Zhejiang Chinese Medical University, Hangzhou, Zhejiang, 310053, PR China.
Affiliated Hangzhou First People's Hospital, Zhejiang University of Medicine, Hangzhou, Zhejiang, 310003, PR China.
BMC Pharmacol Toxicol. 2023 Jan 30;24(1):5. doi: 10.1186/s40360-023-00648-z.
Glycyrrhetinic acid (GA) is a bio-effective component of Licorice. The GA is a monomer and the ingredient is an Oleanane-type pentacyclic triterpenes that has been used as a remedy for years. Due to the abuse of antibiotics, people pay attention to the emergence of Multidrug-resistant Acinetobacter baumannii (MDR-AB). As a conditional pathogen, MDR-AB causes severe infection, endangering human lives. Our previous studies found GA played an important role in Yinhua Pinggan, a Chinese medicine. However, whether GA could protect lung epithelium from MDR-AB-induced cell injury was elusive. Herein, we investigated the effects of GA on MDR-AB-infected A549 cells. The results showed GA had slightly antibacterial activity to MDR-AB in the GA (high concentration) but no impact on drug resistance genes. Notwithstanding, GA could reverse MDR-AB-induced cell apoptosis, hampered adhesion and invasion of MDR-AB to cells, and inhibit pro-inflammatory cytokines expression of IL-1β, IL-6, and TNF. Besides, MDR-AB-induced reactive oxygen species, pro-oxidative protein malonaldehyde, and myeloperoxidase of cells were decreased by GA, while antioxidative proteins were recovered, showing antioxidative capacity of GA might play a critical role. The expressions of toll-like receptor (TLRs) - 1, 2, 4, 5, 6, and 9 were increased by MDR-AB infection, while GA reversed the tendency. Interestingly, GA inhibited MDR-AB induced myeloiddifferentiationfactor88 expression (MYD88), one downstream con-factors of TLRs, but no affection on Interferon regulatory Factor 3 (IRF3), the other one, indicating GA inhibited MDR-AB induced cell injury by impact TLR/MYD88 pathway to attenuate inflammation. Altogether, our results demonstrated that GA protects against MDR-AB-induced cell injury through its antioxidative and anti-inflammatory properties, which deserve further study in the future.
甘草酸(GA)是甘草的一种生物有效成分。GA 是一种单体,其成分是一种齐墩果烷型五环三萜类化合物,多年来一直被用作药物。由于抗生素的滥用,人们开始关注多药耐药鲍曼不动杆菌(MDR-AB)的出现。作为一种条件病原体,MDR-AB 会引起严重的感染,危及人类生命。我们之前的研究发现,GA 在中药银花平安中发挥了重要作用。然而,GA 是否能保护肺上皮细胞免受 MDR-AB 诱导的细胞损伤尚不清楚。在此,我们研究了 GA 对 MDR-AB 感染的 A549 细胞的影响。结果表明,GA(高浓度)对 MDR-AB 有轻微的抗菌活性,但对耐药基因没有影响。尽管如此,GA 可以逆转 MDR-AB 诱导的细胞凋亡,阻碍 MDR-AB 与细胞的黏附和侵袭,并抑制促炎细胞因子 IL-1β、IL-6 和 TNF 的表达。此外,GA 降低了 MDR-AB 诱导的细胞内活性氧、氧化蛋白丙二醛和髓过氧化物酶的表达,同时恢复了抗氧化蛋白,表明 GA 的抗氧化能力可能发挥了关键作用。TLRs(TLR1、2、4、5、6 和 9)的表达在 MDR-AB 感染后增加,而 GA 则逆转了这一趋势。有趣的是,GA 抑制了 MDR-AB 诱导的髓样分化因子 88 表达(MYD88),即 TLRs 的一个下游共同因子,但对干扰素调节因子 3(IRF3)没有影响,IRF3 是另一个共同因子,这表明 GA 通过影响 TLR/MYD88 通路抑制 MDR-AB 诱导的细胞损伤,从而减轻炎症。总之,我们的研究结果表明,GA 通过其抗氧化和抗炎特性来保护细胞免受 MDR-AB 诱导的细胞损伤,这值得在未来进一步研究。