de Araujo Portes Juliana, Achari Anushree, Vinayagam Jayaraman, Bhattacharjee Pinaki, Chatterjee Sourav, Jaisankar Parasuraman, de Souza Wanderley
Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho, Centro de Pesquisa em Medicina de Precisão, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Organic & Medicinal Chemistry Division, CSIR-Indian Institute of Chemical Biology, 4 Raja S. C. Mullick Road, Kolkata, 700032, India.
Exp Parasitol. 2025 Aug;275:108988. doi: 10.1016/j.exppara.2025.108988. Epub 2025 Jul 8.
Toxoplasma gondii is an obligate intracellular protozoan, the causative agent of toxoplasmosis. The current treatment against toxoplasmosis is based on the combination of sulfadiazine and pyrimethamine, which are toxic and unable to clear the infection. Due to the need for new active drugs against T. gondii, we have described here the effects of Furan derivatives on T. gondii in vitro. They were previously used with relevant activity against Leishmania amazonensis and Trypanosoma cruzi. The anti-Toxoplasma effects of the furan derivatives were evaluated using tachyzoites of T. gondii from RH strain and as host cells the human foreskin fibroblast (HFF) and the epithelial lineage from Macaca mulatta LLC-MK2. High-content screening and other microscopy techniques were employed to analyze the infected cells after incubation in the presence of the compounds tested. The most effective derivative was 3g, presenting a 50 % inhibitory concentration (IC50) of 4.3 μM after 48 h of incubation. The 50 % cytotoxic concentration (CC50) in the host cells was 50 μM after a 72-h treatment. The ultrastructural analysis showed that after treatment the parasites presented cytoplasmic emptying, mitochondrial swelling, and interference with cell division. It was revealed by TUNEL assay that the parasites dyed in part due to an apoptosis-like cell death. These findings suggest that the furan derivative 3g is a potential candidate for further studies in vivo to find alternative drugs to treat T. gondii infections.
刚地弓形虫是一种专性细胞内原生动物,是弓形虫病的病原体。目前针对弓形虫病的治疗方法是基于磺胺嘧啶和乙胺嘧啶的联合使用,这两种药物有毒且无法清除感染。由于需要针对刚地弓形虫的新型活性药物,我们在此描述了呋喃衍生物在体外对刚地弓形虫的作用。它们之前被用于对亚马逊利什曼原虫和克氏锥虫具有相关活性的研究。使用来自RH株的刚地弓形虫速殖子以及人包皮成纤维细胞(HFF)和恒河猴上皮细胞系LLC-MK2作为宿主细胞,评估呋喃衍生物的抗弓形虫作用。在存在测试化合物的情况下孵育后,采用高内涵筛选和其他显微镜技术分析感染细胞。最有效的衍生物是3g,孵育48小时后其50%抑制浓度(IC50)为4.3μM。宿主细胞经72小时处理后的50%细胞毒性浓度(CC50)为50μM。超微结构分析表明,处理后寄生虫出现细胞质排空、线粒体肿胀以及对细胞分裂的干扰。TUNEL检测显示,寄生虫部分染色是由于类似凋亡的细胞死亡。这些发现表明,呋喃衍生物3g是进一步体内研究的潜在候选药物,以寻找治疗刚地弓形虫感染的替代药物。