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从藏丹参中提取的改性酸性多糖,具有优异的伤口愈合和增强的生物活性。

Modified acid polysaccharide derived from Salvia przewalskii with excellent wound healing and enhanced bioactivity.

机构信息

College of Material Science and Chemical Engineering, Southwest Forestry University, Kunming, Yunnan 650224, China.

School of Health Preservation and Rehabilitation, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610075, China.

出版信息

Int J Biol Macromol. 2024 Apr;263(Pt 2):129803. doi: 10.1016/j.ijbiomac.2024.129803. Epub 2024 Jan 30.

Abstract

Acid polysaccharide was extracted from Salvia przewalskii root powders (PSP), purified by diethylaminoethyl cellulose column (DEAE-52) and molecular sieve (PSP2). PSPm1 was obtained by modifying PSP2 with nitrite and phosphoric acid. The chemical structure of PSP2 and PSPm1 exhibited notable distinctions, primarily due to the absence of arabinose and promotion of glucuronic acid (GlcA). The structure of PSPm1 was deduced through the utilization of H, C, and 2-D NMR. The main chain was linked by α-D-Galp(1 → 3)-α-Glcp-(1 → fragments and →6)-β-D-Galp fragments, with the presence of →4)-α-D-GlcpA-(1 → 6)-β-D-Galp-(1 → , → 4)-α-D-GalAp-(1 → 2,4)-α-D-Rhap-(1 → fragments and →6)-α-Glcp-(1 → 2,4)-β-D-Manp-(1 → fragments. PSPm1 exhibited different immunoregulatory bioactivity in vitro, including haemostatic effects indicated by activated clotting time of 55.5 % reduction by the activated clotting time (ACT) test and wound healing function in vivo. PSPm1 also displayed better anti-tumor biological effects than unmodified. The structure-activity dissimilarity between PSP2 and PSPm1 primarily stems from variations in molecular weight (Mw), monosaccharide composition, and branching patterns. The modification of polysaccharides from the extract residues of Chinese medicinal materials may be a new form of drug supplements.

摘要

从丹参根粉中提取酸性多糖(PSP),经二乙氨基乙基纤维素柱(DEAE-52)和分子筛(PSP2)纯化。亚硝酸和磷酸对 PSP2 进行改性得到 PSPm1。PSP2 和 PSPm1 的化学结构存在显著差异,主要是由于阿拉伯糖的缺失和半乳糖醛酸(GlcA)的增加。通过 1H、13C 和 2D NMR 推断 PSPm1 的结构。主链由 α-D-Galp(1→3)-α-Glcp-(1→f 片段和 →6)-β-D-Galp 片段连接,存在 →4)-α-D-GlcpA-(1→6)-β-D-Galp-(1→, →4)-α-D-GalAp-(1→2,4)-α-D-Rhap-(1→f 片段和 →6)-α-Glcp-(1→2,4)-β-D-Manp-(1→f 片段。PSPm1 在体外表现出不同的免疫调节生物活性,包括由激活凝血时间(ACT)试验引起的凝血时间减少 55.5%所表明的止血作用和体内伤口愈合功能。PSPm1 还表现出比未改性物更好的抗肿瘤生物效应。PSP2 和 PSPm1 的结构-活性差异主要源于分子量(Mw)、单糖组成和支链模式的变化。对中药材提取物残渣中多糖的修饰可能是一种新的药物补充形式。

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