Yu Jianyuan, Zhou Huifen, Guo Jianwen, Chen Tianhang, Shao Chongyu, Pan Zhiyong, Yang Jiehong, Wan Haitong
School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Key Laboratory of TCM Encephalopathy of Zhejiang Province (grant no. 2020E10012), Hangzhou, China.
J Tradit Complement Med. 2024 Mar 13;15(1):84-92. doi: 10.1016/j.jtcme.2024.03.005. eCollection 2025 Jan.
The NLRP3 inflammasome can be activated after intracerebral hemorrhage (ICH), triggering an inflammatory response in the brain. Chinese herbal medicine Zhongfeng Xingnao Prescription (ZFXN) is commonly used in China for intracerebral hemorrhage treatment. However, the underlying treatment mechanism of it is unclear. The purpose of our study is to investigate whether ZFXN alleviates injury after intracerebral hemorrhage by blocking the activation of CaMKII/NF-κB p65/NLRP3/GSDMD signaling axis.
We evaluated the protective effect of ZFXN in a rat model of collagenase Ⅶ-induced ICH. The neurological deficit score, cerebral hematoma-injury ratio, pathology, and ultrastructure of tissue surrounding the hematoma were evaluated after 5 days of ZFXN treatment, CaMKII/NF-κB p65/NLRP3/GSDMD signaling axis-related protein expression around the hematoma was assessed by Western blot and immunohistochemistry. Meanwhile, ELISA measured the levels of IL-1β, IL-18, IL-6 and TNF-α in serum.
After 5 days of ZFXN treatment, the score of neurological deficit and hematoma damage ratio decreased, and the cell destruction such as edema and vacuole conditions around the hematoma improved. The mechanism investigation results showed that ZFXN down-regulated expressions of CaMKII/NF-κB p65/NLRP3/GSDMD signaling axis-related protein around the hematoma area. In addition, ZFXN could attenuate the inflammatory response by regulating the activation of NLRP3 inflammasome after ICH. For the first time, we found that the efficacy of ZFXN on ICH might be related to the regulation of NLRP3 inflammasome.
脑出血(ICH)后NLRP3炎性小体可被激活,引发脑部炎症反应。中药醒脑静注射液(ZFXN)在中国常用于脑出血治疗。然而,其潜在的治疗机制尚不清楚。本研究的目的是探讨ZFXN是否通过阻断CaMKII/NF-κB p65/NLRP3/GSDMD信号轴的激活来减轻脑出血后的损伤。
我们在胶原酶Ⅶ诱导的脑出血大鼠模型中评估了ZFXN的保护作用。ZFXN治疗5天后,评估神经功能缺损评分、脑血肿损伤率、病理学及血肿周围组织的超微结构,通过蛋白质免疫印迹法和免疫组织化学法评估血肿周围CaMKII/NF-κB p65/NLRP3/GSDMD信号轴相关蛋白表达。同时,酶联免疫吸附测定法检测血清中IL-1β、IL-18、IL-6和TNF-α的水平。
ZFXN治疗5天后,神经功能缺损评分和血肿损伤率降低,血肿周围的细胞破坏如水肿和空泡情况得到改善。机制研究结果表明,ZFXN下调了血肿周围区域CaMKII/NF-κB p65/NLRP3/GSDMD信号轴相关蛋白的表达。此外,ZFXN可通过调节脑出血后NLRP3炎性小体的激活来减轻炎症反应。我们首次发现ZFXN对脑出血的疗效可能与NLRP3炎性小体的调节有关。