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Eurasian Journal of
            Medicine and Oncology                                                  Research on DSY in treating gastritis



            method. The contents of total uronic acid and proteins in   the treatment of gastritis, the polysaccharide of DSY may
            DSY samples were 12.39% and 4.18%, respectively.   play a significant role. Despite this, polysaccharides have
              The   monosaccharide   composition  of   DSY     garnered limited attention in  previous  gastritis  studies
            polysaccharide was analyzed using complete acid hydrolysis   investigating DSY’s mechanisms of action.
            followed by PMP  derivatization  and HPLC  analysis. As   3.6. Network pharmacology analysis
            shown in  Figure  7D, seven kinds of monosaccharides
            were identified, including mannose, rhamnose, glucuronic   A total of 1138 targets related to 67 compounds (15 volatile
            acid, galacturonic acid, glucose, galactose, and arabinose.   and 52 nonvolatile) were obtained through the TCMSP,
            In  addition,  the molar percentages  of  monosaccharide   HERB, and SwissTargetPrediction databases. Concurrently,
            composition were calculated based on their respective   1719 targets related to gastritis were obtained through the
            peak areas (Table 4). The results revealed that DSY   DisGeNet, GeneCards, and MalaCards databases. Venn
            polysaccharide is primarily composed of galactose,   diagram analysis  (Figure  8A) revealed  195 overlapping
            glucose, and galacturonic acid.                    targets, representing potential therapeutic targets of DSY for
                                                               treating gastritis. Subsequently, the compounds identified
              FTIR spectroscopy (Figure 7E) confirmed the presence
            of characteristic polysaccharide functional groups.   in  DSY  decoction  and  these  overlapping  targets  were
                                                               imported into Cytoscape 3.9.1 to construct a compound–
            The O–H stretching vibration at 3431 cm⁻¹ indicates   target–disease interaction network (Figure 8B). Network
            intermolecular hydrogen bonding. The peak at 2931 cm⁻¹   topology parameters–degree, betweenness centrality,
            corresponds to –CH₂– or –CH₃ stretching vibrations,   and closeness centrality value–were used to evaluate
            while the strong absorption at 1606 cm⁻¹ indicates the C=O
            stretch of free carboxyl groups. The peaks at 1396 cm⁻¹,   node importance in the network. As shown in  Table 5,
            926 cm⁻¹, and 871 cm⁻¹ are assigned to C–H bending,   22  compounds (5 volatile and 17 nonvolatile) exhibited
            β-glycosidic, and α-glycosidic bonds, respectively. These   values greater than the corresponding median values,
            results are consistent with typical features of plant-derived   suggesting their potential as key bioactive components of
            polysaccharides.                                   DSY in treating gastritis.
              The relative contents of crude polysaccharides in their   The shared targets DSY compounds and gastritis were
            respective aqueous extracts were 9.8% (DSY), 12.4% (DS),   imported to the STRING database, resulting in a PPI
            16% (SR), and 6.4% (TX), indicating that polysaccharides   network containing 194 nodes and 1142 edges (Figure 8C).
            are important components of DSY, primarily derived from   The CytoNCA plugin in Cytoscape was then used to assess
            SR and DS.                                         the importance of each node. Filtering conditions were
                                                               set as follows: betweenness centrality ≥median, closeness
              Although   polysaccharide  macromolecules  have  centrality  ≥median,  degree  ≥median,  local  average
            complex  structures and poor oral absorbability, studies   connectivity ≥median, eigenvector ≥median, and network
            have  found that  plant  polysaccharides can exhibit   ≥median. Ultimately, 55 core targets, including TNF, IL2,
            biological effects in the gastrointestinal tract.  DS   IL6, AKT1, STAT3, and TP53, were screened from the 195
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            polysaccharides have been shown to regulate the gut   intersecting targets (Figure 8C).
            microbiota homeostasis.  Moreover, the findings of Gao
                                28
            et al.  suggest that disruption of the gut microbiota may   The GO enrichment analysis of these 55 core targets
                29
            be  a  key  factor  contributing  to  the  worsening  of  gastric   returned 1373 terms, including 1234 biological processes,
            mucosal inflammation, and that restoring gut microbiota   52 cellular components, and 87 molecular functions. The
            balance  could  be  a  significant approach to  curing  or   top 10 terms in each category are shown in  Figure  8D.
            preventing the progression from chronic atrophic   In the biological process category, the therapeutic effects
            gastritis to gastric cancer. In addition, Liu  et al.  found   of DSY appear to involve a response to reactive oxygen
                                                    30
            that purified SR polysaccharide (AVLP-2) improved the   species. Membrane raft, transcription regulator complex,
            oxidative stress status of the gastric mucosa by increasing   side  of membrane, and  endoplasmic  reticulum lumen
            superoxide dismutase activity and glutathione levels and   were enriched in the cellular component category. In the
            inhibiting malondialdehyde accumulation. Therefore, in   molecular function category, protein kinase binding, DNA-

            Table 4. Molar percentages of monosaccharide composition in DSY polysaccharide.

            Monosaccharide  Mannose   Rhamnose    Glucuronic acid  Galacturonic acid  Glucose  Galactose  Arabinose
            Molar %           0.21       0.53         0.15            4.12         6.24      18.07      0.84




            Volume 9 Issue 3 (2025)                        178                         doi: 10.36922/EJMO025160124
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