State Key Laboratory of Natural Medicines, Department of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, PR China.
Yangtze River Pharmaceutical Group Beijing Haiyan Pharmaceutical Co., Ltd., Beijing 102206, PR China; Beijing University of Chemical Technology, Beijing 100029, PR China.
Biomed Pharmacother. 2019 Oct;118:109188. doi: 10.1016/j.biopha.2019.109188. Epub 2019 Jul 14.
Pulmonary dysfunction is tightly associated with cough variant asthma (CVA), a respiratory damage disease. Suhuang antitussive capsule (Suhuang), one of traditional Chinese patent medicines, plays a crucial role in the treatment and complication of CVA in the long clinical application. In this study, we aimed to investigate the protective effects and underlying antitussive mechanisms of Suhuang on pulmonary function in ovalbumin (OVA)-induced CVA rats. Administration (i.g.) of Suhuang significantly alleviated pulmonary damage and dysfunction. Suhuang improved ER stress and PKCε translocation via regulation of Ca trafficking. Suhuang also inhibited NLRP3 inflammasome activation, as evidenced by disrupting the assembly of NLRP3 inflammasome and reducing the expression of cleaved caspase-1, and decreased IL-1β secretion. Besides, it's identified that TXNIP induction and RIP1-RIP3-Drp1 pathway were required for the inhibitory routes of Suhuang from ER stress to NLRP3 inflammasome activation. Consistent with the in vivo findings, Suhuang also attenuated ER stress/NLRP3 inflammasome activation, and thereby restored pulmonary homeostasis in vitro. Meantime, these functions were diminished by blocking ER stress, indicating that ER stress is essential for the effects of Suhuang on pulmonary function. A further in vivo analysis showed that Suhuang-driven pharmacological inactivation of NLRP3 inflammasome and amelioration of pulmonary dysfunction were reversed by an ER stress inducer tunicamycin, well confirming the beneficial effects of Suhuang on pulmonary function by regulation of ER stress. Collectively, these results indicated that Suhuang contributed to impairing NLRP3 inflammasome activation via inhibition of ER stress, which was responsible for the protection of pulmonary homeostasis. These findings may provide a pharmacological groundwork and important new experimental data regarding the clinical treatment of Suhuang in CVA patients.
肺部功能障碍与咳嗽变异性哮喘(CVA)密切相关,CVA 是一种呼吸系统损伤疾病。苏黄止咳胶囊(Suhuang)是一种中药方剂,在长期的临床应用中对 CVA 的治疗和并发症发挥着重要作用。本研究旨在探讨苏黄对卵清蛋白(OVA)诱导的 CVA 大鼠肺功能的保护作用及其潜在的镇咳机制。苏黄经口给药(i.g.)可显著减轻肺部损伤和功能障碍。苏黄通过调节钙转运来改善内质网应激和蛋白激酶 Cε易位。苏黄还抑制 NLRP3 炎性体激活,表现在破坏 NLRP3 炎性体的组装,减少切割的半胱天冬酶-1 的表达,降低白细胞介素-1β的分泌。此外,研究发现 TXNIP 诱导和 RIP1-RIP3-Drp1 途径是苏黄从内质网应激到 NLRP3 炎性体激活的抑制途径所必需的。与体内研究结果一致,苏黄也可减轻内质网应激/NLRP3 炎性体激活,从而恢复体外肺内稳态。同时,这些功能通过阻断内质网应激而减弱,表明内质网应激是苏黄对肺功能作用的关键。进一步的体内分析表明,苏黄驱动的 NLRP3 炎性体药理学失活和肺功能障碍改善被内质网应激诱导剂衣霉素逆转,这充分证实了苏黄通过调节内质网应激对肺功能的有益作用。综上所述,苏黄通过抑制内质网应激来损害 NLRP3 炎性体激活,这有助于维持肺内稳态。这些发现可能为苏黄在 CVA 患者中的临床治疗提供药理学基础和重要的新实验数据。