Evaluation of the therapeutic potential and underlying mechanisms of synephrine, a component of Kampo medicine, against allergic rhinitis
The mechanisms of action of Kampo medicines as treatments for allergic rhinitis are unknown. In this study, we aimed to identify novel potential therapeutic agents for allergic rhinitis and to elucidate their underlying mechanisms. Different components of Kampo medicines (crude drugs) were screened...
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Published in | Cogent biology Vol. 5; no. 1; p. 1592274 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
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01.01.2019
Taylor & Francis Ltd |
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Abstract | The mechanisms of action of Kampo medicines as treatments for allergic rhinitis are unknown. In this study, we aimed to identify novel potential therapeutic agents for allergic rhinitis and to elucidate their underlying mechanisms. Different components of Kampo medicines (crude drugs) were screened for their ability to inhibit the secretion of thymic stromal lymphopoietin (TSLP), a cytokine secreted during allergen exposure. Synephrine (SYN) exhibited the strongest inhibitory effect. In an early-phase allergic reaction, histidine decarboxylase (HDC) and its receptor are activated, leading to the secretion of TSLP. Mucins are thought to be produced as a late-phase reaction. We examined the action of SYN in cultures of human nasal epithelial cells both during mono-stimulation and co-stimulation with activating agents. Based on its inhibition of the histamine H1 receptor and HDC mRNA expression, SYN was assumed to reduce the histamine production. Increased expression of the HDC protein was confirmed in tissues of patients with allergic rhinitis via western blotting. In addition, SYN inhibited TSLP at the mRNA and protein levels and inhibited mucin 5AC mRNA expression. Its inhibitory effects on both early- and late-phase allergic reactions indicate that SYN can serve as a novel therapeutic agent with potential leukotriene antagonist-like activity. |
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AbstractList | The mechanisms of action of Kampo medicines as treatments for allergic rhinitis are unknown. In this study, we aimed to identify novel potential therapeutic agents for allergic rhinitis and to elucidate their underlying mechanisms. Different components of Kampo medicines (crude drugs) were screened for their ability to inhibit the secretion of thymic stromal lymphopoietin (TSLP), a cytokine secreted during allergen exposure. Synephrine (SYN) exhibited the strongest inhibitory effect. In an early-phase allergic reaction, histidine decarboxylase (HDC) and its receptor are activated, leading to the secretion of TSLP. Mucins are thought to be produced as a late-phase reaction. We examined the action of SYN in cultures of human nasal epithelial cells both during mono-stimulation and co-stimulation with activating agents. Based on its inhibition of the histamine H1 receptor and HDC mRNA expression, SYN was assumed to reduce the histamine production. Increased expression of the HDC protein was confirmed in tissues of patients with allergic rhinitis via western blotting. In addition, SYN inhibited TSLP at the mRNA and protein levels and inhibited mucin 5AC mRNA expression. Its inhibitory effects on both early- and late-phase allergic reactions indicate that SYN can serve as a novel therapeutic agent with potential leukotriene antagonist-like activity. |
Author | Ogawa, Kaoru Watanabe, Kenji Hommura, Tomoko Dan, Katsuaki Kanzaki, Sho |
Author_xml | – sequence: 1 givenname: Tomoko surname: Hommura fullname: Hommura, Tomoko email: tomokohommura@keio.jp organization: Keio University School of Medicine – sequence: 2 givenname: Katsuaki surname: Dan fullname: Dan, Katsuaki organization: Research Organization of Biological Activity – sequence: 3 givenname: Sho surname: Kanzaki fullname: Kanzaki, Sho organization: Keio University School of Medicine – sequence: 4 givenname: Kenji surname: Watanabe fullname: Watanabe, Kenji organization: Keio University – sequence: 5 givenname: Kaoru surname: Ogawa fullname: Ogawa, Kaoru organization: Keio University School of Medicine |
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CitedBy_id | crossref_primary_10_1016_j_jconrel_2021_05_048 |
Cites_doi | 10.1164/ajrccm.163.2.2004039 10.1177/000348940411300707 10.1097/MLG.0b013e3180383651 10.3390/molecules190811211 10.1007/PL00007616 10.1159/000346609 10.1248/yakushi1947.109.11_835 10.2500/ajra.2016.30.4295 10.1067/mai.2003.1512 10.1113/jphysiol.1910.sp001406 10.1164/ajrccm.161.6.9909098 10.1517/14728222.12.4.415 10.1155/2017/5974574 10.1186/1465-9921-6-100 10.1016/j.ejphar.2003.12.038 10.4049/jimmunol.179.2.1080 10.1097/ACI.0b013e32831d815c 10.1046/j.1365-2222.2001.01045.x 10.1093/intimm/dxv055 10.5631/jibirin.88.389 10.1016/j.phrs.2016.08.001 10.1177/019459989010300406 10.1016/j.alit.2014.11.002 10.1007/BF02484434 |
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Copyright | 2019 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license. 2019 2019 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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SubjectTerms | Allergens Allergic rhinitis Epithelial cells Gene expression Histamine histamine H1 receptor Histamine H1 receptors Histidine Histidine decarboxylase Hypersensitivity Kampo leukotriene antagonist Mucin Nose synephrine Thymic stromal lymphopoietin Thymus Western blotting |
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Title | Evaluation of the therapeutic potential and underlying mechanisms of synephrine, a component of Kampo medicine, against allergic rhinitis |
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