首页|黄芪多糖对缺血性脑损伤大鼠的神经保护作用及机制研究

黄芪多糖对缺血性脑损伤大鼠的神经保护作用及机制研究

Neuroprotective effect of astragalan on ischemic brain injury in rats and its mechanism

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目的:研究分析缺血性脑损伤后海马CA1区神经细胞黏附分子(neural cell adhesion molecule,NCAM)以及细胞癌基因fos(cellular oncogene fos,c-fos)在黄芪多糖(astragalan,AG)影响后的表达.方法:本研究所用大鼠为Wistar雄性大鼠200只,随机分为4组.假手术组(sham operation group,SOG)20只,未进行缺血处理,仅进行假手术;模型组(model group,MG-1 d;MG-3 d;MG-7 d)60只,经过缺血处理,用以模拟脑损伤情况,被进一步细分为1 d、3 d、和7 d 3个时间点;低剂量黄芪多糖治疗组(low-dose astragalus polysaccharides treatment group,L-AGTG,L-AGTG-1 d;L-AGTG-3 d;L-AGTG-7 d)60只,在缺血后接受低剂量的黄芪多糖治疗,被进一步细分为1 d、3 d、和7 d3个时间点;高剂量黄芪多糖治疗组(high-dose astragalus polysaccharides treatment group,H-AGTG,H-AGTG-1 d;H-AGTG-3 d;H-AGTG-7 d)60只,在缺血后接受高剂量的黄芪多糖治疗,被进一步细分为1 d、3 d、和7 d 3个时间点.MG组及AGTG组行颈切口术致大鼠脑组织缺血后,经颈切除术封闭右脑中动脉;AGTG组以5 mg/kg和15 mg/kg的方式分别腹腔注射AG.于第1天、第3天、第7天进行脑血流量的重新灌流;对大鼠的神经损伤程度进行评定后,采集标本,计算凋亡神经元数量;免疫组织化学法和反转录-聚合酶链反应(reverse transcription-polymerase chain reaction,RT-PCR)半定量分析检测海马CA1区神经元NCAM和c-fos的表达.结果:与MG组相比,L-AGTG组及H-AGTG组的脑损伤神经功能缺损指数(NIPs)评分及海马区凋亡神经元NCAM均明显降低,差异有统计学意义(P<0.05,P<0.01).在海马CA1区域,L-AGTG组及H-AGTG组大鼠的NCAM及c-fos蛋白表达量均较高,差异有统计学意义(P<0.05,P<0.01).L-AGTG组及H-AGTG组的海马CA1区域beta-actin和c-fos mRNA的表达谱也显示了显著变化,表明黄芪多糖对c-fos mRNA的表达有正向调节作用.结论:经过研究分析,黄芪多糖可以改善缺血性脑损伤,有可能与促进海马MSAM和c-fos表达、阻止或逆转海马神经元凋亡相关.
Objective:To investigate and analyze the expression of neural cell adhesion molecule(NCAM)and cellu-lar oncogene fos(c-fos)in CA1 region of hippocampus after ischemic brain injury under the influence of astragalan(AG).Methods:In this study,200 Wistar male rats were randomly divided into 4 groups.The rats in sham operation group(SOG,n=20)underwent sham operation without ischemic treatment.The rats in model group(MG,n=60)(MG-1 d;MG-3 d;MG-7 d)were given ischemic treatment to simulate brain injury and further subdivided into 3 time points of 1 day,3 days,and 7 days.The rats in low-dose astragalus polysaccharides treatment group(L-AGTG,n=60)(L-AGTG-1 d;L-AGTG-3 d;L-AGTG-7 d)were given low-dose astragalus polysaccharides treatment after ischemia and further di-vided into 3 time points of 1 day,3 days,and 7 days.The rats in high-dose astragalus polysaccharides treatment group(H-AGTG,n=60)(H-AGTG-1 d;H-AGTG-3 d;H-AGTG-7 d)were given high-dose astragalus polysaccharides treatment after ischemia and further divided into 3 time points of 1 day,3 days,and 7 days.In the MG and AGTG groups,the rat brain tissue was in state of ischemia induced by neck incision,and then the right middle cerebral artery was closed through neck resection.In AGTG group,AG was injected intraperitoneally at 5 mg/kg and 15 mg/kg,respectively.The ce-rebral blood flow was reperfused on the 1st,3rd and 7th day.After the degree of nerve injury was evaluated,the specimens were collected and the number of apoptotic neurons was counted.Immunohistochemistry and reverse transcription-polymerase chain reaction(RT-PCR)were used to detect the expression of NCAM and c-fos in hippocampal CA1 region neurons.Results:Compared with those in MG group,the neurological impairment index(NIPs)scores and the NCAM of apoptotic neurons in hippocampus of L-AGTG group and H-AGTG group were significantly decreased,and the differences were statistically significant(P<0.05,P<0.01).In the CA1 region of hippocampus,the expression levels of NCAM and c-fos protein in L-AGTG group and H-AGTG group were higher,and the differences were statistically significant(P<0.05,P<0.01).The expression profiles of beta-actin and c-fos mRNA in hippocampal CA1 region of L-AGTG group and H-AGTG group also showed significant changes,indicating that AG had a positive regulatory effect on the expression of c-fos mRNA.Conclusion:Studies have shown that AG can improve ischemic brain damage,which may be related to promoting the expression of hippocampal MSAM and c-fos,and preventing or reversing hippocampal neuron apoptosis.

AGhippocampusprotective effectmechanism

唐颖林、徐琼芳、简亚平

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永州职业技术学院,湖南 永州 425000

黄芪多糖 海马 保护作用 机制

2021年湖南省教育厅科学研究项目

21C1521

2024

山西中医药大学学报

山西中医药大学学报

ISSN:
年,卷(期):2024.25(1)
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