Momordica charantia Ameliorates Insulin Resistance and Dyslipidemia with Altered Hepatic Glucose Production and Fatty Acid Synthesis and AMPK Phosphorylation in High‐fat‐fed Mice. (23rd April 2013)
- Record Type:
- Journal Article
- Title:
- Momordica charantia Ameliorates Insulin Resistance and Dyslipidemia with Altered Hepatic Glucose Production and Fatty Acid Synthesis and AMPK Phosphorylation in High‐fat‐fed Mice. (23rd April 2013)
- Main Title:
- Momordica charantia Ameliorates Insulin Resistance and Dyslipidemia with Altered Hepatic Glucose Production and Fatty Acid Synthesis and AMPK Phosphorylation in High‐fat‐fed Mice
- Authors:
- Shih, Chun‐Ching
Shlau, Min‐Tzong
Lin, Cheng‐Hsiu
Wu, Jin‐Bin - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <italic>Momordica charantia</italic> Linn. (Cucurbitaceae) fruit is commonly known as bitter melon. C57BL/6J mice were firstly divided randomly into two groups: the control (CON) group was fed with a low‐fat diet, whereas the experimental group was fed a 45% high‐fat (HF) diet for 8 weeks. Afterwards, the CON group was treated with vehicle, whereas the HF group was subdivided into five groups and still on HF diet and was given orally <italic>M. charantia</italic> extract (MCE) or rosiglitazone (Rosi) or not for 4 weeks. <italic>M. charantia</italic> decreased the weights of visceral fat and caused glucose lowering. AMP‐activated protein kinase (AMPK) is a major cellular regulator of lipid and glucose metabolism. MCE significantly increases the hepatic protein contents of AMPK phosphorylation by 126.2–297.3% and reduces expression of phosphenolpyruvate carboxykinase (PEPCK) and glucose production. Most importantly, MCE decreased expression of hepatic 11beta hydroxysteroid dehydroxygenase (11beta‐HSD1) gene, which contributed in attenuating diabetic state. Furthermore, MCE lowered serum triglycerides (TGs) by inhibition of hepatic fatty acid synthesis by dampening sterol response element binding protein 1c and fatty acid synthase mRNA leading to reduction in TGs synthesis. This study demonstrates <italic>M. charantia</italic> ameliorates diabetic and hyperlipidemic state in HF‐fed mice<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <italic>Momordica charantia</italic> Linn. (Cucurbitaceae) fruit is commonly known as bitter melon. C57BL/6J mice were firstly divided randomly into two groups: the control (CON) group was fed with a low‐fat diet, whereas the experimental group was fed a 45% high‐fat (HF) diet for 8 weeks. Afterwards, the CON group was treated with vehicle, whereas the HF group was subdivided into five groups and still on HF diet and was given orally <italic>M. charantia</italic> extract (MCE) or rosiglitazone (Rosi) or not for 4 weeks. <italic>M. charantia</italic> decreased the weights of visceral fat and caused glucose lowering. AMP‐activated protein kinase (AMPK) is a major cellular regulator of lipid and glucose metabolism. MCE significantly increases the hepatic protein contents of AMPK phosphorylation by 126.2–297.3% and reduces expression of phosphenolpyruvate carboxykinase (PEPCK) and glucose production. Most importantly, MCE decreased expression of hepatic 11beta hydroxysteroid dehydroxygenase (11beta‐HSD1) gene, which contributed in attenuating diabetic state. Furthermore, MCE lowered serum triglycerides (TGs) by inhibition of hepatic fatty acid synthesis by dampening sterol response element binding protein 1c and fatty acid synthase mRNA leading to reduction in TGs synthesis. This study demonstrates <italic>M. charantia</italic> ameliorates diabetic and hyperlipidemic state in HF‐fed mice occurred by regulation of hepatic PEPCK, 11beta‐HSD1 and AMPK phosphorylation. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Phytotherapy research. Volume 28:Number 3(2014:Mar.)
- Journal:
- Phytotherapy research
- Issue:
- Volume 28:Number 3(2014:Mar.)
- Issue Display:
- Volume 28, Issue 3 (2014)
- Year:
- 2014
- Volume:
- 28
- Issue:
- 3
- Issue Sort Value:
- 2014-0028-0003-0000
- Page Start:
- 363
- Page End:
- 371
- Publication Date:
- 2013-04-23
- Subjects:
- Materia medica, Vegetable -- Periodicals
Botany, Medical -- Periodicals
Medicinal plants -- Periodicals
Plant Extracts -- therapeutic use -- Periodicals
Plants, Medicinal -- Periodicals
581.634 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ptr.5003 ↗
- Languages:
- English
- ISSNs:
- 0951-418X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6497.060000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3174.xml