Li Pei-Pei, He Ling, Zhang Li-Miao, Qin Xue-Mei, Hu Jian-Peng
Key Laboratory of Xin'an Medicine, Ministry of Education, Anhui University of Chinese Medicine, Hefei, Anhui 230038, China.
School of Chinese Medicine, Anhui University of Chinese Medicine, Hefei, Anhui 230012, China.
Evid Based Complement Alternat Med. 2022 Apr 11;2022:9341466. doi: 10.1155/2022/9341466. eCollection 2022.
Naoluo Xintong decoction (NLXTD) is a traditional Chinese medicine (TCM) formula which has been used to improve neuronal functional recovery after cerebral ischemic stroke. However, the molecular mechanism underlying NLXTD's amelioration of ischemic stroke remains unclear. The present study was designed to explore the effect and mechanism of NLXTD on brain angiogenesis in a rat model with cerebral ischemia-reperfusion (I/R) injury targeting the hypoxia-inducible factor-1 (HIF-1)/vascular endothelial growth factor (VEGF) pathway.
Cerebral I/R model was established by the classical middle cerebral artery occlusion (MCAO) method. Sprague-Dawley (SD) male rats ( = 80) were randomly divided into the sham-operation group, the model group, the HIF-1 inhibitor 2-methoxyestradiol (2ME2) group, the 2ME2 with NLXTD group, and the NLXTD group. Neurological deficit test, TTC staining, H&E staining, TUNEL staining, immunohistochemistry (IH), immunofluorescence (IF), western blot, and quantitative RT-PCR were performed to evaluate the effect of NLXTD after MCAO.
Administration of NLXTD significantly decreased neuron deficiency scores, reduced brain infarct volume, and lowered damaged and apoptotic cells after brain I/R injury in rats. Meanwhile, NLXTD had a protective effect on angiogenesis by increasing the MVD and the expressions of BrdU and CD34, which enhanced the number of endothelial cells in the ischemic penumbra brain. NLXTD treatment significantly raised the protein and mRNA levels of HIF-1, VEGF, VEGFR2, and Notch1 compared with the model treatment. In contrast, a specific HIF-1 inhibitor, 2ME2, inhibited the improvement of neurological function and angiogenesis in NLXTD-induced rats with cerebral I/R injury, suggesting that NLXTD played a positive role in ischemic brain injury by activating the HIF-1/VEGF signaling pathway.
NLXTD exerts neuroprotection targeting angiogenesis by upregulating the HIF-1/VEGF signaling pathway on cerebral I/R injury rats.
脑络欣通方(NLXTD)是一种中药配方,已被用于改善脑缺血性中风后神经元功能恢复。然而,NLXTD改善缺血性中风的分子机制仍不清楚。本研究旨在探讨NLXTD对脑缺血再灌注(I/R)损伤大鼠脑 angiogenesis 的影响及其机制,靶点为缺氧诱导因子-1(HIF-1)/血管内皮生长因子(VEGF)通路。
采用经典大脑中动脉闭塞(MCAO)法建立脑I/R模型。将80只雄性Sprague-Dawley(SD)大鼠随机分为假手术组、模型组、HIF-1抑制剂2-甲氧基雌二醇(2ME2)组、2ME2与NLXTD联合组和NLXTD组。进行神经功能缺损测试、TTC染色、H&E染色、TUNEL染色、免疫组织化学(IH)、免疫荧光(IF)、蛋白质免疫印迹法和定量逆转录聚合酶链反应,以评估MCAO后NLXTD的作用。
给予NLXTD可显著降低大鼠脑I/R损伤后的神经元缺损评分,减少脑梗死体积,并降低受损和凋亡细胞数量。同时,NLXTD通过增加微血管密度(MVD)以及BrdU和CD34的表达对angiogenesis具有保护作用,从而增加缺血半暗带脑区的内皮细胞数量。与模型组相比,NLXTD治疗显著提高了HIF-1、VEGF、VEGFR2和Notch1的蛋白质和mRNA水平。相反,一种特异性HIF-1抑制剂2ME2抑制了NLXTD诱导的脑I/R损伤大鼠神经功能和angiogenesis的改善,表明NLXTD通过激活HIF-1/VEGF信号通路在缺血性脑损伤中发挥积极作用。
NLXTD通过上调脑I/R损伤大鼠的HIF-1/VEGF信号通路对angiogenesis发挥神经保护作用。