The Potential of VipAlbumin® to Chronic Inflammation in Type 2 Diabetes Mellitus Balb/C Mice Model

D. Dwijayanti, M. S. Djati, Mansur Ibrahim, Muhaimin Rifa’i
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引用次数: 7

Abstract

Diabetes Mellitus (DM) is one of diseases which have increasing number of sufferers every year. Almost all DM patients are type 2 DM. One of the causes of type 2 DM is a chronic inflammation due to an increase of circulating proinflammatory cytokines such as TNF-I±, IFN-I³ and IL-6. VipAlbumin® from snakehead fish extract is expected to be useful as an alternative treatment of type 2 DM because of its proinflammatory activity. The aim of this study was to determine the effect of VipAlbumin® on regulatory T cell activation, macrophage cells, proinflammatory cytokines and NF-IoB. The experiments were done by inducing mice model of type 2 DM with STZ 100 mg/kg BW and then gave them oral administration of VipAlbumin® 0 mg/g BW, 0.01664 mg/g BW, 0.0416 mg/g BW and 10.4 mg/g BW for 14 days. The data were statistically analyzed with one way ANOVA with significance value 0.05% and Tukey test using SPSS version 16 for Windows. The results showed the decreasing number of regulatory T cells in type 2 DM mice, increasing number of macrophage cells and proinflammatory cytokines TNF-I±, IFN-I³ and IL-6 as well as the increasing number of NF-IoB as a transcription factor of inflammatory mediators in CD4+ T cells, CD8+ T cells and macrophages (CD68+) compared to healthy mice (p≤0.05). Oral administration of VipAlbumin®for 14 days was proven to cure type 2 DM mice (K+) by increasing the number of regulatory T cells, decreasing the number of macrophage cells and proinflammatory cytokines TNF-I±, IFN-I³ and IL-6 and inhibiting NF-IoBin T lymphocytes CD4+, CD8+ and macrophages at the level equivalent to healthy mice and significantly different (p
VipAlbumin®对2型糖尿病Balb/C小鼠慢性炎症的影响
糖尿病(DM)是每年发病人数不断增加的疾病之一。几乎所有的糖尿病患者都是2型糖尿病,2型糖尿病的病因之一是由于循环中促炎细胞因子如TNF-I±、IFN-I³和IL-6的增加而引起的慢性炎症。VipAlbumin®从蛇头鱼提取物预计是有用的替代治疗2型糖尿病,因为它的促炎活性。本研究的目的是确定VipAlbumin®对调节性T细胞活化、巨噬细胞、促炎细胞因子和NF-IoB的影响。实验采用STZ 100 mg/kg BW诱导2型糖尿病小鼠模型,然后分别给药VipAlbumin®0 mg/g BW、0.01664 mg/g BW、0.0416 mg/g BW和10.4 mg/g BW,持续14 d。使用SPSS version 16 for Windows软件对数据进行统计学分析,采用显著性值0.05%的单因素方差分析和Tukey检验。结果显示,与健康小鼠相比,2型糖尿病小鼠CD4+ T细胞、CD8+ T细胞和巨噬细胞(CD68+)中调节性T细胞数量减少,巨噬细胞和促炎细胞因子TNF-I±、IFN-I³、IL-6数量增加,炎症介质转录因子NF-IoB数量增加(p < 0.05)。口服VipAlbumin®14天,通过增加调节性T细胞的数量,减少巨噬细胞和促炎细胞因子TNF-I±、IFN-I³和IL-6的数量,抑制NF-IoBin T淋巴细胞CD4+、CD8+和巨噬细胞的水平与健康小鼠相当,并显著差异于健康小鼠(p
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