虎杖苷通过抑制生物膜形成和氧化应激来预防肺上皮细胞免受耐碳青霉烯类肺炎克雷伯菌的损伤。
Polydatin prevent lung epithelial cell from Carbapenem-resistant Klebsiella pneumoniae injury by inhibiting biofilm formation and oxidative stress.
机构信息
Zhejiang Chinese Medical University, No. 548, Binwen Road, Binjiang District, Hangzhou, 310053, Zhejiang, People's Republic of China.
Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.
出版信息
Sci Rep. 2023 Oct 18;13(1):17736. doi: 10.1038/s41598-023-44836-7.
Carbapenem-resistant Klebsiella pneumoniae (CRKP) causes severe inflammation in various infectious diseases, such as bloodstream infections, respiratory and urinary tract infections, which leads to high mortality. Polydatin (PD), an active ingredient of Yinhuapinggan granule, has attracted worldwide attention for its powerful antioxidant, anti-inflammatory, antitumor, and antibacterial capacity. However, very little is known about the effect of PD on CRKP. In this research, we evaluated the inhibitory effects of PD on both the bacterial level and the bacterial-cell co-culture level on anti-biofilm and efflux pumps and the other was the inhibitory effect on apoptosis, reactive oxygen species (ROS), mitochondrial membrane potential (MMP) after CRKP induction. Additionally, we validated the mechanism of action by qRT-PCR and western blot in human lung epithelial cells. Firstly, PD was observed to have an inhibitory effect on the biofilm of CRKP and the efflux pump AcrAB-TolC. Mechanically, CRKP not only inhibited the activation of Nuclear Factor erythroid 2-Related Factor 2 (Nrf-2) but also increased the level of ROS in cells. These results showed that PD could inhibit ROS and activate Nrf-2 production. Together, our research demonstrated that PD inhibited bacterial biofilm formation and efflux pump AcrAB-TolC expression and inhibited CRKP-induced cell damage by regulating ROS and Nrf-2-regulated antioxidant pathways.
耐碳青霉烯肺炎克雷伯菌(CRKP)可引起多种感染性疾病的严重炎症,如血流感染、呼吸道和尿路感染等,导致高死亡率。虎杖苷(PD)是茵黄肝炎颗粒的一种有效成分,因其强大的抗氧化、抗炎、抗肿瘤和抗菌能力而引起了全球关注。然而,关于 PD 对 CRKP 的影响知之甚少。在这项研究中,我们评估了 PD 对 CRKP 的细菌水平和细菌-细胞共培养水平的抗生物膜和外排泵的抑制作用,以及对诱导 CRKP 后细胞凋亡、活性氧(ROS)、线粒体膜电位(MMP)的抑制作用。此外,我们还通过 qRT-PCR 和 Western blot 在人肺上皮细胞中验证了作用机制。首先,观察到 PD 对 CRKP 的生物膜和外排泵 AcrAB-TolC 具有抑制作用。从机制上讲,CRKP 不仅抑制核因子红细胞 2 相关因子 2(Nrf-2)的激活,还增加了细胞内 ROS 的水平。这些结果表明 PD 可以抑制 ROS 并激活 Nrf-2 的产生。总之,我们的研究表明 PD 通过调节 ROS 和 Nrf-2 调节的抗氧化途径抑制细菌生物膜形成和外排泵 AcrAB-TolC 表达,并抑制 CRKP 诱导的细胞损伤。