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Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis
PURPOSE: There is increasing epidemiological evidence of an association between childhood obesity and atopic dermatitis, but little is known about the underlying mechanism(s). In the present study, we used a rat model of atopic dermatitis to assess whether juvenile obesity, induced by reduction of l...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274472/ https://www.ncbi.nlm.nih.gov/pubmed/25553265 http://dx.doi.org/10.4168/aair.2015.7.1.69 |
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author | Jeong, Keun-Yeong Lee, Jaehee Li, Chengjin Han, Taeho Lee, Sat-Byol Lee, Hyunkyoung Back, Seung Keun Na, Heung Sik |
author_facet | Jeong, Keun-Yeong Lee, Jaehee Li, Chengjin Han, Taeho Lee, Sat-Byol Lee, Hyunkyoung Back, Seung Keun Na, Heung Sik |
author_sort | Jeong, Keun-Yeong |
collection | PubMed |
description | PURPOSE: There is increasing epidemiological evidence of an association between childhood obesity and atopic dermatitis, but little is known about the underlying mechanism(s). In the present study, we used a rat model of atopic dermatitis to assess whether juvenile obesity, induced by reduction of litter size, aggravated the signs of atopic dermatitis and, if so, whether this aggravation was associated with changes in plasma concentration of adipokines, such as leptin and adiponectin. METHODS: Dermatitis was induced by neonatal capsaicin treatment. Body weight, dermatitis score, serum IgE, skin nerve growth factor (NGF), serum leptin and adiponectin, and cytokine mRNA expression in the skin lesion were compared between small (SL, 5 pups) and large litters (LL, 15 pups). RESULTS: The body weight of juvenile rats up to 6 weeks of age was significantly heavier in the SL group, compared with those in the LL group. The SL group showed more robust development of dermatitis, and higher levels of serum IgE and skin NGF than the LL group. Additionally, the SL group demonstrated higher levels of leptin and pro-inflammatory cytokine mRNA but lower levels of adiponectin than the LL group. CONCLUSIONS: These results suggest a causal link between a decrease in immunological tolerance, induced by juvenile obesity, and aggravation of atopic dermatitis. |
format | Online Article Text |
id | pubmed-4274472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease |
record_format | MEDLINE/PubMed |
spelling | pubmed-42744722015-01-01 Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis Jeong, Keun-Yeong Lee, Jaehee Li, Chengjin Han, Taeho Lee, Sat-Byol Lee, Hyunkyoung Back, Seung Keun Na, Heung Sik Allergy Asthma Immunol Res Original Article PURPOSE: There is increasing epidemiological evidence of an association between childhood obesity and atopic dermatitis, but little is known about the underlying mechanism(s). In the present study, we used a rat model of atopic dermatitis to assess whether juvenile obesity, induced by reduction of litter size, aggravated the signs of atopic dermatitis and, if so, whether this aggravation was associated with changes in plasma concentration of adipokines, such as leptin and adiponectin. METHODS: Dermatitis was induced by neonatal capsaicin treatment. Body weight, dermatitis score, serum IgE, skin nerve growth factor (NGF), serum leptin and adiponectin, and cytokine mRNA expression in the skin lesion were compared between small (SL, 5 pups) and large litters (LL, 15 pups). RESULTS: The body weight of juvenile rats up to 6 weeks of age was significantly heavier in the SL group, compared with those in the LL group. The SL group showed more robust development of dermatitis, and higher levels of serum IgE and skin NGF than the LL group. Additionally, the SL group demonstrated higher levels of leptin and pro-inflammatory cytokine mRNA but lower levels of adiponectin than the LL group. CONCLUSIONS: These results suggest a causal link between a decrease in immunological tolerance, induced by juvenile obesity, and aggravation of atopic dermatitis. The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2015-01 2014-07-09 /pmc/articles/PMC4274472/ /pubmed/25553265 http://dx.doi.org/10.4168/aair.2015.7.1.69 Text en Copyright © 2015 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease 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 Jeong, Keun-Yeong Lee, Jaehee Li, Chengjin Han, Taeho Lee, Sat-Byol Lee, Hyunkyoung Back, Seung Keun Na, Heung Sik Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis |
title | Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis |
title_full | Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis |
title_fullStr | Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis |
title_full_unstemmed | Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis |
title_short | Juvenile Obesity Aggravates Disease Severity in a Rat Model of Atopic Dermatitis |
title_sort | juvenile obesity aggravates disease severity in a rat model of atopic dermatitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274472/ https://www.ncbi.nlm.nih.gov/pubmed/25553265 http://dx.doi.org/10.4168/aair.2015.7.1.69 |
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