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Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells

Allergic rhinitis (AR) is a non-infectious chronic inflammatory disease of nasal mucosa provoking T helper cell (Th) 17 response. Chlorogenic acid (CGA), one of the most abundant polyphenol compounds in various agricultural products, possesses antiviral, anti-inflammatory, and antibacterial properti...

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Autores principales: Shi, Zhaohui, Jiang, Weihong, Chen, Xiaodong, Xu, Min, Wang, Jian, Lai, Yubin, Zha, Dingjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607190/
https://www.ncbi.nlm.nih.gov/pubmed/33015714
http://dx.doi.org/10.1042/BSR20201643
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author Shi, Zhaohui
Jiang, Weihong
Chen, Xiaodong
Xu, Min
Wang, Jian
Lai, Yubin
Zha, Dingjun
author_facet Shi, Zhaohui
Jiang, Weihong
Chen, Xiaodong
Xu, Min
Wang, Jian
Lai, Yubin
Zha, Dingjun
author_sort Shi, Zhaohui
collection PubMed
description Allergic rhinitis (AR) is a non-infectious chronic inflammatory disease of nasal mucosa provoking T helper cell (Th) 17 response. Chlorogenic acid (CGA), one of the most abundant polyphenol compounds in various agricultural products, possesses antiviral, anti-inflammatory, and antibacterial properties. However, the effect of CGA on AR is unclear. Thus, our study explored the effect of CGA in modulating AR-related symptoms and immunoreaction, especially Th17 response. AR mice were induced by ovalbumin (OVA) administration and further treated with CGA or dexamethasone (Dex). The frequencies of rubbing and sneezing of AR mice were recorded. Histopathological analysis of nasal mucosa was conducted by Hematoxylin–Eosin and Periodic acid–Schiff stainings. The serum and nasal mucosa levels of OVA-immunoglobulin (Ig)E, interferon (IFN)-γ, retinoic acid-associated nuclear orphan receptor (ROR)-γt, and interleukin (IL)-17A were measured by enzyme-linked immunosorbent assay, quantitative reverse-transcription polymerase chain reaction (qRT-PCR), or Western blot. The ratio of CD4(+)IL-17(+)Th17 cells to CD4(+) T cells in peripheral blood of AR mice was assessed by flow cytometer. CGA diminished the frequencies of rubbing and sneezing of AR mice in a concentration-dependent manner. CGA attenuated histopathological abnormalities and decreased goblet cell number in nasal mucosa of AR mice. CGA decreased the serum levels of OVA-IgE, ROR-γt, and IL-17A, while increasing the serum level of IFN-γ in AR mice. Meanwhile, CGA decreased the ratio of CD4(+)IL-17(+)Th17 cells to CD4(+)T cells in peripheral blood and the mRNA and protein levels of IL-17A and ROR-γt in AR mice. CGA ameliorated AR-related symptoms in mice by regulating Th17 cells, which could be a candidate for the treatment of AR.
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spelling pubmed-76071902020-11-05 Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells Shi, Zhaohui Jiang, Weihong Chen, Xiaodong Xu, Min Wang, Jian Lai, Yubin Zha, Dingjun Biosci Rep Immunology & Inflammation Allergic rhinitis (AR) is a non-infectious chronic inflammatory disease of nasal mucosa provoking T helper cell (Th) 17 response. Chlorogenic acid (CGA), one of the most abundant polyphenol compounds in various agricultural products, possesses antiviral, anti-inflammatory, and antibacterial properties. However, the effect of CGA on AR is unclear. Thus, our study explored the effect of CGA in modulating AR-related symptoms and immunoreaction, especially Th17 response. AR mice were induced by ovalbumin (OVA) administration and further treated with CGA or dexamethasone (Dex). The frequencies of rubbing and sneezing of AR mice were recorded. Histopathological analysis of nasal mucosa was conducted by Hematoxylin–Eosin and Periodic acid–Schiff stainings. The serum and nasal mucosa levels of OVA-immunoglobulin (Ig)E, interferon (IFN)-γ, retinoic acid-associated nuclear orphan receptor (ROR)-γt, and interleukin (IL)-17A were measured by enzyme-linked immunosorbent assay, quantitative reverse-transcription polymerase chain reaction (qRT-PCR), or Western blot. The ratio of CD4(+)IL-17(+)Th17 cells to CD4(+) T cells in peripheral blood of AR mice was assessed by flow cytometer. CGA diminished the frequencies of rubbing and sneezing of AR mice in a concentration-dependent manner. CGA attenuated histopathological abnormalities and decreased goblet cell number in nasal mucosa of AR mice. CGA decreased the serum levels of OVA-IgE, ROR-γt, and IL-17A, while increasing the serum level of IFN-γ in AR mice. Meanwhile, CGA decreased the ratio of CD4(+)IL-17(+)Th17 cells to CD4(+)T cells in peripheral blood and the mRNA and protein levels of IL-17A and ROR-γt in AR mice. CGA ameliorated AR-related symptoms in mice by regulating Th17 cells, which could be a candidate for the treatment of AR. Portland Press Ltd. 2020-11-02 /pmc/articles/PMC7607190/ /pubmed/33015714 http://dx.doi.org/10.1042/BSR20201643 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).
spellingShingle Immunology & Inflammation
Shi, Zhaohui
Jiang, Weihong
Chen, Xiaodong
Xu, Min
Wang, Jian
Lai, Yubin
Zha, Dingjun
Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells
title Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells
title_full Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells
title_fullStr Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells
title_full_unstemmed Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells
title_short Chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating Th17 cells
title_sort chlorogenic acid ameliorated allergic rhinitis-related symptoms in mice by regulating th17 cells
topic Immunology & Inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607190/
https://www.ncbi.nlm.nih.gov/pubmed/33015714
http://dx.doi.org/10.1042/BSR20201643
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