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Resveratrol ameliorates 2,4-dinitrofluorobenzene-induced atopic dermatitis-like lesions through effects on the epithelium

Background. Resveratrol is a natural polyphenol that exhibits anti-inflammatory effects. The aim of this study was to investigate the effects of resveratrol treatment on epithelium-derived cytokines and epithelial apoptosis in a murine model of atopic dermatitis-like lesions. Material and Methods. A...

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Published in:PeerJ (San Francisco, CA) CA), 2016-03, Vol.4, p.e1889-e1889, Article e1889
Main Authors: Caglayan Sozmen, Sule, Karaman, Meral, Cilaker Micili, Serap, Isik, Sakine, Arikan Ayyildiz, Zeynep, Bagriyanik, Alper, Uzuner, Nevin, Karaman, Ozkan
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creator Caglayan Sozmen, Sule
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Arikan Ayyildiz, Zeynep
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Uzuner, Nevin
Karaman, Ozkan
description Background. Resveratrol is a natural polyphenol that exhibits anti-inflammatory effects. The aim of this study was to investigate the effects of resveratrol treatment on epithelium-derived cytokines and epithelial apoptosis in a murine model of atopic dermatitis-like lesions. Material and Methods. Atopic dermatitis-like lesions were induced in BALB/c mice by repeated application of 2,4-dinitrofluorobenzene to shaved dorsal skin. Twenty-one BALB/c mice were divided into three groups: group I (control), group II (vehicle control), and group III (resveratrol). Systemic resveratrol (30 mg/kg/day) was administered repeatedly during the 6th week of the experiment. After the mice had been sacrificed, skin tissues were examined histologically for epithelial thickness. Epithelial apoptosis (caspase-3) and epithelium-derived cytokines [interleukin (IL)-25, IL-33, and thymic stromal lymphopoietin (TSLP)] were evaluated immunohistochemically. Results. Epithelial thickness and the numbers of IL-25, IL-33, TSLP and caspase-3-positive cells were significantly higher in group II compared to group I mice. There was significant improvement in epithelial thickness in group III compared with group II mice (p < 0.05). The numbers of IL-25, IL-33, and TSLP-positive cells in the epithelium were lower in group III than in group II mice (p < 0.05). The number of caspase-3-positive cells, as an indicator of apoptosis, in the epithelium was significantly lower in group III than in group II mice (p < 0.05). Conclusion. Treatment with resveratrol was effective at ameliorating histological changes and inflammation by acting on epithelium-derived cytokines and epithelial apoptosis.
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Resveratrol is a natural polyphenol that exhibits anti-inflammatory effects. The aim of this study was to investigate the effects of resveratrol treatment on epithelium-derived cytokines and epithelial apoptosis in a murine model of atopic dermatitis-like lesions. Material and Methods. Atopic dermatitis-like lesions were induced in BALB/c mice by repeated application of 2,4-dinitrofluorobenzene to shaved dorsal skin. Twenty-one BALB/c mice were divided into three groups: group I (control), group II (vehicle control), and group III (resveratrol). Systemic resveratrol (30 mg/kg/day) was administered repeatedly during the 6th week of the experiment. After the mice had been sacrificed, skin tissues were examined histologically for epithelial thickness. Epithelial apoptosis (caspase-3) and epithelium-derived cytokines [interleukin (IL)-25, IL-33, and thymic stromal lymphopoietin (TSLP)] were evaluated immunohistochemically. Results. Epithelial thickness and the numbers of IL-25, IL-33, TSLP and caspase-3-positive cells were significantly higher in group II compared to group I mice. There was significant improvement in epithelial thickness in group III compared with group II mice (p &lt; 0.05). The numbers of IL-25, IL-33, and TSLP-positive cells in the epithelium were lower in group III than in group II mice (p &lt; 0.05). The number of caspase-3-positive cells, as an indicator of apoptosis, in the epithelium was significantly lower in group III than in group II mice (p &lt; 0.05). Conclusion. Treatment with resveratrol was effective at ameliorating histological changes and inflammation by acting on epithelium-derived cytokines and epithelial apoptosis.</description><identifier>ISSN: 2167-8359</identifier><identifier>EISSN: 2167-8359</identifier><identifier>DOI: 10.7717/peerj.1889</identifier><identifier>PMID: 27069818</identifier><language>eng</language><publisher>United States: PeerJ. 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Resveratrol is a natural polyphenol that exhibits anti-inflammatory effects. The aim of this study was to investigate the effects of resveratrol treatment on epithelium-derived cytokines and epithelial apoptosis in a murine model of atopic dermatitis-like lesions. Material and Methods. Atopic dermatitis-like lesions were induced in BALB/c mice by repeated application of 2,4-dinitrofluorobenzene to shaved dorsal skin. Twenty-one BALB/c mice were divided into three groups: group I (control), group II (vehicle control), and group III (resveratrol). Systemic resveratrol (30 mg/kg/day) was administered repeatedly during the 6th week of the experiment. After the mice had been sacrificed, skin tissues were examined histologically for epithelial thickness. Epithelial apoptosis (caspase-3) and epithelium-derived cytokines [interleukin (IL)-25, IL-33, and thymic stromal lymphopoietin (TSLP)] were evaluated immunohistochemically. Results. Epithelial thickness and the numbers of IL-25, IL-33, TSLP and caspase-3-positive cells were significantly higher in group II compared to group I mice. There was significant improvement in epithelial thickness in group III compared with group II mice (p &lt; 0.05). The numbers of IL-25, IL-33, and TSLP-positive cells in the epithelium were lower in group III than in group II mice (p &lt; 0.05). The number of caspase-3-positive cells, as an indicator of apoptosis, in the epithelium was significantly lower in group III than in group II mice (p &lt; 0.05). Conclusion. Treatment with resveratrol was effective at ameliorating histological changes and inflammation by acting on epithelium-derived cytokines and epithelial apoptosis.</description><subject>Allergy and Clinical Immunology</subject><subject>Analysis</subject><subject>Animal experimentation</subject><subject>Apoptosis</subject><subject>Atopic dermatitis</subject><subject>Dermatology</subject><subject>Epithelium</subject><subject>Immunology</subject><subject>Interleukins</subject><subject>Mice</subject><subject>Resveratrol</subject><subject>Skin</subject><subject>Treatment</subject><issn>2167-8359</issn><issn>2167-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptkt9rHCEQx5fS0oRrXvoHlIVCKaV71dVT96UQQn8EAoXSPour451XV6_qBtK_vl4uDXdQfRid-cwXnZmmeYnRknPMP-wA0naJhRieNOc9ZrwTZDU8PTqfNRc5b1FdomdIkOfNWc8RGwQW583dd8i3kFRJ0bdqAu9ivUBu-_e0My64GrB-jimOEP5AgM4FM2swrSpx53RrIE2quOJy590vaD1kF0NuyybFeb1pwVrQJbcxVBe0sHPVeDdPL5pnVvkMFw920fz8_OnH1dfu5tuX66vLm06vaF86i3qLVoYNXClMFWJUAx8UB8oFNcxqSkbOgYHCNW4JMiOzA1OYmZ5Yy8miuT7omqi2cpfcpNKdjMrJe0dMa6lScdqDZJSrkVjBGVZ0YGK0TKGRaD1oTMahr1ofD1q7eZzAaAglKX8iehoJbiPX8VZS0dOh1n7RvH0QSPH3DLnIyWUN3qsAcc4Sc4EEpoiSir4-oGtVn-aCjVVR73F5uapxQWuDK7X8D1W3gcnpGMC66j9JeHOUsAHlyyZHP5d9107BdwdQp5hzAvv4TYzkfvTk_ejJ_ehV-NVxYR7Rf4NG_gJQztbE</recordid><startdate>20160331</startdate><enddate>20160331</enddate><creator>Caglayan Sozmen, Sule</creator><creator>Karaman, Meral</creator><creator>Cilaker Micili, Serap</creator><creator>Isik, Sakine</creator><creator>Arikan Ayyildiz, Zeynep</creator><creator>Bagriyanik, Alper</creator><creator>Uzuner, Nevin</creator><creator>Karaman, Ozkan</creator><general>PeerJ. 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Resveratrol is a natural polyphenol that exhibits anti-inflammatory effects. The aim of this study was to investigate the effects of resveratrol treatment on epithelium-derived cytokines and epithelial apoptosis in a murine model of atopic dermatitis-like lesions. Material and Methods. Atopic dermatitis-like lesions were induced in BALB/c mice by repeated application of 2,4-dinitrofluorobenzene to shaved dorsal skin. Twenty-one BALB/c mice were divided into three groups: group I (control), group II (vehicle control), and group III (resveratrol). Systemic resveratrol (30 mg/kg/day) was administered repeatedly during the 6th week of the experiment. After the mice had been sacrificed, skin tissues were examined histologically for epithelial thickness. Epithelial apoptosis (caspase-3) and epithelium-derived cytokines [interleukin (IL)-25, IL-33, and thymic stromal lymphopoietin (TSLP)] were evaluated immunohistochemically. Results. Epithelial thickness and the numbers of IL-25, IL-33, TSLP and caspase-3-positive cells were significantly higher in group II compared to group I mice. There was significant improvement in epithelial thickness in group III compared with group II mice (p &lt; 0.05). The numbers of IL-25, IL-33, and TSLP-positive cells in the epithelium were lower in group III than in group II mice (p &lt; 0.05). The number of caspase-3-positive cells, as an indicator of apoptosis, in the epithelium was significantly lower in group III than in group II mice (p &lt; 0.05). Conclusion. Treatment with resveratrol was effective at ameliorating histological changes and inflammation by acting on epithelium-derived cytokines and epithelial apoptosis.</abstract><cop>United States</cop><pub>PeerJ. Ltd</pub><pmid>27069818</pmid><doi>10.7717/peerj.1889</doi><oa>free_for_read</oa></addata></record>
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subjects Allergy and Clinical Immunology
Analysis
Animal experimentation
Apoptosis
Atopic dermatitis
Dermatology
Epithelium
Immunology
Interleukins
Mice
Resveratrol
Skin
Treatment
title Resveratrol ameliorates 2,4-dinitrofluorobenzene-induced atopic dermatitis-like lesions through effects on the epithelium
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