Tatli I Irem, Akdemir Zeliha S, Yesilada Erdem, Küpeli Esra
Department of Pharmaceutical Botany, Faculty of Pharmacy, Hacettepe University, 06100 Ankara, Turkey.
Z Naturforsch C J Biosci. 2008 Mar-Apr;63(3-4):196-202. doi: 10.1515/znc-2008-3-406.
The potential effects of flavonoids, phenylethanoid and neolignan glycosides from the aerial parts of Verbascum salviifolium Boiss. were studied in the p-benzoquinone-induced writhing reflex, for the assessment of the antinociceptive activity, and in carrageenan- and PGE1-induced hind paw edema and 12-O-tetradecanoyl-13-acetate (TPA)-induced ear edema models in mice, for the assessment of the anti-inflammatory activity. Through bioassay-guided fractionation and isolation procedures ten compounds from the aqueous extract of the plant, luteolin 7-O-glucoside (1), luteolin 3'-O-glucoside (2), apigenin 7-O-glucoside (3), chrysoeriol 7-O-glucoside (4), beta-hydroxyacteoside (5), martynoside (6), forsythoside B (7), angoroside A (8), dehydrodiconiferyl alcohol-9'-O-beta-D-glucopyranoside (9) and dehydrodiconiferyl alcohol-9-O-beta-D-glucopyranoside (10), were isolated and their structures were elucidated by spectral techniques. Results have shown that 1, 2, 3 and 5 significantly inhibited carrageenan-induced paw edema at a 200 mg/kg dose, while 1, 2 and 5 also displayed anti-inflammatory activity against the PGE1-induced hind paw edema model. However, all the compounds showed no effect in the TPA-induced ear edema model. The compounds 1 and 2 also exhibited significant antinociceptive activity.
研究了绵毛 Verbascum salviifolium Boiss.地上部分的黄酮类、苯乙醇苷和新木脂素苷在对苯醌诱导的扭体反射中的潜在作用,以评估其镇痛活性;并在角叉菜胶和前列腺素 E1诱导的小鼠后爪水肿以及 12 - O - 十四烷酰 - 13 - 乙酸酯(TPA)诱导的小鼠耳水肿模型中进行研究,以评估其抗炎活性。通过生物活性导向的分离和纯化程序,从该植物的水提取物中分离出十种化合物,分别为木犀草素 7 - O - 葡萄糖苷(1)、木犀草素 3'-O - 葡萄糖苷(2)、芹菜素 7 - O - 葡萄糖苷(3)、金圣草素 7 - O - 葡萄糖苷(4)、β - 羟基洋丁香酚苷(5)、紫葳苷(6)、连翘酯苷 B(7)、安格洛苷 A(8)、脱氢二松柏醇 - 9'-O - β - D - 吡喃葡萄糖苷(9)和脱氢二松柏醇 - 9 - O - β - D - 吡喃葡萄糖苷(10),并通过光谱技术确定了它们的结构。结果表明,化合物 1、2、3 和 5 在 200 mg/kg 剂量下能显著抑制角叉菜胶诱导的爪水肿,而化合物 1、2 和 5 对前列腺素 E1诱导的后爪水肿模型也具有抗炎活性。然而,所有化合物在 TPA 诱导的耳水肿模型中均无作用。化合物 1 和 2 还表现出显著镇痛活性。