Gutierrez Rosa Martha Perez, Solis Rosario Vargas, Baez Efren Garcia, Martinez Francisco Martinez
Laboratorio de Investigacion de Productos Naturales, Escuela Superior de Ingeniería Química e Industrias extractivas IPN, Punto fijo 16, col. Torres Lindavista cp 07708, México D.F.
Phytother Res. 2006 Jul;20(7):542-5. doi: 10.1002/ptr.1893.
The methanol soluble fraction of the leaves of Buddleia scordioides after column chromatography resulted in the isolation of two known iridoid glucosides, catalpol and methylcatalpol. The structures were elucidated by extensive 1D-2D-NMR spectroscopy. The structure of methylcatalpol was confirmed by single-crystal x-ray diffraction. These compounds showed protective activity against increased (both chloroform and histamine) skin vascular permeability in rabbits. The protective effect was measured as the reduction in leakage of Evans blue. The results showed that the iridoids produced a significant inhibition of microvascular permeability. A comparison was made between the action of the iridoids and a known inhibitor of vascular permeability, troxerutin (50 mg/kg). Methylcatalpol and catalpol were found to be less effective than troxerutin.
对醉鱼草叶的甲醇可溶部分进行柱色谱分离后,得到了两种已知的环烯醚萜苷,梓醇和甲基梓醇。通过广泛的一维-二维核磁共振光谱对其结构进行了阐明。甲基梓醇的结构通过单晶X射线衍射得以确证。这些化合物对家兔因(氯仿和组胺)引起的皮肤血管通透性增加具有保护活性。以伊文思蓝渗漏减少量来衡量保护效果。结果表明,环烯醚萜对微血管通透性有显著抑制作用。对环烯醚萜与一种已知的血管通透性抑制剂曲克芦丁(50毫克/千克)的作用进行了比较。发现甲基梓醇和梓醇的效果不如曲克芦丁。