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某些黄酮类化合物及其代谢产物的体外抗幽门螺杆菌活性

In vitro anti-Helicobacter pylori activity of some flavonoids and their metabolites.

作者信息

Bae E A, Han M J, Kim D H

出版信息

Planta Med. 1999 Jun;65(5):442-3. doi: 10.1055/s-2006-960805.

Abstract

The inhibitory effect of flavonoids and phenolic acids, which could be transformed from flavonoids by human intestinal microflora, on the growth of Helicobacter pylori (HP) was investigated. Ponciretin, hesperetin, naringenin and diosmetin were active against HP. Among them, ponciretin was the most potent and its MIC was 10-20 micrograms/ml. However, these active compounds against HP did nearly not inhibit the urease activity of HP.

摘要

研究了黄酮类化合物以及可由人体肠道微生物群从黄酮类化合物转化而来的酚酸对幽门螺杆菌(HP)生长的抑制作用。紫铆亭、橙皮素、柚皮素和香叶木素对HP有活性。其中,紫铆亭活性最强,其最低抑菌浓度为10 - 20微克/毫升。然而,这些对HP有活性的化合物几乎不抑制HP的脲酶活性。

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