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Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury
Many preclinical studies show that electroacupuncture (EA) on PC6 and ST36 can reduce infarct size after ischemia-reperfusion (IR) injury. Yet studies to enhance the treatment effect size are limited. The purpose of this study was to explore whether EA has additional myocardial protective effects on...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736192/ https://www.ncbi.nlm.nih.gov/pubmed/26881000 http://dx.doi.org/10.1155/2015/625645 |
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author | Kathy Lee, Seung Min Yoon, Kang Hyun Park, Jimin Kim, Hyun Soo Woo, Jong Shin Lee, So Ra Lee, Kyung Hye Jang, Hyun-Hee Kim, Jin-Bae Kim, Woo Shik Lee, Sanghoon Kim, Weon |
author_facet | Kathy Lee, Seung Min Yoon, Kang Hyun Park, Jimin Kim, Hyun Soo Woo, Jong Shin Lee, So Ra Lee, Kyung Hye Jang, Hyun-Hee Kim, Jin-Bae Kim, Woo Shik Lee, Sanghoon Kim, Weon |
author_sort | Kathy Lee, Seung Min |
collection | PubMed |
description | Many preclinical studies show that electroacupuncture (EA) on PC6 and ST36 can reduce infarct size after ischemia-reperfusion (IR) injury. Yet studies to enhance the treatment effect size are limited. The purpose of this study was to explore whether EA has additional myocardial protective effects on an ischemia-reperfusion (IR) injury rat model when back-shu EA and moxibustion are added. SD rats were divided into several groups and treated with either EA only, EA + back-shu EA (B), or EA + B + moxibustion (M) for 5 consecutive days. Transthoracic echocardiography and molecular and immunohistochemical evaluations were performed. It was found that although myocardial infarct areas were significantly lower and cardiac function was also significantly preserved in the three treatment groups compared to the placebo group, there were no additional differences between the three treatment groups. In addition, HSP20 and HSP27 were expressed significantly more in the treatment groups. The results suggest that adding several treatments does not necessarily increase protection. Our study corroborates previous findings that more treatment, such as prolonging EA duration or increasing EA intensity, does not always lead to better results. Other methods of increasing treatment effect size should be explored. |
format | Online Article Text |
id | pubmed-4736192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47361922016-02-15 Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury Kathy Lee, Seung Min Yoon, Kang Hyun Park, Jimin Kim, Hyun Soo Woo, Jong Shin Lee, So Ra Lee, Kyung Hye Jang, Hyun-Hee Kim, Jin-Bae Kim, Woo Shik Lee, Sanghoon Kim, Weon Evid Based Complement Alternat Med Research Article Many preclinical studies show that electroacupuncture (EA) on PC6 and ST36 can reduce infarct size after ischemia-reperfusion (IR) injury. Yet studies to enhance the treatment effect size are limited. The purpose of this study was to explore whether EA has additional myocardial protective effects on an ischemia-reperfusion (IR) injury rat model when back-shu EA and moxibustion are added. SD rats were divided into several groups and treated with either EA only, EA + back-shu EA (B), or EA + B + moxibustion (M) for 5 consecutive days. Transthoracic echocardiography and molecular and immunohistochemical evaluations were performed. It was found that although myocardial infarct areas were significantly lower and cardiac function was also significantly preserved in the three treatment groups compared to the placebo group, there were no additional differences between the three treatment groups. In addition, HSP20 and HSP27 were expressed significantly more in the treatment groups. The results suggest that adding several treatments does not necessarily increase protection. Our study corroborates previous findings that more treatment, such as prolonging EA duration or increasing EA intensity, does not always lead to better results. Other methods of increasing treatment effect size should be explored. Hindawi Publishing Corporation 2015 2016-01-11 /pmc/articles/PMC4736192/ /pubmed/26881000 http://dx.doi.org/10.1155/2015/625645 Text en Copyright © 2015 Seung Min Kathy Lee et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kathy Lee, Seung Min Yoon, Kang Hyun Park, Jimin Kim, Hyun Soo Woo, Jong Shin Lee, So Ra Lee, Kyung Hye Jang, Hyun-Hee Kim, Jin-Bae Kim, Woo Shik Lee, Sanghoon Kim, Weon Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury |
title | Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury |
title_full | Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury |
title_fullStr | Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury |
title_full_unstemmed | Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury |
title_short | Additional Effects of Back-Shu Electroacupuncture and Moxibustion in Cardioprotection of Rat Ischemia-Reperfusion Injury |
title_sort | additional effects of back-shu electroacupuncture and moxibustion in cardioprotection of rat ischemia-reperfusion injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736192/ https://www.ncbi.nlm.nih.gov/pubmed/26881000 http://dx.doi.org/10.1155/2015/625645 |
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