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Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201

DWP208 is a sodium succinate form of ZYM-201 which is a triterpenoid glycoside isolated from Sanguisorba officinalis, a medicinal plant prescribed for various diseases, such as duodenal ulcers and bleeding in East Asian counties. We demonstrated that this compound is able to normalize the altered li...

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Autores principales: Cho, Jae Youl, Choi, Jongwon, Park, Jae Gwang, Yi, Young-Su, Hossen, Muhammad Jahangir, Kim, Hyeongmin, Ro, Jieun, Cha, Bae Cheon, Yoo, Eun Sook, Kim, Jong-Hoon, Lee, Jaehwi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296035/
https://www.ncbi.nlm.nih.gov/pubmed/25598660
http://dx.doi.org/10.4196/kjpp.2014.18.6.469
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author Cho, Jae Youl
Choi, Jongwon
Park, Jae Gwang
Yi, Young-Su
Hossen, Muhammad Jahangir
Kim, Hyeongmin
Ro, Jieun
Cha, Bae Cheon
Yoo, Eun Sook
Kim, Jong-Hoon
Lee, Jaehwi
author_facet Cho, Jae Youl
Choi, Jongwon
Park, Jae Gwang
Yi, Young-Su
Hossen, Muhammad Jahangir
Kim, Hyeongmin
Ro, Jieun
Cha, Bae Cheon
Yoo, Eun Sook
Kim, Jong-Hoon
Lee, Jaehwi
author_sort Cho, Jae Youl
collection PubMed
description DWP208 is a sodium succinate form of ZYM-201 which is a triterpenoid glycoside isolated from Sanguisorba officinalis, a medicinal plant prescribed for various diseases, such as duodenal ulcers and bleeding in East Asian counties. We demonstrated that this compound is able to normalize the altered lipid metabolism induced by hyperglycemia and a high fat diet. In this study, we determined whether hyperlipidemic conditions induced with chronically treated alcohol can also be restored by DWP208. Similar to our previous results, orally administered DWP208 (1 to 10 mg/kg) also ameliorated the hyperlipidemia that was induced by alcohol. This compound reversed the alcohol-induced hyperlipidemia including (i) up-regulated hyperlipidemic parameters such as low-density lipoprotein (LDL), very low-density lipoprotein (VLDL), atherosclerotic index (AI), triglyceride, and total cholesterol, and (ii) down-regulated hyperlipidemic parameters such as absolute body weight, superoxide dismutase (SOD) activity, and high-density lipoprotein (HDL) in serum and liver. According to our data, the ameliorative activity of DWP208 is due to its indirect anti-oxidative activity as a result of which lipid peroxide and hydroxyl radical levels were reduced and the activity of SOD was enhanced. Therefore, our data strongly suggest that DWP208 can be used as a remedy against alcohol-induced hyperlipidemia.
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spelling pubmed-42960352015-01-16 Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201 Cho, Jae Youl Choi, Jongwon Park, Jae Gwang Yi, Young-Su Hossen, Muhammad Jahangir Kim, Hyeongmin Ro, Jieun Cha, Bae Cheon Yoo, Eun Sook Kim, Jong-Hoon Lee, Jaehwi Korean J Physiol Pharmacol Original Article DWP208 is a sodium succinate form of ZYM-201 which is a triterpenoid glycoside isolated from Sanguisorba officinalis, a medicinal plant prescribed for various diseases, such as duodenal ulcers and bleeding in East Asian counties. We demonstrated that this compound is able to normalize the altered lipid metabolism induced by hyperglycemia and a high fat diet. In this study, we determined whether hyperlipidemic conditions induced with chronically treated alcohol can also be restored by DWP208. Similar to our previous results, orally administered DWP208 (1 to 10 mg/kg) also ameliorated the hyperlipidemia that was induced by alcohol. This compound reversed the alcohol-induced hyperlipidemia including (i) up-regulated hyperlipidemic parameters such as low-density lipoprotein (LDL), very low-density lipoprotein (VLDL), atherosclerotic index (AI), triglyceride, and total cholesterol, and (ii) down-regulated hyperlipidemic parameters such as absolute body weight, superoxide dismutase (SOD) activity, and high-density lipoprotein (HDL) in serum and liver. According to our data, the ameliorative activity of DWP208 is due to its indirect anti-oxidative activity as a result of which lipid peroxide and hydroxyl radical levels were reduced and the activity of SOD was enhanced. Therefore, our data strongly suggest that DWP208 can be used as a remedy against alcohol-induced hyperlipidemia. The Korean Physiological Society and The Korean Society of Pharmacology 2014-12 2014-12-30 /pmc/articles/PMC4296035/ /pubmed/25598660 http://dx.doi.org/10.4196/kjpp.2014.18.6.469 Text en Copyright © 2014 The Korean Physiological Society and The Korean Society of Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cho, Jae Youl
Choi, Jongwon
Park, Jae Gwang
Yi, Young-Su
Hossen, Muhammad Jahangir
Kim, Hyeongmin
Ro, Jieun
Cha, Bae Cheon
Yoo, Eun Sook
Kim, Jong-Hoon
Lee, Jaehwi
Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201
title Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201
title_full Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201
title_fullStr Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201
title_full_unstemmed Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201
title_short Alcohol-induced Hyperlipidemia Is Ameliorated by Orally Administered DWP208, a Sodium Succinate Form of ZYM201
title_sort alcohol-induced hyperlipidemia is ameliorated by orally administered dwp208, a sodium succinate form of zym201
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296035/
https://www.ncbi.nlm.nih.gov/pubmed/25598660
http://dx.doi.org/10.4196/kjpp.2014.18.6.469
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