Li Yumeng, Ye Qingping, Li Jingjing, Zhang Lijuan, Yu Chao, Xue Sujun, Li Shuangping, Duan Xianchun, Peng Daiyin
Department of Pharmacy, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, 230031, China; School of Pharmacy, Anhui University of Chinese Medicine, Hefei, 230012, China.
Department of Pharmacy, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, 230031, China; School of Pharmacy, Anhui University of Chinese Medicine, Hefei, 230012, China; Xin 'an Medical Research Institute, Hefei, 230038, China; Key Laboratory of Xin'An Medicine, Ministry of Education, Hefei, 230012, China; Anhui Province Key Laboratory of Chinese Medicinal Formula, Hefei, 230012, China.
Phytomedicine. 2025 Jan;136:156305. doi: 10.1016/j.phymed.2024.156305. Epub 2024 Nov 28.
Ischemic stroke (IS) is the most prevalent type of cerebrovascular disease. Taohong Siwu Decoction (THSWD) has been demonstrated to have neuroprotective benefits during Cerebral Ischemia-Reperfusion Injury (CIRI). Whether THSWD mitigates CIRI by modulating the circDnajc1/miR-27a-5p/C1qc signaling axis is not known.
Examine how THSWD provides neuroprotective benefits in reducing the damage wrought by IS.
We employed middle cerebral artery occlusion/reperfusion (MCAO/R) rat model and oxygen glucose deprivation/re-oxygenation (OGD/R) in vitro model. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR), Western blot (WB), and immunofluorescence analyses (IF) were utilized to detect microglial activation markers TMEM119, CD11b, and Iba1, inflammatory mediators CCL2, CCL6, IL1, IL6, IL10, and TNF-α, as well as circDnajc1, miR-27a-5p, C1qc, C3, and C5aR.
Our data suggest that THSWD can mitigate inflammatory response, inhibit microglial activation and neuron apoptosis, and exert neuroprotective effects by regulating the circDnajc1/miR-27a-5p/C1qc signaling axis.
缺血性中风(IS)是最常见的脑血管疾病类型。桃红四物汤(THSWD)已被证明在脑缺血再灌注损伤(CIRI)期间具有神经保护作用。THSWD是否通过调节circDnajc1/miR-27a-5p/C1qc信号轴减轻CIRI尚不清楚。
研究THSWD如何在减轻IS造成的损伤方面提供神经保护作用。
我们采用大脑中动脉闭塞/再灌注(MCAO/R)大鼠模型和体外氧糖剥夺/复氧(OGD/R)模型。利用逆转录定量聚合酶链反应(RT-qPCR)、蛋白质免疫印迹法(WB)和免疫荧光分析(IF)检测小胶质细胞激活标志物TMEM119、CD11b和Iba1、炎症介质CCL2、CCL6、IL1、IL6、IL10和TNF-α,以及circDnajc1、miR-27a-5p、C1qc、C3和C5aR。
我们的数据表明,THSWD可以减轻炎症反应,抑制小胶质细胞激活和神经元凋亡,并通过调节circDnajc1/miR-27a-5p/C1qc信号轴发挥神经保护作用。