Adachi Y, Ohno N, Ohsawa M, Oikawa S, Yadomae T
Laboratory of Immunopharmacology of Microbial Products, Tokyo College of Pharmacy, Japan.
Chem Pharm Bull (Tokyo). 1990 Feb;38(2):477-81. doi: 10.1248/cpb.38.477.
Changes of biological activities manifested by (1----6)-branched (1----3)-beta-D-glucans of various molecular weights obtained by heat treatment of the corresponding intact beta-glucan at 150 degrees C (HD-LE) were examined. The activities assessed in this study were as follows: an antitumor activity, activation of alternative complement pathway, glucose consumption by macrophages, macrophage-mediated lysosomal enzyme activity in culture supernatant and cell lysate, interleukin-1 (IL-1) activity, and adjuvant activity. HD-LE could be classified into three groups: 1) HD-LE 0 h (MW 800000) which activated all of the biological activities tested, 2) HD-LE 0.5 and 3 h (MW 250000 and 21000) which lacked or exhibited low levels of activities such as activation of alternative complement pathway and lysosomal enzyme secretion, 3) HD-LE 6 h (MW 6400) which only activated glucose consumption and synthesis of lysosomal enzyme. These results suggest that an antitumor glucan is not always a multiple enhancer of host defense mechanisms and that a large molecular weight is required to augment multiple immunological activities.
研究了通过在150℃对相应的完整β-葡聚糖进行热处理(HD-LE)获得的不同分子量的(1→6)分支(1→3)-β-D-葡聚糖所表现出的生物活性变化。本研究评估的活性如下:抗肿瘤活性、替代补体途径的激活、巨噬细胞的葡萄糖消耗、培养上清液和细胞裂解物中巨噬细胞介导的溶酶体酶活性、白细胞介素-1(IL-1)活性和佐剂活性。HD-LE可分为三组:1)HD-LE 0小时(分子量800000),其激活了所有测试的生物活性;2)HD-LE 0.5小时和3小时(分子量250000和21000),其缺乏或表现出低水平的活性,如替代补体途径的激活和溶酶体酶分泌;3)HD-LE 6小时(分子量6400),其仅激活葡萄糖消耗和溶酶体酶的合成。这些结果表明,抗肿瘤葡聚糖并不总是宿主防御机制的多重增强剂,并且需要大分子量来增强多种免疫活性。