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KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats

BACKGROUND: KBH-1 is an herbal mixture of Saururus chinensis, Curcuma longa and Polygala tenuifolia. Each herb has been reported to have various pharmaceutical activities; however, the synergistic effect of this herbal composition on obesity has not yet been determined. We investigated the alleviati...

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Autores principales: Lee, Ji-Hye, Lee, Jung-Jin, Cho, Won-Kyung, Yim, Nam-Hui, Kim, Hyun-Kyu, Yun, Bora, Ma, Jin Yeul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5020448/
https://www.ncbi.nlm.nih.gov/pubmed/27618865
http://dx.doi.org/10.1186/s12906-016-1265-z
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author Lee, Ji-Hye
Lee, Jung-Jin
Cho, Won-Kyung
Yim, Nam-Hui
Kim, Hyun-Kyu
Yun, Bora
Ma, Jin Yeul
author_facet Lee, Ji-Hye
Lee, Jung-Jin
Cho, Won-Kyung
Yim, Nam-Hui
Kim, Hyun-Kyu
Yun, Bora
Ma, Jin Yeul
author_sort Lee, Ji-Hye
collection PubMed
description BACKGROUND: KBH-1 is an herbal mixture of Saururus chinensis, Curcuma longa and Polygala tenuifolia. Each herb has been reported to have various pharmaceutical activities; however, the synergistic effect of this herbal composition on obesity has not yet been determined. We investigated the alleviation effect of KBH-1 and its possible molecular mechanism in obesity-induced hepatic steatosis and leptin resistance in the hypothalamus. METHODS: We used HepG2 cells, primary neuronal cells and a high-fat diet (HFD)-induced obesity rat model to determine the effect of KBH-1 in vitro and in vivo on hepatic steatosis and leptin resistance accompanied by obesity. To identify the alleviation effect on lipid accumulation, HepG2 cells stimulated by FFA were stained with Oil Red O; in addition, immunoblotting and qPCR were performed to determine the effect of KBH-1 on the activation of proteins and nuclear enzymes in HepG2 cells and the steatotic liver of HFD-induced obesity rats. To examine the effect of KBH-1 on the leptin resistance of the hypothalamus and its possible molecular mechanism, we examined the effect of KBH-1 on the activation of the leptin resistance-related protein in primary cultured cortical neuron cells and the hypothalamus of an HFD-induced obesity rat model. In addition, we used HPLC analysis to identify the standard compound of KBH-1. RESULTS: KBH-1 not only suppressed the lipid deposition in HepG2 cells exposed to free fatty acids (FFA) but also significantly down-regulated major factors in lipogenesis and up-regulated major factors in lipolysis. Similarly, in a HFD-induced obesity model, KBH-1 improved hepatic steatosis by alleviating the effects on lipogenic genes and kinases. In addition, KBH-1 significantly improved the leptin-mediated signals impaired by obesity or FFA in the obesity model and primary cultured cortical neuron cells. In addition, KBH-1 was analyzed to include six standard compounds using HPLC analysis, among these compounds, onji-saponin B and curcumin were potently suppressed the level of triglycerides. CONCLUSIONS: KBH-1 exhibits alleviating effects by improving hepatic steatosis and leptin resistance by up-regulating the activation of AMPK and suppressing the expression of PPARγ. These findings show the potential of KBH-1 as a functional food supplement or preventive agent in the treatment of obesity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1265-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-50204482016-09-14 KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats Lee, Ji-Hye Lee, Jung-Jin Cho, Won-Kyung Yim, Nam-Hui Kim, Hyun-Kyu Yun, Bora Ma, Jin Yeul BMC Complement Altern Med Research Article BACKGROUND: KBH-1 is an herbal mixture of Saururus chinensis, Curcuma longa and Polygala tenuifolia. Each herb has been reported to have various pharmaceutical activities; however, the synergistic effect of this herbal composition on obesity has not yet been determined. We investigated the alleviation effect of KBH-1 and its possible molecular mechanism in obesity-induced hepatic steatosis and leptin resistance in the hypothalamus. METHODS: We used HepG2 cells, primary neuronal cells and a high-fat diet (HFD)-induced obesity rat model to determine the effect of KBH-1 in vitro and in vivo on hepatic steatosis and leptin resistance accompanied by obesity. To identify the alleviation effect on lipid accumulation, HepG2 cells stimulated by FFA were stained with Oil Red O; in addition, immunoblotting and qPCR were performed to determine the effect of KBH-1 on the activation of proteins and nuclear enzymes in HepG2 cells and the steatotic liver of HFD-induced obesity rats. To examine the effect of KBH-1 on the leptin resistance of the hypothalamus and its possible molecular mechanism, we examined the effect of KBH-1 on the activation of the leptin resistance-related protein in primary cultured cortical neuron cells and the hypothalamus of an HFD-induced obesity rat model. In addition, we used HPLC analysis to identify the standard compound of KBH-1. RESULTS: KBH-1 not only suppressed the lipid deposition in HepG2 cells exposed to free fatty acids (FFA) but also significantly down-regulated major factors in lipogenesis and up-regulated major factors in lipolysis. Similarly, in a HFD-induced obesity model, KBH-1 improved hepatic steatosis by alleviating the effects on lipogenic genes and kinases. In addition, KBH-1 significantly improved the leptin-mediated signals impaired by obesity or FFA in the obesity model and primary cultured cortical neuron cells. In addition, KBH-1 was analyzed to include six standard compounds using HPLC analysis, among these compounds, onji-saponin B and curcumin were potently suppressed the level of triglycerides. CONCLUSIONS: KBH-1 exhibits alleviating effects by improving hepatic steatosis and leptin resistance by up-regulating the activation of AMPK and suppressing the expression of PPARγ. These findings show the potential of KBH-1 as a functional food supplement or preventive agent in the treatment of obesity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12906-016-1265-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-13 /pmc/articles/PMC5020448/ /pubmed/27618865 http://dx.doi.org/10.1186/s12906-016-1265-z 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
Lee, Ji-Hye
Lee, Jung-Jin
Cho, Won-Kyung
Yim, Nam-Hui
Kim, Hyun-Kyu
Yun, Bora
Ma, Jin Yeul
KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
title KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
title_full KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
title_fullStr KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
title_full_unstemmed KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
title_short KBH-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
title_sort kbh-1, an herbal composition, improves hepatic steatosis and leptin resistance in high-fat diet-induced obese rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5020448/
https://www.ncbi.nlm.nih.gov/pubmed/27618865
http://dx.doi.org/10.1186/s12906-016-1265-z
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