D. Dwijayanti, M. S. Djati, Mansur Ibrahim, Muhaimin Rifai
{"title":"The Potential of VipAlbumin® to Chronic Inflammation in Type 2 Diabetes Mellitus Balb/C Mice Model","authors":"D. Dwijayanti, M. S. Djati, Mansur Ibrahim, Muhaimin Rifai","doi":"10.3844/AJISP.2015.56.67","DOIUrl":null,"url":null,"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 (pâ¤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","PeriodicalId":88361,"journal":{"name":"American journal of immunology","volume":"11 1","pages":"56-67"},"PeriodicalIF":0.0000,"publicationDate":"2015-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3844/AJISP.2015.56.67","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3844/AJISP.2015.56.67","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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 (pâ¤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