Department of Anesthesiology, Nanchong Central Hospital, The Second Clinical College of North Sichuan Medical College, Nanchong, China; North Sichuan Medical College, Nanchong, China.
North Sichuan Medical College, Nanchong, China.
Int Immunopharmacol. 2021 Oct;99:107972. doi: 10.1016/j.intimp.2021.107972. Epub 2021 Jul 20.
We sought to assess the protective effect of different doses of Fingolimod (FTY720) in a rat model of acute lung injury (ALI) induced by intratracheal instillation of lipopolysaccharide (LPS) and explored the underlying mechanisms. The ALI model was established in rats and different doses of FTY720 (0.1 mg/kg, 0.2 mg/kg, 0.5 mg/kg, 1 mg/kg, or 2 mg/kg) were injected intraperitoneally. Lung computed tomography and blood gas analyses were performed at 6 h, 24 h, and 48 h after intraperitoneal injection, and the lung tissues were extracted to prepare paraffin sections for histopathological examination. The levels of inflammatory cytokines (TNF-α, IL-6, and IL-1β) were detected by ELISA, and the expressions of inflammatory pathway proteins in each group were measured by Western blot analysis. A single intraperitoneal injection of FTY720 inhibited LPS-induced NF-κB activation, reduced the level of inflammatory cytokines, and decreased the infiltration of inflammatory cells. Moreover, it alleviated lung tissue injury, as shown by marked attenuation of pulmonary oedema and improved arterial partial pressure of oxygen (PaO) and the general condition of ALI rats. In conclusion, our results demonstrate the protective effect of FTY720 against LPS-induced ALI. The underlying mechanism of the protective effect may involve inhibition of LPS-induced activation of NF-κB and regulation of the inflammatory pathway to alleviate barrier dysfunction of alveolar capillaries.
我们旨在评估不同剂量的芬戈莫德(FTY720)在脂多糖(LPS)气管内滴注诱导的大鼠急性肺损伤(ALI)模型中的保护作用,并探讨其潜在机制。在大鼠中建立了 ALI 模型,并通过腹腔内注射给予不同剂量的 FTY720(0.1mg/kg、0.2mg/kg、0.5mg/kg、1mg/kg 或 2mg/kg)。在腹腔内注射后 6h、24h 和 48h 进行肺部计算机断层扫描和血气分析,并提取肺组织制备石蜡切片进行组织病理学检查。通过 ELISA 检测炎症细胞因子(TNF-α、IL-6 和 IL-1β)的水平,通过 Western blot 分析测量各组中炎症途径蛋白的表达。单次腹腔内注射 FTY720 抑制 LPS 诱导的 NF-κB 激活,降低炎症细胞因子水平,并减少炎症细胞浸润。此外,它还减轻了肺组织损伤,表现为肺水肿明显减轻,动脉部分氧分压(PaO)和 ALI 大鼠一般状况得到改善。总之,我们的结果表明 FTY720 对 LPS 诱导的 ALI 具有保护作用。其保护作用的潜在机制可能涉及抑制 LPS 诱导的 NF-κB 激活和调节炎症途径,以减轻肺泡毛细血管的屏障功能障碍。