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: Skin wounds can occur for many reasons, including UV radiation, mechanical burns, trauma, and chronic inflammation caused by metabolic factors. In Mongolia, as of 2022, household burns were the top 5 causes of injuries, the leading cause of injuries in children aged 0-5, and accounted for 18.4% of all illnesses in children aged 0-5. Skin burns and wounds take a long time to heal, which causes emotional, aesthetic, and economic stress for doctors. Developing in novative, effective, and low-side effects therapeutic products to improve wound healing is of great clinical and economic importance. The lack of research on the effects of bacterial metabolites and aloe vera (Aloe barbadensis Miller) on burn wounds was the basis for our research. Aim: To determine the effects of a mixture of bacterial metabolites and aloe vera on burn wounds in experimental animals. Materials and Methods: Eight-week-old BALB/c mice were divided into three groups: control group, bacterial metabo lite group, and aloe vera group. The mice were anesthetized, and the dorsal hair was shaved over a 2×2 cm area using an electric clipper. A second-degree burn wound model was created by exposing the shaved dorsal skin to hot air at 200°C for 10 seconds. A total of 100 μL of a bacterial metabolite suspension mixed with aloe vera at a 1:1 ratio was applied evenly to the center of the wound. Wound images were captured daily, and wound areas were measured using ImageJ software. Healing was evaluated on days 7, 14, and 21 of treatment and compared with the control group. The initial wound size was defined as 100%, and wound closure percentages were calculated accordingly. Burn skin tissues from both experimen tal and control groups were subjected to immunofluorescence staining for the vascular marker α-SMA (Thermo Fisher Scientific). Statistical analysis: The differences between the control and experimental groups were analyzed using an independent t-test using GraphPad Prism 10 software, and the mean, standard deviation, and statistical correlation were calculated. Results: The effect of the mixture of bacterial metabolites and aloe vera (Aloe barbadensis Miller) on the healing of burn wounds in experimental mice was compared with the control group. The wound size at 7 days was 82.1% in the control group and 83.7% in the experimental group (p<0.197), at 14 days was 62.6% in the control group and 58.1% in the exper imental group (p<0.0001), at 21 days was 50.7% in the control group and 32.7% in the experimental group (p<0.0001). No statistically significant difference in wound healing was observed between the groups at day 7; however, significant differences were observed at days 14 and 21. Immunofluorescence analysis revealed uniform expression of α-SMA-pos itive cells in the experimental group at 7, 14, and 21 days of treatment, whereas α-SMA expression was not detected in the control group. Conclusion The combination of bacterial metabolites and aloe vera promotes wound healing in experimental mouse burn wounds.

Background: Hemophilia is a congenital bleeding disorder caused by a lack of clotting factor in the blood. Hemophilia A, B, and C are caused by congenital deficiencies of clotting factors VIII, IX, and IX which are involved in thrombin generation of intrinsic coagulation pathway. Hemophilia A and B is a recessive X-linked congenital bleeding disorder but hemophilia C is typically inherited in an autosomal recessive, these are rare inherited coagulation disorders. This study was conducted based on the lack of database on the epidemiology, clinical type and severity in hemophilia in Mongolia. Aim: The aim of this study was to investigate the relationship between clotting factor levels and bleeding severity of hemophilia. Materials and Methods: A cross sectional study included a total of 30 patients with hemophilia who were registered from May to October 2025 at the Comprehensive Hemophilia Center, MNUMS. The study was approved by the Research Ethics Committee of MNUMS. Result: In this study 30 patients with hemophilia mean age was 18.4±15.7 years, and 96.7% were male. When categorized by age group, 13.4% (n=4) were under 4 years, 40% (n=12) were 5–13 years, 10% (n=3) were 14–18 years, 33.3% (n=10) were 19–44 years, and 3.3% (n=1) were over 45 years. Of the total cases, 83.3% (n=25) had Hemophilia A and 16.7% (n=5) had Hemophilia B. Of the total case, 80% of cases were classified as severe and 20% as moderate hemophilia. Additionally, 40% of cases had joint complications. Conclusion Joint bleeding was observed in 41.6% of patients with severe hemophilia and in 33.3% of those with moderate hemophilia. Target joint damage was found in 40% of the study population because 86.6% of patients were not able to receive prophylactic factor replacement therapy. Joint damage, joint deformities, reduced range of motion, and deterioration in quality of life were all adverse outcomes related to the early onset of joint bleeding.

Background: Skin diseases are highly prevalent worldwide. Although plant-derived medicinal materials continue to be used among Mongolians for the traditional and household management of dermatological conditions, studies that systematically quantify their frequency of use, informant consensus, and cultural significance remain limited. Aim: To determine the traditional knowledge, patterns of use, and cultural significance of plant-derived medicinal materials used for dermatological conditions among residents of Ulaanbaatar using quantitative ethnobotanical indices. Materials and Methods: Information was collected on the diversity of plant species used for dermatological conditions, modes and frequency of use, perceived effectiveness, adverse effects, and methods of preparation and processing. The collected data were evaluated using quantitative ethnobotanical indices, including the Use Value (UV), Relative Frequency of Citation (RFC), Informant Consensus Factor (ICF), Fidelity Level (FL), Relative Popularity Level (RPL), Rank Order Priority (ROP), Cultural Importance Index (CII), Jaccard Index (JI), and Shannon–Wiener Diversity Index (SDI). Statistical analyses were performed using Microsoft Excel 2016. The study was conducted with the approval of the Research Ethics Review Committee of the Mongolian National University of Medical Sciences (Approval Protocol No. 25-06/03-03 and Ethical Opinion Protocol No. 26/03-B02). Result: A total of 73 plant species belonging to 36 families were documented, with species from the Asteraceae, Rosaceae, Apiaceae, and Liliaceae families being predominant. Regarding modes of use, 29.6% of the remedies were prepared as infusions or decoctions and applied as washes or topical applications, 18.9% involved the direct application of plant juice, and 18.1% were applied as mashed plant material or poultices. Aloe barbadensis showed the highest ethnobotanical importance, with UV= 0.19, RFC=0.128, CII=0.19, RPL=1.00, and ROP=100. Nugaraa altan tovch, Gobi thyme, yashilduu sea buckthorn, and greater plantain were also highly ranked. The Informant Consensus Factor was highest for thermal burns (ICF=0.82), followed by open wounds (ICF=0.77) and pustular acne (ICF=0.76). Eighteen species overlapped with the 126 medicinal materials recorded in traditional medicinal prescriptions, yielding a Jaccard Index of JI=10%. The Shannon–Wiener diversity index was H′=3.4184, with an evenness value of E=0.7967. Among the informants, 40.8% reported a reduction in symptoms, while 61.9% reported no adverse effects associated with the use of plant-derived medicinal materials. Conclusion 1. Among residents of Ulaanbaatar, information was documented on the use of 73 plant species belonging to 36 families for skin diseases. Knowledge of these plants was transmitted mainly within families, and topical methods of use, including washing with herbal infusions, rinsing, and direct application of expressed plant juice, were predominant. 2. According to the quantitative ethnobotanical indices, Aloe vera showed the highest values for use, citation frequency, and cultural importance. Matricaria chamomilla L., Thymus gobicus Tschern., Hippophae rhamnoides L., and Plantago major L. also ranked highly. The highest Informant Consensus Factor (ICF) values were observed for thermal burns, open skin wounds, and acne vulgaris.

Background: Panzerina lanata (L.) is widely distributed across various ecosystems in the mountain, steppe, and Gobi regions of Mongolia and has traditionally been used in folk medicine to alleviate joint and muscle inflammation, reduce liver heat, lower blood pressure, promote diuresis, and treat edema and tumors. Its similar applications in Mongolian and Chinese traditional medicine suggest considerable therapeutic potential and biological activity. Studies conducted since 2019 have reported that P.lanata (L.) is rich in phenolic compounds, flavonoids, and antioxidant-active constituents; however, studies on the microscopic and histochemical characteristics of the species growing under Mongolian conditions remain limited, providing the rationale for this study. Aim: To characterize the microscopic features of Panzerina lanata (L.), determine the distribution of starch, polysaccharides, and phenolic compounds using histochemical methods, and evaluate the total polyphenol and flavonoid contents and antioxidant activity. Materials and Methods: For microscopic analysis, plant materials were softened by soaking for 24 h in a 1:1:1 water–ethanol–glycerin mixture (Strich–Fleming solution), followed by preparation of manual transverse and longitudinal sections of the stems, roots, and petals. A 10% chloral hydrate solution was used for clearing. Histochemical analyses were performed using potassium dichromate (K₂Cr₂O₇), ferric chloride (FeCl₃), Lugol’s solution (I₂/KI), thymol (C₁₀H₁₄O) with concentrated sulfuric acid (H₂SO₄), methylene blue (C₁₆H₁₈ClN₃S), and Dragendorff’s reagent. The prepared sections were cleared with glycerin and examined under an Olympus light microscope at ×40 and ×100 magnifications, with images documented using a 12-MP camera. Result: Microscopic examination of the roots, stems, and petals revealed that the root stele exhibited a polyarchy arrangement, with clearly differentiated xylem, phloem, and cambial tissues in both transverse and longitudinal sections. Scalariform tracheary elements in the xylem contributed to water and mineral transport and mechanical support. The stem xylem contained both spiral and scalariform tracheary elements. The petals consisted of cells with double walls and single nuclei, while the floral seed tissue was composed of meristematic tissue associated with continuous cell division, growth, and tissue differentiation. Histochemical analysis of transverse and longitudinal sections of the stems and roots, as well as petal sections, revealed the presence of essential oils, polyphenolic compounds (tannins and flavonoids), and starch. Conclusion Microscopic, histochemical, and phytochemical analyses of Panzerina lanata (L.) revealed the presence of biologically active compounds, indicating its potential for use in the quality evaluation of medicinal plant raw materials.

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: Numerous experimental and clinical studies have investigated the therapeutic potential of Silybum marianum (L.) Gaertn., mainly attributing its biological activities to antioxidant, anti-inflammatory, antifibrotic, and hepatoprotective effects. In particular, silymarin has been reported to exert hepatoprotective effects by reducing oxidative stress, protecting cell membranes from certain toxic insults, and modulating protein synthesis. Therefore, cultivation of S. marianum and utilization of its seeds for industrial and research purposes are important for establishing a sustainable source of pharmacologically valuable bioactive compounds and increasing the availability of high-quality medicinal plant material. Aim: To evaluate the feasibility of cultivating S. marianum from seeds and to determine seed germination, seedling growth and development, survival after transplantation to open-field conditions, phenological stages, and seed yield characteristics. Materials and Methods: Seeds of S. marianum were germinated under indoor conditions, and normally developed seedlings were subsequently raised in a greenhouse and transplanted to a cultivation site near Tamgan Öndör, Erdene sum, Töv Province, Mongolia. Germination percentage (GP), mean germination time (MGT), seedling growth based on morphometric parameters, and survival rate after transplantation were evaluated. At harvest, the number and diameter of capitula, seed weight per plant, 1000-seed weight, and seed yield per unit area were determined. Data were expressed as mean±SD, and statistical significance was evaluated at p < 0.05. Result: Of the 1,000 seeds sown, 852 germinated, resulting in a germination percentage of 85.2% and a mean germination time of 11 days. Under greenhouse conditions, plant height increased from 1.0 to 3.0 cm, while rosette diameter increased from 1.2 to 7.0 cm. Of the 452 seedlings transplanted to the open field, 353 survived, corresponding to a survival rate of 78.1%. The first flowering was observed on June 12, full flowering on July 9, and full seed maturation on August 30, with 175 days from sowing to seed maturity. On average, each plant produced 18 branches and 20 capitula, with a capitulum diameter of 4.4 cm, seed weight per plant of 15.5 g, 1000-seed weight of 11.5 g, and seed yield of 195.325 kg/ha. Conclusion S. marianum was able to germinate, establish, complete its major growth, flowering, and seed maturation stages, and produce seeds under the cultivation conditions of the Tamgan Öndör area, Erdene sum, Töv Province. These findings indicate that S. marianum can potentially be cultivated in this specific area as a source of medicinal plant material.

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.