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补体抑制活性柴胡多糖及其作用靶点研究(英文)
引用本文:狄宏晔,章蕴毅,陈道峰.补体抑制活性柴胡多糖及其作用靶点研究(英文)[J].中国天然药物,2013(2):177-184.
作者姓名:狄宏晔  章蕴毅  陈道峰
作者单位:复旦大学药学院,上海201203
基金项目:国家自然科学基金(Nos.30925042,30572315),科技部“重大新药创制”重大科技专项课题(NOS.2009ZX09502-0132012ZX09301001-003)和上海市科委项目(10XDl405900)资助
摘    要:目的:从北柴胡根中分离表征具有抗补体活性的多糖成分。方法:以抗补体活性为导向从北柴胡根水提物中分离纯化活性多糖;化学和谱学方法表征多糖的理化性质;采用体外细胞溶血试验法测定抗补体活性;并利用补体成分缺失血清鉴定补体激活过程中的作用靶点。结果:获得一个均一多糖BC-PS2,是一个具分支结构的杂多糖,平均分子量2000KDa,其单糖摩尔比为:葡萄糖/阿拉伯糖/半乳糖/甘露糖=3.5:2.4:2.0:1.0,并含有少量的鼠李糖和木糖以及蛋白(1.11%);单糖的主要连接方式包括:末端、1,3-、1,6-和1,3,6-连接的葡萄糖,末端、1,5-连接的阿拉伯糖,末端、1,4-、1,6-和1,4,6-连接的半乳糖,末端、1,4-和1,4,6-连接的甘露糖;BC-PS2对补体激活的经典和旁路途径均有抑制作用,CH50和AP50分别为(0.222±0.013)和(0.356±0.032)mg·mL-1;靶点研究结果表明BC-PS2作用于补体成分C1q,C2和C9。结论:BC-PS2是一个具有抗补体活性的多糖成分,应该是柴胡治疗与补体过度激活相关疾病的药效成分之一。

关 键 词:北柴胡  多糖  BC-PS2  补体抑制剂

Isolation of an anti-complementary polysaccharide from . the root of Bupleurum chinense and identification of its targets in complement activation cascade
DI Hong-Ye,ZHANG Yun-Yi,CHEN Dao-Feng.Isolation of an anti-complementary polysaccharide from . the root of Bupleurum chinense and identification of its targets in complement activation cascade[J].Chinese JOurnal of Natural Medicines,2013(2):177-184.
Authors:DI Hong-Ye  ZHANG Yun-Yi  CHEN Dao-Feng
Institution:School of Pharmacy, Fudan University, Shanghai 201203, China
Abstract:AIM: To isolate and characterize the anti-complementary polysaccharide from the root of Bupleurum chinense. METHODS: Bioactivity-guided fractionation and purification was used to obtain the anti-complementary polysaccharide from the hot-water extract of the root of Bupleurum chinense. The polysaccharide was characterized by various chemical and spectral analyses. The anti-complementary activities were evaluated by hemolytic assay in vitro. The action targets were identified in the system with individual complement-depleted sera. RESULTS: A homogeneous polysaccharide BC-PS2 was isolated as an anti-complementary agent. It was identified as a branched polysaccharide with an average molecular weight about 2 000 KDa, composed of Glc, Ara, Gal, and Man in the ratio 3.5 : 2.4 : 2.0 : 1.0, respectively, along with a trace of Rha and Xyl, and only 1.11% of protein. The main linkages of the residues of BC-PS2 include terminal, 1, 6-1inked, 1, 3-1inked and 1, 3, 6-1inked Glcp, terminal and 1, 5-1inked Araf, terminal, 1, 4-1inked, 1, 6-1inked and 1, 4, 6-1inked Galp, terminal, and, 1, 4-1inked and 1, 4, 6-1inked Manp. The bioassay experiments revealed that BC-PS2 inhibited complement activation on both the classical and alternative pathways, with CHs0 and APs0 of (0.222 ± 0.013) and (0.356 ± 0.032) mg·mL^-1, respectively. Preliminary mechanism studies indicated that BC-PS2 interacted with Clq, C2, and C9 components. CONCLUSION: The results demonstrated that BC-PS2 is an anti-complementary polysaccharide, and should be important constituent of the root ofBupleurum chinense for its application in the treatment of diseases associated with the excessive activation of complement system.
Keywords:Bupleurum chinense  Polysaccharide  BC-PS2  Complement inhibitor
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