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HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice
BACKGROUND: HOX-7 is a newly developed dietary formula composed of traditional oriental herbal medicines. The formula was developed with the aim of improving weight control. We investigated the anti-obesity effect of HOX-7 on high-fat-diet (HFD)-induced obesity in C57BL/6 mice. METHODS: The mice wer...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320579/ https://www.ncbi.nlm.nih.gov/pubmed/25515293 http://dx.doi.org/10.1186/1472-6882-14-505 |
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author | Lee, Heon-Myung Rim, Hong-Kun Seo, Jong-Hwan Kook, Yoon-Bum Kim, Sung-Kew Oh, Chang-Hyun Yoo, Kyung Ho Jin, Jong-Sik An, Hyo-Jin |
author_facet | Lee, Heon-Myung Rim, Hong-Kun Seo, Jong-Hwan Kook, Yoon-Bum Kim, Sung-Kew Oh, Chang-Hyun Yoo, Kyung Ho Jin, Jong-Sik An, Hyo-Jin |
author_sort | Lee, Heon-Myung |
collection | PubMed |
description | BACKGROUND: HOX-7 is a newly developed dietary formula composed of traditional oriental herbal medicines. The formula was developed with the aim of improving weight control. We investigated the anti-obesity effect of HOX-7 on high-fat-diet (HFD)-induced obesity in C57BL/6 mice. METHODS: The mice were divided into four groups and were fed a normal diet (ND), HFD, or HFD with oral administration of HOX-7 at 100 or 200 mg/kg/day for 12 weeks. Body and fat weight, histological changes of fat tissue, and the expression of key adipogenic transcription factors were investigated. RESULTS: The body weight of mice fed the HFD with HOX-7 was significantly decreased compared to the HFD group. There were no obvious differences in weekly food intake among the 4 groups. The weight of the epididymal and total fat pads was reduced in mice fed the HFD with HOX-7. Treatment with HOX-7 also substantially attenuated the expression of key adipogenic transcription factors, including peroxisome proliferatoractivated receptor γ, CCAAT/enhancer binding protein α, sterol regulatory element binding protein 1c, adipocyte P2, liver X receptor, and lipoprotein lipase in the epididymal adipose tissue. CONCLUSION: Overall, this study highlighted the anti-obesity effects of HOX-7, a finding that could contribute to the development of natural anti-obesity herbal medicines. |
format | Online Article Text |
id | pubmed-4320579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43205792015-02-08 HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice Lee, Heon-Myung Rim, Hong-Kun Seo, Jong-Hwan Kook, Yoon-Bum Kim, Sung-Kew Oh, Chang-Hyun Yoo, Kyung Ho Jin, Jong-Sik An, Hyo-Jin BMC Complement Altern Med Research Article BACKGROUND: HOX-7 is a newly developed dietary formula composed of traditional oriental herbal medicines. The formula was developed with the aim of improving weight control. We investigated the anti-obesity effect of HOX-7 on high-fat-diet (HFD)-induced obesity in C57BL/6 mice. METHODS: The mice were divided into four groups and were fed a normal diet (ND), HFD, or HFD with oral administration of HOX-7 at 100 or 200 mg/kg/day for 12 weeks. Body and fat weight, histological changes of fat tissue, and the expression of key adipogenic transcription factors were investigated. RESULTS: The body weight of mice fed the HFD with HOX-7 was significantly decreased compared to the HFD group. There were no obvious differences in weekly food intake among the 4 groups. The weight of the epididymal and total fat pads was reduced in mice fed the HFD with HOX-7. Treatment with HOX-7 also substantially attenuated the expression of key adipogenic transcription factors, including peroxisome proliferatoractivated receptor γ, CCAAT/enhancer binding protein α, sterol regulatory element binding protein 1c, adipocyte P2, liver X receptor, and lipoprotein lipase in the epididymal adipose tissue. CONCLUSION: Overall, this study highlighted the anti-obesity effects of HOX-7, a finding that could contribute to the development of natural anti-obesity herbal medicines. BioMed Central 2014-12-17 /pmc/articles/PMC4320579/ /pubmed/25515293 http://dx.doi.org/10.1186/1472-6882-14-505 Text en © Lee et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. 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 work is properly credited. 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 Lee, Heon-Myung Rim, Hong-Kun Seo, Jong-Hwan Kook, Yoon-Bum Kim, Sung-Kew Oh, Chang-Hyun Yoo, Kyung Ho Jin, Jong-Sik An, Hyo-Jin HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice |
title | HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice |
title_full | HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice |
title_fullStr | HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice |
title_full_unstemmed | HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice |
title_short | HOX-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice |
title_sort | hox-7 suppresses body weight gain and adipogenesis-related gene expression in high-fat-diet-induced obese mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320579/ https://www.ncbi.nlm.nih.gov/pubmed/25515293 http://dx.doi.org/10.1186/1472-6882-14-505 |
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