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Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression

Beneficial effects of glycyrrhizic acid (GA), a bioactive extract of licorice root, in the prevention of metabolic syndrome have been consistently reported while advanced glycation end products (AGE) and receptor for advanced glycation end product (RAGE) are the leading factors in the development of...

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Autores principales: Cheng, Hong Sheng, Kong, Joana Magdelene Xiao Fang, Ng, Athena Xin Hui, Chan, Weng Keong, Ton, So Ha, Abdul Kadir, Khalid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250570/
https://www.ncbi.nlm.nih.gov/pubmed/25369772
http://dx.doi.org/10.1007/s13659-014-0044-0
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author Cheng, Hong Sheng
Kong, Joana Magdelene Xiao Fang
Ng, Athena Xin Hui
Chan, Weng Keong
Ton, So Ha
Abdul Kadir, Khalid
author_facet Cheng, Hong Sheng
Kong, Joana Magdelene Xiao Fang
Ng, Athena Xin Hui
Chan, Weng Keong
Ton, So Ha
Abdul Kadir, Khalid
author_sort Cheng, Hong Sheng
collection PubMed
description Beneficial effects of glycyrrhizic acid (GA), a bioactive extract of licorice root, in the prevention of metabolic syndrome have been consistently reported while advanced glycation end products (AGE) and receptor for advanced glycation end product (RAGE) are the leading factors in the development of diabetes mellitus. The aim of this study was to investigate the effects of GA on the AGE-RAGE axis using high-fat/high-sucrose (HF/HS) diet-induced metabolic syndrome rat models. Twenty four male Sprague–Dawley rats were randomly assigned into three groups for 4 weeks: (1) Group A, normal diet with standard rat chow; (2) Group B, HF/HS diet; (3) Group C, HF/HS diet and oral administration of 100 mg/kg GA per day. The results showed that HF/HS diet elevated the fasting blood glucose level and insulin resistance index which was prevented by GA supplementation. GA treatment significantly lowered the circulating AGE independent of its glucose-lowering effect. HF/HS diet also triggered RAGE upregulation in the abdominal muscles while GA administration downregulated RAGE expression in the abdominal muscles, aorta and subcutaneous adipose tissues. In conclusion, HF/HS diet could cause glucose intolerance, insulin resistance and upregulation of RAGE expression while GA ameliorated the metabolic dysregulation besides exhibiting inhibitory effects on the AGE-RAGE axis. [Image: see text]
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spelling pubmed-42505702014-12-04 Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression Cheng, Hong Sheng Kong, Joana Magdelene Xiao Fang Ng, Athena Xin Hui Chan, Weng Keong Ton, So Ha Abdul Kadir, Khalid Nat Prod Bioprospect Original Article Beneficial effects of glycyrrhizic acid (GA), a bioactive extract of licorice root, in the prevention of metabolic syndrome have been consistently reported while advanced glycation end products (AGE) and receptor for advanced glycation end product (RAGE) are the leading factors in the development of diabetes mellitus. The aim of this study was to investigate the effects of GA on the AGE-RAGE axis using high-fat/high-sucrose (HF/HS) diet-induced metabolic syndrome rat models. Twenty four male Sprague–Dawley rats were randomly assigned into three groups for 4 weeks: (1) Group A, normal diet with standard rat chow; (2) Group B, HF/HS diet; (3) Group C, HF/HS diet and oral administration of 100 mg/kg GA per day. The results showed that HF/HS diet elevated the fasting blood glucose level and insulin resistance index which was prevented by GA supplementation. GA treatment significantly lowered the circulating AGE independent of its glucose-lowering effect. HF/HS diet also triggered RAGE upregulation in the abdominal muscles while GA administration downregulated RAGE expression in the abdominal muscles, aorta and subcutaneous adipose tissues. In conclusion, HF/HS diet could cause glucose intolerance, insulin resistance and upregulation of RAGE expression while GA ameliorated the metabolic dysregulation besides exhibiting inhibitory effects on the AGE-RAGE axis. [Image: see text] Springer Berlin Heidelberg 2014-11-05 /pmc/articles/PMC4250570/ /pubmed/25369772 http://dx.doi.org/10.1007/s13659-014-0044-0 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/This article is published under license to BioMed Central Ltd. Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Cheng, Hong Sheng
Kong, Joana Magdelene Xiao Fang
Ng, Athena Xin Hui
Chan, Weng Keong
Ton, So Ha
Abdul Kadir, Khalid
Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression
title Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression
title_full Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression
title_fullStr Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression
title_full_unstemmed Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression
title_short Novel Inhibitory Effects of Glycyrrhizic Acid on the Accumulation of Advanced Glycation End Product and Its Receptor Expression
title_sort novel inhibitory effects of glycyrrhizic acid on the accumulation of advanced glycation end product and its receptor expression
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250570/
https://www.ncbi.nlm.nih.gov/pubmed/25369772
http://dx.doi.org/10.1007/s13659-014-0044-0
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