EMSA Eritin Blocks Nuclear Factor-Kappa B in Diabetes Mellitus Mice Model

Authors

  • Maic Audo Lin Sihombing Brawijaya University
  • Sutiman B. Sumitro Dept. of Biology, University of Brawijaya
  • Muhaimin Rifa'i Dept. of Biology, University of Brawijaya

DOI:

https://doi.org/10.21776/ub.jels.2015.005.01.05

Abstract

Diabetes mellitus is one of the common metabolic disorders with increasing prevalence during recent years with hyperglycemia as its characteristic. DM has been shown to be a state of free radicals over production resulted from hyperglycemia that can activate cellular signaling pathways transcription of factor NF-κB which stimulates the production of several inflammatory mediators andl lead to chronic inflammation. Chronic inflammation is implicated in β-cell damage and function and promotes apoptosis. EMSA Eritin is a polyherbal consisting of soy bean extracts, coconut water extract and red rice extract that assumed to be antidiabetic and anti-inflammatory. This study will assess the effectiveness of EMSA Eritin against inflammation in diabetes mellitus by measuring levels of NF-κB produced by immunocompetent cells in DM mice model. Streptozotocin 100 mg.kg-1 BW is used to induce diabetes mellitus in mice. Oral administration of EMSA Eritin was given for 14 days with dose of 0.3125 mg.g-1 BW, 3.125 mg.g-1 BW and 31.25 mg.g-1 BW. Data were analyzed using One-way ANOVA (p<0.05) and Duncan test using SPSS 16.0 for Windows. The results showed that EMSA Eritin can be used as an alternative therapy for the treatment of DM. The level of NF-κB in diabetic mice significantly decreased when the mice received EMSA Eritin.

Keywords: Diabetes Mellitus, EMSA Eritin, NF-κB, ROS

Author Biography

Maic Audo Lin Sihombing, Brawijaya University

Postgraduate program of Biology, Faculty of Mathematics and Natural Sciences, University of Brawijaya, Malang, Indonesia.

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Published

2015-09-30

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Articles