Alves Alex Barbosa, da Silva Bortoleti Bruna Taciane, Tomiotto-Pellissier Fernanda, Ganaza Ana Flávia Marques, Gonçalves Manoela Daiele, Carloto Amanda Cristina Machado, Rodrigues Ana Carolina Jacob, Silva Taylon Felipe, Nakazato Gerson, Kobayashi Renata Katsuko Takayama, Lazarin-Bidóia Danielle, Miranda-Sapla Milena Menegazzo, Costa Idessania Nazareth, Pavanelli Wander Rogério, Conchon-Costa Ivete
Laboratory of Immunoparasitology of Neglected Diseases and Cancer, Department of Pathological Sciences, Center of Biological Sciences, State University of Londrina, Londrina 86057-970, PR, Brazil.
Carlos Chagas Institute (ICC-Fiocruz-Pr), Curitiba 81310-020, PR, Brazil.
Pathogens. 2023 Apr 29;12(5):660. doi: 10.3390/pathogens12050660.
American tegumentary leishmaniasis, a zoonotic disease caused by the genus, poses significant challenges in treatment, including administration difficulty, low efficacy, and parasite resistance. Novel compounds or associations offer alternative therapies, and natural products such as oregano essential oil (OEO), extracted from , have been extensively researched due to biological effects, including antibacterial, antifungal, and antiparasitic properties. Silver nanoparticles (AgNp), a nanomaterial with compelling antimicrobial and antiparasitic activity, have been shown to exhibit potent leishmanicidal properties. We evaluated the in vitro effect of OEO and AgNp-Bio association on and the death mechanisms of the parasite involved. Our results demonstrated a synergistic antileishmanial effect of OEO + AgNp on promastigote forms and -infected macrophages, which induced morphological and ultrastructural changes in promastigotes. Subsequently, we investigated the mechanisms underlying parasite death and showed an increase in NO, ROS, mitochondrial depolarization, accumulation of lipid-storage bodies, autophagic vacuoles, phosphatidylserine exposure, and damage to the plasma membrane. Moreover, the association resulted in a reduction in the percentage of infected cells and the number of amastigotes per macrophage. In conclusion, our findings establish that OEO + AgNp elicits a late apoptosis-like mechanism to combat promastigote forms and promotes ROS and NO production in infected macrophages to target intracellular amastigote forms.
美洲皮肤利什曼病是一种由该属引起的人畜共患病,在治疗方面面临重大挑战,包括给药困难、疗效低和寄生虫耐药性。新型化合物或组合提供了替代疗法,从牛至中提取的牛至精油(OEO)等天然产物因其具有抗菌、抗真菌和抗寄生虫等生物学效应而受到广泛研究。银纳米颗粒(AgNp)是一种具有强大抗菌和抗寄生虫活性的纳米材料,已被证明具有强大的杀利什曼原虫特性。我们评估了OEO和AgNp-Bio组合对利什曼原虫的体外作用以及所涉及的寄生虫死亡机制。我们的结果表明,OEO + AgNp对前鞭毛体形式和感染的巨噬细胞具有协同抗利什曼原虫作用,这会诱导前鞭毛体的形态和超微结构变化。随后,我们研究了寄生虫死亡的潜在机制,结果显示一氧化氮(NO)、活性氧(ROS)增加、线粒体去极化、脂质储存体积累、自噬泡、磷脂酰丝氨酸暴露以及质膜受损。此外,这种组合导致感染细胞百分比和每个巨噬细胞内无鞭毛体数量减少。总之,我们的研究结果表明,OEO + AgNp引发一种类似晚期凋亡的机制来对抗前鞭毛体形式,并促进感染巨噬细胞中ROS和NO的产生,以靶向细胞内无鞭毛体形式。