Pós-doutoranda em Ciências Farmacêuticas, Departamento de Farmácia e Farmacologia, Universidade Estadual de Maringá, Av. Colombo 5790, 87020-900 Maringá, PR, Brazil.
Phytomedicine. 2012 Feb 15;19(3-4):223-30. doi: 10.1016/j.phymed.2011.10.008. Epub 2012 Jan 28.
We have previously demonstrated antileishmanial activity on Leishmania amazonensis of the natural (1-2), synthetic (7) and derivatives of coumarin (-) mammea A/BB (3-6) isolated from the dichloromethane extract of Calophyllum brasiliense leaves. The aim of the present study was to evaluate morphological and ultrastructural alterations in Leishmania amazonensis induced by these compounds. In promastigote forms, all seven compounds produced significant morphological and ultrastructural alterations, as revealed by scanning and transmission electron microscopy. The compound 5,7-dihydroxy-8-(2-methylbutanoyl)-6-(3-methylbutyl)-4-phenyl-chroman-2-one (3), the most active antileishmanial with LD₅₀ of 0.9 μM), induced cell shrinkage and a rounded appearance of the cells. Parasites incubated in the presence of compound (3) showed ultrastructural changes, such as the appearance of mitochondrial swelling with a reduction in the density of the mitochondrial matrix and the presence of vesicles inside the mitochondrion, indicating damage and significant change in this organelle; abnormal chromatin condensation, alterations in the nuclear envelope, intense atypical cytoplasmic vacuolization, and the appearance of autophagic vacuoles were also observed. In addition, the compound (3) may be acting to depolarize the mitochondrial membrane potential of the cells, leading to death of the parasite.
我们之前已经证明了天然(1-2)、合成(7)和香豆素衍生物(-)mammea A/BB(3-6)对亚马逊利什曼原虫具有抗利什曼原虫活性,这些化合物均从巴西苏木叶的二氯甲烷提取物中分离得到。本研究的目的是评估这些化合物对亚马逊利什曼原虫形态和超微结构的影响。在前鞭毛体形式中,所有七种化合物都通过扫描和透射电子显微镜显示出显著的形态和超微结构改变。化合物 5,7-二羟基-8-(2-甲基丁酰基)-6-(3-甲基丁基)-4-苯基-色满-2-酮(3)是最具抗利什曼原虫活性的化合物,LD₅₀ 为 0.9 μM),导致细胞收缩和细胞呈圆形外观。在存在化合物(3)的情况下孵育的寄生虫显示出超微结构变化,例如线粒体肿胀,线粒体基质密度降低,线粒体内部出现囊泡,表明该细胞器受损且发生了重大变化;还观察到异常染色质凝聚、核膜改变、强烈的非典型细胞质空泡化和自噬空泡的出现。此外,化合物(3)可能作用于使线粒体膜电位去极化,导致寄生虫死亡。