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甘遂烷醇类化合物(瑞香科)对体外培养的溶组织内阿米巴和十二指肠贾第鞭毛虫的活性。

Activity of methylgerambullin from Glycosmis species (Rutaceae) against Entamoeba histolytica and Giardia duodenalis in vitro.

机构信息

Institute of Specific Prophylaxis and Tropical Medicine, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, A-1090, Vienna, Austria.

Chemodiversity Research Group, Faculty of Life Sciences, University of Vienna, A-1030, Vienna, Austria.

出版信息

Int J Parasitol Drugs Drug Resist. 2019 Aug;10:109-117. doi: 10.1016/j.ijpddr.2019.08.001. Epub 2019 Aug 10.

Abstract

Entamoeba histolytica and Giardia duodenalis are widespread intestinal protozoan parasites which both spread via cysts that have to be ingested to infect a new host. Their environment, the small intestine for G. duodenalis and the colon for E. histolytica, contains only very limited amounts of oxygen, so both parasites generate energy by fermentation and substrate level phosphorylation rather than by oxidative phosphorylation. They both contain reducing agents able to reduce and activate nitroimidazole drugs such as metronidazole which is the gold standard drug to treat Entamoeba or Giardia infections. Although metronidazole works well in the majority of cases, it has a number of drawbacks. In animal models, the drug has carcinogenic activity, and concerns about a possible teratogenic activity remain. In addition, the treatment of G. duodenalis infections is hampered by emerging metronidazole resistance. Plant-derived drugs play a dominant role in human medicine, therefore we tested the activity of 14 isolated plant compounds belonging to seven different classes in vitro against both parasites. The tests were performed in a new setting in microtiter plates under anaerobic conditions. The compound with the highest activity was methylgerambullin, a sulphur-containing amide found in Glycosmis species of the family Rutaceae with an EC of 14.5 μM (6.08 μg/ml) after 24 h treatment for E. histolytica and 14.6 μM (6.14 μg/ml) for G. duodenalis. The compound was successfully synthesised in the laboratory which opens the door for the generation of new derivatives with higher activity.

摘要

溶组织内阿米巴原虫和十二指肠贾第鞭毛虫是广泛存在的肠道原生动物寄生虫,它们都通过必须摄入才能感染新宿主的包囊传播。它们的生存环境——十二指肠贾第鞭毛虫的小肠和溶组织内阿米巴原虫的结肠——只含有非常有限量的氧气,因此两种寄生虫都通过发酵和底物水平磷酸化而不是氧化磷酸化来产生能量。它们都含有还原剂,能够还原和激活硝基咪唑类药物,如甲硝唑,甲硝唑是治疗溶组织内阿米巴原虫或贾第鞭毛虫感染的金标准药物。尽管甲硝唑在大多数情况下都很有效,但它也有一些缺点。在动物模型中,该药物具有致癌活性,并且对其可能的致畸活性仍存在担忧。此外,由于甲硝唑耐药性的出现,十二指肠贾第鞭毛虫感染的治疗受到阻碍。植物来源的药物在人类医学中占主导地位,因此我们在体外测试了属于七个不同类别的 14 种分离的植物化合物对这两种寄生虫的活性。这些测试是在微滴定板中在厌氧条件下进行的。活性最高的化合物是甲基革拉明,一种在芸香科 Glycosmis 属植物中发现的含硫酰胺,对溶组织内阿米巴原虫的 EC 为 14.5 μM(6.08 μg/ml),作用 24 h;对十二指肠贾第鞭毛虫的 EC 为 14.6 μM(6.14 μg/ml)。该化合物已在实验室中成功合成,为生成具有更高活性的新衍生物开辟了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a130/6722286/43639400c266/fx1.jpg

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