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桦木酸及其衍生物对恶性疟原虫的体外抗疟活性以及对感染伯氏疟原虫小鼠的体内抗疟活性。

Antimalarial activity of betulinic acid and derivatives in vitro against Plasmodium falciparum and in vivo in P. berghei-infected mice.

作者信息

de Sá Matheus Santos, Costa José Fernando Oliveira, Krettli Antoniana Ursine, Zalis Mariano Gustavo, Maia Gabriela Lemos de Azevedo, Sette Ivana Maria Fechine, Câmara Celso de Amorim, Filho José Maria Barbosa, Giulietti-Harley Ana Maria, Ribeiro Dos Santos Ricardo, Soares Milena Botelho Pereira

机构信息

Centro de Pesquisas Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Bahia, Brazil.

出版信息

Parasitol Res. 2009 Jul;105(1):275-9. doi: 10.1007/s00436-009-1394-0. Epub 2009 Apr 15.

Abstract

Malaria is one of the most important tropical diseases and mainly affects populations living in developing countries. Reduced sensitivity of Plasmodium sp. to formerly recommended antimalarial drugs places an increasing burden on malaria control programs as well as on national health systems in endemic countries. The present study aims to evaluate the antimalarial activity of betulinic acid and its derivative compounds, betulonic acid, betulinic acid acetate, betulinic acid methyl ester, and betulinic acid methyl ester acetate. These substances showed antiplasmodial activity against chloroquine-resistant Plasmodium falciparum parasites in vitro, with IC(50) values of 9.89, 10.01, 5.99, 51.58, and 45.79 microM, respectively. Mice infected with Plasmodium berghei and treated with betulinic acid acetate had a dose-dependent reduction of parasitemia. Our results indicate that betulinic acid and its derivative compounds are candidates for the development of new antimalarial drugs.

摘要

疟疾是最重要的热带疾病之一,主要影响生活在发展中国家的人群。疟原虫对先前推荐的抗疟药物的敏感性降低,给疟疾控制项目以及疟疾流行国家的国家卫生系统带来了越来越大的负担。本研究旨在评估桦木酸及其衍生物桦木酮酸、醋酸桦木酸、桦木酸甲酯和醋酸桦木酸甲酯的抗疟活性。这些物质在体外对氯喹耐药的恶性疟原虫表现出抗疟原虫活性,IC(50)值分别为9.89、10.01、5.99、51.58和45.79微摩尔。感染伯氏疟原虫并用醋酸桦木酸治疗的小鼠,其寄生虫血症呈剂量依赖性降低。我们的结果表明,桦木酸及其衍生物是开发新型抗疟药物的候选物。

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