Da Silva B J M, Da Silva R R P, Rodrigues A P D, Farias L H S, Do Nascimento J L M, Silva E O
Federal University of Pará, Institute of Biological Sciences, Laboratory of Parasitology and Laboratory of Structural Biology, Belém, Pará, Brazil; National Institute of Science and Technology in Structural Biology and Bioimaging, Rio de Janeiro, Rio de Janeiro, Brazil.
National Institute of Science and Technology in Structural Biology and Bioimaging, Rio de Janeiro, Rio de Janeiro, Brazil; Evandro Chagas Institute, Laboratory of Electron Microscopy, Department of Health Surveillance, Ministry of Health, Belém, Pará, Brazil.
Micron. 2016 Mar;82:25-32. doi: 10.1016/j.micron.2015.12.001. Epub 2015 Dec 29.
Leishmaniasis are a neglected group of emerging diseases that have been found in 98 countries and are caused by protozoa of the genus Leishmania. The therapy for leishmaniasis causes several side effects and leads to drug-resistant strains. Natural products from plants have exhibited activities against Leishmania in various experimental models. Physalis angulata is a widely used plant in popular medicine, and in the literature it has well-documented leishmanicidal activity. However, its mechanism of action is still unknown. Thus, this study aims to evaluate the mechanism driving the leishmanicidal activity of an aqueous extract of P. angulata root (AEPa). AEPa was effective against both promastigotes and intracellular amastigote forms of Leishmania amazonensis. This effect was mediated by an increase of reactive oxygen species (ROS), but not of nitric oxide (NO). The increased production of ROS induces cell death by phenotypes seems by apoptosis cell death in Leishmania, but not autophagy or necrosis. In addition, morphological analysis of macrophages showed that AEPa induced a high number of cytoplasmic projections, increased the volume of cytoplasm and number of vacuoles, caused cytoskeleton alterations and resulted in high spreading ability. AEPa also promoted superoxide anion (O2(-)) production in both uninfected macrophages and those infected with Leishmania. Therefore, these results revealed that AEPa causes cell death by phenotypes seems by apoptosis cell death in L. amazonensis and modulates macrophage activation through morphofunctional alterations and O2(-) generation to induce Leishmania death.
利什曼病是一组被忽视的新发疾病,已在98个国家被发现,由利什曼原虫属的原生动物引起。利什曼病的治疗会产生多种副作用,并导致耐药菌株的出现。植物来源的天然产物在各种实验模型中已显示出对利什曼原虫的活性。酸浆是一种在民间医学中广泛使用的植物,文献中已充分证明其具有杀利什曼原虫活性。然而,其作用机制仍不清楚。因此,本研究旨在评估酸浆根水提取物(AEPa)杀利什曼原虫活性的作用机制。AEPa对亚马逊利什曼原虫的前鞭毛体和细胞内无鞭毛体形式均有效。这种作用是由活性氧(ROS)的增加介导的,而不是一氧化氮(NO)。ROS产生的增加通过凋亡导致利什曼原虫细胞死亡,但不是自噬或坏死。此外,巨噬细胞的形态学分析表明,AEPa诱导了大量的细胞质突起,增加了细胞质体积和液泡数量,引起细胞骨架改变,并导致高扩散能力。AEPa还促进了未感染巨噬细胞和感染利什曼原虫的巨噬细胞中超氧阴离子(O2(-))的产生。因此,这些结果表明,AEPa通过凋亡导致亚马逊利什曼原虫细胞死亡,并通过形态功能改变和O2(-)的产生调节巨噬细胞活化以诱导利什曼原虫死亡。