Modulation of lung local immune responses by oral administration of a herbal medicine Sho-saiko-to

Nobuhiro Ohtake , Rie Suzuki , Haruyuki Daikuhara , Youichiro Nakai , Masahiro Yamamoto , Sakae Amagaya , Atsushi Ishige , Hiroshi Sasaki , Yasuhiro Komatsu , Kazunori Fukuda , Seiji Hayashi
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引用次数: 39

Abstract

Sho-saiko-to (SST), a Chinese/Japanese herbal medicine (Kampo medicine) widely used to treat chronic hepatitis in Japan, is known to modulate immune responses, and thus its immunomodulating activity may be responsible for its bi-directional effects on the lungs as therapeutic efficacy in various lung diseases and involvement in development of interstitial pneumonia. We administered SST to BALB/c mice orally and examined the lung tissue levels of pro/anti-inflammatory cytokines, interleukin-1beta (IL-1β), tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6), and the effects of SST on acute lung injury induced by instillation of lipopolysaccharide (LPS) or IL-1. Although SST had no effect on lung TNF-α or IL-1β level, it increased IL-6. Investigation of active fractions of SST suggested that multiple ingredients were supposed to be responsible for IL-6-inducing activity. Liquiritigenin, a metabolite of liquiritin which is one of the major ingredients in SST enhanced in vitro IL-6 production in anti-CD3 monoclonal antibody (anti-CD3 mAb)-stimulated lung mononuclear cells in a cell-type specific and dose-dependent manner. SST suppressed LPS-induced lung injury at the later phase when lung leak was evident while being ineffective on initial neutrophil sequestration to the lung in these models. These findings suggest that SST modulates lung inflammation by regulating local immune response.

口服中草药shoo -saiko-to对肺局部免疫反应的调节
shoo -saiko-to (SST)是一种在日本广泛用于治疗慢性肝炎的中草药(汉布药),已知可以调节免疫反应,因此其免疫调节活性可能是其对肺的双向作用的原因,作为治疗各种肺部疾病的疗效和参与间质性肺炎的发展。我们给BALB/c小鼠口服SST,检测肺组织中促炎性因子、白细胞介素-1β (IL-1β)、肿瘤坏死因子-α (TNF-α)和白细胞介素-6 (IL-6)的水平,以及SST对脂多糖(LPS)或IL-1诱导的急性肺损伤的影响。虽然SST对肺TNF-α和IL-1β水平无影响,但可使IL-6升高。对SST活性组分的研究表明,多种成分可能对il -6的诱导活性起作用。Liquiritigenin是liquiritin的代谢物,liquiritin是SST的主要成分之一,在抗cd3单克隆抗体(anti-CD3 mAb)刺激的肺单核细胞中,以细胞类型特异性和剂量依赖性的方式促进IL-6的体外产生。在这些模型中,SST在肺渗漏明显的后期抑制lps诱导的肺损伤,但对初始中性粒细胞对肺的隔离无效。这些发现表明,SST通过调节局部免疫反应来调节肺部炎症。
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