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Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats

Electroacupuncture (EA) is a modified form of acupuncture that utilizes electrical stimulation. We previously showed that EA stimulated rats were divided into responders that were sensitive to EA and non-responders that were insensitive to EA based on the tail flick latency (TFL) test. The dopamine...

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Autores principales: Kim, Soo-Jeong, Chung, Eun Sook, Lee, Jun-Ho, Lee, Chang Hoon, Kim, Sun Kwang, Lee, Hye-Jung, Bae, Hyunsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874437/
https://www.ncbi.nlm.nih.gov/pubmed/24381499
http://dx.doi.org/10.4196/kjpp.2013.17.6.505
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author Kim, Soo-Jeong
Chung, Eun Sook
Lee, Jun-Ho
Lee, Chang Hoon
Kim, Sun Kwang
Lee, Hye-Jung
Bae, Hyunsu
author_facet Kim, Soo-Jeong
Chung, Eun Sook
Lee, Jun-Ho
Lee, Chang Hoon
Kim, Sun Kwang
Lee, Hye-Jung
Bae, Hyunsu
author_sort Kim, Soo-Jeong
collection PubMed
description Electroacupuncture (EA) is a modified form of acupuncture that utilizes electrical stimulation. We previously showed that EA stimulated rats were divided into responders that were sensitive to EA and non-responders that were insensitive to EA based on the tail flick latency (TFL) test. The dopamine beta-hydroxylase (DBH) gene was more abundantly expressed in the hypothalamus of responder rats than non-responder rats. To determine whether overexpression of DBH gene expression in the hypothalamus modulate EA analgesia, we constructed a DBH encoding adenovirus and which was then injected into the hypothalamus of SD rats. Microinjection of DBH or control GFP virus into the hypothalamus had no changes on the basal pain threshold measured by a TFL test without EA treatment. However, the analgesic effect of EA was significantly enhanced from seven days after microinjection of the DBH virus, but not after injection of the control GFP virus. DBH expression was significantly higher in the hypothalamus of DBH virus injected rat than control GFP virus or PBS injected rats. Moreover, expression of the DBH gene did not affect the body core temperature, body weight, motor function or learning and memory ability. Although the functional role of DBH in the hypothalamus in the analgesic effect of EA remains unclear, our findings suggest that expression of the DBH gene in the hypothalamus promotes EA analgesia without obvious side-effects.
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spelling pubmed-38744372013-12-31 Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats Kim, Soo-Jeong Chung, Eun Sook Lee, Jun-Ho Lee, Chang Hoon Kim, Sun Kwang Lee, Hye-Jung Bae, Hyunsu Korean J Physiol Pharmacol Original Article Electroacupuncture (EA) is a modified form of acupuncture that utilizes electrical stimulation. We previously showed that EA stimulated rats were divided into responders that were sensitive to EA and non-responders that were insensitive to EA based on the tail flick latency (TFL) test. The dopamine beta-hydroxylase (DBH) gene was more abundantly expressed in the hypothalamus of responder rats than non-responder rats. To determine whether overexpression of DBH gene expression in the hypothalamus modulate EA analgesia, we constructed a DBH encoding adenovirus and which was then injected into the hypothalamus of SD rats. Microinjection of DBH or control GFP virus into the hypothalamus had no changes on the basal pain threshold measured by a TFL test without EA treatment. However, the analgesic effect of EA was significantly enhanced from seven days after microinjection of the DBH virus, but not after injection of the control GFP virus. DBH expression was significantly higher in the hypothalamus of DBH virus injected rat than control GFP virus or PBS injected rats. Moreover, expression of the DBH gene did not affect the body core temperature, body weight, motor function or learning and memory ability. Although the functional role of DBH in the hypothalamus in the analgesic effect of EA remains unclear, our findings suggest that expression of the DBH gene in the hypothalamus promotes EA analgesia without obvious side-effects. The Korean Physiological Society and The Korean Society of Pharmacology 2013-12 2013-12-16 /pmc/articles/PMC3874437/ /pubmed/24381499 http://dx.doi.org/10.4196/kjpp.2013.17.6.505 Text en Copyright © 2013 The Korean Physiological Society and The Korean Society of Pharmacology 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
Kim, Soo-Jeong
Chung, Eun Sook
Lee, Jun-Ho
Lee, Chang Hoon
Kim, Sun Kwang
Lee, Hye-Jung
Bae, Hyunsu
Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats
title Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats
title_full Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats
title_fullStr Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats
title_full_unstemmed Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats
title_short Electroacupuncture Analgesia Is Improved by Adenoviral Gene Transfer of Dopamine Beta-hydroxylase into the Hypothalamus of Rats
title_sort electroacupuncture analgesia is improved by adenoviral gene transfer of dopamine beta-hydroxylase into the hypothalamus of rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874437/
https://www.ncbi.nlm.nih.gov/pubmed/24381499
http://dx.doi.org/10.4196/kjpp.2013.17.6.505
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