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巴西黑黄皮果实中的天然产物可抑制利什曼原虫蛋白酶。

Natural products from Garcinia brasiliensis as Leishmania protease inhibitors.

机构信息

Department of Pharmacy, Laboratory of Phytochemistry and Medicinal Chemistry, Federal University of Alfenas, Minas Gerais, Brazil.

出版信息

J Med Food. 2011 Jun;14(6):557-62. doi: 10.1089/jmf.2010.0018. Epub 2011 May 9.

Abstract

The infections by protozoans of the genus Leishmania are a major worldwide health problem, with high endemicity in developing countries. The drugs of choice for the treatment of leishmaniasis are the pentavalent antimonials, which cause renal and cardiac toxicity. As part of a search for new drugs against leishmaniasis, we evaluated the in vitro Leishmania protease inhibition activity of extracts (hexanic, ethyl-acetate, and ethanolic) and fukugetin, a bioflavonoid purified from the ethyl-acetate extract of the pericarp of the fruit of Garcinia brasiliensis, a tree native to Brazilian forests. The isolated compound was characterized by using spectral analyses with nuclear magnetic resonance, mass spectroscopy, ultraviolet, and infrared techniques. The ethyl-acetate extract and the compound fukugetin showed significant activity as inhibitors of Leishmania's proteases, with mean (±SD) IC(50) (50% inhibition concentration of protease activity) values of 15.0±1.3 μg/mL and 3.2±0.5 μM/mL, respectively, characterizing a bioguided assay. In addition, this isolated compound showed no activity against promastigote and amastigote forms of L. (L.) amazonensis and mammalian cells. These results suggest that fukugetin is a potent protease inhibitor of L. (L.) amazonensis and does not cause toxicity in mammalian or Leishmania cells in vitro. This study provides new perspectives on the development of novel drugs that have leishmanicidal activity obtained from natural products and that target the parasite's proteases.

摘要

利什曼原虫属原生动物的感染是一个全球性的主要健康问题,在发展中国家流行率很高。治疗利什曼病的首选药物是五价锑,它会导致肾和心脏毒性。作为寻找治疗利什曼病的新药的一部分,我们评估了提取物(己烷、乙酸乙酯和乙醇)和福果汀对利什曼原虫蛋白酶的体外抑制活性,福果汀是从巴西野牡丹果皮的乙酸乙酯提取物中分离得到的生物类黄酮。该分离化合物通过使用核磁共振、质谱、紫外和红外技术的光谱分析进行了表征。乙酸乙酯提取物和福果汀化合物对利什曼原虫蛋白酶表现出显著的抑制活性,平均(±SD)IC50(蛋白酶活性的 50%抑制浓度)值分别为 15.0±1.3μg/mL 和 3.2±0.5μM/mL,这是一种生物导向测定法。此外,该分离化合物对前鞭毛体和无鞭毛体形式的 L.(L.)amazonensis 和哺乳动物细胞没有活性。这些结果表明,福果汀是 L.(L.)amazonensis 的一种有效的蛋白酶抑制剂,在体外对哺乳动物或利什曼原虫细胞没有毒性。本研究为开发具有杀利什曼原虫活性的新型药物提供了新的视角,这些药物来源于天然产物,并针对寄生虫的蛋白酶。

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