• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

头花蓼黄酮苷对幽门螺杆菌感染相关炎症具有保护作用。

Flavonoid Glycosides of Polygonum capitatum Protect against Inflammation Associated with Helicobacter pylori Infection.

作者信息

Zhang Shu, Mo Fei, Luo Zhaoxun, Huang Jian, Sun Chaoqin, Zhang Ran

机构信息

Guiyang medical college, Guiyang, 550004, China.

Affiliated hospital of Guiyang Medical College, Guiyang, 550004, China.

出版信息

PLoS One. 2015 May 18;10(5):e0126584. doi: 10.1371/journal.pone.0126584. eCollection 2015.

DOI:10.1371/journal.pone.0126584
PMID:25993258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4436306/
Abstract

The antibacterial and anti-inflammatory activities, and protective effects of extracts (flavonoid glycosides) of Polygonum capitatum were investigated to detect the evidence for the utilization of the herb in the clinical therapy of gastritis caused by H. pylori. A mouse gastritis model was established using H. pylori. According to treating methods, model mice were random assigned into a model group (MG group), a triple antibiotics group (TG group, clarithromycin, omeprazole and amoxicillin), low/middle/high concentrations of flavonoid glycosides groups (LF, MF and HF groups) and low/middle/high concentrations of flavonoid glycosides and amoxicillin groups (LFA, MFA and HFA groups). A group with pathogen-free mice was regarded as a control group (CG group). The eradicate rates of H. pylori were 100%, 93%, 89% in TG, MFA and HF groups. The serum levels of IFN-gamma and gastrin were higher in a MG group than those from all other groups (P < 0.05). The serum levels of IFN-gamma and gastrin were reduced significantly in LF, MF and HF groups (P < 0.05) while little changes were observed in LFA, MFA and HFA groups. In contrast, the serum levels of IL-4 were lower and higher in MG and CG groups compared with other groups (P<0.05). The serum levels of IL-4 were increased significantly in LF, MF and HF groups (P < 0.05) while little changes were found in LFA, MFA and HFA groups. According to pathological scores, flavonoid glycosides therapy showed better protection for gastric injuries than the combination of flavonoid glycoside and amoxicillin (P < 0.05). The results suggested that flavonoid glycoside has repairing functions for gastric injuries. The results suggest that the plant can treat gastritis and protect against gastric injuries. The flavonoid glycosides from Polygonum capitatum should be developed as a potential drug for the therapy of gastritis caused by H. pylori.

摘要

研究了头花蓼提取物(黄酮苷)的抗菌、抗炎活性及保护作用,以探寻该草药用于幽门螺杆菌引起的胃炎临床治疗的依据。采用幽门螺杆菌建立小鼠胃炎模型。根据治疗方法,将模型小鼠随机分为模型组(MG组)、三联抗生素组(TG组,克拉霉素、奥美拉唑和阿莫西林)、低/中/高浓度黄酮苷组(LF、MF和HF组)以及低/中/高浓度黄酮苷与阿莫西林组(LFA、MFA和HFA组)。将无病原体小鼠组作为对照组(CG组)。TG、MFA和HF组的幽门螺杆菌根除率分别为100%、93%、89%。MG组的血清干扰素-γ和胃泌素水平高于其他所有组(P<0.05)。LF、MF和HF组的血清干扰素-γ和胃泌素水平显著降低(P<0.05),而LFA、MFA和HFA组变化不大。相比之下,MG组和CG组的血清白细胞介素-4水平与其他组相比更低和更高(P<0.05)。LF、MF和HF组的血清白细胞介素-4水平显著升高(P<0.05),而LFA、MFA和HFA组变化不大。根据病理评分,黄酮苷治疗对胃损伤的保护作用优于黄酮苷与阿莫西林联合治疗(P<0.05)。结果表明黄酮苷对胃损伤具有修复作用。结果表明该植物可治疗胃炎并预防胃损伤。头花蓼中的黄酮苷应开发为治疗幽门螺杆菌引起的胃炎的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/b351458b36ba/pone.0126584.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/75fac25133a0/pone.0126584.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/653351f800c9/pone.0126584.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/a687fa632879/pone.0126584.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/fd5238117279/pone.0126584.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/7a21a6f9fdcd/pone.0126584.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/18cfc126a52e/pone.0126584.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/cd5e8f45a989/pone.0126584.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/32e1d5a97d8b/pone.0126584.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/b351458b36ba/pone.0126584.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/75fac25133a0/pone.0126584.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/653351f800c9/pone.0126584.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/a687fa632879/pone.0126584.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/fd5238117279/pone.0126584.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/7a21a6f9fdcd/pone.0126584.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/18cfc126a52e/pone.0126584.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/cd5e8f45a989/pone.0126584.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/32e1d5a97d8b/pone.0126584.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4af/4436306/b351458b36ba/pone.0126584.g009.jpg

相似文献

1
Flavonoid Glycosides of Polygonum capitatum Protect against Inflammation Associated with Helicobacter pylori Infection.头花蓼黄酮苷对幽门螺杆菌感染相关炎症具有保护作用。
PLoS One. 2015 May 18;10(5):e0126584. doi: 10.1371/journal.pone.0126584. eCollection 2015.
2
Quercetin from Polygonum capitatum Protects against Gastric Inflammation and Apoptosis Associated with Helicobacter pylori Infection by Affecting the Levels of p38MAPK, BCL-2 and BAX.头花蓼中的槲皮素通过影响 p38MAPK、BCL-2 和 BAX 的水平,防止幽门螺杆菌感染引起的胃炎症和凋亡。
Molecules. 2017 May 6;22(5):744. doi: 10.3390/molecules22050744.
3
Gastroprotective effects of Hwanglyeonhaedok-tang against Helicobacter pylori-induced gastric cell injury.黄莲解毒汤对幽门螺杆菌诱导的胃细胞损伤的胃保护作用。
J Ethnopharmacol. 2018 Apr 24;216:239-250. doi: 10.1016/j.jep.2018.01.025. Epub 2018 Feb 2.
4
Relation of lactoferrin levels in gastric mucosa with Helicobacter pylori infection and with the degree of gastric inflammation.胃黏膜乳铁蛋白水平与幽门螺杆菌感染及胃炎症程度的关系。
Am J Gastroenterol. 1997 Jun;92(6):1005-11.
5
Effect of Helicobacter pylori eradication on gastric histology, serum gastrin and pepsinogen I levels, and gastric emptying in patients with gastric ulcer.幽门螺杆菌根除对胃溃疡患者胃组织学、血清胃泌素和胃蛋白酶原I水平以及胃排空的影响。
Am J Gastroenterol. 1997 Oct;92(10):1844-8.
6
Anti-Helicobacter pylori activities of Chenopodium ambrosioides L. in vitro and in vivo.土荆芥对幽门螺杆菌的体内外抗菌活性
World J Gastroenterol. 2015 Apr 14;21(14):4178-83. doi: 10.3748/wjg.v21.i14.4178.
7
Eradication therapy of Helicobacter pylori directly induces apoptosis in inflammation-related immunocytes in the gastric mucosa--possible mechanism for cure of peptic ulcer disease and MALT lymphoma with a low-grade malignancy.幽门螺杆菌根除治疗直接诱导胃黏膜中炎症相关免疫细胞凋亡——这可能是消化性溃疡疾病和低度恶性黏膜相关淋巴组织淋巴瘤治愈的机制。
Hepatogastroenterology. 2003 May-Jun;50(51):607-9.
8
Mechanism underlying Polygonum capitatum effect on Helicobacter pylori-associated gastritis based on network pharmacology.基于网络药理学的头花蓼对幽门螺杆菌相关性胃炎作用机制研究。
Bioorg Chem. 2021 Sep;114:105044. doi: 10.1016/j.bioorg.2021.105044. Epub 2021 Jun 5.
9
How to eradicate Helicobacter pylori using amoxicillin and omeprazole in the remnant stomach.如何在残胃中使用阿莫西林和奥美拉唑根除幽门螺杆菌。
Hepatogastroenterology. 2003 Nov-Dec;50(54):2267-9.
10
Effect of probiotics and triple eradication therapy on the cyclooxygenase (COX)-2 expression, apoptosis, and functional gastric mucosal impairment in Helicobacter pylori-infected Mongolian gerbils.益生菌和三联根除疗法对幽门螺杆菌感染的蒙古沙鼠环氧化酶(COX)-2表达、细胞凋亡及胃黏膜功能损伤的影响
Helicobacter. 2006 Feb;11(1):10-20. doi: 10.1111/j.0083-8703.2006.00373.x.

引用本文的文献

1
Plant-derived extracts or compounds for Helicobacter-associated gastritis: a systematic review of their anti-Helicobacter activity and anti-inflammatory effect in animal experiments.用于幽门螺杆菌相关性胃炎的植物提取物或化合物:动物实验中其抗幽门螺杆菌活性和抗炎作用的系统评价
Chin Med. 2025 Apr 22;20(1):53. doi: 10.1186/s13020-025-01093-2.
2
Hyperoside Alleviates -Induced Gastric Epithelial Cell Injury by Regulating Nrf2/HO-1 Signaling.金丝桃苷通过调节Nrf2/HO-1信号通路减轻[具体因素]诱导的胃上皮细胞损伤。
Pol J Microbiol. 2025 Mar 26;74(1):60-70. doi: 10.33073/pjm-2025-005. eCollection 2025 Mar 1.
3
Mechanisms of intestinal pharmacokinetic natural product-drug interactions.

本文引用的文献

1
Association between Helicobacter pylori burden and Alzheimer's disease.幽门螺杆菌负荷与阿尔茨海默病之间的关联。
Eur J Neurol. 2014 Dec;21(12):e100. doi: 10.1111/ene.12563.
2
Antioxidant and antibacterial activities of flavonoid glycosides from Ficus exasperata Vahl-Holl (moraceae) leaves.粗叶榕(桑科)叶中黄酮苷的抗氧化和抗菌活性
Afr J Tradit Complement Altern Med. 2014 Apr 3;11(3):97-101. doi: 10.4314/ajtcam.v11i3.14. eCollection 2014.
3
Association between Helicobacter pylori genotypes and severity of chronic gastritis, peptic ulcer disease and gastric mucosal interleukin-8 levels: Evidence from a study in the Middle East.
肠道药代动力学天然产物-药物相互作用的机制。
Drug Metab Rev. 2024 Aug;56(3):285-301. doi: 10.1080/03602532.2024.2386597. Epub 2024 Aug 12.
4
Progress in traditional Chinese medicine against chronic gastritis: From chronic non-atrophic gastritis to gastric precancerous lesions.中医治疗慢性胃炎的进展:从慢性非萎缩性胃炎到胃癌前病变
Heliyon. 2023 May 27;9(6):e16764. doi: 10.1016/j.heliyon.2023.e16764. eCollection 2023 Jun.
5
Bidirectional Effects of Mao Jian Green Tea and Its Flavonoid Glycosides on Gastrointestinal Motility.毛尖绿茶及其黄酮苷对胃肠动力的双向作用
Foods. 2023 Feb 16;12(4):854. doi: 10.3390/foods12040854.
6
, the Hmong Medicinal Flora: A Comprehensive Review of Its Phytochemical, Pharmacological and Pharmacokinetic Characteristics.《苗药本草:其植物化学、药理学和药代动力学特征的全面综述》。
Molecules. 2022 Sep 28;27(19):6407. doi: 10.3390/molecules27196407.
7
Interruption of -Induced NLRP3 Inflammasome Activation by Chalcone Derivatives.查尔酮衍生物对诱导的NLRP3炎性小体激活的阻断作用
Biomol Ther (Seoul). 2021 Jul 1;29(4):410-418. doi: 10.4062/biomolther.2020.192.
8
Pharmacological Effects of against Gastritis Using a Network Pharmacology Approach.基于网络药理学探讨 对胃炎的药理作用
Biomolecules. 2020 Sep 9;10(9):1298. doi: 10.3390/biom10091298.
9
A Systematic Review of the Mechanisms Underlying Treatment of Gastric Precancerous Lesions by Traditional Chinese Medicine.中医药治疗胃癌前病变机制的系统评价
Evid Based Complement Alternat Med. 2020 Apr 26;2020:9154738. doi: 10.1155/2020/9154738. eCollection 2020.
10
New Insights into Bioactive Compounds from the Medicinal Plant P. Beauv. and Their Activity against .药用植物P. Beauv.生物活性化合物的新见解及其对……的活性
Antibiotics (Basel). 2020 May 15;9(5):258. doi: 10.3390/antibiotics9050258.
幽门螺杆菌基因型与慢性胃炎、消化性溃疡病严重程度及胃黏膜白细胞介素-8 水平的关系:来自中东地区的研究证据。
Gut Pathog. 2014 Sep 26;6(1):41. doi: 10.1186/s13099-014-0041-1. eCollection 2014.
4
Mycobacterium tuberculosis decreases human macrophage IFN-γ responsiveness through miR-132 and miR-26a.结核分枝杆菌通过miR-132和miR-26a降低人类巨噬细胞对干扰素-γ的反应性。
J Immunol. 2014 Nov 1;193(9):4537-47. doi: 10.4049/jimmunol.1400124. Epub 2014 Sep 24.
5
Clarithromycin-based standard triple therapy can still be effective for Helicobacter pylori eradication in some parts of the Korea.在韩国的某些地区,基于克拉霉素的标准三联疗法对根除幽门螺杆菌仍可能有效。
J Korean Med Sci. 2014 Sep;29(9):1240-6. doi: 10.3346/jkms.2014.29.9.1240. Epub 2014 Sep 2.
6
Rifabutin-based high-dose proton-pump inhibitor and amoxicillin triple regimen as the rescue treatment for Helicobacter pylori.基于利福布汀的高剂量质子泵抑制剂和阿莫西林三联疗法作为幽门螺杆菌的挽救治疗方案。
Helicobacter. 2014 Dec;19(6):455-61. doi: 10.1111/hel.12147. Epub 2014 Sep 18.
7
Helicobacter pylori infection activates Src homology-2 domain-containing phosphatase 2 to suppress IFN-γ signaling.幽门螺杆菌感染激活含Src同源2结构域的磷酸酶2以抑制γ-干扰素信号传导。
J Immunol. 2014 Oct 15;193(8):4149-58. doi: 10.4049/jimmunol.1400594. Epub 2014 Sep 15.
8
Interaction of omeprazole and Helicobacter pylori-induced nuclear factor-κB activation and mediators in gastric epithelial cells.奥美拉唑与幽门螺杆菌诱导的胃上皮细胞核因子-κB激活及介质之间的相互作用。
J Chin Med Assoc. 2014 Nov;77(11):567-72. doi: 10.1016/j.jcma.2014.07.006. Epub 2014 Sep 7.
9
Periodontal disease and Helicobacter pylori infection: a community-based study using serology and rapid urease test.牙周病与幽门螺杆菌感染:一项基于社区的血清学和快速尿素酶试验研究
J Investig Clin Dent. 2016 Feb;7(1):37-45. doi: 10.1111/jicd.12122. Epub 2014 Aug 30.
10
CagA status & genetic characterization of metronidazole resistant strains of H. pylori from: A region at high risk of gastric cancer.CagA 状态与来自高胃癌风险地区的甲硝唑耐药幽门螺杆菌菌株的遗传特征。
Pak J Med Sci. 2014 Jul;30(4):804-8. doi: 10.12669/pjms.304.4840.