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从欧洲槲寄生中分离出的黄酮类化合物的抗炎和镇痛活性。

Anti-inflammatory and antinociceptive activity of flavonoids isolated from Viscum album ssp. album.

作者信息

Orhan Didem Deliorman, Küpeli Esra, Yesilada Erdem, Ergun Fatma

机构信息

Gazi University, Faculty of Pharmacy, Department of Pharmacognosy, 06330 Etiler, Ankara, Turkey.

出版信息

Z Naturforsch C J Biosci. 2006 Jan-Feb;61(1-2):26-30. doi: 10.1515/znc-2006-1-205.

Abstract

Viscum album L. has been used in the indigenous systems of medicine for treatment of headache and some inflammatory diseases. In order to evaluate this information, antinociceptive and anti-inflammatory activities of the five flavonoids (5,7-dimethoxy naringenin or 4',6'-dimethoxy chalcononaringenin) derivatives, isolated from the ethyl acetate fraction of the extract from V. album ssp. album, were investigated, namely 5,7-dimethoxy-flavanone-4'-O-beta-D-glucopyranoside (1), 2'-hydroxy-4',6'-dimethoxy-chalcone-4-O-beta-D-glucopyranoside (2), 5,7-dimethoxy-flavanone-4'-O-[2"-O-(5"'-O-trans-cinnamoyl)-beta-D-apiofuranosyl]-beta-D-glucopyranoside (3), 2'-hydroxy-4',6'-dimethoxy-chalcone-4-O-[2"-O-(5"'-O-trans-cinnamoyl)-beta-Dapiofuranosyl]-beta-D-glucopyranoside (4), 5,7-dimethoxy-flavanone-4'-O-[beta-D-apiofuranosyl-(1 --> 2)]-beta-D-glucopyranoside (5). For the antinociceptive activity assessment the p-benzoquinone-induced writhing test and for the anti-inflammatory activity the carrageenan-induced hind paw edema model in mice were used. The ethyl acetate fraction in a dose of 250 mg/kg as well as compounds 2 and 5 in a 30 mg/kg dose were shown to possess remarkable antinociceptive and anti-inflammatory activities per os without inducing any apparent acute toxicity as well as gastric damage.

摘要

白果槲寄生已被用于传统医学体系中治疗头痛和一些炎症性疾病。为了评估这些信息,对从白果槲寄生提取物的乙酸乙酯部分分离出的五种黄酮类(5,7-二甲氧基柚皮素或4',6'-二甲氧基查耳酮柚皮素)衍生物的镇痛和抗炎活性进行了研究,即5,7-二甲氧基黄烷酮-4'-O-β-D-吡喃葡萄糖苷(1)、2'-羟基-4',6'-二甲氧基查耳酮-4-O-β-D-吡喃葡萄糖苷(2)、5,7-二甲氧基黄烷酮-4'-O-[2''-O-(5'''-O-反式肉桂酰基)-β-D-芹菜呋喃糖基]-β-D-吡喃葡萄糖苷(3)、2'-羟基-4',6'-二甲氧基查耳酮-4-O-[2''-O-(5'''-O-反式肉桂酰基)-β-D-芹菜呋喃糖基]-β-D-吡喃葡萄糖苷(4)、5,7-二甲氧基黄烷酮-4'-O-[β-D-芹菜呋喃糖基-(1→2)]-β-D-吡喃葡萄糖苷(5)。对于镇痛活性评估,采用对苯醌诱导的扭体试验;对于抗炎活性,采用角叉菜胶诱导的小鼠后足肿胀模型。乙酸乙酯部分以250mg/kg的剂量以及化合物2和5以30mg/kg的剂量经口给药时,显示出显著的镇痛和抗炎活性,且未诱导任何明显的急性毒性以及胃损伤。

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