Núcleo de Pesquisas em Plantas Medicinais, Universidade Federal do Piauí, Avenida Universitária lado ímpar, Teresina, 64049-550, Piauí, Brazil.
Laboratório de Sanidade Animal, Universidade Federal do Piauí, Teresina, Piauí, Brazil.
Naunyn Schmiedebergs Arch Pharmacol. 2017 Sep;390(9):893-903. doi: 10.1007/s00210-017-1387-y. Epub 2017 Jun 22.
Leishmaniasis is a complex of parasitic protozoan diseases caused by more than 20 different species of parasites from Leishmania genus. Conventional treatments are high costly, and promote a sort of side effects. Besides, protozoan resistance to treatments has been reported. Natural products have been investigated as a source of new therapeutic alternatives, not only acting directly against the parasite but also being able to synergistically act on the host immune system in order to control parasitemia. Gallic acid (GA) and ellagic acid (EA) are plant-derived phenolic compounds which are able to induce antiinflammatory, gastroprotective, and anticarcinogenic activities. Therefore, the antileishmania, cytotoxic, and immunomodulatory activities of GA and EA were evaluated in this study. Both GA and EA were able to inhibit the growth of Leishmania major promastigotes (effective concentration (EC) values 16.4 and 9.8 μg/mL, respectively). The cytotoxicity against BALB/c murine macrophages for GA and EA was also assessed (CC values 126.6 and 23.8 μg/mL, respectively). Interestingly, GA and EA also significantly reduced the infection and infectivity of macrophages infected by L. major (EC values 5.0 and 0.9 μg/mL, respectively), with selectivity index higher than 20. Furthermore, both GA and EA induced high immunomodulatory activity evidenced by the increase of phagocytic capability, lysosomal volume, nitrite release, and intracellular calcium [Ca] in macrophages. Further investigations are reinforced in order to evaluate the therapeutic effects of GA and EA in in vivo experimental infection model of leishmaniasis.
利什曼病是由利什曼属的 20 多种不同寄生虫引起的寄生虫原生动物病的复杂疾病。传统的治疗方法成本高,并会引起一定的副作用。此外,已经报道了原生动物对治疗的耐药性。天然产物已被研究作为新的治疗替代物的来源,不仅可以直接作用于寄生虫,还可以协同作用于宿主免疫系统,以控制寄生虫血症。没食子酸(GA)和鞣花酸(EA)是植物来源的酚类化合物,能够诱导抗炎、胃保护和抗癌活性。因此,本研究评估了 GA 和 EA 的抗利什曼原虫、细胞毒性和免疫调节活性。GA 和 EA 均能抑制利什曼原虫大滋养体的生长(有效浓度(EC)值分别为 16.4 和 9.8μg/mL)。还评估了 GA 和 EA 对 BALB/c 小鼠巨噬细胞的细胞毒性(CC 值分别为 126.6 和 23.8μg/mL)。有趣的是,GA 和 EA 还显著降低了被大滋养体感染的巨噬细胞的感染和感染力(EC 值分别为 5.0 和 0.9μg/mL),其选择性指数高于 20。此外,GA 和 EA 均能诱导吞噬能力、溶酶体体积、亚硝酸盐释放和巨噬细胞内钙[Ca]增加,从而表现出高免疫调节活性。为了评估 GA 和 EA 在利什曼病体内实验感染模型中的治疗效果,进一步加强了研究。