首页> 美国卫生研究院文献>Toxins >Anti-Helicobacter pylori Properties of the Ant-Venom Peptide Bicarinalin
【2h】

Anti-Helicobacter pylori Properties of the Ant-Venom Peptide Bicarinalin

机译:蚂蚁毒肽Bicarinalin的抗幽门螺杆菌特性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The venom peptide bicarinalin, previously isolated from the ant Tetramorium bicarinatum, is an antimicrobial agent with a broad spectrum of activity. In this study, we investigate the potential of bicarinalin as a novel agent against Helicobacter pylori, which causes several gastric diseases. First, the effects of synthetic bicarinalin have been tested against Helicobacter pylori: one ATCC strain, and forty-four isolated from stomach ulcer biopsies of Peruvian patients. Then the cytoxicity of bicarinalin on human gastric cells and murine peritoneal macrophages was measured using XTT and MTT assays, respectively. Finally, the preventive effect of bicarinalin was evaluated by scanning electron microscopy using an adherence assay of H. pylori on human gastric cells treated with bicarinalin. This peptide has a potent antibacterial activity at the same magnitude as four antibiotics currently used in therapies against H. pylori. Bicarinalin also inhibited adherence of H. pylori to gastric cells with an IC50 of 0.12 μg·mL−1 and had low toxicity for human cells. Scanning electron microscopy confirmed that bicarinalin can significantly decrease the density of H. pylori on gastric cells. We conclude that Bicarinalin is a promising compound for the development of a novel and effective anti-H. pylori agent for both curative and preventive use.
机译:毒肽双香豆素以前从蚂蚁四甲螨中分离出来,是一种具有广泛活性的抗菌剂。在这项研究中,我们调查了双香豆素作为抗幽门螺杆菌(一种引起几种胃部疾病)的新型药物的潜力。首先,已经测试了合成的双香豆素对幽门螺杆菌的作用:一种ATCC菌株,以及从秘鲁患者的胃溃疡活检物中分离出的四十四种。然后分别使用XTT和MTT分析法测定了双香豆素对人胃细胞和鼠腹膜巨噬细胞的细胞毒性。最后,使用幽门螺杆菌的粘附测定法通过扫描电子显微镜评价了比卡洛林的预防作用对用比卡洛林处理的人胃细胞的粘附作用。该肽具有强大的抗菌活性,其强度与目前用于治疗幽门螺杆菌的四种抗生素相同。 Bicarinalin还抑制幽门螺杆菌对胃细胞的粘附,IC50为0.12μg·mL -1 ,对人体细胞毒性低。扫描电子显微镜证实,双香豆素可显着降低胃细胞上幽门螺杆菌的密度。我们得出的结论是,Bicarinalin是开发新型且有效的抗H的有前途的化合物。用于治疗和预防的幽门螺杆菌制剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号