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芪归药对中一种多糖的结构表征及其对结肠癌细胞的抗肿瘤活性

Structural characterization of a polysaccharide from Qi-Gui herb pair and its anti-tumor activity in colon cancer cells.

作者信息

Liu Wen-Juan, Ma Ye-Zi, Li Jia-Xin, Fan Bei-Sheng, Li Xiao-Qiang, Cao Wei, Tang Yu-Ping

机构信息

Key Laboratory of Shaanxi Administration of Traditional Chinese Medicine for TCM Compatibility, Shaanxi University of Chinese Medicine, Xianyang, China.

Department of Pharmacology and Key Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, School of Pharmacy, Air Force Medical University, Xi'an, China.

出版信息

Front Pharmacol. 2025 Mar 24;16:1557151. doi: 10.3389/fphar.2025.1557151. eCollection 2025.

Abstract

(Fisch.) Bunge and (Oliv.) Diels forms a classic herb pair (Qi-Gui her pair) in Chinese medicine, which was commonly used for treating menstrual anemia and microvascular ischemic diseases. While polysaccharides are known to be key bioactive components of the Qi-Gui herb pair, their structural characteristics and pharmacological activities remain underexplored. In this research, a homogeneous polysaccharide with a molecular weight of 18.1 kDa was isolated, and its structure was analyzed via high pressure size exclusion chromatography, high performance liquid chromatography, gas chromatography mass spectrometry, and nuclear magnetic resonance spectroscopy. The structural analysis revealed that AAPS-1a was composed of α-T-Glc (5.9%), β-1,3-Gal (3.9%), α-1,4-Man (3.6%), α-1,4-Gal (2.1%), α-1,4-Glc (2.8%), and α-1,6-Glc (81.7%). Furthermore, NMR analysis revealed that AAPS-1a consists of a repeat unit: α-T-Glc-(1→4)-α-Gal-(1→4)-α-Man-(1→4)-α-Glc-(1→[6)-α-Glc-(1]→3)-β-Gal-(1→. studies showed that AAPS-1a could significantly inhibit the proliferation of HCT116 cells, and induces G1 arrest and G2/M arrest, as well as apoptosis of HCT116 cells. This study presents the inaugural report establishing a connection between the structural characteristics of Qi-Gui herbal polysaccharides and their anti-colon cancer activity, demonstrating that AAPS-1a holds promise as a therapeutic agent for the treatment of colon cancer.

摘要

( Fisch.) Bunge和(Oliv.) Diels在中国医学中形成了经典的药对(芪归药对),常用于治疗月经性贫血和微血管缺血性疾病。虽然已知多糖是芪归药对的关键生物活性成分,但其结构特征和药理活性仍未得到充分研究。在本研究中,分离出一种分子量为18.1 kDa的均一多糖,并通过高压尺寸排阻色谱、高效液相色谱、气相色谱 - 质谱和核磁共振光谱对其结构进行了分析。结构分析表明,AAPS - 1a由α - T - Glc(5.9%)、β - 1,3 - Gal(3.9%)、α - 1,4 - Man(3.6%)、α - 1,4 - Gal(2.1%)、α - 1,4 - Glc(2.8%)和α - 1,6 - Glc(81.7%)组成。此外,核磁共振分析表明,AAPS - 1a由一个重复单元组成:α - T - Glc - (1→4) - α - Gal - (1→4) - α - Man - (1→4) - α - Glc - (1→[6) - α - Glc - (1]→3) - β - Gal - (1→。研究表明,AAPS - 1a可显著抑制HCT116细胞的增殖,并诱导HCT116细胞的G1期阻滞和G2/M期阻滞以及凋亡。本研究首次报道了芪归草药多糖的结构特征与其抗结肠癌活性之间的联系,表明AAPS - 1a有望成为治疗结肠癌的治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/524c/11973367/f25da7110104/fphar-16-1557151-g001.jpg

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