Aminin Dmitry L, Silchenko Alexandra S, Avilov Sergey A, Stepanov Vadim G, Kalinin Vladimir I
Pacific Institute of Bioorganic Chemistry, Vladivostok, 690022, Russian Federation.
Nat Prod Commun. 2009 Jun;4(6):773-6.
Four triterpene glycosides from sea cucumbers belonging to the genus Cucumaria, okhotoside A(1)-1 (1), cucumarioside A(0)-1 (2), frondoside A (3) and cucumarioside A(2)-2 (4) inhibit the activity of nonspecific esterase of mouse spleen lymphocytes. The dependence of the inhibitory activity of the glycosides on their structure is similar to that for hemolytic activity. The absence of inhibitory activity for the preparation Cumaside, which is a complex of cucumarioside A(2)-2 and related compounds with cholesterol, shows a cholesterol-dependent character of the inhibitory action of the glycosides. The effective inhibitory concentrations of frondoside A and cucumarioside A(2)-2 are significantly higher than the immunomodulatory doses of these glycosides.
从瓜参属海参中提取的四种三萜糖苷,即奥霍托苷A(1)-1(1)、瓜参苷A(0)-1(2)、叶苷A(3)和瓜参苷A(2)-2(4),可抑制小鼠脾脏淋巴细胞的非特异性酯酶活性。这些糖苷的抑制活性对其结构的依赖性与溶血活性相似。制备物Cumaside是瓜参苷A(2)-2与相关化合物和胆固醇的复合物,对其无抑制活性,这表明糖苷的抑制作用具有胆固醇依赖性。叶苷A和瓜参苷A(2)-2的有效抑制浓度显著高于这些糖苷的免疫调节剂量。