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Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway
Anisodamine, an antagonist of muscarinic receptor, has been used therapeutically to improve blood flow in circulatory disorders such as septic shock in China since 1965. The main mechanism of anisodamine for anti-shock proposed in Pharmacology for Chinese medical students is to improve blood flow in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108475/ https://www.ncbi.nlm.nih.gov/pubmed/21687515 http://dx.doi.org/10.3389/fphar.2011.00023 |
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author | Zhao, Ting Li, Dong-Jie Liu, Chong Su, Ding-Feng Shen, Fu-Ming |
author_facet | Zhao, Ting Li, Dong-Jie Liu, Chong Su, Ding-Feng Shen, Fu-Ming |
author_sort | Zhao, Ting |
collection | PubMed |
description | Anisodamine, an antagonist of muscarinic receptor, has been used therapeutically to improve blood flow in circulatory disorders such as septic shock in China since 1965. The main mechanism of anisodamine for anti-shock proposed in Pharmacology for Chinese medical students is to improve blood flow in the microcirculation. Here, we suggest a new mechanism for its anti-shock effect. That is, anisodamine, by blocking muscarinic receptor, results in rerouting of acetylcholine to α7 nicotinic acetylcholine receptor (α7nAChR) bringing about increased acetylcholine-mediated activation of α7nAChR and the cholinergic anti-inflammatory pathway. |
format | Online Article Text |
id | pubmed-3108475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31084752011-06-16 Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway Zhao, Ting Li, Dong-Jie Liu, Chong Su, Ding-Feng Shen, Fu-Ming Front Pharmacol Pharmacology Anisodamine, an antagonist of muscarinic receptor, has been used therapeutically to improve blood flow in circulatory disorders such as septic shock in China since 1965. The main mechanism of anisodamine for anti-shock proposed in Pharmacology for Chinese medical students is to improve blood flow in the microcirculation. Here, we suggest a new mechanism for its anti-shock effect. That is, anisodamine, by blocking muscarinic receptor, results in rerouting of acetylcholine to α7 nicotinic acetylcholine receptor (α7nAChR) bringing about increased acetylcholine-mediated activation of α7nAChR and the cholinergic anti-inflammatory pathway. Frontiers Research Foundation 2011-05-02 /pmc/articles/PMC3108475/ /pubmed/21687515 http://dx.doi.org/10.3389/fphar.2011.00023 Text en Copyright © 2011 Zhao, Li, Liu, Su and Shen. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with. |
spellingShingle | Pharmacology Zhao, Ting Li, Dong-Jie Liu, Chong Su, Ding-Feng Shen, Fu-Ming Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway |
title | Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway |
title_full | Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway |
title_fullStr | Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway |
title_full_unstemmed | Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway |
title_short | Beneficial Effects of Anisodamine in Shock Involved Cholinergic Anti-Inflammatory Pathway |
title_sort | beneficial effects of anisodamine in shock involved cholinergic anti-inflammatory pathway |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108475/ https://www.ncbi.nlm.nih.gov/pubmed/21687515 http://dx.doi.org/10.3389/fphar.2011.00023 |
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