School of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen, 518107, Guangdong, China.
Regenerative Medicine Research Center, Future Homo Sapiens Institute of Regenerative Medicine Co., Ltd, Guangzhou, China.
J Ethnopharmacol. 2024 Feb 10;320:117428. doi: 10.1016/j.jep.2023.117428. Epub 2023 Nov 18.
Terminalia chebula Retz., known as the King of Traditional Tibetan Medicine, is widely used for treating various ailments, particularly stomach disorders. It exhibited inhibitory activity against helicobacter pylori.
The exact mechanism by which T. chebula combats H. pylori infection remains unclear. Therefore, this study aimed to investigate its mechanism of action and the key pathways and targets involved.
Minimum inhibitory concentration (MIC) assay, scanning electron microscope, and inhibiting kinetics curves were conducted. The mRNA expressions were measured by RNA-seq analysis and RT-QPCR. ELISA and Western blot were used to detect the changes in proteins. The main compounds were analyzed by High-performance Liquid Chromatography. The interaction between the compound and target was predicted by Molecular Docking.
The study revealed that T. chebula disrupted the structure of H. pylori bacteria and inhibited Cag A protein expression. Additionally, T. chebula can reduce the expression of flaA, flaB, babA, alpA, alpB, ureE, and ureF genes. Furthermore, T. chebula demonstrated its effectiveness in inhibiting the H. pylori-induced inflammatory response by regulating the inflammasome signaling and ER-stress pathway. Moreover, the study discovered that chebulagic acid has anti-HP activity and inhibits the expression of Cag A protein.
T. chebula acts as a natural remedy for combating H. pylori infection. Its ability to disrupt the bacterial structure, inhibit key proteins, regulate inflammatory pathways, and the presence of chebulagic acid contribute to its anti-H. pylori activity.
诃子(Terminalia chebula Retz.),又称传统藏药之王,被广泛用于治疗各种疾病,特别是胃病。它对幽门螺杆菌具有抑制活性。
诃子对抗幽门螺杆菌感染的确切机制尚不清楚。因此,本研究旨在探讨其作用机制以及涉及的关键途径和靶点。
进行最低抑菌浓度(MIC)测定、扫描电子显微镜观察和抑制动力学曲线测定。通过 RNA-seq 分析和 RT-QPCR 测量 mRNA 表达。ELISA 和 Western blot 用于检测蛋白变化。采用高效液相色谱分析主要化合物。通过分子对接预测化合物与靶标的相互作用。
研究表明,诃子破坏了幽门螺杆菌的结构并抑制了 Cag A 蛋白的表达。此外,诃子可以降低 flaA、flaB、babA、alpA、alpB、ureE 和 ureF 基因的表达。此外,诃子通过调节炎症小体信号和内质网应激途径,显示出抑制幽门螺杆菌诱导的炎症反应的有效性。此外,研究发现诃子酸具有抗 HP 活性并抑制 Cag A 蛋白的表达。
诃子是一种天然的抗幽门螺杆菌感染的药物。它破坏细菌结构、抑制关键蛋白、调节炎症途径以及存在诃子酸的能力,使其具有抗幽门螺杆菌的活性。