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Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats
Eucommia ulmoides Oliv. (EU) has been used for treatment of liver diseases. The protective effects of Eucommia Ulmoides Oliv. cortex extracts (EUCE) on the carbon tetrachloride- (CCl(4)-) induced hepatic lipid accumulation were examined in this study. Rats were orally treated with EUCE in different...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762164/ https://www.ncbi.nlm.nih.gov/pubmed/24027582 http://dx.doi.org/10.1155/2013/751854 |
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author | Jin, Chang-Feng Li, Bo Lin, Shun-Mei Yadav, Raj-Kumar Kim, Hyung-Ryong Chae, Han-Jung |
author_facet | Jin, Chang-Feng Li, Bo Lin, Shun-Mei Yadav, Raj-Kumar Kim, Hyung-Ryong Chae, Han-Jung |
author_sort | Jin, Chang-Feng |
collection | PubMed |
description | Eucommia ulmoides Oliv. (EU) has been used for treatment of liver diseases. The protective effects of Eucommia Ulmoides Oliv. cortex extracts (EUCE) on the carbon tetrachloride- (CCl(4)-) induced hepatic lipid accumulation were examined in this study. Rats were orally treated with EUCE in different doses prior to an intraperitoneal injection of 1 mg/kg CCl(4). Acute injection of CCl(4) decreased plasma triglyceride but increased hepatic triglyceride and cholesterol as compared to control rats. On the other hand, the pretreatment with EUCE diminished these effects at a dose-dependent manner. CCl(4) treatment decreased glutathione (GSH) and increased malondialdehyde (MDA) accompanied by activated P450 2E1. The pretreatment with EUCE significantly improved these deleterious effects of CCl(4). CCl(4) treatment increased P450 2E1 activation and ApoB accumulation. Pretreatment with EUCE reversed these effects. ER stress response was significantly increased by CCl(4), which was inhibited by EUCE. One of the possible ER stress regulatory mechanisms, lysosomal activity, was examined. CCl(4) reduced lysosomal enzymes that were reversed with the EUCE. The results indicate that oral pretreatment with EUCE may protect liver against CCl(4)-induced hepatic lipid accumulation. ER stress and its related ROS regulation are suggested as a possible mechanism in the antidyslipidemic effect of EUCE. |
format | Online Article Text |
id | pubmed-3762164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37621642013-09-11 Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats Jin, Chang-Feng Li, Bo Lin, Shun-Mei Yadav, Raj-Kumar Kim, Hyung-Ryong Chae, Han-Jung Int J Endocrinol Research Article Eucommia ulmoides Oliv. (EU) has been used for treatment of liver diseases. The protective effects of Eucommia Ulmoides Oliv. cortex extracts (EUCE) on the carbon tetrachloride- (CCl(4)-) induced hepatic lipid accumulation were examined in this study. Rats were orally treated with EUCE in different doses prior to an intraperitoneal injection of 1 mg/kg CCl(4). Acute injection of CCl(4) decreased plasma triglyceride but increased hepatic triglyceride and cholesterol as compared to control rats. On the other hand, the pretreatment with EUCE diminished these effects at a dose-dependent manner. CCl(4) treatment decreased glutathione (GSH) and increased malondialdehyde (MDA) accompanied by activated P450 2E1. The pretreatment with EUCE significantly improved these deleterious effects of CCl(4). CCl(4) treatment increased P450 2E1 activation and ApoB accumulation. Pretreatment with EUCE reversed these effects. ER stress response was significantly increased by CCl(4), which was inhibited by EUCE. One of the possible ER stress regulatory mechanisms, lysosomal activity, was examined. CCl(4) reduced lysosomal enzymes that were reversed with the EUCE. The results indicate that oral pretreatment with EUCE may protect liver against CCl(4)-induced hepatic lipid accumulation. ER stress and its related ROS regulation are suggested as a possible mechanism in the antidyslipidemic effect of EUCE. Hindawi Publishing Corporation 2013 2013-08-20 /pmc/articles/PMC3762164/ /pubmed/24027582 http://dx.doi.org/10.1155/2013/751854 Text en Copyright © 2013 Chang-Feng Jin et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jin, Chang-Feng Li, Bo Lin, Shun-Mei Yadav, Raj-Kumar Kim, Hyung-Ryong Chae, Han-Jung Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats |
title | Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats |
title_full | Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats |
title_fullStr | Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats |
title_full_unstemmed | Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats |
title_short | Mechanism of the Inhibitory Effects of Eucommia ulmoides Oliv. Cortex Extracts (EUCE) in the CCl(4)-Induced Acute Liver Lipid Accumulation in Rats |
title_sort | mechanism of the inhibitory effects of eucommia ulmoides oliv. cortex extracts (euce) in the ccl(4)-induced acute liver lipid accumulation in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762164/ https://www.ncbi.nlm.nih.gov/pubmed/24027582 http://dx.doi.org/10.1155/2013/751854 |
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