Synthesis and structure-activity relationships of skin ceramides
Language English Country United Arab Emirates Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
20459376
DOI
10.2174/092986710791331068
PII: BSP/CMC/E-Pub/142
Knihovny.cz E-resources
- MeSH
- Ceramides chemical synthesis chemistry physiology MeSH
- Epidermis chemistry MeSH
- Skin Diseases metabolism MeSH
- Humans MeSH
- Sphingolipids chemistry MeSH
- Sphingosine analogs & derivatives chemical synthesis chemistry MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- 6-hydroxy-4-sphingenine MeSH Browser
- Ceramides MeSH
- Sphingolipids MeSH
- Sphingosine MeSH
Ceramides are a complex group of lipids that has gained much attention as cell signaling molecules and skin barrier constituents. In the skin, these sphingolipids form a major part of the stratum corneum intercellular lipid matrix, which is the barrier for penetration of most compounds. The development of such a protective layer was a critical step in the evolution of life on a dry land. Moreover, prominent skin diseases such as psoriasis and atopic dermatitis are associated with diminished ceramide levels and may be effectively improved by exogenous ceramides or their analogues. Since ceramides are not obtained from natural sources in pure form, they are of synthetic interest since 1950's. In this review, we describe sphingosine syntheses from 1998 until 2008, and the synthetic approaches to the unique epidermal ceramides, including the 6-hydroxysphingosine-based ones, the alpha- and omega-hydroxy forms and the omega-acyloxy species. Moreover, the structural requirements of ceramides for a competent skin barrier are discussed, including acyl chain length, trans double bond, acyl alpha-hydroxyl, stereochemistry, omega-linoleyloxy species and ceramide conformation.
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