Laboratory of Histology and Embriology, Institute of Biomedical Sciences, Federal University of Uberlândia, 38405-320 Uberlândia, MG, Brazil.
Vet Parasitol. 2012 Jun 8;187(1-2):44-52. doi: 10.1016/j.vetpar.2011.12.039. Epub 2012 Jan 10.
Currently, toxoplasmosis is treated with sulfadiazine and pyrimethamine. However, this treatment presents several adverse side effects; thus, there is a critical need for the development and evaluation of new drugs, which do not present the same problems of the standard therapy. Enrofloxacin is a fluoroquinolone antibiotic known to control infection against several bacteria in veterinary medicine. Recently, this drug has demonstrated protective effects against protozoan parasites such as Neospora caninum. The present study aimed to determine the effect of enrofloxacin in the control of Toxoplasma gondii infection. For this purpose, human foreskin fibroblast (HFF) cells were infected with T. gondii RH strain and treated with sulfadiazine, penicillin/streptomycin, pyrimethamine, or enrofloxacin. Following treatment, we analyzed the infection index, parasite intracellular proliferation and the number of plaques. Additionally, tissue parasitism and histological changes were investigated in the brain of Calomys callosus that were infected with T. gondii (ME49 strain) and treated with either sulfadiazine or enrofloxacin. Enrofloxacin was able to reduce the infection index, intracellular proliferation and the number of plaques in HFF cells infected by T. gondii in comparison with untreated or penicillin/streptomycin-treated ones. Enrofloxacin was more protective against T. gondii in HFF infected cells than sulfadiazine treatment (P<0.001). In addition, pyrimethamine, enrofloxacin or the associations of sulfadiazine plus pyrimethamine, enrofloxacin plus sulfadiazine or enrofloxacin plus pyrimethamine-treatments were able to reduce the plaque numbers in HFF cells infected by T. gondii when compared to medium, penicillin/streptomycin or sulfadiazine alone. In vivo experiments demonstrated that enrofloxacin diminished significantly the tissue parasitism as well as the inflammatory alterations in the brain of C. callosus infected with T. gondii when compared with untreated animals. Based on our findings, it can be concluded that enrofloxacin is a potential alternative drug for the treatment of toxoplasmosis.
目前,弓形虫病的治疗方法是使用磺胺嘧啶和乙胺嘧啶。然而,这种治疗方法存在许多不良反应;因此,迫切需要开发和评估新的药物,这些药物不会带来标准治疗的相同问题。恩诺沙星是一种氟喹诺酮类抗生素,已知在兽医领域可控制多种细菌感染。最近,这种药物已被证明对新孢子虫等原生动物寄生虫具有保护作用。本研究旨在确定恩诺沙星在控制弓形虫感染中的作用。为此,用人包皮成纤维细胞(HFF)感染弓形虫 RH 株,并用磺胺嘧啶、青霉素/链霉素、乙胺嘧啶或恩诺沙星进行治疗。治疗后,我们分析了感染指数、寄生虫细胞内增殖和菌斑数量。此外,还研究了用磺胺嘧啶或恩诺沙星治疗感染弓形虫(ME49 株)的毛丝鼠脑组织中的组织寄生和组织学变化。与未处理或青霉素/链霉素处理的细胞相比,恩诺沙星能够降低 HFF 细胞感染弓形虫的感染指数、细胞内增殖和菌斑数量。恩诺沙星对 HFF 感染细胞的保护作用优于磺胺嘧啶(P<0.001)。此外,与培养基、青霉素/链霉素或磺胺嘧啶单独治疗相比,嘧啶胺、恩诺沙星或磺胺嘧啶加嘧啶胺、恩诺沙星加磺胺嘧啶或恩诺沙星加嘧啶胺联合治疗能够降低 HFF 细胞感染弓形虫的菌斑数量。体内实验表明,与未处理的动物相比,恩诺沙星显著降低了感染弓形虫的毛丝鼠脑组织中的组织寄生和炎症改变。根据我们的发现,可以得出结论,恩诺沙星是治疗弓形虫病的一种潜在替代药物。