Abolfazl Shakeri, Mehrangiz Tajvar, Ghazaleh Tabriznia Tabrizi, Saman Soleimanpour, Javid Davoodi, Javad Asili, Mohammad Sadegh Amiri, Seyed Ahmad Emami
{"title":"生物测定指导下从 Galatella grimmii (Regel & Schmalh.) Sennikov 中分离抗结核分枝杆菌化合物并阐明其结构。","authors":"Abolfazl Shakeri, Mehrangiz Tajvar, Ghazaleh Tabriznia Tabrizi, Saman Soleimanpour, Javid Davoodi, Javad Asili, Mohammad Sadegh Amiri, Seyed Ahmad Emami","doi":"10.1186/s12906-024-04632-w","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Galatella is a genus in the family Asteraceae, represented by 35-45 species. Considering the high effectiveness of the ethyl acetate (EtOAc) fraction of G. grimmii against Mycobacterium tuberculosis (MIC = 0.5 µg/mL), a bioassay-directed fractionation of this extract was carried out.</p><p><strong>Methods: </strong>The methanolic extract of the aerial parts of G. grimmii was obtained using maceration, then it was suspended in water and partitioned with petroleum ether, dichloromethane (CH<sub>2</sub>Cl<sub>2</sub>), EtOAc, and n-butanol (n-BuOH), successively. The most potent fraction (EtOAc), was selected for further isolation by Sephadex LH-20 and semi-preparative HPLC to obtain active compounds.</p><p><strong>Results: </strong>Fractionation of the EtOAc solvent fraction resulted in the characterization of five compounds, among them, compounds 1 and 2 showed the highest anti-mycobacterial effects with MICs of 0.062 and 1.00 µg/mL against H37Rv M. tuberculosis, respectively, which were higher than those of rifampin (MIC of 1.25 µg/mL) and isoniazid (MIC of 0.31 µg/mL), as positive controls. Also, compound 1 inhibited all tested strains of drug-resistant Mycobacterium (MDR and XDR). Notably, the isolated compounds have been reported for the first time from G. grimmii.</p><p><strong>Conclusion: </strong>Due to the potent anti-mycobacterial effect of isolated compounds from G. grimmii, this study could pave the way for developing a novel class of natural anti-tuberculosis compounds.</p>","PeriodicalId":9128,"journal":{"name":"BMC Complementary Medicine and Therapies","volume":"24 1","pages":"345"},"PeriodicalIF":3.3000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11443940/pdf/","citationCount":"0","resultStr":"{\"title\":\"Bioassay-guided isolation and structure elucidation of anti-mycobacterium tuberculosis compounds from Galatella grimmii (Regel & Schmalh.) 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The most potent fraction (EtOAc), was selected for further isolation by Sephadex LH-20 and semi-preparative HPLC to obtain active compounds.</p><p><strong>Results: </strong>Fractionation of the EtOAc solvent fraction resulted in the characterization of five compounds, among them, compounds 1 and 2 showed the highest anti-mycobacterial effects with MICs of 0.062 and 1.00 µg/mL against H37Rv M. tuberculosis, respectively, which were higher than those of rifampin (MIC of 1.25 µg/mL) and isoniazid (MIC of 0.31 µg/mL), as positive controls. Also, compound 1 inhibited all tested strains of drug-resistant Mycobacterium (MDR and XDR). 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引用次数: 0
摘要
背景介绍Galatella属菊科,有35-45个种。考虑到 G. grimmii 的乙酸乙酯(EtOAc)馏分对结核分枝杆菌(MIC = 0.5 µg/mL)具有很高的药效,我们对这种提取物进行了生物测定定向分馏:采用浸渍法获得 G. grimmii 的气生部分甲醇提取物,然后将其悬浮于水中,依次用石油醚、二氯甲烷 (CH2Cl2)、EtOAc 和正丁醇 (n-BuOH) 进行分配。选出效力最强的馏分(EtOAc),通过 Sephadex LH-20 和半制备高效液相色谱进一步分离,以获得活性化合物:结果:对 EtOAc 溶剂馏分进行分馏后,鉴定出 5 种化合物,其中化合物 1 和 2 对 H37Rv 结核杆菌的抗霉菌效果最好,其 MIC 分别为 0.062 和 1.00 µg/mL,高于作为阳性对照的利福平(MIC 为 1.25 µg/mL)和异烟肼(MIC 为 0.31 µg/mL)。此外,化合物 1 还能抑制所有测试的耐药分枝杆菌(MDR 和 XDR)菌株。值得注意的是,这些化合物是首次从 G. grimmii 中分离出来:结论:由于从 G. grimmii 中分离出的化合物具有强效抗结核作用,该研究可为开发新型天然抗结核化合物铺平道路。
Bioassay-guided isolation and structure elucidation of anti-mycobacterium tuberculosis compounds from Galatella grimmii (Regel & Schmalh.) Sennikov.
Background: Galatella is a genus in the family Asteraceae, represented by 35-45 species. Considering the high effectiveness of the ethyl acetate (EtOAc) fraction of G. grimmii against Mycobacterium tuberculosis (MIC = 0.5 µg/mL), a bioassay-directed fractionation of this extract was carried out.
Methods: The methanolic extract of the aerial parts of G. grimmii was obtained using maceration, then it was suspended in water and partitioned with petroleum ether, dichloromethane (CH2Cl2), EtOAc, and n-butanol (n-BuOH), successively. The most potent fraction (EtOAc), was selected for further isolation by Sephadex LH-20 and semi-preparative HPLC to obtain active compounds.
Results: Fractionation of the EtOAc solvent fraction resulted in the characterization of five compounds, among them, compounds 1 and 2 showed the highest anti-mycobacterial effects with MICs of 0.062 and 1.00 µg/mL against H37Rv M. tuberculosis, respectively, which were higher than those of rifampin (MIC of 1.25 µg/mL) and isoniazid (MIC of 0.31 µg/mL), as positive controls. Also, compound 1 inhibited all tested strains of drug-resistant Mycobacterium (MDR and XDR). Notably, the isolated compounds have been reported for the first time from G. grimmii.
Conclusion: Due to the potent anti-mycobacterial effect of isolated compounds from G. grimmii, this study could pave the way for developing a novel class of natural anti-tuberculosis compounds.