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Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration

Aspalathin is a rooibos flavonoid with established blood glucose lowering properties, however, its efficacy to moderate complications associated with hepatic insulin resistance is unknown. To study such effects, C3A liver cells exposed to palmitate were used as a model of hepatic insulin resistance....

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Autores principales: Mazibuko-Mbeje, Sithandiwe E., Dludla, Phiwayinkosi V., Johnson, Rabia, Joubert, Elizabeth, Louw, Johan, Ziqubu, Khanyisani, Tiano, Luca, Silvestri, Sonia, Orlando, Patrick, Opoku, Andy R., Muller, Christo J. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497260/
https://www.ncbi.nlm.nih.gov/pubmed/31048842
http://dx.doi.org/10.1371/journal.pone.0216172
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author Mazibuko-Mbeje, Sithandiwe E.
Dludla, Phiwayinkosi V.
Johnson, Rabia
Joubert, Elizabeth
Louw, Johan
Ziqubu, Khanyisani
Tiano, Luca
Silvestri, Sonia
Orlando, Patrick
Opoku, Andy R.
Muller, Christo J. F.
author_facet Mazibuko-Mbeje, Sithandiwe E.
Dludla, Phiwayinkosi V.
Johnson, Rabia
Joubert, Elizabeth
Louw, Johan
Ziqubu, Khanyisani
Tiano, Luca
Silvestri, Sonia
Orlando, Patrick
Opoku, Andy R.
Muller, Christo J. F.
author_sort Mazibuko-Mbeje, Sithandiwe E.
collection PubMed
description Aspalathin is a rooibos flavonoid with established blood glucose lowering properties, however, its efficacy to moderate complications associated with hepatic insulin resistance is unknown. To study such effects, C3A liver cells exposed to palmitate were used as a model of hepatic insulin resistance. These hepatocytes displayed impaired substrate metabolism, including reduced glucose transport and free fatty acid uptake. These defects included impaired insulin signaling, evident through reduced phosphatidylinositol-4,5-bisphosphate 3-kinase/ protein kinase B (PI3K/AKT) protein expression, and mitochondrial dysfunction, depicted by a lower mitochondrial respiration rate. Aspalathin was able to ameliorate these defects by correcting altered substrate metabolism, improving insulin signaling and mitochondrial bioenergetics. Activation of 5ʹ-adenosine monophosphate-activated protein kinase (AMPK) may be a plausible mechanism by which aspalathin increases hepatic energy expenditure. Overall, these results encourage further studies assessing the potential use of aspalathin as a nutraceutical to improve hepatocellular energy expenditure, and reverse metabolic disease-associated complications.
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spelling pubmed-64972602019-05-17 Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration Mazibuko-Mbeje, Sithandiwe E. Dludla, Phiwayinkosi V. Johnson, Rabia Joubert, Elizabeth Louw, Johan Ziqubu, Khanyisani Tiano, Luca Silvestri, Sonia Orlando, Patrick Opoku, Andy R. Muller, Christo J. F. PLoS One Research Article Aspalathin is a rooibos flavonoid with established blood glucose lowering properties, however, its efficacy to moderate complications associated with hepatic insulin resistance is unknown. To study such effects, C3A liver cells exposed to palmitate were used as a model of hepatic insulin resistance. These hepatocytes displayed impaired substrate metabolism, including reduced glucose transport and free fatty acid uptake. These defects included impaired insulin signaling, evident through reduced phosphatidylinositol-4,5-bisphosphate 3-kinase/ protein kinase B (PI3K/AKT) protein expression, and mitochondrial dysfunction, depicted by a lower mitochondrial respiration rate. Aspalathin was able to ameliorate these defects by correcting altered substrate metabolism, improving insulin signaling and mitochondrial bioenergetics. Activation of 5ʹ-adenosine monophosphate-activated protein kinase (AMPK) may be a plausible mechanism by which aspalathin increases hepatic energy expenditure. Overall, these results encourage further studies assessing the potential use of aspalathin as a nutraceutical to improve hepatocellular energy expenditure, and reverse metabolic disease-associated complications. Public Library of Science 2019-05-02 /pmc/articles/PMC6497260/ /pubmed/31048842 http://dx.doi.org/10.1371/journal.pone.0216172 Text en © 2019 Mazibuko-Mbeje et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mazibuko-Mbeje, Sithandiwe E.
Dludla, Phiwayinkosi V.
Johnson, Rabia
Joubert, Elizabeth
Louw, Johan
Ziqubu, Khanyisani
Tiano, Luca
Silvestri, Sonia
Orlando, Patrick
Opoku, Andy R.
Muller, Christo J. F.
Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration
title Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration
title_full Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration
title_fullStr Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration
title_full_unstemmed Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration
title_short Aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration
title_sort aspalathin, a natural product with the potential to reverse hepatic insulin resistance by improving energy metabolism and mitochondrial respiration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497260/
https://www.ncbi.nlm.nih.gov/pubmed/31048842
http://dx.doi.org/10.1371/journal.pone.0216172
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