首页> 外文期刊>International journal of immunopharmacology >Intragastric administration of ursodeoxycholic acid suppresses immunoglobulin secretion by lymphocytes from liver, but not from peripheral blood, spleen or Peyer's patches in mice.
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Intragastric administration of ursodeoxycholic acid suppresses immunoglobulin secretion by lymphocytes from liver, but not from peripheral blood, spleen or Peyer's patches in mice.

机译:熊去氧胆酸胃内给药可抑制小鼠淋巴细胞的免疫球蛋白分泌,但不能抑制小鼠外周血,脾脏或Peyer斑块的免疫球蛋白分泌。

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摘要

Ursodeoxycholic acid (UDCA) has been recognized as a therapeutic drug for primary biliary cirrhosis (PBC) and chronic viral hepatitis. As one of the mechanisms by which UDCA improves liver function tests in those patients, its immunomodulatory effect is currently considered important. Although the suppressive effects of UDCA on some cytokine productions, T-cell mediated cytotoxicity and immunoglobulin production were observed from in vitro studies, the immunomodulation in vivo by UDCA remains unclear. In the present study, we investigated the effect of UDCA administration on the number of immunoglobulin secreting cells in liver, peripheral blood, spleen and Peyer's patches in mice using the enzyme linked immunospot assay and assessed whether the UDCA-mediated immunomodulation is liver-specific. It was demonstrated that intragastric administration of UDCA reduced immunoglobulin secretion by lymphocytes from liver, but not from peripheral blood, spleen, or Peyer's patches. However, immunoglobulin production of those lymphocytes cultured in the presence of UDCA was suppressed, irrespective of their distribution sites, in a UDCA dose-dependent manner. When the concentrations of UDCA in portal and peripheral blood were measured using high performance liquid chromatography, UDCA was detectable in the portal blood in UDCA-treated mice, but not in peripheral blood, suggesting that the concentrations of UDCA in the environment surrounding lymphocytes may be an important factor for the modulation of lymphocyte functions.
机译:熊去氧胆酸(UDCA)被公认为治疗原发性胆汁性肝硬化(PBC)和慢性病毒性肝炎的药物。作为UDCA改善这些患者肝功能测试的机制之一,目前认为其免疫调节作用很重要。尽管从体外研究中观察到了UDCA对某些细胞因子产生,T细胞介导的细胞毒性和免疫球蛋白产生的抑制作用,但UDCA在体内的免疫调节仍不清楚。在本研究中,我们使用酶联免疫斑点法研究了UDCA给药对小鼠肝脏,外周血,脾脏和Peyer斑块中免疫球蛋白分泌细胞数量的影响,并评估了UDCA介导的免疫调节是否为肝特异性的。已证明胃内施用UDCA可减少肝脏淋巴细胞的免疫球蛋白分泌,但不能减少外周血,脾脏或Peyer斑块的免疫球蛋白分泌。然而,以UDCA剂量依赖性方式,抑制了在UDCA存在下培养的那些淋巴细胞的免疫球蛋白产生,而不论其分布部位如何。当使用高效液相色谱法测量门静脉和外周血中UDCA的浓度时,在经UDCA处理的小鼠的门静脉血中可检测到UDCA,而在外周血中则未检测到,这表明淋巴细胞周围环境中UDCA的浓度可能是调节淋巴细胞功能的重要因素。

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