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Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver
BACKGROUND: Plasma free fatty acids (FFA) are involved in blood lipid metabolism as well as many health complications. The present study was conducted to evaluate the potential role of chlorogenic acid complex from green coffee bean (CGA7) on FFA metabolism in high fat diet fed rats. METHODS: Hyperl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974694/ https://www.ncbi.nlm.nih.gov/pubmed/27495925 http://dx.doi.org/10.1186/s12906-016-1258-y |
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author | H.V., Sudeep K, Venkatakrishna Patel, Dipak K, Shyamprasad |
author_facet | H.V., Sudeep K, Venkatakrishna Patel, Dipak K, Shyamprasad |
author_sort | H.V., Sudeep |
collection | PubMed |
description | BACKGROUND: Plasma free fatty acids (FFA) are involved in blood lipid metabolism as well as many health complications. The present study was conducted to evaluate the potential role of chlorogenic acid complex from green coffee bean (CGA7) on FFA metabolism in high fat diet fed rats. METHODS: Hyperlipidemia was induced in Wistar rats using high-fat diet. The animals were given CGA7/orlistat concurrently for 42 days. The parameters analysed during the study include plasma and liver total cholesterol (TC), Triglycerides (TG) and FFA. AMPK activation in the liver was analysed through ELISA. The multiple factors involved in AMPK mediated FFA metabolism were analysed using western blotting. RESULTS: CGA7 (50, 100, 150 mg/kg BW) decreased triglycerides (TG) and FFA levels in plasma and liver. CGA7 administration led to the activation of AMP-activated protein kinase (AMPK) and a subsequent increase in the levels of carnitine palmitoyltransferase 1 (CPT-1). There was a decrease in acetyl-CoA carboxylase (ACC) activity as evident by the increase in its phosphorylation level. CONCLUSION: Chlorogenic acids improved the blood lipid metabolism in rats by alleviating the levels of FFA and TG, modulating the multiple factors in liver through AMPK pathway. The study concludes that CGA7 complex can be promoted as an active ingredient in nutrition for obesity management. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1258-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4974694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49746942016-08-06 Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver H.V., Sudeep K, Venkatakrishna Patel, Dipak K, Shyamprasad BMC Complement Altern Med Research Article BACKGROUND: Plasma free fatty acids (FFA) are involved in blood lipid metabolism as well as many health complications. The present study was conducted to evaluate the potential role of chlorogenic acid complex from green coffee bean (CGA7) on FFA metabolism in high fat diet fed rats. METHODS: Hyperlipidemia was induced in Wistar rats using high-fat diet. The animals were given CGA7/orlistat concurrently for 42 days. The parameters analysed during the study include plasma and liver total cholesterol (TC), Triglycerides (TG) and FFA. AMPK activation in the liver was analysed through ELISA. The multiple factors involved in AMPK mediated FFA metabolism were analysed using western blotting. RESULTS: CGA7 (50, 100, 150 mg/kg BW) decreased triglycerides (TG) and FFA levels in plasma and liver. CGA7 administration led to the activation of AMP-activated protein kinase (AMPK) and a subsequent increase in the levels of carnitine palmitoyltransferase 1 (CPT-1). There was a decrease in acetyl-CoA carboxylase (ACC) activity as evident by the increase in its phosphorylation level. CONCLUSION: Chlorogenic acids improved the blood lipid metabolism in rats by alleviating the levels of FFA and TG, modulating the multiple factors in liver through AMPK pathway. The study concludes that CGA7 complex can be promoted as an active ingredient in nutrition for obesity management. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1258-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-05 /pmc/articles/PMC4974694/ /pubmed/27495925 http://dx.doi.org/10.1186/s12906-016-1258-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article H.V., Sudeep K, Venkatakrishna Patel, Dipak K, Shyamprasad Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver |
title | Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver |
title_full | Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver |
title_fullStr | Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver |
title_full_unstemmed | Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver |
title_short | Biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver |
title_sort | biomechanism of chlorogenic acid complex mediated plasma free fatty acid metabolism in rat liver |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974694/ https://www.ncbi.nlm.nih.gov/pubmed/27495925 http://dx.doi.org/10.1186/s12906-016-1258-y |
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