Skin Pharmacology and Physiology

Original Paper

Increase in Ceramide Level after Application of Various Sizes of Sphingomyelin Liposomes to a Cultured Human Skin Model

Tokudome Y.a · Jinno M.a · Todo H.a · Kon T.b · Sugibayashi K.a · Hashimoto F.a

Author affiliations

aFaculty of Pharmaceutical Sciences, Josai University, Sakado, and bShalom Ltd., Oshino, Japan

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Skin Pharmacol Physiol 2011;24:218–223

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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: August 06, 2010
Accepted: January 22, 2011
Published online: March 26, 2011
Issue release date: May 2011

Number of Print Pages: 6
Number of Figures: 5
Number of Tables: 0

ISSN: 1660-5527 (Print)
eISSN: 1660-5535 (Online)

For additional information: https://www.karger.com/SPP

Abstract

Sphingomyelin-based liposomes (SPM-L) that were sized (or not) by extrusion through a filter with pores of 100, 200, or 400 nm were applied to a three-dimensional cultured human skin model in order to evaluate which size of SPM-L was most effective at increasing its ceramide level. The diameters of the SPM-L in PBS were 102.7, 181.0, 224.0, and 380.1 nm. The diameters of the liposomes in the culture medium were 117.5, 199.2, 242.1, and 749.8 nm. The diameter of the small liposomes (<200 nm in diameter) did not change much, at least for 7 days. SPM-L in saline or culture medium were applied to the basal layer side or stratum corneum side of the cultured skin model, and ceramide II, III, V, and VI were then extracted from it. The extracted ceramide molecules were separated by HPTLC, and the concentration of each type of ceramide was quantified using a densitometer. When the small SPM-L (110 or 190 nm in diameter) were applied to the basal layer side, the levels of ceramide III and V were increased. When they were applied to the stratum corneum side, the levels of ceramide II, III, V, and VI were significantly increased compared to those of the PBS group, especially after the application of the small SPM-L (110 nm in diameter). Thus, the application of small SPM-L was useful for increasing the ceramide II, III, V, and VI levels of a cultured human skin model.

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References

  1. Elias PM, Friend DS: The permeability barrier in mammalian epidermis. J Cell Biol 1975;65:180–191.
  2. Madison KC: Barrier function of the skin: ‘la raison d’être’ of the epidermis. J Invest Dermatol 2003;121:231–241.
  3. Elias, PM: Epidermal lipids, barrier function, and desquamation. J Invest Dermatol 1983;80(suppl):445–495.
  4. Uchida Y, Iwamori M, Nagai Y: Distinct differences in lipid composition between epidermis and dermis from footpad and dorsal skin of guinea pigs. J Exp Med 1988;58:153–161.
  5. Swartzendruber DC, Wertz PW, Kitko DJ, Madison KC, Downing DT: Molecular models of the intercellular lipid lamellae in mammalian stratum corneum. J Invest Dermatol 1989;92:251–257.
  6. Bouwstra JA, Gooris GS, Bras W, Downing DT: Lipid organization in pig stratum corneum. J Lipid Res 1995;36:685–695.
  7. Imokawa G, Hattori M: A possible function of structural lipid in the water-holding properties of the stratum corneum. J Invest Dermatol 1985;84:282–284.
  8. Imokawa G, Abe A, Jin K, Higaki Y, Kawashima M, Hidano A: Decreased level of ceramides in stratum corneum of atopic dermatitis: an etiologic factor in atopic dry skin? J Invest Dermatol 1991;96:523–526.
  9. Jensen JM, Fölster-Holst R, Baranowsky A, Schunck M, Winoto-Morbach S, Neumann C, Schütze S, Proksch E: Impaired sphingomyelinase activity and epidermal differentiation in atopic dermatitis. J Invest Dermatol 2004;122:1423–1431.
  10. Farwanah H, Raith K, Neubert RH, Wohlrab J: Ceramide profiles of the uninvolved skin in atopic dermatitis and psoriasis are comparable to those of healthy skin. Arch Dermatol Res 2005;296:514–521.
  11. Gray GM, Yardley HJ: Different populations of pig epidermal cells: isolation and lipid composition. J Lipid Res 1975;16:441–447.
  12. Weerheim A, Ponec M: Determination of stratum corneum lipid profile by tape stripping in combination with high-performance thin-layer chromatography. Arch Dermatol Res 2001;293:191–199.
  13. Motta S, Sesana S, Ghidoni R, Monti M: Content of the different lipid classes in psoriatic scale. Arch Dermatol Res 1995;287:691–694.
  14. Vicanová J, Boyce ST, Harriger MD, Weerheim AM, Bouwstra JA, Ponec M: Stratum corneum lipid composition and structure in cultured skin substitutes is restored to normal after grafting onto athymic mice. J Invest Dermatol Symp Proc 1998;3:114–120.
  15. Grayson S, Johnson-Winegar AG, Wintroub BU, Isseroff RR, Epstein EH Jr, Elias PM: Lamellar body-enriched fractions from neonatal mice: preparative techniques and partial characterization. J Invest Dermatol 1985;85:289–294.
  16. Grégoire S, Patouillet C, Noé C, Fossa I, Benech Kieffer F, Ribaud C: Improvement of the experimental setup for skin absorption screening studies with reconstructed skin EPISKIN®. Skin Pharmacol Physiol 2008;21:89–97
  17. Tokudome Y, Uchida R, Yokote T, Todo H, Hada N, Kon T, Yasuda J, Hayashi H, Hashimoto F, Sugibayashi K: Effect of topically applied sphingomyelin-based liposomes on the ceramide level in a three-dimensional cultured human skin model. J Liposome Res 2010;20:49–54.
  18. Mayer LD, Hope MJ, Cullis PR: Vesicles of variable sizes produced by a rapid extrusion procedure. Biochim Biophys Acta 1986;858:161–168.
  19. Bligh EG, Dyer WJ: A rapid method of total lipid extraction and purification. Can J Biochem Physiol 1959;37:911–917.
  20. Yada Y, Higuchi K, Imokawa G: Purification and biochemical characterization of membrane-bound epidermal ceramidases from guinea pig skin. J Biol Chem 1995;270:12677–12684.

Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: August 06, 2010
Accepted: January 22, 2011
Published online: March 26, 2011
Issue release date: May 2011

Number of Print Pages: 6
Number of Figures: 5
Number of Tables: 0

ISSN: 1660-5527 (Print)
eISSN: 1660-5535 (Online)

For additional information: https://www.karger.com/SPP


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