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An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation
The effects of an ethanolic extract of Angelica gigas (EAG) on the vascular smooth muscle cell (VSMC) proliferation and high-cholesterol diet-induced hypercholesterolemia and atherosclerosis were investigated. Rat aortic VSMCs were stimulated with platelet-derived growth factor-BB (25 ng/mL) for the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079836/ https://www.ncbi.nlm.nih.gov/pubmed/24999363 http://dx.doi.org/10.5625/lar.2014.30.2.84 |
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author | Jang, Ja Young Kim, Jihyun Cai, Jingmei Kim, Youngeun Shin, Kyungha Kim, Tae-Su Lee, Sung-Pyo Park, Sung Kyeong Choi, Ehn-Kyoung Kim, Yun-Bae |
author_facet | Jang, Ja Young Kim, Jihyun Cai, Jingmei Kim, Youngeun Shin, Kyungha Kim, Tae-Su Lee, Sung-Pyo Park, Sung Kyeong Choi, Ehn-Kyoung Kim, Yun-Bae |
author_sort | Jang, Ja Young |
collection | PubMed |
description | The effects of an ethanolic extract of Angelica gigas (EAG) on the vascular smooth muscle cell (VSMC) proliferation and high-cholesterol diet-induced hypercholesterolemia and atherosclerosis were investigated. Rat aortic VSMCs were stimulated with platelet-derived growth factor-BB (25 ng/mL) for the induction of DNA synthesis and cell proliferation. EAG (1-10 µg/mL) significantly inhibited both the thymidine incorporation and cell proliferation in a concentration-dependent manner. Hypercholesterolemia was induced by feeding male New Zealand white rabbits with 0.5% cholesterol in diet for 10 weeks, during which EAG (1% in diet) was given for the final 8 weeks after 2-week induction of hypercholesterolemia. Hypercholesterolemic rabbits exhibited great increases in serum total cholesterol and low-density lipoproteins (LDL) levels, and finally severe atheromatous plaque formation covering 28.4% of the arterial walls. EAG significantly increased high-density lipoproteins (HDL), slightly decreased LDL, and potentially reduced the atheroma area to 16.6%. The results indicate that EAG attenuates atherosclerosis not only by inhibiting VASC proliferation, but also by increasing blood HDL levels. Therefore, it is suggested that EAG could be an alternative or an adjunct therapy for the improvement of hypercholesterolemia and atherosclerosis. |
format | Online Article Text |
id | pubmed-4079836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40798362014-07-04 An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation Jang, Ja Young Kim, Jihyun Cai, Jingmei Kim, Youngeun Shin, Kyungha Kim, Tae-Su Lee, Sung-Pyo Park, Sung Kyeong Choi, Ehn-Kyoung Kim, Yun-Bae Lab Anim Res Letter The effects of an ethanolic extract of Angelica gigas (EAG) on the vascular smooth muscle cell (VSMC) proliferation and high-cholesterol diet-induced hypercholesterolemia and atherosclerosis were investigated. Rat aortic VSMCs were stimulated with platelet-derived growth factor-BB (25 ng/mL) for the induction of DNA synthesis and cell proliferation. EAG (1-10 µg/mL) significantly inhibited both the thymidine incorporation and cell proliferation in a concentration-dependent manner. Hypercholesterolemia was induced by feeding male New Zealand white rabbits with 0.5% cholesterol in diet for 10 weeks, during which EAG (1% in diet) was given for the final 8 weeks after 2-week induction of hypercholesterolemia. Hypercholesterolemic rabbits exhibited great increases in serum total cholesterol and low-density lipoproteins (LDL) levels, and finally severe atheromatous plaque formation covering 28.4% of the arterial walls. EAG significantly increased high-density lipoproteins (HDL), slightly decreased LDL, and potentially reduced the atheroma area to 16.6%. The results indicate that EAG attenuates atherosclerosis not only by inhibiting VASC proliferation, but also by increasing blood HDL levels. Therefore, it is suggested that EAG could be an alternative or an adjunct therapy for the improvement of hypercholesterolemia and atherosclerosis. Korean Association for Laboratory Animal Science 2014-06 2014-06-23 /pmc/articles/PMC4079836/ /pubmed/24999363 http://dx.doi.org/10.5625/lar.2014.30.2.84 Text en Copyright © 2014 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 | Letter Jang, Ja Young Kim, Jihyun Cai, Jingmei Kim, Youngeun Shin, Kyungha Kim, Tae-Su Lee, Sung-Pyo Park, Sung Kyeong Choi, Ehn-Kyoung Kim, Yun-Bae An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation |
title | An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation |
title_full | An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation |
title_fullStr | An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation |
title_full_unstemmed | An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation |
title_short | An ethanolic extract of Angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation |
title_sort | ethanolic extract of angelica gigas improves atherosclerosis by inhibiting vascular smooth muscle cell proliferation |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079836/ https://www.ncbi.nlm.nih.gov/pubmed/24999363 http://dx.doi.org/10.5625/lar.2014.30.2.84 |
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