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Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats

OBJECTIVES: Cultivated wild ginseng (cWG), called SanYangSanSam, has been used clinically in patients with chronic fatigue in Korea. Little is known about effects of the ginseng distilled (volatile) components produced during evaporizaiton. Recently, we first identified one major component from cWG...

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Autores principales: Shin, Il-Soo, Kim, Do-Hee, Jang, Eun Young, Kim, Hee Young, Yoo, Hwa-Seung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pharmacopuncture Institute (KPI) 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645343/
https://www.ncbi.nlm.nih.gov/pubmed/31338245
http://dx.doi.org/10.3831/KPI.2019.22.008
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author Shin, Il-Soo
Kim, Do-Hee
Jang, Eun Young
Kim, Hee Young
Yoo, Hwa-Seung
author_facet Shin, Il-Soo
Kim, Do-Hee
Jang, Eun Young
Kim, Hee Young
Yoo, Hwa-Seung
author_sort Shin, Il-Soo
collection PubMed
description OBJECTIVES: Cultivated wild ginseng (cWG), called SanYangSanSam, has been used clinically in patients with chronic fatigue in Korea. Little is known about effects of the ginseng distilled (volatile) components produced during evaporizaiton. Recently, we first identified one major component from cWG distilled extract, panaxydol, by using mass spectrometry. However, functional properties of cWG distilled extract and panaxydol remains elusive. Therefore, the present study evaluated the effect of cWG distilled extract or panaxydol on exercise-induced fatigue in rats. METHODS: Fatigue was induced by forced swimming and the immobility time was analyzed in male Sprague-Dawley rats. The animals received intraperitoneally either vehicle, cWG distilled extract, or panaxydol 10 min prior to beginning of the forced swimming test (FST) once daily for 5 days. After the FST on day 5, we also analyzed fatigue-related biochemical levels including blood urea nitrogen (BUN), lactate acid (LAC), and lactate dehydrogenase (LDH) in serum and levels of glycogen in liver and soleus muscle. RESULTS: The forced swimming time in cWG distilled extract (0.6 mL/kg)-treated group was significantly longer than that of control group on day 4 and 5. Panaxydol (0.1 and 0.25 mg/kg)-treated groups showed significantly enhanced performance in the forced swimming, compared to control. In addition, a significant decrease in serum LDH level was found in panaxydol-treated group, while there were no alternations in levels of serum BUN and LAC and glycogen in liver or soleus muscle. CONCLUSION: The present study demonstrated cWG distilled extract and its active component panaxydol have a function of anti-fatigue.
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spelling pubmed-66453432019-07-23 Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats Shin, Il-Soo Kim, Do-Hee Jang, Eun Young Kim, Hee Young Yoo, Hwa-Seung J Pharmacopuncture Original Article OBJECTIVES: Cultivated wild ginseng (cWG), called SanYangSanSam, has been used clinically in patients with chronic fatigue in Korea. Little is known about effects of the ginseng distilled (volatile) components produced during evaporizaiton. Recently, we first identified one major component from cWG distilled extract, panaxydol, by using mass spectrometry. However, functional properties of cWG distilled extract and panaxydol remains elusive. Therefore, the present study evaluated the effect of cWG distilled extract or panaxydol on exercise-induced fatigue in rats. METHODS: Fatigue was induced by forced swimming and the immobility time was analyzed in male Sprague-Dawley rats. The animals received intraperitoneally either vehicle, cWG distilled extract, or panaxydol 10 min prior to beginning of the forced swimming test (FST) once daily for 5 days. After the FST on day 5, we also analyzed fatigue-related biochemical levels including blood urea nitrogen (BUN), lactate acid (LAC), and lactate dehydrogenase (LDH) in serum and levels of glycogen in liver and soleus muscle. RESULTS: The forced swimming time in cWG distilled extract (0.6 mL/kg)-treated group was significantly longer than that of control group on day 4 and 5. Panaxydol (0.1 and 0.25 mg/kg)-treated groups showed significantly enhanced performance in the forced swimming, compared to control. In addition, a significant decrease in serum LDH level was found in panaxydol-treated group, while there were no alternations in levels of serum BUN and LAC and glycogen in liver or soleus muscle. CONCLUSION: The present study demonstrated cWG distilled extract and its active component panaxydol have a function of anti-fatigue. The Korean Pharmacopuncture Institute (KPI) 2019-06 2019-06-30 /pmc/articles/PMC6645343/ /pubmed/31338245 http://dx.doi.org/10.3831/KPI.2019.22.008 Text en © 2019 Korean Pharmacopuncture Institute This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Shin, Il-Soo
Kim, Do-Hee
Jang, Eun Young
Kim, Hee Young
Yoo, Hwa-Seung
Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats
title Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats
title_full Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats
title_fullStr Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats
title_full_unstemmed Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats
title_short Anti-Fatigue Properties of Cultivated Wild Ginseng Distilled Extract and Its Active Component Panaxydol in Rats
title_sort anti-fatigue properties of cultivated wild ginseng distilled extract and its active component panaxydol in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645343/
https://www.ncbi.nlm.nih.gov/pubmed/31338245
http://dx.doi.org/10.3831/KPI.2019.22.008
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