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首页> 外文期刊>Phytotherapy research: PTR >Antimycobacterial and synergistic effects of 18β-glycyrrhetinic acid or glycyrrhetinic acid-30-piperazine in combination with isoniazid, rifampicin or streptomycin against Mycobacterium bovis
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Antimycobacterial and synergistic effects of 18β-glycyrrhetinic acid or glycyrrhetinic acid-30-piperazine in combination with isoniazid, rifampicin or streptomycin against Mycobacterium bovis

机译:18β-甘草次酸或甘草次酸-30-哌嗪与异烟肼,利福平或链霉素联合使用对牛分枝杆菌的抗分枝作用和协同作用

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18β-Glycyrrhetinic acid (18βGA) is a major bioactive component of liquorice with known activity. In this study, we found that both 18βGA and its derivative glycyrrhetinic acid-30-piperazine (PGA), have potent antimycobacterial properties against the drug-susceptible and drug-resistant Mycobacterium bovis. More importantly, they exhibited synergistic effects with the first-line drugs isoniazid (INH), rifampicin (RIF) and streptomycin (SM) against clinical M. bovis isolates, including drug-resistant strains. In combination with a subinhibitory concentration of 18βGA, the minimum inhibitory concentrations (MICs) of the anti-tuberculosis agents decreased, ranging from 4- to 16-, 4- to 8- and 4- to 8-fold for INH (fractional inhibitory concentration index (FICI) 0.125-0.375), RIF (FICI 0.118-0.281) and SM (FICI 0.094-0.275), respectively. In the presence of PGA, MICs for the first-line agents resulted in a 4-16-fold decrease for INH (FICI 0.094-0.266, RIF (FICI 0.114-0.313) and SM (FICI 0.094-0.281). Additionally, the MICs of 18βGA or PGA alone showed significant decreases ranging from 8- to 16-, 8- to 64- and 8- to 128-fold in the presence of INH, RIF and SM, respectively. These findings indicate that 18βGA and its derivatives might serve as potential therapeutic compounds for future antimycobacterial drug development.
机译:18β-甘草次酸(18βGA)是甘草的主要生物活性成分,具有已知的活性。在这项研究中,我们发现18βGA及其衍生物甘草次酸30-哌嗪(PGA)对药物敏感性和耐药性牛分枝杆菌均​​具有有效的抗分枝杆菌特性。更重要的是,它们与一线药物异烟肼(INH),利福平(RIF)和链霉素(SM)对临床牛分枝杆菌分离株(包括耐药株)具有协同作用。与18βGA的亚抑制浓度结合使用时,抗结核药的最低抑制浓度(MIC)降低,INH的最低抑制浓度为4至16倍,4至8倍和4至8倍(分数抑制浓度)指数(FICI)0.125-0.375),RIF(FICI 0.118-0.281)和SM(FICI 0.094-0.275)。在存在PGA的情况下,一线药物的MIC导致INH(FICI 0.094-0.266,RIF(FICI 0.114-0.313)和SM(FICI 0.094-0.281))降低4-16倍。在存在INH,RIF和SM的情况下,单独的18βGA或PGA的显着降低分别为8至16倍,8至64倍和8至128倍,这些发现表明18βGA及其衍生物可能起作用作为未来抗分枝杆菌药物开发的潜在治疗化合物。

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