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Gold nanoparticles improve metabolic profile of mice fed a high-fat diet
BACKGROUND: Obesity is a high risk for multiple metabolic disorders due to excessive influx of energy, glucose and lipid, often from a western based diet. Low-grade inflammation plays a key role in the progression of such metabolic disorders. The anti-inflammatory property of gold compounds has been...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800098/ https://www.ncbi.nlm.nih.gov/pubmed/29409496 http://dx.doi.org/10.1186/s12951-018-0338-1 |
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author | Chen, Hui Ng, Jane P. M. Tan, Yi McGrath, Kristine Bishop, David P. Oliver, Brian Chan, Yik Lung Cortie, Michael B. Milthorpe, Bruce K. Valenzuela, Stella M. |
author_facet | Chen, Hui Ng, Jane P. M. Tan, Yi McGrath, Kristine Bishop, David P. Oliver, Brian Chan, Yik Lung Cortie, Michael B. Milthorpe, Bruce K. Valenzuela, Stella M. |
author_sort | Chen, Hui |
collection | PubMed |
description | BACKGROUND: Obesity is a high risk for multiple metabolic disorders due to excessive influx of energy, glucose and lipid, often from a western based diet. Low-grade inflammation plays a key role in the progression of such metabolic disorders. The anti-inflammatory property of gold compounds has been used in treating rheumatoid arthritis in the clinic. Previously we found that pure gold nanoparticles (AuNPs, 21 nm) also possess anti-inflammatory effects on the retroperitoneal fat tissue following intraperitoneal injection, by downregulating tumor necrosis factor (TNF) α. However, whether such an effect can change the risk of metabolic disorders in the obese has not been well studied. The study employed C57BL/6 mice fed a pellet high fat diet (HFD, 43% as fat) that were treated daily with AuNPs [low (HFD-LAu) or high (HFD-HAu) dose] via intraperitoneal injection for 9 weeks. In the in vitro study, RAW264.7 macrophages and 3T3-L1 adipocytes were cultured with low and high concentrations of AuNPs alone or together. RESULTS: The HFD-fed mice showed a significant increase in fat mass, glucose intolerance, dyslipidemia, and liver steatosis. The HFD-LAu group showed an 8% reduction in body weight, ameliorated hyperlipidemia, and normal glucose tolerance; while the HFD-HAu group had a 5% reduction in body weight with significant improvement in their glucose intolerance and hyperlipidemia. The underlying mechanism may be attributed to a reduction in adipose and hepatic local proinflammatory cytokine production, e.g. TNFα. In vitro studies of co-cultured murine RAW264.7 macrophage and 3T3-L1 adipocytes supported this proposed mechanism. CONCLUSION: AuNPs demonstrate a promising profile for potential management of obesity related glucose and lipid disorders and are useful as a research tool for the study of biological mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0338-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5800098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58000982018-02-13 Gold nanoparticles improve metabolic profile of mice fed a high-fat diet Chen, Hui Ng, Jane P. M. Tan, Yi McGrath, Kristine Bishop, David P. Oliver, Brian Chan, Yik Lung Cortie, Michael B. Milthorpe, Bruce K. Valenzuela, Stella M. J Nanobiotechnology Research BACKGROUND: Obesity is a high risk for multiple metabolic disorders due to excessive influx of energy, glucose and lipid, often from a western based diet. Low-grade inflammation plays a key role in the progression of such metabolic disorders. The anti-inflammatory property of gold compounds has been used in treating rheumatoid arthritis in the clinic. Previously we found that pure gold nanoparticles (AuNPs, 21 nm) also possess anti-inflammatory effects on the retroperitoneal fat tissue following intraperitoneal injection, by downregulating tumor necrosis factor (TNF) α. However, whether such an effect can change the risk of metabolic disorders in the obese has not been well studied. The study employed C57BL/6 mice fed a pellet high fat diet (HFD, 43% as fat) that were treated daily with AuNPs [low (HFD-LAu) or high (HFD-HAu) dose] via intraperitoneal injection for 9 weeks. In the in vitro study, RAW264.7 macrophages and 3T3-L1 adipocytes were cultured with low and high concentrations of AuNPs alone or together. RESULTS: The HFD-fed mice showed a significant increase in fat mass, glucose intolerance, dyslipidemia, and liver steatosis. The HFD-LAu group showed an 8% reduction in body weight, ameliorated hyperlipidemia, and normal glucose tolerance; while the HFD-HAu group had a 5% reduction in body weight with significant improvement in their glucose intolerance and hyperlipidemia. The underlying mechanism may be attributed to a reduction in adipose and hepatic local proinflammatory cytokine production, e.g. TNFα. In vitro studies of co-cultured murine RAW264.7 macrophage and 3T3-L1 adipocytes supported this proposed mechanism. CONCLUSION: AuNPs demonstrate a promising profile for potential management of obesity related glucose and lipid disorders and are useful as a research tool for the study of biological mechanisms. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-018-0338-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-06 /pmc/articles/PMC5800098/ /pubmed/29409496 http://dx.doi.org/10.1186/s12951-018-0338-1 Text en © The Author(s) 2018 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 Chen, Hui Ng, Jane P. M. Tan, Yi McGrath, Kristine Bishop, David P. Oliver, Brian Chan, Yik Lung Cortie, Michael B. Milthorpe, Bruce K. Valenzuela, Stella M. Gold nanoparticles improve metabolic profile of mice fed a high-fat diet |
title | Gold nanoparticles improve metabolic profile of mice fed a high-fat diet |
title_full | Gold nanoparticles improve metabolic profile of mice fed a high-fat diet |
title_fullStr | Gold nanoparticles improve metabolic profile of mice fed a high-fat diet |
title_full_unstemmed | Gold nanoparticles improve metabolic profile of mice fed a high-fat diet |
title_short | Gold nanoparticles improve metabolic profile of mice fed a high-fat diet |
title_sort | gold nanoparticles improve metabolic profile of mice fed a high-fat diet |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800098/ https://www.ncbi.nlm.nih.gov/pubmed/29409496 http://dx.doi.org/10.1186/s12951-018-0338-1 |
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