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Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets
BACKGROUND: Arctium lappa L. (Asteraceae), burdock, is a medicinal plant that is popularly used for treating hypertension, gout, hepatitis, and other inflammatory disorders. This study was performed to test the effect of ethanol extract of Arctium lappa L. (EAL) seeds on vascular reactivity and infl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517347/ https://www.ncbi.nlm.nih.gov/pubmed/22866890 http://dx.doi.org/10.1186/1472-6882-12-116 |
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author | Lee, Yun Jung Choi, Deok Ho Cho, Guk Hyun Kim, Jin Sook Kang, Dae Gill Lee, Ho Sub |
author_facet | Lee, Yun Jung Choi, Deok Ho Cho, Guk Hyun Kim, Jin Sook Kang, Dae Gill Lee, Ho Sub |
author_sort | Lee, Yun Jung |
collection | PubMed |
description | BACKGROUND: Arctium lappa L. (Asteraceae), burdock, is a medicinal plant that is popularly used for treating hypertension, gout, hepatitis, and other inflammatory disorders. This study was performed to test the effect of ethanol extract of Arctium lappa L. (EAL) seeds on vascular reactivity and inflammatory factors in rats fed a high fat/cholesterol diet (HFCD). METHOD: EAL-I (100 mg·kg(−1)/day), EAL-II (200 mg·kg(−1)/day), and fluvastatin (3 mg·kg(−1)/day) groups initially received HFCD alone for 8 weeks, with EAL supplementation provided during the final 6 weeks. RESULTS: Treatment with low or high doses of EAL markedly attenuated plasma levels of triglycerides and augmented plasma levels of high-density lipoprotein (HDL) in HFCD-fed rats. Chronic treatment with EAL markedly reduced impairments of acetylcholine (ACh)-induced relaxation of aortic rings. Furthermore, chronic treatment with EAL significantly lowered systolic blood pressure (SBP) and maintained smooth and flexible intimal endothelial layers in HFCD-fed rats. Chronic treatment with EAL suppressed upregulation of intercellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1, and E-selectin in the aorta. Chronic treatment with EAL also suppressed increases in matrix metalloproteinase (MMP)-2 expression. These results suggested that EAL can inhibit HFCD-induced vascular inflammation in the rat model. CONCLUSION: The present study provides evidence that EAL ameliorates HFCD-induced vascular dysfunction through protection of vascular relaxation and suppression of vascular inflammation. |
format | Online Article Text |
id | pubmed-3517347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35173472012-12-08 Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets Lee, Yun Jung Choi, Deok Ho Cho, Guk Hyun Kim, Jin Sook Kang, Dae Gill Lee, Ho Sub BMC Complement Altern Med Research Article BACKGROUND: Arctium lappa L. (Asteraceae), burdock, is a medicinal plant that is popularly used for treating hypertension, gout, hepatitis, and other inflammatory disorders. This study was performed to test the effect of ethanol extract of Arctium lappa L. (EAL) seeds on vascular reactivity and inflammatory factors in rats fed a high fat/cholesterol diet (HFCD). METHOD: EAL-I (100 mg·kg(−1)/day), EAL-II (200 mg·kg(−1)/day), and fluvastatin (3 mg·kg(−1)/day) groups initially received HFCD alone for 8 weeks, with EAL supplementation provided during the final 6 weeks. RESULTS: Treatment with low or high doses of EAL markedly attenuated plasma levels of triglycerides and augmented plasma levels of high-density lipoprotein (HDL) in HFCD-fed rats. Chronic treatment with EAL markedly reduced impairments of acetylcholine (ACh)-induced relaxation of aortic rings. Furthermore, chronic treatment with EAL significantly lowered systolic blood pressure (SBP) and maintained smooth and flexible intimal endothelial layers in HFCD-fed rats. Chronic treatment with EAL suppressed upregulation of intercellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1, and E-selectin in the aorta. Chronic treatment with EAL also suppressed increases in matrix metalloproteinase (MMP)-2 expression. These results suggested that EAL can inhibit HFCD-induced vascular inflammation in the rat model. CONCLUSION: The present study provides evidence that EAL ameliorates HFCD-induced vascular dysfunction through protection of vascular relaxation and suppression of vascular inflammation. BioMed Central 2012-08-06 /pmc/articles/PMC3517347/ /pubmed/22866890 http://dx.doi.org/10.1186/1472-6882-12-116 Text en Copyright ©2012 Lee et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lee, Yun Jung Choi, Deok Ho Cho, Guk Hyun Kim, Jin Sook Kang, Dae Gill Lee, Ho Sub Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets |
title | Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets |
title_full | Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets |
title_fullStr | Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets |
title_full_unstemmed | Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets |
title_short | Arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets |
title_sort | arctium lappa ameliorates endothelial dysfunction in rats fed with high fat/cholesterol diets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3517347/ https://www.ncbi.nlm.nih.gov/pubmed/22866890 http://dx.doi.org/10.1186/1472-6882-12-116 |
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