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甘草次酸通过调节炎症和氧化应激来保护肺上皮细胞免受耐多药鲍曼不动杆菌诱导的损伤。

Glycyrrhetinic acid protects against Multidrug-resistant Acinetobacter baumannii-induced lung epithelial cells injury by regulating inflammation and oxidative stress.

机构信息

Zhejiang Chinese Medical University, Hangzhou, Zhejiang, 310053, PR China.

Affiliated Hangzhou First People's Hospital, Zhejiang University of Medicine, Hangzhou, Zhejiang, 310003, PR China.

出版信息

BMC Pharmacol Toxicol. 2023 Jan 30;24(1):5. doi: 10.1186/s40360-023-00648-z.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d937/9887834/b76280f3330c/40360_2023_648_Fig1_HTML.jpg

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