急性缺血性脑卒中瘀毒互结证大鼠模型"脑-脾炎症耦联"机制探讨OACSTPCD
Mechanism of brain-spleen inflammation coupling in a rat model of acute ischemic stroke stasis toxin syndrome
目的 探讨急性缺血性脑卒中瘀毒互结证大鼠模型脑损伤与脾损害的相关性,分析对MCP-1/CCR2趋化因子信号轴的影响.方法 40只雄性SD大鼠随机分为假手术组(sham)、角叉菜胶联合干酵母菌瘀毒互结证(Carrageenan/Yeast,CA/Y)组(单纯证候组)、大脑中动脉阻塞(middle cerebral artery occlusion,MCAO)组(单纯疾病组)、大脑中动脉阻塞瘀毒互结证(MCAO+CA/Y)组(病证结合组),每组10只.CA/Y组与MCAO+CA/Y组于造模首日经腹腔注射角叉菜胶10 mg/kg、第2日背部皮下注射干酵母悬液2 mg/kg,MCAO组及MCAO+CA/Y组于第2日采用线栓法建立大脑中动脉阻塞模型.脑梗死模型术后24 h,对各组大鼠进行神经功能缺损评分,采用TTC染色法观察脑梗死面积百分比,取脾测定脾重量,采用Spearman相关系数分析脑梗死面积百分比与脾重量的相关性,苏木素-伊红(HE)染色法观察脑组织及脾组织病理形态,酶联免疫吸附实验(ELISA)检测大鼠血浆中单核细胞趋化蛋白-1(monocyte chemotactic protein 1,MCP-1)、干扰素-γ(interferon-γ,IFN-γ)含量,Western blot 法检测缺血侧脑组织趋化因子C-C-基元受体2(chemokine C-C-motif receptor 2,CCR2)蛋白表达.结果 与sham组比较,MCAO组和MCAO+CA/Y组的神经功能缺损评分、脑梗死面积、血浆中MCP-1与IFN-γ含量均显著升高(P<0.01),脾重量显著下降(P<0.01),脑组织中CCR2蛋白表达明显上调(P<0.05);与CA/Y组比较,MCAO组和MCAO+CA/Y组的神经功能缺损评分、脑梗死面积显著升高(P<0.01),脾重量显著下降(P<0.01),脑组织和脾组织中CCR2蛋白表达均明显上调(P<0.05);与MCAO组比较,MCAO+CA/Y组的脑梗死面积显著升高(P<0.01),脾重量明显下降(P<0.05).Spearman相关分析显示,脾重量与脑梗死面积百分比呈负相关(P<0.01,r=-0.9711).病理形态学观察结果显示,MCAO+CA/Y组病理改变最为严重,脑组织皮层中可见大脑液化坏死灶,病灶中神经元细胞排列稀疏、紊乱,体积萎缩,少部分空泡化和核固缩,大部分神经元细胞红色变性、坏死,小胶质细胞增生明显,小血管明显增多,间质脂质变性;脾组织部分动脉周围淋巴鞘细胞密度减低,边缘区增宽.结论 急性缺血性脑卒中瘀毒互结证大鼠模型脑损伤与脾损害存在相关性,可能与MCP-1/CCR2趋化因子信号轴参与"脑-脾炎症耦联"机制有关.
Objective To investigate the correlation between brain injury and spleen damage in a rat model of acute ischemic stroke and stasis interaction,and its effect on the MCP-1/CCR2 axis,and to provide an experimental basis for the mechanism of brain-spleen inflammatory coupling in spleen lesions caused by acute ischemic stroke.Methods Forty male SD rats were randomly divided into a sham group,carrageenan/yeast stasis syndrome group(carrageenan/yeast,CA/Y),middle cerebral artery occlusion group(MCAO),and middle cerebral artery stasis syndrome group(MCAO CA/Y)with 10 rats in each group.CA/Y and MCAO CA/Y groups were injected with 10 mg/kg carrageenan and 10 mg/kg intraperitoneally on the first day of modeling.2 mg/kg of dry yeast suspension were injected subcutaneously on the second day.MCAO and MCAO CA/Y groups were established by wire embolism on the second day.At 24 h after cerebral infarction modeling,the neurological deficit score was calculated in each group,the percentage of the cerebral infarction area was determined by TTC staining,the spleen weight was measured,and the correlation between the percentage of the cerebral infarction area and spleen weight was analyzed by the Spearman correlation coefficient.Furthermore,the pathological morphology of brain and spleen tissues was observed by hematoxylin-eosin(HE)staining,and chemotactic protein 1(MCP-1)and interferon-γ(IFN-γ)contents were measured in rat plasma by enzyme-linked immunosorbent assays.Western blot was used to detect chemokine C-C-motif receptor 2(CCR2)protein expression in the ischemic side of brain tissue.Results Compared with the sham group,the neurological deficit score,cerebral infarction area,and MCP-1 and IFN-γ contents in plasma were significantly increased(P<0.01),spleen weight was decreased significantly(P<0.01),and CCR2 protein expression in brain tissue was significantly upregulated(P<0.05)in MCAO and MCAO CA/Y groups.Moreover,the area of cerebral infarction was increased significantly(P<0.01),the spleen weight was decreased significantly(P<0.01),and CCR2 protein expression in brain and spleen tissues was significantly upregulated(P<0.05)Compared with the MCAO group,the area of cerebral infarction in the MCAO CA/Y group was significantly increased(P<0.01)and the spleen weight was decreased significantly(P<0.05).Spearman correlation analysis showed that the spleen weight was negatively correlated to the percentage of the cerebral infarction area(P<0.01,r=-0.9711).Pathological morphology observation revealed that the pathological changes in the MCAO CA/Y group were the most serious,cerebral liquefaction necrosis foci were seen in the brain tissue cortex,arrangement of neuronal cells in the lesions was sparse and disordered with volume atrophy and a small number of vacuoles and nuclear solidification,most neuronal cells were degenerated and necrotic,microglia hyperplasia was obvious,small blood vessels were significantly increased,and interstitial lipid degeneration was severe.The density of periarterial lymph sheath cells in some of the spleen tissue was reduced and the marginal area is widened.Conclusions A correlation between brain and spleen injury was found after acute ischemic stroke with stasis and toxin syndrome,and the chemokine signaling axis of MCP-1/CCR2 might be involved in the mechanism of brain-spleen inflammation coupling.
董一蕾;刘悦;李珺媛;付建华;张允岭;姚明江
中国中医科学院西苑医院基础医学研究所,中药药理北京市重点实验室,北京 100091中国中医科学院西苑医院基础医学研究所,中药药理北京市重点实验室,北京 100091||中国中医科学院西苑医院,北京 100091中国中医科学院西苑医院,北京 100091
急性缺血性脑卒中瘀毒互结证脑-脾炎症耦联趋化因子
acute ischemic strokestasis toxin syndromebrain-spleen inflammatory couplingchemokines
《中国比较医学杂志》 2024 (002)
45-54 / 10
北京市自然科学基金面上项目(7232317);中国中医科学院科技创新工程重大攻关项目(C12021A01305);国家中医药管理局中医药创新团队及人才支持计划项目(ZYYCXTD-C-202007);中国中医科学院创新团队项目(CI2021B006).
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