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首页> 外文期刊>Experimental and therapeutic medicine >Protective function of Bu Shen Huo Xue formula on the immunity of B6AF1 mice with experimental autoimmune premature ovarian failure
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Protective function of Bu Shen Huo Xue formula on the immunity of B6AF1 mice with experimental autoimmune premature ovarian failure

机译:Bu Shen Huo Xue公式对B6AF1小鼠免疫的保护功能,实验性自身免疫早期卵巢衰竭

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摘要

Autoimmune abnormality is one of the main causes of premature ovarian failure (POF). Bu Shen Huo Xue formula (BSHXF), a traditional Chinese medicine formula, has been clinically used for the treatment of patients with POF in China. Regulatory T cells (Tregs) are important in the pathogenesis of autoimmune POF. The aim of the present study was to evaluate the immunoprotective effects of BSHXF on POF and the underlying mechanisms. An experimental autoimmune POF model was induced in B6AF1 mice with zona pellucida 3 (ZP3) fragments. Following modeling, BSHXF (31.53 g/kg/day) was orally administered for 4 weeks. CD4(+) T lymphocytes, Tregs, anti-zona pellucida (anti-ZP) antibodies and cytokines were detected using flow cytometry, enzyme-linked immunosorbent assays, reverse transcription-quantitative polymerase chain reaction and immunohistochemistry. The results revealed that BSHXF exhibited an immunoprotective function and reduced inflammatory cell infiltration and damage to the ovary. BSHXF upregulated the percentage of CD4(+) CD25(+) forkhead box P3(+) T cells in the spleen, effectively inhibiting the activation of CD4(+) T lymphocytes. The proliferation of Tregs was increased in serum obtained from mice in the BSHXF group in vitro. Anti-ZP antibodies and interleukin-10 and interferon- levels were decreased in the serum in the BSHXF-treated group. The present study demonstrated that BSHXF had an immunoprotective effect on POF model mice. Additionally, it indicated that the protective mechanisms of BSHXF may be associated with an increase in Treg cells.
机译:自身免疫异常是过早卵巢衰竭(POF)的主要原因之一。中医配方的Bu Shen Huo Xue公式(BSHXF)已临床上用于治疗中国POF的患者。调节性T细胞(Tregs)在自身免疫POF的发病机制中是重要的。本研究的目的是评估BSHXF对POF和潜在机制的免疫保护作用。用Zona Pellucida 3(ZP3)碎片在B6AF1小鼠中诱导了实验性自身免疫POF模型。在建模下,口服BSHXF(31.53克/千克/天)施用4周。使用流式细胞术,酶联免疫吸附试验,逆转录定量聚合酶链反应和免疫组化检测CD4(+)T淋巴细胞,Tregs,抗Zona薄膜肽(抗ZP)抗体和细胞因子。结果表明,BSHXF表现出免疫保护功能,降低炎症细胞浸润和对卵巢的损伤。 BSHXF上调了脾脏中CD4(+)CD25(+)孔箱P3(+)T细胞的百分比,有效地抑制CD4(+)T淋巴细胞的活化。在体外BSHXF组的小鼠中获得的血清中,Tregs的增殖增加。在BSHXF处理基团的血清中,抗ZP抗体和白细胞介素-10和干扰素水平降低。本研究表明,BSHXF对POF模型小鼠进行了免疫保护作用。另外,它表明BSHXF的保护机制可以与Treg细胞的增加相关。

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