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Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats
Hangover is characterized by a number of unpleasant physical and mental symptoms that occur after heavy alcohol drinking. In addition, consistently excessive alcohol intake is considered as a major reason causes liver disease. The present study investigated the in vivo effects of DA-5513 (Morning ca...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010400/ https://www.ncbi.nlm.nih.gov/pubmed/29937911 http://dx.doi.org/10.5625/lar.2018.34.2.49 |
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author | Yu, Jae Young Nguyen, Hanh Thuy Yong, Chul Soon Park, Hyoung Geun Jun, Joon Ho Kim, Jong Oh |
author_facet | Yu, Jae Young Nguyen, Hanh Thuy Yong, Chul Soon Park, Hyoung Geun Jun, Joon Ho Kim, Jong Oh |
author_sort | Yu, Jae Young |
collection | PubMed |
description | Hangover is characterized by a number of unpleasant physical and mental symptoms that occur after heavy alcohol drinking. In addition, consistently excessive alcohol intake is considered as a major reason causes liver disease. The present study investigated the in vivo effects of DA-5513 (Morning care® Kang Hwang) on biological parameters relevant to hangover relief and alcoholic fatty liver. Blood alcohol and acetaldehyde concentrations were determined in rats administered a single dose of alcohol and treated with DA-5513 or commercially available hangover relief beverages (Yeomyung® and Ukon®). The effects of DA-5513 on alcoholic fatty liver were also determined in rats fed alcohol-containing Lieber-DeCarli diets for 4 weeks. Serum liver function markers (aspartate and alanine aminotransferase activities) and serum/liver lipid levels were assessed. Blood alcohol and acetaldehyde concentrations were lower in the groups treated with DA-5513 or Yeomyung®, as compared with control rats. However, Ukon® did not produce any significant effects on these parameters. Treatment with DA-5513 significantly reduced serum aspartate and alanine aminotransferase activities and markedly reduced serum cholesterol and triglyceride levels, as compared with control rats. Histological observations using Oil Red O staining found that DA-5513 delayed the development of alcoholic fatty liver by reversing hepatic fat accumulation. These findings suggest that DA-5513 could have a beneficial effect on alcohol-induced hangovers and has the potential to ameliorate alcoholic fatty liver. |
format | Online Article Text |
id | pubmed-6010400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60104002018-06-22 Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats Yu, Jae Young Nguyen, Hanh Thuy Yong, Chul Soon Park, Hyoung Geun Jun, Joon Ho Kim, Jong Oh Lab Anim Res Original Article Hangover is characterized by a number of unpleasant physical and mental symptoms that occur after heavy alcohol drinking. In addition, consistently excessive alcohol intake is considered as a major reason causes liver disease. The present study investigated the in vivo effects of DA-5513 (Morning care® Kang Hwang) on biological parameters relevant to hangover relief and alcoholic fatty liver. Blood alcohol and acetaldehyde concentrations were determined in rats administered a single dose of alcohol and treated with DA-5513 or commercially available hangover relief beverages (Yeomyung® and Ukon®). The effects of DA-5513 on alcoholic fatty liver were also determined in rats fed alcohol-containing Lieber-DeCarli diets for 4 weeks. Serum liver function markers (aspartate and alanine aminotransferase activities) and serum/liver lipid levels were assessed. Blood alcohol and acetaldehyde concentrations were lower in the groups treated with DA-5513 or Yeomyung®, as compared with control rats. However, Ukon® did not produce any significant effects on these parameters. Treatment with DA-5513 significantly reduced serum aspartate and alanine aminotransferase activities and markedly reduced serum cholesterol and triglyceride levels, as compared with control rats. Histological observations using Oil Red O staining found that DA-5513 delayed the development of alcoholic fatty liver by reversing hepatic fat accumulation. These findings suggest that DA-5513 could have a beneficial effect on alcohol-induced hangovers and has the potential to ameliorate alcoholic fatty liver. Korean Association for Laboratory Animal Science 2018-06 2018-06-18 /pmc/articles/PMC6010400/ /pubmed/29937911 http://dx.doi.org/10.5625/lar.2018.34.2.49 Text en Copyright © 2018 Korean Association for Laboratory Animal Science 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 Yu, Jae Young Nguyen, Hanh Thuy Yong, Chul Soon Park, Hyoung Geun Jun, Joon Ho Kim, Jong Oh Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats |
title | Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats |
title_full | Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats |
title_fullStr | Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats |
title_full_unstemmed | Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats |
title_short | Effects of DA-5513 on alcohol metabolism and alcoholic fatty liver in rats |
title_sort | effects of da-5513 on alcohol metabolism and alcoholic fatty liver in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010400/ https://www.ncbi.nlm.nih.gov/pubmed/29937911 http://dx.doi.org/10.5625/lar.2018.34.2.49 |
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