physical growth and development Z-scores between children with and without ECG abnormalities revealed no statistically significant differences. However, total calcium levels tended to be lower among children with normal growth compared with those with growth retardation in the case group (p < 0.05). No statistically significant differences were observed in serum total or albumin-corrected calcium levels between the study groups (p > 0.05). When height measurements in the study groups were categorized into quartiles, no statistically significant differences in total or albumin-corrected calcium levels were observed between the groups. This suggests that calcium levels alone may not be a decisive determinant of physical growth in children of the same age.

Background: Indirect immunofluorescence (IIF) using HEp-2 cells is internationally recognized as the gold-standard method for detecting antinuclear antibodies (ANAs), which are widely used in the diagnosis of systemic autoimmune diseases. Developing and evaluating a standardized experimental protocol for ANA detection is important for improving the diagnosis of systemic autoimmune diseases. Aim: To detect serum ANAs using an HEp-2 cell-based indirect immunofluorescence assay. Materials and Methods: Frozen HEp-2 cells were thawed, recovered, and cultured. Cells were seeded at a density of 5x10⁵ cells per reaction well and incubated at 37°C in a humidified atmosphere containing 5% CO₂ for 24 hours, followed by fixation. The fixed cells were incubated with serum samples from patients diagnosed with systemic lupus erythematosus (SLE) and Sjögren’s syndrome (SjS), diluted at 1:80 and 1:160. A fluorescein isothiocyanate (FITC)-conjugated secondary antibody was subsequently applied at a dilution of 1:500. Fluorescence patterns were examined using an immunofluorescence microscope at 20× and 40× magnifications. Nuclear staining patterns observed at a serum dilution of 1:160 under 40× magnification were evaluated with reference to the International Consensus on ANA Patterns (ICAP) classification. Results: HEp-2 cells were evaluated using the indirect immunofluorescence (IIF) assay with ANA-positive and ANA-negative sera. No fluorescence was observed in the negative control serum. In contrast, serum positive for anti-dsDNA from a patient with systemic lupus erythematosus (SLE) produced a distinct homogeneous nuclear staining pattern, whereas anti-SSA/SSB-positive serum from a patient with Sjögren’s syndrome (SjS) produced a speckled nuclear staining pattern. The homogeneous and speckled staining patterns observed in the respective SLE and SjS sera were consistent with the expected morphological characteristics of the corresponding reference patterns, supporting the applicability of the established HEp-2 cell-based IIF protocol for ANA detection and nuclear staining pattern assessment. Conclusion The HEp-2 cell-based indirect immunofluorescence (IIF) assay enabled the detection of serum ANAs and the differentiation of homogeneous and speckled nuclear staining patterns. The observed staining patterns were morphologically consistent with the corresponding reference patterns described in the International Consensus on ANA Patterns (ICAP) classification. These findings support the potential applicability of the established protocol for ANA detection and nuclear staining pattern assessment.

Background: Ephedra przewalskii Stapf. is a perennial shrubby plant of the family Ephedraceae, naturally distributed in the dry and cold desert regions of Mongolia. In traditional medicine, the stems and roots of this plant have been used as decoctions for the treatment of gastrointestinal spasms, abdominal distension, urinary retention, and general fatigue. Members of the Ephedraceae family are known to contain sympathomimetic alkaloids such as ephedrine and pseudoephedrine, which exert strong physiological effects on the central nervous system, respiratory tract, and cardiovascular system. However, detailed information on the tissue- and cell-level localization of biologically active compounds and the microstructural characteristics of E. przewalskii remains limited. Aim: This study aimed to investigate the microanatomical structure and histochemical characteristics of the stem and root of Ephedra przewalskii Stapf., with particular emphasis on the localization of biologically active compounds. Materials and Methods: Plant samples were collected in July from Chandmani soum, Govi-Altai province, Mongolia. The collected material was air-dried in the shade and softened using Ostrich and Fleming solution prior to sectioning. Transverse sections of the stem and root were prepared using a hand microtome and examined under an Olympus light microscope. Histochemical analyses were performed using standard reagents to detect alkaloids, phenolic compounds, tannins, essential oils, polysaccharides, and starch. Results: The stem epidermis consisted of thin-walled, quadrangular cells with a surface covered by spherical protuberances. The stomatal apparatus exhibited a tetracytic structure, and photosynthetic activity was primarily localized in the stem chlorenchyma. The vascular bundles were collateral, with phloem located externally and xylem internally. Idioblasts containing reddish-brown crystalline inclusions were observed in the central pith of the stem. The root showed a polyarch central cylinder, with uniformly distributed, rounded parenchymal cells, and idioblasts similar to those observed in the stem. Histochemical analysis revealed the presence of flavonoids, alkaloids, polysaccharides, and tannins in the stem, predominantly localized in parenchymal and chlorenchymal tissues. In the root, polysaccharides, tannins, and starch were detected, whereas alkaloid accumulation was more prominent in the stem parenchyma. Conclusion The microscopic examination of Ephedra przewalskii Stapf. revealed the characteristic structures of the stem epidermis, stomata, chlorenchyma, vascular tissues, and crystal-containing idioblasts, as well as a polyarch central cylinder in the root. Histochemical reactions detected flavonoids, alkaloids, tannins, starch, and polysaccharides in the stem, whereas tannins, starch, and polysaccharides were identified in the root. These findings provide a comprehensive characterization of the anatomical and chemical features of the different plant organs.

Background: Nuclear factor erythroid 2-related factor 2 (NRF2) is a transcription factor that plays a crucial role in regulating cellular responses to oxidative stress and xenobiotic exposure. However, excessive NRF2 activation can enhance cancer cell survival and contribute to chemoresistance. Therefore, increasing attention has been directed toward naturally occurring flavonoids that may modulate NRF2 activity. Molecular docking provides a computational approach for predicting potential interactions between flavonoids and NRF2 and may help identify candidate compounds for further investigation in cancer therapy. Objective: To evaluate the potential interactions of five naturally occurring flavonoids—daidzin, rutin, luteolin, apigenin, and quercetin—with the Neh1 domain of NRF2 using molecular docking and to identify promising candidates for further investigation based on docking scores and ligand efficiency. Materials and Methods: The potential interactions of five natural flavonoids, namely daidzin, rutin, luteolin, apigenin, and quercetin, with the target region of NRF2 were investigated using molecular docking. Three-dimensional structures of the flavonoids were retrieved from the PubChem database, while the NRF2 protein structure was obtained from the Protein Data Bank (PDB). Molecular docking calculations were performed using the CB-Dock2 web platform, which incorporates the AutoDock Vina algorithm. Results: The docking scores of the selected flavonoids ranged from −64.9 to −77.2. Daidzin exhibited the most favorable docking score (−77.2), followed by apigenin (−72.0) and luteolin (−71.4), whereas rutin showed the least favorable score (−64.9). The calculated RMSD values ranged from 14.766 to 15.344 Å, with relatively small differences among the ligands. Daidzin and apigenin exhibited comparatively lower RMSD values. The reported pose-clustering analysis indicated that all ligands occupied similar binding regions. In terms of ligand efficiency, apigenin (−2.40), luteolin (−2.30), and quercetin (−2.20) showed comparatively favorable values. Although daidzin had the most favorable docking score, its ligand efficiency relative to molecular size was comparatively lower. Conclusion The results suggest that daidzin and apigenin may be candidate compounds for further investigation of potential interactions with the Neh1 domain of NRF2. However, these findings are based solely on computational analysis. Further molecular dynamics simulations and experimental studies are required to validate the predicted interactions and determine their actual effects on NRF2 activity.

Background: HepG2 cells are widely used as an in vitro model for investigating alterations in hepatic cellular metabolism. Studies evaluating the biological activities of plant-derived compounds using HepG2 cells have also increased. Strawberry (Fragaria orientalis), lingonberry (Vaccinium vitis-idaea), radish (Raphanus sativus), and blue honeysuckle (Lonicera caerulea L.) contain polyphenols, flavonoids, anthocyanins, and other secondary metabolites. The biological activities of these plants may vary depending on species, plant tissue, growing conditions, and extraction methods. Prior to evaluating the biological activities of plant extracts, it is essential to assess their cytotoxic effects on cells and determine appropriate concentrations for subsequent experiments. Therefore, evaluating the effects of plant extracts on the viability of HepG2 cells, a human hepatocellular carcinoma cell line, is of considerable importance. Aim: To evaluate the effects of aqueous and ethanolic extracts of strawberry, lingonberry, radish, and cultivated and wild blue honeysuckle on HepG2 cell viability and to determine concentrations exhibiting cytotoxic effects. Materials and Methods: A total of 18 plant extracts were prepared using water and ethanol as extraction solvents. The extracts were obtained from strawberry leaves, lingonberry leaves, radish, and the fruits, stems, and leaves of cultivated and wild blue honeysuckle. The extracts were subsequently dried. HepG2 cells maintained in the Cell Biology Laboratory of the Institute of Biomedical Sciences were revived, stabilized, and used for the experiments. The plant extracts were prepared at concentrations of 6.25, 12.5, 25, 50, 100, 200, and 300 μg/mL and used to treat HepG2 cells. Cell viability was assessed using the Cell Counting Kit-8 (CCK-8) assay. Cytotoxicity was defined as a reduction in cell viability of more than 30% compared with the control group. Results: The aqueous extract of cultivated blue honeysuckle and the ethanolic extracts of its fruits and stems maintained HepG2 cell viability above 70% across the concentration range of 6.25–300 μg/mL, indicating relatively low cytotoxicity. In contrast, the ethanolic extract of cultivated blue honeysuckle leaves reduced cell viability at higher concentrations. The aqueous and ethanolic extracts of fruits and stems of wild blue honeysuckle showed no apparent cytotoxic effects, whereas both aqueous and ethanolic extracts of its leaves reduced cell viability to approximately 65% at 300 μg/mL, indicating relatively higher cytotoxicity. Most aqueous and ethanolic extracts of strawberry, radish, and lingonberry maintained cell viability above 70% and showed no cytotoxic effects. The ethanolic extract of strawberry leaves reduced cell viability to approximately 63% even at the lowest concentration of 6.25 μg/mL; however, cell viability tended to increase with increasing extract concentration. Conclusion The effects of plant extracts on HepG2 cell viability varied depending on plant species, tissue type, extraction solvent, and concentration. Most extracts of strawberry, lingonberry, radish, and the fruits and stems of cultivated and wild blue honeysuckle exhibited relatively low cytotoxicity at concentrations ranging from 6.25 to 300 μg/mL. However, the ethanolic extract of cultivated blue honeysuckle leaves at 200 μg/mL and the aqueous and ethanolic extracts of wild blue honeysuckle leaves at 300 μg/mL reduced cell viability by more than 30%, indicating relatively higher cytotoxicity.

Background: The first confirmed case of COVID-19 in Mongolia was reported on November 11, 2020. In response, the government imposed a nationwide lockdown, which significantly impacted the population’s mental health. Heightened levels of stress, anxiety, loneliness, and depression during the pandemic altered individuals’ psychological stability and behavior. Personality traits—defined as relatively stable patterns of emotion, cognition, and behavior—play a key role in stress responses and emotional regulation under pressure. Emerging evidence suggests that these psychological factors may influence the immune system’s responsiveness, including vaccine-induced antibody production. Aim: To evaluate the association between post-vaccination antibody responses and personality types following two doses of COVID-19 vaccines. Materials and Methods: A total of 738 participants who received two doses of COVID-19 vaccines (AstraZeneca ChAdOx1, n=29; Pfizer-BioNTech, n=119; Sinopharm BBIBP, n=590) and had no prior SARS-CoV-2 infection were enrolled. Serum samples were collected 21–28 days after the second dose, and SARS-CoV-2 RBD (S) IgG antibodies were measured using ELISA (Proteintech Inc., USA). Personality types were assessed using a 56-item temperament questionnaire developed by A. Belov, categorizing individuals into classical temperament types (choleric, phlegmatic, sanguine, melancholic). Logistic regression and ROC analysis were used to examine associations between personality types and antibody response. Results: The presence of an antibody response was significantly higher among individuals with a melancholic temperament, and significantly lower among those with a phlegmatic temperament. Furthermore, antibody titers were higher in participants with melancholic and sanguine temperaments and lower in those with a phlegmatic type. Conclusions 1. During the early period following the second dose of COVID-19 vaccination, the antibody response was higher in individuals with a pure melancholic temperament, while it was lower in those with a phlegmatic temperament. 2. After the second dose of the Sinopharm BBIBP COVID-19 vaccine, antibody titers were higher in individuals with pure melancholic and sanguine temperaments, and lower in those with a phlegmatic temperament.