Department of Parasitology, Faculty of Medicine, Brawijaya University, Veteran Road, Malang, East Java, 65145, Indonesia.
Doctoral Program in Biomedical Sciences, Faculty of Medicine, Brawijaya University, Malang, East Java, Indonesia.
BMC Complement Altern Med. 2017 Sep 25;17(1):468. doi: 10.1186/s12906-017-1973-z.
Mango mistletoes Dendrophthoe pentandra (MMDP) extract has attracted interest due to its pharmacological properties, including gastro protective effects. The aim of this study was to investigate whether MMDP extract could increase Foxp3 regulatory T cells and inhibits development of Th17 cells.
Colitis was induced in Balb/c mice by rectal administration of 2,4,6-trinitrobenzene sulfonic acid (TNBS). The mice were randomly divided into five groups comprising group1 receiving vehicle (the negative control), group 2-5 receiving TNBS, group 3-5 orally receiving either MMDP extract 150, 300 and 600 mg/kgBW for 7 days after TNBS administration. On day 8 of the experiment, the colon tissues were removed for histological examination, cytokine and myeloperoxidase (MPO) measurement. T-cells sub-population in mesenteric lymph nodes were analyzed by flow cytometer.
MMDP extract potently suppressed colon shortening and MPO in mice with TNBS-induced colitis. Administration of the extract significantly decreased the severity of TNBS-induced colitis in a dose-dependent manner. The extract significantly attenuated the loss of body weight (p < 0.05). These effects were associated with a remarkable amelioration of the disruption of the colonic architecture, significant reduction of the colonic MPO (p < 0.05). The extract lowered the levels of Th17-associated cytokines but increased the production of Treg-associated cytokines in mesenteric lymph node cells.
Our results suggest that MMDP has the therapeutic potential to ameliorate TNBS-induced colitis symptoms revealed by histological change and inhibit IL-17 production.
番石榴曼陀罗(MMDP)提取物因其具有胃保护作用等药理学特性而受到关注。本研究旨在探讨 MMDP 提取物是否能增加 Foxp3 调节性 T 细胞并抑制 Th17 细胞的发展。
通过直肠给予 2,4,6-三硝基苯磺酸(TNBS)诱导 Balb/c 小鼠结肠炎。将小鼠随机分为五组,包括接受载体(阴性对照)的组 1、接受 TNBS 的组 2-5、接受 TNBS 后分别口服 MMDP 提取物 150、300 和 600mg/kgBW 的组 3-5,共 7 天。实验第 8 天,取出结肠组织进行组织学检查、细胞因子和髓过氧化物酶(MPO)测定。通过流式细胞仪分析肠系膜淋巴结中的 T 细胞亚群。
MMDP 提取物能有效抑制 TNBS 诱导的结肠炎小鼠的结肠缩短和 MPO。提取物以剂量依赖性方式显著降低 TNBS 诱导的结肠炎的严重程度。该提取物显著减轻了体重减轻(p<0.05)。这些作用与结肠结构破坏的明显改善、结肠 MPO 的显著减少(p<0.05)有关。提取物降低了 Th17 相关细胞因子的水平,但增加了肠系膜淋巴结细胞中 Treg 相关细胞因子的产生。
我们的结果表明,MMDP 具有通过组织学变化改善 TNBS 诱导的结肠炎症状和抑制 IL-17 产生的治疗潜力。