Ueda-Nakamura Tânia, Mendonça-Filho Ricardo R, Morgado-Díaz José Andrés, Korehisa Maza Paloma, Prado Dias Filho Benedito, Aparício Garcia Cortez Diógenes, Alviano Daniela Sales, Rosa Maria do Socorro S, Lopes Angela Hampshire C S, Alviano Celuta Sales, Nakamura Celso Vataru
Programa de Pós-graduação em Ciências Farmacêuticas, Universidade Estadual de Maringá, Brazil.
Parasitol Int. 2006 Jun;55(2):99-105. doi: 10.1016/j.parint.2005.10.006. Epub 2005 Dec 15.
Leishmaniasis is a group of diseases with a large spectrum of clinical manifestations caused by protozoans of the genus Leishmania. Here we demonstrate the leishmanicidal activity of the essential oil of Ocimum gratissimum as well as its main constituent, eugenol. The eugenol-rich essential oil of O. gratissimum progressively inhibited Leishmania amazonensis growth at concentrations ranging from 100 to 1000 microg/ml. The IC50 (sub-inhibitory concentration) of the essential oil for promastigotes and amastigotes were respectively 135 and 100 microg/ml and the IC50 of eugenol was 80 microg/ml for promastigote forms. L. amazonensis exposed to essential oil at concentrations corresponding to IC50 for promastigotes and for amastigotes underwent considerable ultrastructural alterations, as shown by transmission electron microscopy. Two or more nuclei or flagella were observed in 31% and 23.3% of treated amastigote and promastigote forms, respectively, suggesting interference in cell division. Considerable mitochondrial swelling was observed in essential oil-treated promastigotes and amastigotes, which had the inner mitochondrial membrane altered, with a significant increase in the number of cristae; in some amastigotes the mitochondrial matrix became less electron-dense. The minimum inhibitory concentration for both promastigotes and amastigotes was 150 microg/ml. Pretreatment of mouse peritoneal macrophages with 100 and 150 microg/ml essential oil reduced the indices of association between promastigotes and the macrophages, followed by increased in nitric oxide production by the infected macrophages. The essential oil showed no cytototoxic effects against mammalian cells. This set of results suggests that O. gratissimum essential oil and its compounds could be used as sources for new antileishmanial drugs.
利什曼病是由利什曼原虫属的原生动物引起的一组具有广泛临床表现的疾病。在此,我们展示了丁香罗勒精油及其主要成分丁香酚的杀利什曼原虫活性。富含丁香酚的丁香罗勒精油在浓度为100至1000微克/毫升范围内逐渐抑制亚马逊利什曼原虫的生长。该精油对前鞭毛体和无鞭毛体的IC50(亚抑制浓度)分别为135和100微克/毫升,丁香酚对前鞭毛体形式的IC50为80微克/毫升。如透射电子显微镜所示,暴露于对应前鞭毛体和无鞭毛体IC50浓度的精油中的亚马逊利什曼原虫发生了相当大的超微结构改变。在分别经处理的无鞭毛体和前鞭毛体形式中,观察到31%和23.3%的虫体有两个或更多的细胞核或鞭毛,提示对细胞分裂有干扰。在经精油处理的前鞭毛体和无鞭毛体中观察到相当大的线粒体肿胀,线粒体内膜发生改变,嵴的数量显著增加;在一些无鞭毛体中,线粒体基质的电子密度降低。对前鞭毛体和无鞭毛体的最低抑菌浓度均为150微克/毫升。用100和150微克/毫升精油预处理小鼠腹腔巨噬细胞可降低前鞭毛体与巨噬细胞之间的结合指数,随后感染的巨噬细胞产生一氧化氮增加。该精油对哺乳动物细胞无细胞毒性作用。这一系列结果表明,丁香罗勒精油及其化合物可作为新型抗利什曼病药物的来源。