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首页> 外文期刊>Traditional medicine research. >Research on Xijiao Dihuang Decoction suppressing platelet apoptosis in immune-mediated aplastic anemia based on mitochondrial mediated pathway
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Research on Xijiao Dihuang Decoction suppressing platelet apoptosis in immune-mediated aplastic anemia based on mitochondrial mediated pathway

机译:西交地黄汤基于线粒体介导途径抑制免疫介导的再生障碍性贫血中血小板凋亡的研究

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Highlights Excessive platelet apoptosis is one of the pathogenic cause for immune-induced aplastic anemia. In the present study, we established an immune-induced aplastic anemia model and gave Xijiao Dihuang Decoction lavage daily. The results of this study indicated Xijiao Dihuang Decoction could increase platelet number and prevent its apoptosis through the mitochondrial pathway. The aplastic anemia mice model was established in this study. BALB/c mice shall be treated with whole body irradiation with 60 Co-γradiation (5.5Gy, 1.1Gy/min × 5 min). then within 4 h, DBA/2 mice were injected lymphocyte suspension 1 × 106 cells /mouse through caudal vein. Grouping of testing animals Normal control mice were healthy C57BL/6 mice without AA modeling. AA control group mice were exposed to radiation and cell transfusion and had no treatment with either CSA or XDD. CSA group mice received daily lavage with 0.027g/kg (0.1ml/10g) of CSA whereas XDD group mice received daily lavage with 19.5g/kg of XDD. The experimental result indicated CSA and XDD lavage mice had significantly higher platelet count and ΔΨm than AA mice (P 2+ were significantly lower in CSA and XDD groups compare with AA group. More specifically, compared to CSA group, XDD group also had lower level of ΔΨm and higher level of Cyt C and Ca2+ (both P P P 0.05). Therefore, we hypothesized XDD was possible to increase platelet number and prevent its apoptosis in immune-induced AA via the mitochondrial pathway.
机译:要点血小板过度凋亡是免疫性再生障碍性贫血的病因之一。在本研究中,我们建立了免疫诱导的再生障碍性贫血模型,并每天给予西郊地黄汤灌洗。本研究结果表明,西郊地黄汤可通过线粒体途径增加血小板数量并阻止其凋亡。在该研究中建立了再生障碍性贫血小鼠模型。对BALB / c小鼠进行60Co-γ射线全身照射(5.5Gy,1.1Gy / min×5分钟)。然后在4小时内,通过尾静脉向DBA / 2小鼠注射1×106细胞/小鼠的淋巴细胞悬液。测试动物的分组正常对照小鼠是没有AA模型的健康的C57BL / 6小鼠。 AA对照组小鼠暴露于放射线和细胞输血,并且未使用CSA或XDD进行治疗。 CSA组小鼠每天灌洗0.027g / kg(0.1ml / 10g)CSA,而XDD组小鼠每天灌洗19.5g / kg XDD。实验结果表明,CSA和XDD灌洗小鼠的血小板计数和ΔΨm明显高于AA小鼠(CSA和XDD组的P 2+明显低于AA组,更具体地说,与CSA组相比,XDD组的水平也较低) ΔΨm和Cyt C和Ca2 +的较高水平(均为PPP <0.05),因此,我们推测XDD可能通过线粒体途径增加血小板数量并阻止其在免疫诱导的AA中凋亡。

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