Yoshida I, Kiho T, Usui S, Sakushima M, Ukai S
Gifu Prefectural Health and Environment Research Center, Pharmaceutical University.
Biol Pharm Bull. 1996 Jan;19(1):114-21. doi: 10.1248/bpb.19.114.
Immunomodulating activities of three carboxymethylated derivatives (AG-AL-CMS, AG-AL-CMI, and AM-APP-CM) of linear (1-->3)-alpha-D-glucans from Agrocybe cylindracea and Amanita muscaria were evaluated with murine peritoneal macrophages playing an important role in tumor immunity. The ratio of macrophages in peritoneal exudate cells increased more than 50% after the administration of three carboxymethylated (1-->3)-alpha-D-glucans. These carboxymethylated (1-->3)-alpha-D-glucans exhibited higher potentiating activities for macrophages than carboxymethylated linear (1-->3)-beta-D-glucan (CMPS) in the potency of reduction of nitro blue tetrazolium, products of nitric oxide and the soluble cytotoxic factor, the amount of glucose consumption, and the activation of acid phosphatase. AG-AL-CMS, AG-AL-CMI, and AM-APP-CM were found to induce the tumor regressing factor in mouse serum, although the ability of the induction of this factor was weaker than that of CMPS. The reticuloendothelial system-potentiating activation of three carboxymethylated alpha-D-glucans was similar to that of the carboxymethylated beta-D-glucan. AG-AL-CMS and AG-AL-CMI, but not AM-APP-CM, were suggested to possess a higher-order structure, resulting from the formation of a fluorescent complex with aniline blue.
对来自柱状田头菇和毒蝇伞的线性(1→3)-α-D-葡聚糖的三种羧甲基化衍生物(AG-AL-CMS、AG-AL-CMI和AM-APP-CM)的免疫调节活性进行了评估,其中小鼠腹膜巨噬细胞在肿瘤免疫中起重要作用。给予三种羧甲基化(1→3)-α-D-葡聚糖后,腹膜渗出细胞中巨噬细胞的比例增加了50%以上。在还原硝基蓝四氮唑、一氧化氮产物和可溶性细胞毒性因子、葡萄糖消耗量以及酸性磷酸酶激活方面,这些羧甲基化(1→3)-α-D-葡聚糖对巨噬细胞的增强活性高于羧甲基化线性(1→3)-β-D-葡聚糖(CMPS)。虽然AG-AL-CMS、AG-AL-CMI和AM-APP-CM诱导小鼠血清中肿瘤消退因子的能力比CMPS弱,但仍被发现能诱导该因子。三种羧甲基化α-D-葡聚糖对网状内皮系统的增强激活作用与羧甲基化β-D-葡聚糖相似。AG-AL-CMS和AG-AL-CMI,而非AM-APP-CM,被认为具有更高阶结构,这是由与苯胺蓝形成荧光复合物所致。