Beijing Tide Pharmaceutical Co., Ltd., Beijing Economic Technological Development Area (BDA), No. 8 East Rongjing Street, Beijing, 100176, P. R. China.
Beijing Key Laboratory of Environmental and Viral Oncology, Faculty of Environment and Life, Beijing University of Technology, Beijing, 100124, P. R. China.
Chem Biodivers. 2021 Sep;18(9):e2100338. doi: 10.1002/cbdv.202100338. Epub 2021 Aug 9.
AIDS, caused by HIV-1, is one of the most dangerous infectious diseases in the world. Therefore, it is necessary to develop new drugs with more potent bioactivities, less toxicity and higher tolerability for controlling the viral load, particularly by using the raw materials that are widely available. Agaricus blazei Murill (AbM), known in China as jisongrong, is of great importance as a food source and as a health-promoting supplement for immunomodulation. The polysaccharides of AbM exhibit various biological activities, such as regulating cellular immunity and providing anti-oxidative, anti-infective, and anti-inflammatory effects. At present, to our knowledge, no report has explored the chemically sulfated and anti-HIV-1 activity of AbM polysaccharides. Herein, the sulfated AbM polysaccharides with different sulfur contents were prepared by the chlorosulfonic acid-pyridine method. The characteristics of sulfated derivatives were established by the determination of the sulfur content, the relative molecular weight, and the Fourier-transform infrared spectroscopy. The anti-HIV activities of the sulfated AbM polysaccharides were evaluated by CCK-8 and the single-cycle pseudovirus infection (TZM-bl) assay. The sulfated AbM polysaccharides had strong antiviral properties, and the half-maximal inhibitory concentrations approached that of the positive control, azidothymidine. Sulfated modification of AbM polysaccharides can increase their anti-HIV pharmacological activity, which makes them promising alternative candidates as bioactive macromolecules for biomedical applications in HIV/AIDS.
艾滋病(AIDS)由 HIV-1 引起,是世界上最危险的传染病之一。因此,有必要开发具有更强生物活性、更低毒性和更高耐受性的新药来控制病毒载量,特别是使用广泛可用的原材料。姬松茸(Agaricus blazei Murill),在中国被称为姬松茸,作为一种食物来源和免疫调节的保健品具有重要意义。姬松茸多糖具有多种生物活性,如调节细胞免疫和提供抗氧化、抗感染和抗炎作用。目前,据我们所知,尚未有研究探索姬松茸多糖的化学硫酸化和抗 HIV-1 活性。在此,采用氯磺酸-吡啶法制备了具有不同硫含量的硫酸化姬松茸多糖。通过测定硫含量、相对分子量和傅里叶变换红外光谱来确定硫酸化衍生物的特征。通过 CCK-8 和单循环假病毒感染(TZM-bl)测定评估了硫酸化姬松茸多糖的抗 HIV 活性。硫酸化姬松茸多糖具有很强的抗病毒活性,半数最大抑制浓度接近阳性对照物叠氮胸苷。硫酸化修饰姬松茸多糖可以提高其抗 HIV 药理活性,使它们成为治疗艾滋病的生物活性大分子的有前途的替代候选物。