4.0 Article

Fermentation of purple Jerusalem artichoke extract to improve the α-glucosidase inhibitory effect in vitro and ameliorate blood glucose in db/db mice

Journal

NUTRITION RESEARCH AND PRACTICE
Volume 10, Issue 3, Pages 282-287

Publisher

KOREAN NUTRITION SOC
DOI: 10.4162/nrp.2016.10.3.282

Keywords

alpha-Glucosidase; diabetes mellitus; Jerusalem artichoke; Lactobacillus plantarum; fructan

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [NRF-2012R1A1A2008842]
  2. Priority Research Centers Program through the National Research Foundation of Korea (NRF) - Ministry of Education, Science and Technology [NRF-2009-0094071]
  3. Hallym University Research Fund [HRF-201510-013]

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BACKGROUND/OBJECTIVES: Jerusalem artichoke has inhibitory activity against a-glucosidase and decreases fasting serum glucose levels, which may be related to its fructan content. The biological activity of fructan can be influenced by the degree of polymerization. Thus, in this study, the inhibitory effects of original and fermented purple Jerusalem artichoke (PJA) on alpha-glucosidase were compared in vitro. Additionally, the anti-diabetes effect of Lactobacillus plantarum-fermented PJA (LJA) was studied in a non-insulin-dependent diabetes mellitus animal model (C57BIKsJ db/db). MATERIALS/METHODS: The water extract of PJA was fermented by L. plantarum, and two strains of Bacillus subtilis to compare their anti-alpha-glucosidase activities in vitro by a-glucosidase assays. The anti-diabetes effect of LJA was studied in a non-insulin-dependent diabetes mellitus animal model (C57BIKsJ db/db) for seven weeks. During the experiment, food intake, body weight, and fasting blood glucose were measured every, week. At the end of the treatment period, several diabetic parameters and the intestinal alpha-glucosidase activity were measured. RESULTS: The LJA showed the highest alpha-glucosidase inhibitory activity in vitro. In the in vivo study, it resulted in a significantly lower blood glucose concentration than the control. Serum insulin and HDL cholesterol levels were significantly higher and the concentrations of triglycerides, non-esterified fatty acids, and total cholesterol were significant lower in mice treated with UA after seven weeks. In addition, the intestinal a-glucosidase activity was partially inhibited. CONCLUSIONS: These results suggested that UA regulates blood glucose and has potential use as a dietary supplement.

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