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当归中一种可溶碱性多糖的结构特征及其体内抗肿瘤活性。

Structural Characterization of an Alkali-Soluble Polysaccharide from Angelica sinensis and Its Antitumor Activity in Vivo.

机构信息

College of Food Science and Engineering, Tianjin University of Science and Technology, Tianjin, 300457, P. R. China.

出版信息

Chem Biodivers. 2021 Jun;18(6):e2100089. doi: 10.1002/cbdv.202100089. Epub 2021 May 11.

Abstract

A novel alkali-soluble polysaccharide (AASP) was isolated from Angelica sinensis (Oliv.) Diels under aqueous alkali treatment, and its structural characterization and antitumor activity in Vivo were evaluated in present study. Results of HPGPC and IC revealed that AASP was a neutral polysaccharide containing Ara, Gal and Glc in the mole ratio of 1.00 : 2.26 : 24.43, with the average molecular weight of 4.7 kDa. Periodate oxidation, Smith degradation, methylation, FT-IR, and NMR analyses further demonstrated that a preliminary structure of AASP was proposed as follows: (1→3)-linked arabinose, (1→6)-linked galactose, and (1→), (1→4), (1→6), (1→3,6)-linked glucose with α- and β-configuration. In Vivo antitumor assays, AASP exhibited prominent antitumor effects on H22 hepatoma cells with an inhibitory ratio of 48.57 % and effectively protected thymuses and spleens of tumor-bearing mice. Besides, AASP displayed a proliferation stimulating activity of immunocytes (splenocytes, peritoneal macrophages and natural killer cells), and an auxo-action for cytokines release (TNF-α, IL-2 and IFN-γ), leading to the apoptosis of H22 solid tumors cells via G0/G1 phase arrested. The above data demonstrated that AASP holds great application potential to be a safe and effective antitumor supplement in the future.

摘要

本研究从当归中提取到一种新型的堿溶性多糖(AASP),并对其结构特征和体内抗肿瘤活性进行了评价。HPGPC 和 IC 的结果表明,AASP 是一种中性多糖,含有阿拉伯糖、半乳糖和葡萄糖,摩尔比为 1.00:2.26:24.43,平均分子量为 4.7 kDa。高碘酸氧化、Smith 降解、甲基化、FT-IR 和 NMR 分析进一步表明,AASP 的初步结构如下:(1→3)-连接的阿拉伯糖、(1→6)-连接的半乳糖和(1→)、(1→4)、(1→6)、(1→3,6)-连接的葡萄糖,具有α-和β-构型。体内抗肿瘤实验表明,AASP 对 H22 肝癌细胞具有显著的抗肿瘤作用,抑制率为 48.57%,有效保护荷瘤小鼠的胸腺和脾脏。此外,AASP 对免疫细胞(脾细胞、腹腔巨噬细胞和自然杀伤细胞)具有增殖刺激活性,并对细胞因子释放(TNF-α、IL-2 和 IFN-γ)具有辅助作用,通过 G0/G1 期阻滞导致 H22 实体肿瘤细胞凋亡。上述数据表明,AASP 具有很大的应用潜力,有望成为未来安全有效的抗肿瘤补充剂。

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