念珠菌水溶性(1→3)-β-d-葡聚糖CSBG的免疫药理和免疫毒理学活性

Kazuhiro Tokunaka , Naohito Ohno , Yoshiyuki Adachi , Shigenori Tanaka , Hiroshi Tamura , Toshiro Yadomae
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引用次数: 107

摘要

我们建立了一种简便的两步溶酵母细胞壁(1→3)-β-d-葡聚糖的方法,采用NaClO氧化和DMSO萃取相结合的方法。念珠菌可溶性β-d-葡聚糖(CSBG)主要由线性β-1,3葡聚糖和线性β-1,6葡聚糖组成。在本研究中,我们对CSBG的几种免疫药理活性进行了筛选,发现其具有以下活性:(1)体外巨噬细胞的白细胞介素-6合成;(2)对酵素介导的巨噬细胞肿瘤坏死因子合成的拮抗作用;(3)提高脂多糖介导的肿瘤坏死因子和巨噬细胞氮氧化物合成;(4)补体替代通路的激活;(5)环磷酰胺所致白细胞减少的造血反应;(6)对腹水形成肿瘤的抗肿瘤作用;(7)血管通透性增强;(8)脂多糖引发TNF-α合成的启动效应;(9)佐剂对抗体产生的影响。这些结果强烈提示CSBG具有多种免疫药理活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunopharmacological and immunotoxicological activities of a water-soluble (1→3)-β-d-glucan, CSBG from Candida spp.

We have established a convenient, two-step procedure to solubilize the yeast cell wall (1→3)-β-d-glucan using the combination of NaClO oxidation and DMSO extraction. Candida soluble β-d-glucan (CSBG) was mainly composed of a linear β-1,3 glucan with a linear β-1,6-glucan moiety. In this study, we screened for several immunopharmacological activities of CSBG and found the following activities: (1) interleukin-6 synthesis of macrophages in vitro; (2) antagonistic effect for zymosan mediated-tumor necrosis factor synthesis of macrophages; (3) augmentation for lipopolysaccharide mediated tumor necrosis factor and nitrogen oxide syntheses of macrophages; (4) activation of alternative pathway of complement; (5) hematopoietic response on cyclophosphamide induced leukopenia; (6) the antitumor effect on ascites form tumor; (7) Enhanced vascular permeability; (8) priming effect on lipopolysaccharide triggered TNF-α synthesis; and (9) adjuvant effect on antibody production. These results strongly suggested that CSBG possessed various immunopharmacological activity.

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