<?xml version='1.0' encoding='utf-8'?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2 20190208//EN" "http://jats.nlm.nih.gov/publishing/1.2/JATS-journalpublishing1.dtd">
<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2658-6533-2026-12-1-0-6</article-id><article-id pub-id-type="publisher-id">4039</article-id><article-categories><subj-group subj-group-type="heading"><subject>Pharmacology</subject></subj-group></article-categories><title-group><article-title>Mitigation of indomethacin-induced gastric inflammation in mice through the administration of ethanol extract from Hedyotis capitellata Wall. leaves</article-title><trans-title-group xml:lang="en"><trans-title>Mitigation of indomethacin-induced gastric inflammation in mice through the administration of ethanol extract from Hedyotis capitellata Wall. leaves</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Nhung</surname><given-names>Tran T.P.</given-names></name><name xml:lang="en"><surname>Nhung</surname><given-names>Tran T.P.</given-names></name></name-alternatives><email>tranthiphuongnhung@iuh.edu.vn</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Quoc</surname><given-names>Le P.T.</given-names></name><name xml:lang="en"><surname>Quoc</surname><given-names>Le P.T.</given-names></name></name-alternatives><email>lephamtanquoc@iuh.edu.vn</email></contrib></contrib-group><pub-date pub-type="epub"><year>2026</year></pub-date><volume>12</volume><issue>1</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2026/1/Биомед_исследования-82-100.pdf" /><abstract xml:lang="ru"><p>Background: Gastritis, a prevalent global malady, stems from various factors such as unhealthy lifestyles, bacterial infections, or non-steroidal anti-inflammatory drug usage. If untreated, it leads to severe complications. Hedyotis capitellata Wall., recognized for its medicinal properties, is traditionally acknowledged for its effectiveness in pain relief, neutralizing gastric acid, reducing acid reflux, and promoting ulcer healing. The aim of the study: This study delves into exploring the preventive and protective prowess of H. capitellata leaf ethanol extract (EEHC) against indomethacin (IND)-induced gastric mucosal damage in mice. Materials and methods: EEHC administered at 300, 350, and 400 mg/kg doses, with omeprazole (OME) (20 mg/kg) as the reference standard, EEHC&amp;#39;s impact was assessed on gastric acid levels, mucosal damage, malondialdehyde (MDA) content, antioxidant activity (catalase, myeloperoxidase, glutathione, total antioxidant capacity), cytokine levels (TNF-&amp;alpha;, IL-1&amp;beta;, IL-6, IL-10), and histopathology. Results: EEHC, particularly at 400 mg/kg, exhibited maximal inhibition of total gastric acid (8.58 &amp;plusmn; 0.16 mEq/l), decreased MDA content (5.29&amp;plusmn;0.15 nM/g tissue), and lowered pro-inflammatory cytokines (TNF-&amp;alpha;: 224.04&amp;plusmn;17.56 pg/ml) compared to IND-treated mice (p&amp;lt;0.05). Dose-dependent EEHC enhanced the antioxidant defense system by reducing catalase and myeloperoxidase activity and increasing glutathione and total antioxidant capacity levels (p&amp;lt;0.05). Mice treated with EEHC displayed significantly lower gastric ulcer indices across all experimental models compared to the IND-treated group (p&amp;lt;0.05). Histopathological examinations further affirmed EEHC&amp;#39;s anti-inflammatory efficacy. Conclusion: The study establishes that oral administration of EEHC exerts a positive protective influence on the gastric mucosa, augmenting the antioxidant defense system and anti-inflammatory effects. H. capitellata emerges as a promising resource for managing gastric inflammation due to its potent antioxidant properties</p></abstract><trans-abstract xml:lang="en"><p>Background: Gastritis, a prevalent global malady, stems from various factors such as unhealthy lifestyles, bacterial infections, or non-steroidal anti-inflammatory drug usage. If untreated, it leads to severe complications. Hedyotis capitellata Wall., recognized for its medicinal properties, is traditionally acknowledged for its effectiveness in pain relief, neutralizing gastric acid, reducing acid reflux, and promoting ulcer healing. The aim of the study: This study delves into exploring the preventive and protective prowess of H. capitellata leaf ethanol extract (EEHC) against indomethacin (IND)-induced gastric mucosal damage in mice. Materials and methods: EEHC administered at 300, 350, and 400 mg/kg doses, with omeprazole (OME) (20 mg/kg) as the reference standard, EEHC&amp;#39;s impact was assessed on gastric acid levels, mucosal damage, malondialdehyde (MDA) content, antioxidant activity (catalase, myeloperoxidase, glutathione, total antioxidant capacity), cytokine levels (TNF-&amp;alpha;, IL-1&amp;beta;, IL-6, IL-10), and histopathology. Results: EEHC, particularly at 400 mg/kg, exhibited maximal inhibition of total gastric acid (8.58 &amp;plusmn; 0.16 mEq/l), decreased MDA content (5.29&amp;plusmn;0.15 nM/g tissue), and lowered pro-inflammatory cytokines (TNF-&amp;alpha;: 224.04&amp;plusmn;17.56 pg/ml) compared to IND-treated mice (p&amp;lt;0.05). Dose-dependent EEHC enhanced the antioxidant defense system by reducing catalase and myeloperoxidase activity and increasing glutathione and total antioxidant capacity levels (p&amp;lt;0.05). Mice treated with EEHC displayed significantly lower gastric ulcer indices across all experimental models compared to the IND-treated group (p&amp;lt;0.05). Histopathological examinations further affirmed EEHC&amp;#39;s anti-inflammatory efficacy. Conclusion: The study establishes that oral administration of EEHC exerts a positive protective influence on the gastric mucosa, augmenting the antioxidant defense system and anti-inflammatory effects. H. capitellata emerges as a promising resource for managing gastric inflammation due to its potent antioxidant properties</p></trans-abstract><kwd-group xml:lang="ru"><kwd>acute gastric injury</kwd><kwd>antioxidant activity</kwd><kwd>indomethacin</kwd><kwd>mucosal protection</kwd><kwd>ulcer index</kwd></kwd-group><kwd-group xml:lang="en"><kwd>acute gastric injury</kwd><kwd>antioxidant activity</kwd><kwd>indomethacin</kwd><kwd>mucosal protection</kwd><kwd>ulcer index</kwd></kwd-group></article-meta></front><back><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>De Ara&amp;uacute;jo ERD, Guerra GCB, Andrade AWL, et al. Gastric ulcer healing property of Bryophyllum pinnatum leaf extract in chronic model in vivo and gastroprotective activity of its major flavonoid. Frontiers in&amp;nbsp;Pharmacology. 2021;12:744192. DOI: http://doi.org/10.3389/fphar.2021.744192</mixed-citation></ref><ref id="B2"><mixed-citation>Qureshi MS, Reddy AV, Kumar GS. Protective effect of Hydrolea zeylanica Vahl. leaf extract in ethanol and cold restraint stress induced ulcers in rats. Research Journal of Pharmacy and Technology. 2017;10(1):49-54. DOI: http://doi.org/10.5958/0974-360X.2017.00012.9</mixed-citation></ref><ref id="B3"><mixed-citation>Nabil M, Raey MAE, Abdo W, et al. Gastro-protective effects of Albizia anthelmintica leaf extract on indomethacin-induced gastric ulcer in wistar rats: in silico and in vivo studies. Antioxidants. 2021;10(2):176. DOI: http://doi.org/10.3390/antiox10020176</mixed-citation></ref><ref id="B4"><mixed-citation>Park JU, Kang JH, Rahman MAA, et al. Gastroprotective effects of plants extracts on gastric mucosal injury in experimental sprague-dawley rats. BioMed Research International. 2019;2019:8759708. DOI: http://doi.org/10.1155/2019/8759708</mixed-citation></ref><ref id="B5"><mixed-citation>Huyen LT, Hau NTT, Son VH, et al. A new &amp;beta;-carboline alkaloid from the aerial part of Hedyotis capitellata. Natural Product Communications. 2021;16(10):1-4. DOI: http://doi.org/10.1177/1934578X211047705</mixed-citation></ref><ref id="B6"><mixed-citation>Rohaya A. Biological activity of Hedyotis spp. and chemical constituents of Hedyotis capitellata. Malaysia: Universiti Putra Malaysia; 2005.</mixed-citation></ref><ref id="B7"><mixed-citation>Hung HY, Cheng KC, Kuo PC, et al. Chemical constituents of Hedyotis diffusa and their anti-inflammatory bioactivities. Antioxidants. 2022;11(2):335. DOI:&amp;nbsp; http://doi.org/10.3390/antiox11020335</mixed-citation></ref><ref id="B8"><mixed-citation>Artanti N, Hanafi M, Andriyani R, et al. Isolation of an anti-cancer asperuloside from Hedyotis corymbosa L. Journal of Tropical Life Science. 2015;5(2):98-101. DOI: https://doi.org/10.11594/jtls.05.02.06</mixed-citation></ref><ref id="B9"><mixed-citation>Duc LV, Thanh TB, Giang NP, et al. Anti-inflammatory and anticancer activities of Hedyotis capitellata growing in Vietnam. World Journal of Medical Sciences. 2017;14(2):22-28. DOI: http://doi.org/10.5829/idosi.wjms.2017.22.28</mixed-citation></ref><ref id="B10"><mixed-citation>Loi DT. Vietnamese Medicinal Plants and Herbs. Hanoi: Medical Publisher; 2006. Vietnamese.</mixed-citation></ref><ref id="B11"><mixed-citation>Muhamad M, Sze WA, Zulkifli NS, et al. Qualitative analysis on the phytochemical compounds and total phenolic content of Cissus hastata (semperai) leaf extract. International Journal of Plant Biology. 2023;14(1):53-62. DOI: http://doi.org/10.3390/ijpb14010005</mixed-citation></ref><ref id="B12"><mixed-citation>Mansoori A, Singh N, Dubey SK, et al. Phytochemical characterization and assessment of crude extracts from Lantana camara L. for antioxidant and antimicrobial activity. Frontiers in Agronomy. 2020;2:582268. DOI: http://doi.org/10.3389/fagro.2020.582268</mixed-citation></ref><ref id="B13"><mixed-citation>World Health Organization (WHO). General guidelines for methodologies on research and evaluation of traditional medicine; 2000.</mixed-citation></ref><ref id="B14"><mixed-citation>Hurst SA. Declaration of Helsinki and protection for vulnerable research participants. JAMA. 2014;311(12):1252. DOI: http://doi.org/10.1001/jama.2014.1272</mixed-citation></ref><ref id="B15"><mixed-citation>Luyen LT, Quang NN. National guideline on ethics in biomedical research. Hanoi: Ministry of Health of Vietnam; 2013. Vietnamese.</mixed-citation></ref><ref id="B16"><mixed-citation>Tastekin E, Ayvaz S, Usta U, et al. Indomethacin-induced gastric damage in rats and the protective effect of donkey milk. Archives of Medical Science. 2018;14(3):671-678. DOI: http://doi.org/10.5114/aoms.2016.59645</mixed-citation></ref><ref id="B17"><mixed-citation>Jong-Min L, Chang-Hyun S, Dong-Chan P, et al. Protective effects of triple fermented barley extract (FBe) on indomethacin-induced gastric mucosal damage in rats. BMC Complementary and Alternative Medicine. 2019;19:49. DOI: http://doi.org/10.1186/s12906-019-2457-0</mixed-citation></ref><ref id="B18"><mixed-citation>Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman&amp;#39;s reagent. Analytical Biochemistry. 1968;25:192-205. DOI: http://doi.org/10.1016/0003-2697(68)90092-4</mixed-citation></ref><ref id="B19"><mixed-citation>Popović D, Kocić G, Katić V, et al. Anthocyanins protect hepatocytes against CCl4-induced acute liver injury in rats by inhibiting pro-inflammatory mediators, polyamine catabolism, lipocalin-2, and excessive proliferation of kupffer cells. Antioxidants. 2019;8(10):451. DOI: http://doi.org/10.3390/antiox8100451</mixed-citation></ref><ref id="B20"><mixed-citation>Danisman B, Cicek B, Yildirim S, et al. Carnosic acid ameliorates indomethacin-induced gastric ulceration in rats by alleviating oxidative stress and inflammation. Biomedicines. 2023;11(3):829. DOI: http://doi.org/10.3390/biomedicines11030829</mixed-citation></ref><ref id="B21"><mixed-citation>K&amp;auml;hk&amp;ouml;nen MP, Hopia AI, Vuorela HJ, et al. Antioxidant activity of plant extracts containing phenolic compounds. Journal of Agricultural and Food Chemistry. 1999;47:3954-3962. DOI: http://doi.org/10.3390/10.1021/jf990146l</mixed-citation></ref><ref id="B22"><mixed-citation>Ullah A, Munir S, Badshah SL, et al. Important flavonoids and their role as a therapeutic agent. Molecules. 2020;25(22):5243. DOI: http://doi.org/10.3390/molecules25225243</mixed-citation></ref><ref id="B23"><mixed-citation>Ajayi AF, Olaleye BS. Age-related changes in haematological parameters and biochemical markers of healing in the stomach of rats with acetic acid induced injury. Toxicology Reports. 2020;7:1272-1281. DOI: http://doi.org/10.1016/j.toxrep.2020.09.007</mixed-citation></ref><ref id="B24"><mixed-citation>Adefisayo MA, Akomolafe RO, Akinsomisoye SO, et al. Gastroprotective effect of methanol extract of Vernonia amygdalina (del.) leaf on aspirin-induced gastric ulcer in Wistar rats. Toxicology&amp;nbsp;Reports. 2017;4:625-633. DOI: http://doi.org/10.1016/j.toxrep.2017.11.004s</mixed-citation></ref><ref id="B25"><mixed-citation>Mornet E, Stura E, Lia-Baldini AS, et al. Structural evidence for a functional role of human tissue nonspecific alkaline phosphatase in bone mineralization. Journal of Biological Chemistry. 2001;276(33):31171-31178. DOI: http://doi.org/10.1074/jbc.M102788200</mixed-citation></ref><ref id="B26"><mixed-citation>Ajayi AF, Olaleye SB. Age-related changes in the response of the rat gastric mucosa to acetic acid- and indomethacin-induced ulceration. Archives of Basic and Applied&amp;nbsp;Medicine. 2015;3:79-88.</mixed-citation></ref><ref id="B27"><mixed-citation>Lim JM, Song CH, Park SJ, et al. Protective effects of triple fermented barley extract (FBe) on indomethacin-induced gastric mucosal damage in rats. BMC Complementary and Alternative Medicine. 2019;19:49-60. DOI: http://doi.org/10.1186/s12906-019-2457-0</mixed-citation></ref><ref id="B28"><mixed-citation>Abbas AM, Sakr HF. Effect of selenium and grape seed extract on indomethacin-induced gastric ulcers in rats. Journal of Physiology and Biochemistry. 2013;69(3):527-537. DOI: http://doi.org/10.1007/s13105-013-0241-z</mixed-citation></ref><ref id="B29"><mixed-citation>Fahmy SR, Amer MA, Mohannad H, et al. Ameliorative effect of the sea cucumber Holothuria arenicola extract against gastric ulcer in rats. Journal of Basic and Applied Zoology. 2015;72:16-25. DOI: http://doi.org/10.1016/j.jobaz.2015.03.001</mixed-citation></ref><ref id="B30"><mixed-citation>K&amp;uuml;&amp;ccedil;&amp;uuml;kler S, Kandemir FM, Yıldırım S. Protective effect of chrysin on indomethacin induced gastric ulcer in rats: Role of multi-pathway regulation. Biotechnic and Histochemistry. 2022;97(7):490-503. DOI: http://doi.org/10.1080/10520295.2021.2014569</mixed-citation></ref><ref id="B31"><mixed-citation>Gilani SJ, Bin-Jumah MN, Al-Abbasi FA, et al. Protective effect of fustin against ethanol-activated gastric ulcer via downregulation of biochemical parameters in rats. ACS Omega. 2022;7(27):23245-23254. DOI: http://doi.org/10.1021/acsomega.2c01341</mixed-citation></ref><ref id="B32"><mixed-citation>El-Rady NMA, Dahpy MA, Ahmed A, et al. Interplay of biochemical, genetic, and immunohistochemical factors in the etio-pathogenesis of gastric ulcer in rats: a comparative study of the effect of pomegranate loaded nanoparticles versus pomegranate peel extract. Frontiers in Physiology. 2021;12:649462. DOI: http://doi.org/10.3389/fphys.2021.649462</mixed-citation></ref><ref id="B33"><mixed-citation>Kobayashi T, Ohta Y, Yoshino J, et al. Teprenone promotes the healing of acetic acid-induced chronic gastric ulcer in rats by inhibiting neutrophils infiltration and lipid peroxidation in ulcerated gastric tissue. Pharmacological Research. 2001;43(1):23-30. DOI: http://doi.org/10.1006/phrs.2000.0748</mixed-citation></ref></ref-list></back></article>