Ishige okamurae reduces blood glucose levels in high-fat diet mice and improves glucose metabolism in the skeletal muscle and pancreas

Brown alga ( Ishige okamurae ; IO) dietary supplements have been reported to possess anti-diabetic properties. However, the effects of IO supplements have not been evaluated on glucose metabolism in the pancreas and skeletal muscle. C57BL/6 N male mice (age, 7 weeks) were arranged in five groups: a...

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Published inFisheries and aquatic sciences Vol. 23; no. 1; pp. 1 - 9
Main Authors Yang, Hye-Won, Son, Myeongjoo, Choi, Junwon, Oh, Seyeon, Jeon, You-Jin, Byun, Kyunghee, Ryu, Bo Mi
Format Journal Article
LanguageEnglish
Published London BioMed Central 09.09.2020
Springer
The Korean Society of Fisheries and Aquatic Science
한국수산과학회
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ISSN2234-1757
2234-1749
2234-1757
DOI10.1186/s41240-020-00168-5

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Summary:Brown alga ( Ishige okamurae ; IO) dietary supplements have been reported to possess anti-diabetic properties. However, the effects of IO supplements have not been evaluated on glucose metabolism in the pancreas and skeletal muscle. C57BL/6 N male mice (age, 7 weeks) were arranged in five groups: a chow diet with 0.9% saline (NFD/saline group), high-fat diet (HFD) with 0.9% saline (HFD/saline group). high-fat diet with 25 mg/kg IO extract (HFD/25/IOE). high-fat diet with 50 mg/kg IO extract (HFD/50/IOE), and high-fat diet with 75 mg/kg IO extract (HFD/75/IOE). After 4 weeks, the plasma, pancreas, and skeletal muscle samples were collected for biochemical analyses. IOE significantly ameliorated glucose tolerance impairment and fasting and 2 h blood glucose level in HFD mice. IOE also stimulated the protein expressions of the glucose transporters (GLUTs) including GLUT2 and GLUT4 and those of their related transcription factors in the pancreases and skeletal muscles of HFD mice, enhanced glucose metabolism, and regulated blood glucose level. Our results suggest Ishige okamurae extract may reduce blood glucose levels by improving glucose metabolism in the pancreas and skeletal muscle in HFD-induced diabetes.
ISSN:2234-1757
2234-1749
2234-1757
DOI:10.1186/s41240-020-00168-5