Osuna L, Pereda-Miranda R, Tortoriello J, Villarreal M L
Centro de Investigación Bomédica del Sur, Instituto Mexicano del Seguro Social, Xochitepec, Morelos, México.
Planta Med. 1999 Mar;65(2):149-52. doi: 10.1055/s-1999-14057.
A tissue culture method is described for callus formation from Galphimia glauca (Mapighiaceae) in MS (Murashige & Skoog) medium supplemented with various growth regulators. Best induction was achieved when using hypocotyls as explants in medium supplemented with 2 mg/l of 2,4-dichlorophenoxyacetic acid (2,4-D). Major cellular growth of calluses was obtained with naphthaleneacetic acid (2 mg/l) + kinetin (1 mg/l). Subcultivation of calluses using various concentrations of 2,4-D allowed the production of the sedative nor-seco-triterpenoid, galphimine B and a new related compound. The structure of the new constituent was elucidated as 6-acetoxygalphimine B. The highest accumulation of active constituent 1 (1.5 x 10(-2) dry weight) was achieved when 4 mg/l of the hormone were used, and this experimental condition allowed the detection of only galphimine B. A preliminary screening of the methanolic extracts prepared from calluses, using the isolated guinea-pig ileum as a general test system for pharmacological effects, demonstrated that the most active material was the one with the highest concentration of galphimine B. Total accumulation of this sedative triterpene, in the optimized tissue culture conditions, was in the same order of magnitude as the value quantified for wild plants (4.5 x 10(-2) dry weight).
本文描述了一种组织培养方法,用于在添加了各种生长调节剂的MS(Murashige & Skoog)培养基中从白花假金丝桃(金虎尾科)诱导愈伤组织形成。以2mg/L的2,4-二氯苯氧乙酸(2,4-D)添加到培养基中,使用下胚轴作为外植体时诱导效果最佳。愈伤组织的主要细胞生长是在添加萘乙酸(2mg/L)+激动素(1mg/L)的培养基中获得的。使用不同浓度的2,4-D对愈伤组织进行继代培养,能够产生镇静剂去甲-裂-三萜类化合物galphimine B和一种新的相关化合物。新成分的结构被鉴定为6-乙酰氧基galphimine B。当使用4mg/L的激素时,活性成分1的积累量最高(1.5×10⁻²干重),并且在此实验条件下仅检测到galphimine B。以离体豚鼠回肠作为药理作用的通用测试系统,对愈伤组织制备的甲醇提取物进行初步筛选,结果表明活性最强的物质是galphimine B浓度最高的提取物。在优化的组织培养条件下,这种镇静三萜类化合物的总积累量与野生植物定量值(4.5×10⁻²干重)处于同一数量级。