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螺旋山绿豆中的抗氧化类黄酮糖苷。

Antioxidant flavonoid glycosides from Evolvulus alsinoides.

机构信息

Division of Medicinal and Process Chemistry, Central Drug Research Institute CSIR, Lucknow 226001, India.

出版信息

Fitoterapia. 2010 Jun;81(4):234-42. doi: 10.1016/j.fitote.2009.09.003. Epub 2009 Sep 11.

Abstract

Oxidative damage is an established outcome of chronic stress. Thus, the present study was designed to investigate the modulatory role of ethanolic extract of Evolvulus alsinoides (EA) in terms of oxidative alterations at peripheral and central level in rats subjected to chronic unpredictable stress (CUS). CUS exposure for 7 days reduced Cu, Zn superoxide dismutase and catalase activity with increase in glutathione peroxidase activity and lipid peroxidation, while decrease in reduced glutathione level in blood plasma, frontal cortex and hippocampus regions of brain. Oral administration of EA extract at 200mg/kg p.o. normalized these stress induced oxidative alterations with an efficacy similar to that of melatonin. Further, EA extract was taken up for detailed chemical investigation. Two new flavonol-4'-glycoside, kaempferol 4'-O-beta-D-glucopyranosyl-(1-->2)-beta-D-glucopyranoside (3) and kaempferol 4'-O-alpha-L-rhamnopyranosyl-(1-->6)-beta-D-glucopyranoside (5) were isolated, along with eight known compounds (1, 2, 4 and 6-10). The structures of new compounds were established by detailed spectroscopic studies, while known compounds were characterized by direct comparison of their reported NMR data. All these compounds were evaluated for their in vitro antioxidant activity. Compounds 3, 5, 9 and 10 at 100 and 200 microg/ml showed significant in vitro antioxidant activity. Therefore, EA may hold great potential in preventing clinical deterioration in stress induced oxidative load and related disorders.

摘要

氧化损伤是慢性应激的既定结果。因此,本研究旨在探讨醉蝶花乙醇提取物(EA)在慢性不可预测应激(CUS)大鼠外周和中枢水平氧化改变方面的调节作用。7 天的 CUS 暴露降低了 Cu、Zn 超氧化物歧化酶和过氧化氢酶的活性,增加了谷胱甘肽过氧化物酶的活性和脂质过氧化,同时降低了血浆、额叶皮质和海马区的还原型谷胱甘肽水平。EA 提取物以 200mg/kg 口服给药可使这些应激诱导的氧化改变正常化,其功效与褪黑素相似。此外,还对 EA 提取物进行了详细的化学研究。分离得到两种新的黄酮醇-4'-糖苷,山柰酚 4'-O-β-D-吡喃葡萄糖基-(1-->2)-β-D-吡喃葡萄糖苷(3)和山柰酚 4'-O-α-L-鼠李吡喃糖基-(1-->6)-β-D-吡喃葡萄糖苷(5),以及八种已知化合物(1、2、4 和 6-10)。新化合物的结构通过详细的光谱研究确定,而已知化合物则通过与其报道的 NMR 数据的直接比较来表征。所有这些化合物都评估了它们的体外抗氧化活性。化合物 3、5、9 和 10 在 100 和 200μg/ml 时表现出显著的体外抗氧化活性。因此,EA 可能具有很大的潜力,可以预防应激诱导的氧化负荷和相关疾病的临床恶化。

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