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Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract

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...

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Autores principales: Kim, Da-Hye, Kim, Sang Jun, Yu, Kang-Yeol, Jeong, Seung-Il, Kim, Seon-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Nutrition Society and the Korean Society of Community Nutrition 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792252/
https://www.ncbi.nlm.nih.gov/pubmed/29399293
http://dx.doi.org/10.4162/nrp.2018.12.1.20
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author Kim, Da-Hye
Kim, Sang Jun
Yu, Kang-Yeol
Jeong, Seung-Il
Kim, Seon-Young
author_facet Kim, Da-Hye
Kim, Sang Jun
Yu, Kang-Yeol
Jeong, Seung-Il
Kim, Seon-Young
author_sort Kim, Da-Hye
collection PubMed
description 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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spelling pubmed-57922522018-02-02 Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract Kim, Da-Hye Kim, Sang Jun Yu, Kang-Yeol Jeong, Seung-Il Kim, Seon-Young Nutr Res Pract Original Research 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. The Korean Nutrition Society and the Korean Society of Community Nutrition 2018-02 2018-01-12 /pmc/articles/PMC5792252/ /pubmed/29399293 http://dx.doi.org/10.4162/nrp.2018.12.1.20 Text en ©2018 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Kim, Da-Hye
Kim, Sang Jun
Yu, Kang-Yeol
Jeong, Seung-Il
Kim, Seon-Young
Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract
title Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract
title_full Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract
title_fullStr Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract
title_full_unstemmed Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract
title_short Anti-hyperglycemic effects and signaling mechanism of Perilla frutescens sprout extract
title_sort anti-hyperglycemic effects and signaling mechanism of perilla frutescens sprout extract
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792252/
https://www.ncbi.nlm.nih.gov/pubmed/29399293
http://dx.doi.org/10.4162/nrp.2018.12.1.20
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