Wang Jiamian, Cheng Chen, Gao Yujin, Li Yina, Zhang Xijun, Yao Dan, Zhang Yong
College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730070, China.
Gansu Key Laboratory of Animal Generational Physiology and Reproductive Regulation, Lanzhou 730070, China.
Vet Sci. 2025 Mar 2;12(3):227. doi: 10.3390/vetsci12030227.
(1) Background: Bovine mastitis is a lactational disease caused by infection and milk stagnation in the mammary glands. Danggui buxue decoction (DBD), a traditional remedy for blood tonification, anti-inflammation, and antioxidation, has not been used previously to treat mastitis. (2) Methods: In this study, an mastitis model was established by infecting lactating Kunming mice with clinically isolated bovine mastitis-derived . Based on this, the effects of DBD on inflammation and oxidative stress in mastitis model mice were evaluated by conducting routine blood tests, H&E staining, qRT-PCR analysis, ELISA, and microcolorimetry. (3) Results: We found that DBD treatment reduced body weight loss, abnormal organ indices, abnormal blood cell counts, pathological damage to breast tissue, and the upregulation of the expression of inflammatory factor in mice caused by infection. We also found that DBD increased the expression of antioxidants and antioxidant genes and decreased the expression of oxidation products and oxidation-related genes in breast tissue. The therapeutic effect of DBD on inflammation and oxidative stress (OS) in mice occurred through the regulation of the TLR4/NF-κB and Nrf2/HO-1 signaling pathways. (4) Conclusions: DBD imparted its anti-inflammatory and antioxidant effects by inhibiting the TLR4/NF-κB signaling pathway and activating the antioxidant Nrf2/HO-1 signaling pathway.
(1) 背景:牛乳腺炎是一种由乳腺感染和乳汁淤积引起的泌乳期疾病。当归补血汤(DBD)是一种传统的补血、抗炎和抗氧化药物,此前尚未用于治疗乳腺炎。(2) 方法:在本研究中,通过用临床分离的牛乳腺炎源感染泌乳期昆明小鼠建立乳腺炎模型。在此基础上,通过常规血液检测、苏木精-伊红(H&E)染色、实时定量聚合酶链反应(qRT-PCR)分析、酶联免疫吸附测定(ELISA)和微量比色法评估DBD对乳腺炎模型小鼠炎症和氧化应激的影响。(3) 结果:我们发现,DBD治疗减轻了感染引起的小鼠体重减轻、器官指数异常、血细胞计数异常、乳腺组织病理损伤以及炎症因子表达上调。我们还发现,DBD增加了乳腺组织中抗氧化剂和抗氧化基因的表达,并降低了氧化产物和氧化相关基因的表达。DBD对小鼠炎症和氧化应激(OS)的治疗作用是通过调节Toll样受体4(TLR4)/核因子κB(NF-κB)和核因子E2相关因子2(Nrf2)/血红素加氧酶-1(HO-1)信号通路实现的。(4) 结论:DBD通过抑制TLR4/NF-κB信号通路和激活抗氧化剂Nrf2/HO-1信号通路发挥其抗炎和抗氧化作用。