Wei Yu-Heng, Zhou Shu-Mian, Zhao Wen, Chen Qi, Wang Qiu-Hua, Yu Mei-Ling, Wei Ying-Yi, Hu Ting-Jun
College of Animal Science and Technology, Guangxi University, Nanning, China.
Guangxi Zhuang Autonomous Region Engineering Research Center of Veterinary Biologics, Nanning, China.
Front Vet Sci. 2025 Feb 4;12:1539448. doi: 10.3389/fvets.2025.1539448. eCollection 2025.
The normal butanol fraction of L. flavonoids (FNB) exhibits significant anti-inflammatory effects. This study investigated FNB's impact on inflammatory responses induced by Porcine circovirus type 2 (PCV2) in cell and mouse models.
An inflammatory model was established in RAW264.7 cells infected with varying PCV2 concentrations. And assigning both RAW264.7 cells and 108 SPF-grade KM mice to Control, PCV2, Rutin, and various dosages of FNB groups. Inflammatory factors such as Monocyte Chemoattractant Protein-1 (MCP-1), interleukin-6 (IL-6), IL-8, IL-10, Tumor Necrosis Factor-alpha (TNF-α), Reactive Oxygen Species (ROS), and Nitric Oxide (NO) were quantified using ELISA, RT-qPCR and immunohistochemistry.
Results showed that a PCV2 titer of 10 TCID/0.1 mL when applied to RAW264.7 cells effectively established an inflammatory model at 12 and 24 h post-infection. Following PCV2 infection, all the inflammatory factors displayed a significant increased both in culture supernatant and intracellular mRNA expression levels ( < 0.05 or < 0.01), but these levels were reduced by FNB treatment ( < 0.05 or < 0.01). In mouse sera post-PCV2 infection also showed elevated levels of IL-6, IL-8 IL-10, TNF-α, and MCP-1 ( < 0.05 or < 0.01). Additionally, mRNA and protein levels for TNF-α, IL-8, IL-10, IL-6, and iNOS rose significantly in lung tissues ( < 0.01) but decreased with FNB treatment ( < 0.05 or < 0.01).
These findings suggest that FNB reduces inflammatory factor production and modulates the inflammatory response triggered by PCV2 infection, potentially enhancing host resistance against it.
黄灯笼辣椒黄酮类化合物的正丁醇馏分(FNB)具有显著的抗炎作用。本研究在细胞和小鼠模型中研究了FNB对2型猪圆环病毒(PCV2)诱导的炎症反应的影响。
在感染不同浓度PCV2的RAW264.7细胞中建立炎症模型。将RAW264.7细胞和108只SPF级KM小鼠分为对照组、PCV2组、芦丁组和不同剂量的FNB组。使用酶联免疫吸附测定(ELISA)、逆转录-定量聚合酶链反应(RT-qPCR)和免疫组织化学对单核细胞趋化蛋白-1(MCP-1)、白细胞介素-6(IL-6)、IL-8、IL-10、肿瘤坏死因子-α(TNF-α)、活性氧(ROS)和一氧化氮(NO)等炎症因子进行定量分析。
结果表明,当将10 TCID/0.1 mL的PCV2滴度应用于RAW264.7细胞时,在感染后12小时和24小时有效地建立了炎症模型。PCV2感染后,所有炎症因子在培养上清液和细胞内mRNA表达水平上均显著升高(<0.05或<0.01),但FNB处理后这些水平降低(<0.05或<0.01)。PCV2感染后的小鼠血清中IL-6、IL-8、IL-10、TNF-α和MCP-1水平也升高(<0.05或<0.01)。此外,肺组织中TNF-α、IL-8、IL-10、IL-6和诱导型一氧化氮合酶(iNOS)的mRNA和蛋白水平显著升高(<0.01),但FNB处理后降低(<0.05或<0.01)。
这些发现表明,FNB可减少炎症因子的产生,并调节PCV2感染引发的炎症反应,可能增强宿主对其的抵抗力。