{"title":"具有哌嗪分子的黄酮衍生物类抗菌剂和抗生物膜剂,对抗药性幽门螺旋杆菌菌株具有活性。","authors":"","doi":"10.1016/j.bioorg.2024.107755","DOIUrl":null,"url":null,"abstract":"<div><p><em>Helicobacter pylori</em> (<em>H. pylori</em>) cause chronic inflammation of the gastric mucosa which can lead to epithelial atrophy and metaplasia resulting in peptic ulcer disease and gastric cancer. The increasing resistance of <em>H. pylori</em> to antibiotics and chemotherapeutics used to treat the infection is a serious problem. However, it has been confirmed that the introduction of effective anti-<em>H. pylori</em> therapy can prevent the progression to cancerous changes. This problem calls for the search for new and effective therapies. Xanthones are a group of compounds with extensive biological activities, including antibacterial activity, also against <em>H. pylori.</em> Addressing this issue, the aim of the study was to evaluate the potential of a group of 13 xanthone derivatives against susceptible and resistant <em>H. pylori</em> strains. Moreover, our objective was to conduct tests aimed at determining their ability to inhibit biofilm formation.</p><p>The antimicrobial evaluation revealed that benzylpiperazine coupled at the C-2 position to xanthone (compounds <strong>C11</strong> and <strong>C12</strong>) had good selective bacteriostatic activity against reference and clinical <em>H. pylori</em> strains (MBC/MIC ratio >4) but with no activity against other bacteria such as <em>Staphylococcus aureus</em>, <em>Escherichia coli</em>, and <em>Lactobacillus paracasei.</em> Analysis of the activity of compounds <strong>C11</strong> and <strong>C12</strong> against the biofilm formed by <em>H. pylori</em> strain ATCC 700684, and the clinical strain showed that these compounds caused a significant reduction in the amount of biofilm produced (5–20×). Moreover, cell viability analysis confirmed a 3–4× reduction in the viability of cells forming biofilm after treatment with <strong>C11</strong> and <strong>C12</strong>. Finally,<!--> <!-->both compounds did not impair human fibroblast viability at tested concentrations and were not mutagenic in the Ames test. Therefore, they could be promising leads as antibacterial candidates for multidrug-resistant strains of <em>H. pylori.</em></p></div>","PeriodicalId":257,"journal":{"name":"Bioorganic Chemistry","volume":null,"pages":null},"PeriodicalIF":4.5000,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0045206824006606/pdfft?md5=a1e9b6810000174a9a1b8b6276a76403&pid=1-s2.0-S0045206824006606-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Antibacterial and antibiofilm agents in the group of xanthone derivatives with piperazine moiety active against drug-resistant Helicobacter pylori strains\",\"authors\":\"\",\"doi\":\"10.1016/j.bioorg.2024.107755\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Helicobacter pylori</em> (<em>H. pylori</em>) cause chronic inflammation of the gastric mucosa which can lead to epithelial atrophy and metaplasia resulting in peptic ulcer disease and gastric cancer. The increasing resistance of <em>H. pylori</em> to antibiotics and chemotherapeutics used to treat the infection is a serious problem. However, it has been confirmed that the introduction of effective anti-<em>H. pylori</em> therapy can prevent the progression to cancerous changes. This problem calls for the search for new and effective therapies. Xanthones are a group of compounds with extensive biological activities, including antibacterial activity, also against <em>H. pylori.</em> Addressing this issue, the aim of the study was to evaluate the potential of a group of 13 xanthone derivatives against susceptible and resistant <em>H. pylori</em> strains. Moreover, our objective was to conduct tests aimed at determining their ability to inhibit biofilm formation.</p><p>The antimicrobial evaluation revealed that benzylpiperazine coupled at the C-2 position to xanthone (compounds <strong>C11</strong> and <strong>C12</strong>) had good selective bacteriostatic activity against reference and clinical <em>H. pylori</em> strains (MBC/MIC ratio >4) but with no activity against other bacteria such as <em>Staphylococcus aureus</em>, <em>Escherichia coli</em>, and <em>Lactobacillus paracasei.</em> Analysis of the activity of compounds <strong>C11</strong> and <strong>C12</strong> against the biofilm formed by <em>H. pylori</em> strain ATCC 700684, and the clinical strain showed that these compounds caused a significant reduction in the amount of biofilm produced (5–20×). Moreover, cell viability analysis confirmed a 3–4× reduction in the viability of cells forming biofilm after treatment with <strong>C11</strong> and <strong>C12</strong>. Finally,<!--> <!-->both compounds did not impair human fibroblast viability at tested concentrations and were not mutagenic in the Ames test. Therefore, they could be promising leads as antibacterial candidates for multidrug-resistant strains of <em>H. pylori.</em></p></div>\",\"PeriodicalId\":257,\"journal\":{\"name\":\"Bioorganic Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2024-08-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0045206824006606/pdfft?md5=a1e9b6810000174a9a1b8b6276a76403&pid=1-s2.0-S0045206824006606-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0045206824006606\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0045206824006606","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Antibacterial and antibiofilm agents in the group of xanthone derivatives with piperazine moiety active against drug-resistant Helicobacter pylori strains
Helicobacter pylori (H. pylori) cause chronic inflammation of the gastric mucosa which can lead to epithelial atrophy and metaplasia resulting in peptic ulcer disease and gastric cancer. The increasing resistance of H. pylori to antibiotics and chemotherapeutics used to treat the infection is a serious problem. However, it has been confirmed that the introduction of effective anti-H. pylori therapy can prevent the progression to cancerous changes. This problem calls for the search for new and effective therapies. Xanthones are a group of compounds with extensive biological activities, including antibacterial activity, also against H. pylori. Addressing this issue, the aim of the study was to evaluate the potential of a group of 13 xanthone derivatives against susceptible and resistant H. pylori strains. Moreover, our objective was to conduct tests aimed at determining their ability to inhibit biofilm formation.
The antimicrobial evaluation revealed that benzylpiperazine coupled at the C-2 position to xanthone (compounds C11 and C12) had good selective bacteriostatic activity against reference and clinical H. pylori strains (MBC/MIC ratio >4) but with no activity against other bacteria such as Staphylococcus aureus, Escherichia coli, and Lactobacillus paracasei. Analysis of the activity of compounds C11 and C12 against the biofilm formed by H. pylori strain ATCC 700684, and the clinical strain showed that these compounds caused a significant reduction in the amount of biofilm produced (5–20×). Moreover, cell viability analysis confirmed a 3–4× reduction in the viability of cells forming biofilm after treatment with C11 and C12. Finally, both compounds did not impair human fibroblast viability at tested concentrations and were not mutagenic in the Ames test. Therefore, they could be promising leads as antibacterial candidates for multidrug-resistant strains of H. pylori.
期刊介绍:
Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry.
For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature.
The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.