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            <header>
                <identifier>oai:data.mendeley.com/9443yrtkn9.1</identifier>
                <datestamp>2019-11-25T10:17:29Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Ishida, Koichi</dc:creator>
    <dc:title>Ceramide Plays a Major Role in the Pathogenesis of Atopic Dermatitis.</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Little is known about the pathophysiological linkages between altered ceramide profiles in the stratum corneum (SC) of patients with atopic dermatitis (AD) and their impaired skin barrier and water-holding functions. We studied that pathophysiological linkage by microanalysis of ceramides using NPLC-ESI Mass Spectrometry comparing before and after topical application of a designed synthetic pseudo-ceramide (pCer). Four weeks of treatment with pCer significantly reduced skin symptoms, accompanied by significant decreases in trans-epidermal water loss (TEWL) and increases in water content. In the SC ceramide profiles, Cer[NH/NP] increased and Cer[NS/AS] decreased with larger alkyl chain lengths in Cer[NS], distinctly representing a switch from an AD to a healthy skin phenotype. The levels of pCer that penetrated into the SC were significantly correlated with the SC water content but not with TEWL. The levels of Cer[NS] and the average carbon chain length of Cer[NS] were closely correlated with the pCer level in the SC. These findings indicate that the penetrated pCer contributes to shift the ceramide profile from an AD to a healthy skin phenotype. Taken together, the observed clinical efficacy of treatment with pCer provides a deep insight into the pathogenesis of AD as a ceramide-deficient disease.</dc:description>
    <dc:subject>Ceramide</dc:subject>
    <dc:subject>Atopic Dermatitis</dc:subject>
    <dc:subject>Biophysical Profile</dc:subject>
    <dc:contributor>Takahashi, Akihiko</dc:contributor>
    <dc:contributor>Bito, Kotatsu</dc:contributor>
    <dc:contributor>Draelos, Zoe</dc:contributor>
    <dc:contributor>Imokawa, Genji</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/9443yrtkn9.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/9443yrtkn9.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:relation>https://data.mendeley.com/datasets/9443yrtkn9</dc:relation>
    <dc:date>2019-11-25T10:17:29Z</dc:date>
</oai_dc:dc></metadata>
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