Laboratório de Parasitologia, Departamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto FCFRP-USP, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
Parasite Immunol. 2010 Apr;32(4):245-51. doi: 10.1111/j.1365-3024.2009.01185.x.
The aim of this study was to evaluate a possible synergism between melatonin and meloxicam in up-regulating the immune response in male Wistar rats infected with Trypanosoma cruzi during immunosuppression phenomenon, which characterizes the acute phase of the Chagas' disease. Male Wistar rats were infected with the Y strain of T. cruzi. Experiments were performed on 7, 14 and 21 days post-infection. Several immunological parameters were evaluated including gamma-interferon (IFN-gamma), interleukin-2 (IL-2), nitric oxide (NO) and prostaglandin E(2) (PGE(2)). The combined treatment with melatonin and meloxicam significantly enhanced the release of IL-2 and INF-gamma into animals' serum, when compared with the infected control groups during the course of infection. Furthermore, the blockade of PGE(2) synthesis and the increased release of NO by macrophage cells from T. cruzi-infected animals contributed to regulate the production of Th1 subset cytokines significantly reducing the parasitaemia in animals treated with the combination of both substances. Therefore, our results suggest that the association of melatonin and meloxicam was more effective in protecting animals against the harmful actions of T. cruzi infection as compared with the treatments of meloxicam or melatonin alone.
本研究旨在评估褪黑素和美洛昔康在调节感染恰加斯病急性期免疫抑制现象的雄性 Wistar 大鼠中免疫反应方面的可能协同作用。雄性 Wistar 大鼠感染 T. cruzi 的 Y 株。实验在感染后 7、14 和 21 天进行。评估了几种免疫参数,包括γ-干扰素(IFN-γ)、白细胞介素 2(IL-2)、一氧化氮(NO)和前列腺素 E2(PGE2)。与感染对照组相比,褪黑素和美洛昔康联合治疗在感染过程中显著增加了 IL-2 和 INF-γ向动物血清中的释放。此外,阻断 PGE2 合成和增加感染 T. cruzi 的巨噬细胞细胞释放的 NO 有助于调节 Th1 亚群细胞因子的产生,显著降低了联合治疗动物的寄生虫血症。因此,我们的结果表明,与单独使用美洛昔康或褪黑素相比,褪黑素和美洛昔康的联合使用在保护动物免受 T. cruzi 感染的有害作用方面更有效。