Zhang Xuefeng, Li Xuanyi, Wang Peng, Zhao Shuqin, Zhao Yuanyuan
Pulmonary and Critical Care Medicine, Yantaishan Hospital, Yantai, Shandong, China.
Department of Center for Laboratory Diagnosis, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, Shandong, China.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Mar 31. doi: 10.1007/s00210-025-03943-0.
Safranal is an active ingredient with pharmacological anti-inflammatory effects derived from Crocus sativus essential oil. To explore the comprehensive effects of Safranal on airway inflammation, airway hyperreactivity, and remodeling and its potential mechanisms through the allergic asthma model, an in vitro model of ASMC cells stimulated by TNF-α was established. The cells were transfected with si-RUNX3 and RUNX3 overexpression plasmids, and DEX was used as a positive control. The expression of RUNX3 was detected by western blot and immunofluorescence. The levels of inflammatory factors were measured by ELISA, while flow cytometry detected the anti-apoptotic effects and ROS production. Subsequently, OVA-sensitized WT mice and RUNX3-KO mice were administered with DEX and Safranal for 2 weeks to establish a mouse model of allergic asthma, and changes in airway hyperresponsiveness, inflammatory manifestations, and airway remodeling were detected. The mechanism of Safranal was verified by detecting the expression of RUNX3, inflammation, and fibrosis-related proteins in the lung tissues. By modulating the NLRP3/Caspase-1 pathway, Safranal significantly alleviated the negative effects caused by RUNX3 suppression in vivo and in vitro. We propose that Safranal is a potential active compound for the treatment of asthma, and its clinical application value in allergic asthma should be further explored.
藏红花醛是一种具有药理抗炎作用的活性成分,源自藏红花精油。为了通过过敏性哮喘模型探讨藏红花醛对气道炎症、气道高反应性和重塑的综合影响及其潜在机制,建立了肿瘤坏死因子-α刺激的气道平滑肌细胞(ASMC)体外模型。细胞用小干扰RNA(si-RUNX3)和RUNX3过表达质粒转染,地塞米松(DEX)用作阳性对照。通过蛋白质免疫印迹法和免疫荧光检测RUNX3的表达。用酶联免疫吸附测定法(ELISA)测量炎症因子水平,同时用流式细胞术检测抗凋亡作用和活性氧(ROS)产生。随后,对卵清蛋白致敏的野生型(WT)小鼠和RUNX3基因敲除(RUNX3-KO)小鼠给予地塞米松和藏红花醛2周以建立过敏性哮喘小鼠模型,并检测气道高反应性、炎症表现和气道重塑的变化。通过检测肺组织中RUNX3、炎症和纤维化相关蛋白的表达来验证藏红花醛的作用机制。通过调节NLRP3/半胱天冬酶-1途径,藏红花醛显著减轻了体内和体外RUNX3抑制引起的负面影响。我们认为藏红花醛是一种治疗哮喘的潜在活性化合物,其在过敏性哮喘中的临床应用价值有待进一步探索。