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Neuroprotective Effect of Xueshuantong for Injection (Lyophilized) in Transient and Permanent Rat Cerebral Ischemia Model

机译:血栓通注射液(冻干)对短暂性和永久性大鼠脑缺血模型的神经保护作用

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摘要

Xueshuantong for Injection (Lyophilized) (XST), a Chinese Materia Medica standardized product extracted from Panax notoginseng (Burk.), is used extensively for the treatment of cerebrovascular diseases such as acutely cerebral infarction clinically in China. In the present study, we evaluated the acute and extended protective effects of XST in different rat cerebral ischemic model and explored its effect on peroxiredoxin (Prx) 6-toll-like receptor (TLR) 4 signaling pathway. We found that XST treatment for 3 days could significantly inhibit transient middle cerebral artery occlusion (MCAO) induced infarct volume and swelling percent and regulate the mRNA expression of interleukin-1β (IL-1β), IL-17, IL-23p19, tumor necrosis factor-α (TNFα), and inducible nitric oxide synthase (iNOS) in brain. Further study demonstrated that treatment with XST suppressed the protein expression of peroxiredoxin (Prx) 6-toll-like receptor (TLR) 4 and phosphorylation level of p38 and upregulated the phosphorylation level of STAT3. In permanent MCAO rats, XST could reduce the infarct volume and swelling percent. Moreover, our results revealed that XST treatment could increase the rats' weight and improve a batch of functional outcomes. In conclusion, the present data suggested that XST could protect against ischemia injury in transient and permanent MCAO rats, which might be related to Prx6-TLR4 pathway.
机译:注射用血栓通(冻干)(XST)是从三七(Burax)提取的中药标准化产品,在中国临床上广泛用于治疗脑血管疾病,例如急性脑梗塞。在本研究中,我们评估了XST在不同大鼠脑缺血模型中的急性和扩展保护作用,并探讨了其对过氧化物酶(Prx)6-toll样受体(TLR)4信号通路的影响。我们发现,XST治疗3天可以显着抑制短暂性脑中动脉阻塞(MCAO)引起的梗塞体积和肿胀百分率,并调节白介素1β(IL-1β),IL-17,IL-23p19,肿瘤坏死的mRNA表达。因子-α(TNFα)和脑中诱导型一氧化氮合酶(iNOS)。进一步的研究表明,XST处理可抑制过氧化物酶(Prx)6-toll样受体(TLR)4的蛋白表达和p38的磷酸化水平,并上调STAT3的磷酸化水平。在永久性MCAO大鼠中,XST可以减少梗塞体积和肿胀百分比。此外,我们的结果表明,XST治疗可以增加大鼠的体重并改善一批功能结果。总之,目前的数据表明,XST可以预防短暂和永久MCAO大鼠的缺血性损伤,这可能与Prx6-TLR4途径有关。

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