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Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs
BACKGROUND: Previously, we evaluated a minimally invasive epidermal lipid sampling method called skin scrub, which achieved reproducible and comparable results to skin scraping. The present study aimed at investigating regional variations in canine epidermal lipid composition using the skin scrub te...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107596/ https://www.ncbi.nlm.nih.gov/pubmed/25012966 http://dx.doi.org/10.1186/1746-6148-10-152 |
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author | Angelbeck-Schulze, Mandy Mischke, Reinhard Rohn, Karl Hewicker-Trautwein, Marion Naim, Hassan Y Bäumer, Wolfgang |
author_facet | Angelbeck-Schulze, Mandy Mischke, Reinhard Rohn, Karl Hewicker-Trautwein, Marion Naim, Hassan Y Bäumer, Wolfgang |
author_sort | Angelbeck-Schulze, Mandy |
collection | PubMed |
description | BACKGROUND: Previously, we evaluated a minimally invasive epidermal lipid sampling method called skin scrub, which achieved reproducible and comparable results to skin scraping. The present study aimed at investigating regional variations in canine epidermal lipid composition using the skin scrub technique and its suitability for collecting skin lipids in dogs suffering from certain skin diseases. Eight different body sites (5 highly and 3 lowly predisposed for atopic lesions) were sampled by skin scrub in 8 control dogs with normal skin. Additionally, lesional and non-lesional skin was sampled from 12 atopic dogs and 4 dogs with other skin diseases by skin scrub. Lipid fractions were separated by high performance thin layer chromatography and analysed densitometrically. RESULTS: No significant differences in total lipid content were found among the body sites tested in the control dogs. However, the pinna, lip and caudal back contained significantly lower concentrations of ceramides, whereas the palmar metacarpus and the axillary region contained significantly higher amounts of ceramides and cholesterol than most other body sites. The amount of total lipids and ceramides including all ceramide classes were significantly lower in both lesional and non-lesional skin of atopic dogs compared to normal skin, with the reduction being more pronounced in lesional skin. The sampling by skin scrub was relatively painless and caused only slight erythema at the sampled areas but no oedema. Histological examinations of skin biopsies at 2 skin scrubbed areas revealed a potential lipid extraction from the transition zone between stratum corneum and granulosum. CONCLUSIONS: The present study revealed regional variations in the epidermal lipid and ceramide composition in dogs without skin abnormalities but no connection between lipid composition and predilection sites for canine atopic dermatitis lesions. The skin scrub technique proved to be a practicable sampling method for canine epidermal lipids, revealed satisfying results regarding alterations of skin lipid composition in canine atopic dermatitis and might be suitable for epidermal lipid investigations of further canine skin diseases. Although the ceramide composition should be unaffected by the deeper lipid sampling of skin scrub compared to other sampling methods, further studies are required to determine methodological differences. |
format | Online Article Text |
id | pubmed-4107596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41075962014-07-24 Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs Angelbeck-Schulze, Mandy Mischke, Reinhard Rohn, Karl Hewicker-Trautwein, Marion Naim, Hassan Y Bäumer, Wolfgang BMC Vet Res Research Article BACKGROUND: Previously, we evaluated a minimally invasive epidermal lipid sampling method called skin scrub, which achieved reproducible and comparable results to skin scraping. The present study aimed at investigating regional variations in canine epidermal lipid composition using the skin scrub technique and its suitability for collecting skin lipids in dogs suffering from certain skin diseases. Eight different body sites (5 highly and 3 lowly predisposed for atopic lesions) were sampled by skin scrub in 8 control dogs with normal skin. Additionally, lesional and non-lesional skin was sampled from 12 atopic dogs and 4 dogs with other skin diseases by skin scrub. Lipid fractions were separated by high performance thin layer chromatography and analysed densitometrically. RESULTS: No significant differences in total lipid content were found among the body sites tested in the control dogs. However, the pinna, lip and caudal back contained significantly lower concentrations of ceramides, whereas the palmar metacarpus and the axillary region contained significantly higher amounts of ceramides and cholesterol than most other body sites. The amount of total lipids and ceramides including all ceramide classes were significantly lower in both lesional and non-lesional skin of atopic dogs compared to normal skin, with the reduction being more pronounced in lesional skin. The sampling by skin scrub was relatively painless and caused only slight erythema at the sampled areas but no oedema. Histological examinations of skin biopsies at 2 skin scrubbed areas revealed a potential lipid extraction from the transition zone between stratum corneum and granulosum. CONCLUSIONS: The present study revealed regional variations in the epidermal lipid and ceramide composition in dogs without skin abnormalities but no connection between lipid composition and predilection sites for canine atopic dermatitis lesions. The skin scrub technique proved to be a practicable sampling method for canine epidermal lipids, revealed satisfying results regarding alterations of skin lipid composition in canine atopic dermatitis and might be suitable for epidermal lipid investigations of further canine skin diseases. Although the ceramide composition should be unaffected by the deeper lipid sampling of skin scrub compared to other sampling methods, further studies are required to determine methodological differences. BioMed Central 2014-07-10 /pmc/articles/PMC4107596/ /pubmed/25012966 http://dx.doi.org/10.1186/1746-6148-10-152 Text en Copyright © 2014 Angelbeck-Schulze et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Article Angelbeck-Schulze, Mandy Mischke, Reinhard Rohn, Karl Hewicker-Trautwein, Marion Naim, Hassan Y Bäumer, Wolfgang Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs |
title | Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs |
title_full | Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs |
title_fullStr | Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs |
title_full_unstemmed | Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs |
title_short | Canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs |
title_sort | canine epidermal lipid sampling by skin scrub revealed variations between different body sites and normal and atopic dogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107596/ https://www.ncbi.nlm.nih.gov/pubmed/25012966 http://dx.doi.org/10.1186/1746-6148-10-152 |
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