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논문 기본 정보

자료유형
학술저널
저자정보
Da-Hye Kim (Jeonju AgroBio-Materials Institute) Sang Jun Kim (Jeonju AgroBio-Materials Institute) Kang-Yeol Yu (Jeonju AgroBio-Materials Institute) Seung-Il Jeong (Jeonju AgroBio-Materials Institute) Seon-Young Kim (Jeonju AgroBio-Materials Institute)
저널정보
대한지역사회영양학회 Nutrition Research and Practice Nutrition Research and Practice Vol.12 No.1
발행연도
2018.2
수록면
20 - 28 (9page)

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초록· 키워드

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BACKGROUND/OBJECTIVES: Perilla frutescens (L.) Britton var. (PF) sprout is a plant of the labiate family. We have previously reported the protective effects of PF sprout extract on cytokine-induced β-cell damage. However, the mechanism of action of the PF sprout extract in type 2 diabetes (T2DM) has not been investigated. The present study was designed to study the effects of PF sprout extract and signaling mechanisms in the T2DM mice model using C57BL/KsJ-db/db (db/db) mice.
MATERIALS/METHODS: Male db/db mice were orally administered PF sprout extract (100, 300, and 1,000 mg/kg of body weight) or rosiglitazone (RGZ, positive drug, 1 mg/kg of body weight) for 4 weeks. Signaling mechanisms were analyzed using liver tissues and HepG2 cells.
RESULTS: The PF sprout extract (300 and 1,000 mg/kg) significantly reduced the fasting blood glucose, serum insulin, triglyceride and total cholesterol levels in db/db mice. PF sprout extract also significantly improved glucose intolerance and insulin sensitivity, decreased hepatic gluconeogenic protein expression, and ameliorated histological alterations of the pancreas and liver. Levels of phosphorylated AMP-activated protein kinase (AMPK) protein expression also increased in the liver after treatment with the extract. In addition, an increase in the phosphorylation of AMPK and decrease in the phosphoenolpyruvate carboxykinase and glucose 6-phosphatase proteins in HepG2 cells were also observed.
CONCLUSIONS: Our results sugges that PF sprout displays beneficial effects in the prevention and treatment of type 2 diabetes via modulation of the AMPK pathway and inhibition of gluconeogenesis in the liver.

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INTRODUCTION
MATERALS AND METHODS
RESULTS
DISCUSSCION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2018-594-001756825