Professor Instituto Rene Rachou - Fundação Instituto Oswaldo Cruz -FIOCRUZ, Malaria Laboratory, Avenue Augusto de Lima 1715, Belo Horizonte, MG, CEP 30190 002, Brazil +55 31 3349 7770 ; +55 31 3295 3115 ;
Expert Opin Drug Discov. 2009 Feb;4(2):95-108. doi: 10.1517/17530050802678127.
Malaria is the most important parasitic disease and its control depends on specific chemotherapy, now complicated by Plasmodium falciparum that has become resistant to most commonly available antimalarials. Treatment of the disease requires quinine or drug combinations of artemisinin derivatives and other antimalarials. Further drug resistance is expected. New active compounds need to be discovered.
OBJECTIVE/METHOD: To find new antimalarials from medicinal and randomly collected plants, crude extracts are screened against P. falciparum in cultures and in malaria animal models, following bioassays of purified fractions, and cytotoxicity tests.
For antimalarial research, screening medicinal plants is more efficient than screening randomly chosen plants. Biomonitored fractionation allows selection of new active molecules identified as potential antimalarials in multidisciplinary projects in Brazil; no new molecule is available for human testing. The advantages of projects based on ethnopharmacology are discussed.
疟疾是最重要的寄生虫病,其防治依赖于特效化学疗法,而现在恶性疟原虫已经对大多数现有的抗疟药物产生了耐药性,使得情况更为复杂。治疗该疾病需要用到奎宁或青蒿素衍生物和其他抗疟药物的联合用药。预计还会出现进一步的耐药性。需要发现新的有效化合物。
目的/方法:从药用植物和随机采集的植物中寻找新的抗疟药物,针对培养的疟原虫和疟疾动物模型筛选粗提取物,随后对纯化部分进行生物测定,并进行细胞毒性测试。
对于抗疟药物研究,筛选药用植物比随机选择植物更为高效。生物监测的分步提取方法可用于在巴西的多学科项目中选择新的活性分子,这些分子被确定为潜在的抗疟药物;目前还没有可供人体测试的新分子。本文还讨论了基于民族药理学的项目的优势。