Wang Qi, Hou Ziwen, Liu Yaoyao, Wei Dan, Kong Qingjie, Chen Xia
Department of Acupuncture and Moxibustion, First Teaching Hospital of Tianjin University of TCM, Tianjin 300193, China; National Clinical Research Center for Chinese Medicine Acupuncture and Moxibustion, Tianjin 300193.
School of Acupuncture-Moxibustion and Tuina, Tianjin University of TCM.
Zhongguo Zhen Jiu. 2025 Aug 12;45(8):1099-1110. doi: 10.13703/j.0255-2930.20240703-k0003. Epub 2025 May 14.
To explore the neuroprotective effect and underlying mechanism of acupuncture (acupuncture for regaining consciousness and opening orifices) in the rat models of cerebral ischemia-reperfusion injury (CIRI) based on the p53 protein (p53)/solute carrier family 7 member 11 (SLC7A11)/glutathione peroxidase 4 (GPX4) signaling pathway.
Of 102 male Wistar rats, 20 rats were randomly collected as a sham-operation group. Using a modified external carotid artery filament insertion method, CIRI models were prepared by occluding the middle cerebral artery in the rest rats. After modeling and excluding 1 non-successfully modeled rat and 1 dead one, the other modeled rats were randomized into a model group, an agonist group, an acupuncture group, and an acupuncture + agonist group, 20 rats in each one. acupuncture therapy was delivered in the rats of the acupuncture group and the acupuncture + agonist group. The acupoints included "Shuigou" (GV26), bilateral "Neiguan" (PC6), and "Sanyinjiao" (SP6) on the affected side. Electroacupuncture was attached to "Neiguan" (PC6) and "Sanyinjiao" (SP6) on the affected side, with dense-disperse wave, a frequency of 2 Hz/15 Hz and intensity of 1 mA. The intervention was delivered twice daily, 20 min each time and for 7 consecutive days. In the agonist group and acupuncture+agonist group, p53 agonist, COTI-2 was intraperitoneally injected (15 mg/kg), once daily for 7 consecutive days. Neurological deficit was evaluated using Zausinger's six-point scale. Cerebral infarction volume was quantified by triphenyl tetrazolium chloride (TTC) staining. Histopathological changes were observed using hematoxylin-eosin (HE) staining. Iron deposition was assessed by Prussian blue staining. Mitochondrial ultrastructure in the ischemic cortex was examined under transmission electron microscopy (TEM). Serum iron (Fe) was measured with chromometry. Malondialdehyde (MDA) and glutathione (GSH) levels in the ischemic hippocampus were determined using thiobarbituric acid and microplate assays, respectively. The mean fluorescence intensity of reactive oxygen species (ROS) in the ischemic cortex was analyzed by flow cytometry. The mRNA and protein expression of GPX4, SLC7A11, and p53 in the ischemic hippocampus were evaluated using quantitative real-time PCR (qRT-PCR) and Western blotting, respectively.
Compared with the sham-operated group, the model group exhibited the decrease in neurological deficit score (<0.01), and the increase in cerebral infarction volume percentage (<0.01). The changes of brain tissue were presented in extensive cellular necrosis, pyknotic and deeply-stained nuclei, and vacuolar degeneration. The iron deposition was elevated in cortex and hippocampus (<0.01), mitochondrial membrane density increased, the cristae was broken or reduced, and the outer membrane ruptured. The levels of Fe and MDA, as well as the mean flourscence intensity of ROS were elevated (<0.01) and the level of GSH was reduced (<0.01). The mRNA and protein expression of GPX4 and SLC7A11 was reduced (<0.01), while that of p53 rose (<0.01). When compared with the model group, in the agonist group, the neurological deficit score was reduced (<0.05), the percentage of infarction volume was higher (<0.01), the histopathological damage was further exacerbated, and the percentage of iron deposition increased in the cortex and hippocampus (<0.01). The mitochondrial quantity decreased, the membrane density increased, the mitochondrial cristae were broken or reduced, and the outer membrane was ruptured. The levels of Fe and MDA, as well as the mean flourscence intensity of ROS were higher (<0.01, <0.05) and the level of GSH was reduced (<0.05). The mRNA and protein expression of GPX4 and SLC7A11 decreased (<0.01, <0.05), while that of p53 was elevated (<0.01). Besides, in comparison with the model group, the neurological deficit score was higher in the acupuncture group and the acupuncture + agonist group (<0.01, <0.05), the percentage of cerebral infarction volume was lower in the acupuncture group (<0.01), the pathological damage of brain tissue was alleviated in the acupuncture group and the acupuncture + agonist group, and the percentage of iron depositiondecreased in the cortex and hippocampus (<0.01). The mitochondrial structure was relatively clear, the mitochondrial cristae were fractured or reduced mildly in the acupuncture group and the acupuncture + agonist group. The levels of Fe and MDA, as well as the mean flourscence intensity of ROS were lower (<0.01) and the level of GSH was higher (<0.01) in the acupuncture group. The mean fluorescence intensity of ROS were dropped (<0.01) in the acupuncture + agonist group. The mRNA expression of GPX4 and SLC7A11 was elevated (<0.01) and that of p53 was reduced (<0.01, <0.05) in either the acupuncture group or the acupuncture + agonist group; the protein expression of GPX4 and SLC7A11 rose (<0.05, <0.01) and that of p53 was dropped (<0.01) in the acupuncture group; and the protein expression of p53 was also lower in the acupuncture + agonist group (<0.05). When compared with the agonist group, in the acupuncture + agonist group, neurological deficit score increased (<0.01), the percentage of cerebral infarction volume decreased (<0.01), the pathological brain tissue damage was reduced, the percentage of iron deposition in cortex and hippocampus decreased (<0.01), the mitochondrial structure was relatively clear and the cristae broken or reduced slightly; the levels of Fe and MDA, as well as the mean fluorescence intensity of ROS were dropped (<0.01), while the level of GSH increased (<0.05); the mRNA and protein expression of GPX4 and SLC7411 was elevated (<0.01, <0.05), and that of p53 reduced (<0.01). In comparison with the acupuncture + agonist group, in the acupuncture group, the neurological deficit score increased (<0.05), the percentage of cerebral infarction volume decreased (<0.05), the pathological brain tissue damage was alleviated, the percentage of iron deposition in cortex and hippocampus decreased (<0.01), the mitochondrial structure was normal in tendency; the levels of Fe and MDA, as well as the mean fluorescence intensity of ROS were reduced (<0.05), while the level of GSH rose (<0.01); the mRNA and protein expression of GPX4 and SLC7411 was elevated (<0.01, <0.05), and that of p53 reduced (<0.01, <0.05).
acupuncture can alleviate neurological damage in CIRI rats, which is obtained probably by inhibiting ferroptosis through p53/SLC7A11/GPX4 pathway.
基于p53蛋白(p53)/溶质载体家族7成员11(SLC7A11)/谷胱甘肽过氧化物酶4(GPX4)信号通路,探讨醒脑开窍针法对脑缺血再灌注损伤(CIRI)大鼠模型的神经保护作用及潜在机制。
将102只雄性Wistar大鼠中的20只随机选取作为假手术组。其余大鼠采用改良的颈外动脉线栓法制备CIRI模型,通过阻塞大脑中动脉来实现。建模后,排除1只建模未成功的大鼠和1只死亡大鼠,将其余建模成功的大鼠随机分为模型组、激动剂组、针刺组和针刺+激动剂组,每组20只。对针刺组和针刺+激动剂组的大鼠进行针刺治疗。穴位包括患侧的“水沟”(GV26)、双侧“内关”(PC6)和“三阴交”(SP6)。将电针连接到患侧的“内关”(PC6)和“三阴交”(SP6),采用疏密波,频率为2Hz/15Hz,强度为1mA。每天干预2次,每次20分钟,连续7天。在激动剂组和针刺+激动剂组中,腹腔注射p53激动剂COTI-2(15mg/kg),每天1次,连续7天。使用Zausinger六点量表评估神经功能缺损。通过氯化三苯基四氮唑(TTC)染色定量脑梗死体积。采用苏木精-伊红(HE)染色观察组织病理学变化。通过普鲁士蓝染色评估铁沉积。在透射电子显微镜(TEM)下检查缺血皮层的线粒体超微结构。用比色法测量血清铁(Fe)。分别使用硫代巴比妥酸和微孔板法测定缺血海马中的丙二醛(MDA)和谷胱甘肽(GSH)水平。通过流式细胞术分析缺血皮层中活性氧(ROS)的平均荧光强度。分别使用定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法评估缺血海马中GPX4、SLC7A11和p53的mRNA和蛋白表达。
与假手术组相比,模型组神经功能缺损评分降低(<0.01),脑梗死体积百分比增加(<0.01)。脑组织变化表现为广泛的细胞坏死、核固缩和深染以及空泡变性。皮层和海马中的铁沉积升高(<0.01),线粒体膜密度增加,嵴断裂或减少,外膜破裂。Fe和MDA水平以及ROS的平均荧光强度升高(<0.01),GSH水平降低(<0.01)。GPX4和SLC7A11的mRNA和蛋白表达降低(<0.01),而p53的表达升高(<0.01)。与模型组相比,激动剂组神经功能缺损评分降低(<0.05),梗死体积百分比更高(<0.01),组织病理学损伤进一步加重,皮层和海马中的铁沉积百分比增加(<0.01)。线粒体数量减少,膜密度增加,线粒体嵴断裂或减少,外膜破裂。Fe和MDA水平以及ROS的平均荧光强度更高(<0.01,<0.05),GSH水平降低(<0.05)。GPX