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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Leishmanicidal activity of polysaccharides and their oxovanadium(IV/V) complexes
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Leishmanicidal activity of polysaccharides and their oxovanadium(IV/V) complexes

机译:多糖及其氧钒(IV / V)配合物的杀菌活性

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The parasites of the genus Leishmania cause a range of leishmaniasis diseases, whose treatment is impaired due to intramacrophage parasites living in the mammalian host. Immunostimulation has been considered an important strategy to leishmaniasis treatment. The immunomodulatory effects of the polysaccharides arabinogalactan (ARAGAL), galactomannan (GMPOLY), and xyloglucan (XGJ), as well as their oxovanadium (IV/V) complexes (ARAGAL:VO, GMPOLY:VO, and XGJ:VO) were evaluated on peritoneal macrophages. At 25 mu g/mL of GMPOLY:VO and of XGJ:VO, and 10 mu g/mL of ARAGAL:VO, nitric oxide (NO) production by the macrophages was not altered compared with the control group. All polymers increased the production of interleukins 1 beta and 6 (IL-1 beta and IL-6), but the oxovanadium complexes were more potent activators of these mediators. ARAGAL:VO 10 mu g/mL, GMPOLY:VO and XGJ:VO 25 mu g/mL led to an increase of 562%, 1054%, and 523% for IL-1 beta, respectively. For IL-6 at the same concentration, the levels increased by 539% and 794% for ARAGAL:VO and GMPOLY:VO, respectively. Polysaccharides and their oxovanadium complexes exhibited important leishmanicidal effects on amastigotes of Leishmania (L.) amazonensis. The native and complexed polymers reduced the growth of promastigote-form Leishmania by similar to 60%. This effect was reached at concentrations 12 times lower than that observed for Glucantime (300 mu g/mL promoted an inhibition of -60%). The 50% inhibitory concentration (IC50) values for the complexes were determined. XGJ:VO showed the lowest IC50 value (6.2 mu g/mL; 0.07 mu g/mL of vanadium), which for ARAGAL:VO was 6.5 mu g/mL (0.21 mu g/mL of vanadium) and 7.3 mu g/mL (0.06 mu g/mL of vanadium) for GMPOLY:VO. The upregulation of IL-1 beta and IL-6 release and downregulation of NO production by macrophages and the important leishmanicidal effect are essential to stablish their potential use against this pathology. (C) 2014 Elsevier Masson SAS. All rights reserved.
机译:利什曼原虫属的寄生虫引起多种利什曼病,由于哺乳动物体内的巨噬细胞内寄生虫,其治疗受到损害。免疫刺激被认为是利什曼病治疗的重要策略。评估了阿拉伯糖半乳糖(ARAGAL),半乳甘露聚糖(GMPOLY)和木葡聚糖(XGJ)以及它们的氧钒(IV / V)复合物(ARAGAL:VO,GMPOLY:VO和XGJ:VO)的免疫调节作用。腹膜巨噬细胞。与对照组相比,在25μg / mL的GMPOLY:VO和XGJ:VO,以及10μg / mL的ARAGAL:VO时,巨噬细胞产生的一氧化氮(NO)并未改变。所有聚合物均增加了白介素1β和6(IL-1β和IL-6)的产生,但氧钒络合物是这些介体的更有效活化剂。 ARAGAL:VO 10μg / mL,GMPOLY:VO和XGJ:VO 25μg/ mL导致IL-1 beta分别增加562%,1054%和523%。对于相同浓度的IL-6,ARAGAL:VO和GMPOLY:VO的水平分别增加了539%和794%。多糖及其氧杂钒配合物对利什曼原虫(亚马逊利什曼原虫)的变形虫表现出重要的利什曼杀菌作用。天然和复杂的聚合物使前鞭毛体形式的利什曼原虫的生长减少了约60%。在浓度比葡聚糖时间所观察到的浓度低12倍(300μg / mL促进了-60%的抑制)时,达到了这种效果。测定复合物的50%抑制浓度(IC50)值。 XGJ:VO显示最低的IC50值(6.2μg / mL; 0.07μg / mL钒),对于ARAGAL:VO为6.5μg / mL(0.21μg/ mL钒)和7.3μg / mL GMPOLY:VO(0.06μg / mL钒)。 IL-1β和IL-6释放的上调和巨噬细胞NO生成的下调以及重要的杀人作用对于稳定其针对这种病理的潜在用途至关重要。 (C)2014 Elsevier Masson SAS。版权所有。

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