茜草单个化合物对体外止血的影响

V. Luzhanin, A. Samorodov, A. K. Whaley, A. Whaley, G. P. Yakovlev, I. A. Samylina
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As a result of our previous phytochemical research of R. chamaemorus leaves, five polyphenolic secondary metabolites belonging to the classes of tannins and flavonoids were isolated and characterized.Aim. Screening of previously isolated from R. chamaemorus individual compounds for the hemostasis system in vitro and identification of the most promising compounds for subsequent pharmaceutical development.Materials and methods. Experiments under in vitro conditions were performed on the blood of healthy male donors. The research of the effect on platelet aggregation was carried out according to the Born method on an AT-02 aggregometer (LLC \"SPF \"Medtech\", Russia). Determination of anticoagulant activity was carried out by conventional clotting tests on a Solar CGL 2110 turbidimetric hemocoagulometer (CJSC \"SOLAR\", Russia). Cytofluorimetric analysis was performed on a NovoCyte instrument (Agilent Technologies, USA).Result and discussion. 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引用次数: 0

摘要

导言。制药业的主要任务之一是寻找新的有前途的化合物--潜在的候选药物。天然物,尤其是植物,一直以来都是新分子的丰富来源,并被广泛应用于全球食品和制药行业。云莓(Rubus chamaemorus L.)是蔷薇科多年生草本植物。云莓的果实和叶子含有多种多酚次生代谢物--可水解/缩合单宁和黄酮类化合物。富含多酚的提取物具有显著的抗增殖活性,能抑制细胞生长,还能诱导细胞凋亡。我们之前对 R. chamaemorus 叶片进行了植物化学研究,结果分离并鉴定了属于单宁酸和黄酮类的五种多酚次生代谢物。筛选之前从 R. chamaemorus 中分离出的体外止血系统单个化合物,并确定最有希望用于后续药物开发的化合物。对健康男性献血者的血液进行了体外条件下的实验。根据 Born 方法,在 AT-02 聚集仪(LLC "SPF "Medtech",俄罗斯)上研究了对血小板聚集的影响。抗凝血活性的测定是通过 Solar CGL 2110 比浊血凝仪(CJSC "SOLAR",俄罗斯)上的传统凝血试验进行的。细胞荧光分析在 NovoCyte 仪器(美国安捷伦科技公司)上进行。研究了分离出的化合物 1-5 对活化、血小板聚集和止血凝固成分参数的影响。浓度为 1.0 毫克/毫升时,化合物 1-5 不影响纤维蛋白原浓度和凝血酶原时间。在研究浓度下,化合物 1、3 和 5 完全抑制了血小板的活化。化合物 1 和 3 显示出与乙酰水杨酸相当的抗聚集活性,并且包含在 R. сhamaemorus 叶片的所有水提取物和酒精提取物中;它们的定量含量因提取条件而异。因此,通过对从 R. сhamaemorus 叶子中分离出来的单个化合物 1-5 的筛选,确定了它们的抗凝血和抗凝血特性。化合物 1(4-O-α-L-阿拉伯呋喃木苷酸)和化合物 3(槲皮素-3-O-β-D-葡萄糖醛酸)显示出与乙酰水杨酸相当的抗凝血活性,是所研究的系列化合物中最有希望用于后续抗血小板药物开发的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Individual Compounds from Rubus chamaemoruson Hemostasis in vitro
Introduction. One of the key tasks of the pharmaceutical industry is the search for new promising compounds – potential drug candidates. Natural objects, especially plants, have long been rich sources of new molecules and are widely used in the global food and pharmaceutical industries. Cloudberry (Rubus chamaemorus L.) is a perennial herb from the Rosaceae family. The fruits and leaves of R. chamaemorus contain a wide variety of polyphenolic secondary metabolites – hydrolysable/condensed tannins and flavonoids. Extracts enriched by polyphenols showed significant antiproliferative activity and inhibition of cell growth, and also induce cell apoptosis. As a result of our previous phytochemical research of R. chamaemorus leaves, five polyphenolic secondary metabolites belonging to the classes of tannins and flavonoids were isolated and characterized.Aim. Screening of previously isolated from R. chamaemorus individual compounds for the hemostasis system in vitro and identification of the most promising compounds for subsequent pharmaceutical development.Materials and methods. Experiments under in vitro conditions were performed on the blood of healthy male donors. The research of the effect on platelet aggregation was carried out according to the Born method on an AT-02 aggregometer (LLC "SPF "Medtech", Russia). Determination of anticoagulant activity was carried out by conventional clotting tests on a Solar CGL 2110 turbidimetric hemocoagulometer (CJSC "SOLAR", Russia). Cytofluorimetric analysis was performed on a NovoCyte instrument (Agilent Technologies, USA).Result and discussion. The influence of the isolated compounds 1–5 on the parameters of activation, platelet aggregation and the coagulation component of hemostasis was studied. At a concentration of 1.0 mg/ml, compounds 1–5 did not affect the fibrinogen concentration and prothrombin time. Compounds 1, 3 and 5 completely suppressed platelet activation at the studied concentrations. Compounds 1 and 3 showed antiaggregation activity comparible to the values of acetylsalicylic acid and are contained in all aqueous and alcoholic extracts of R. сhamaemorus leaves; their quantitative content varies depending on the extraction conditions.Conclusion. Thus, as a result of the screening of individual compounds 1–5 isolated from the leaves of R. chamaemorus their antiaggregating and anticoagulation properties were established. Compounds 1 (4-O-α-L-arabinofuranosylellagic acid) and 3 (quercetin-3-O-β-D-glucuronide) showed antiaggregation activity comparible to that of acetylsalicylic acid, and are the most promising of the studied series of compounds for the subsequent pharmaceutical development of new antiplatelet agents.
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