Effects of environmentally realistic levels of ozone on stratum corneum function

International Journal of Cosmetic Science

Volumn 28, Issue 5, 2006, Pages 349-357

  He, Q C ^a   Tavakkol, A ^a,b   Wietecha, K ^a   Begum Gafur, R ^a   Ansari, S A ^a   Polefka, T ^a  

^a Global Personal Care and Skin Health R D   (United States)

^b NOVARTIS PHARMA AG   (Switzerland)

Author keywords

Cutaneous oxidative stress; Human clinical; Lipid hydroperoxide; Ozone; Stratum corneum enzymes; Vitamin E

Indexed keywords

ALPHA TOCOPHEROL; LIPID HYDROPEROXIDE; OZONE; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE; PROTEINASE; TRYPTASE;

ADULT; ANTIOXIDANT ACTIVITY; ARTICLE; CONTROLLED STUDY; DATA ANALYSIS; DRY SKIN; ENZYME ACTIVITY; ERYTHEMA; FEMALE; HOMEOSTASIS; HUMAN; LONG TERM EXPOSURE; LOW ENERGY RADIATION; NORMAL HUMAN; OUTCOME ASSESSMENT; OXIDATIVE STRESS; PROTEIN DETERMINATION; RADIATION EXPOSURE; RADIATION RESPONSE; SKIN FLORA; SKIN FUNCTION; SKIN PENETRATION; SKIN PROTECTION; STATISTICAL SIGNIFICANCE; STRATUM CORNEUM; ULTRAVIOLET RADIATION; WATER AVAILABILITY;

EID: 33748860325     PISSN: 01425463     EISSN: 14682494     Source Type: Journal    
DOI: 10.1111/j.1467-2494.2006.00347.x     Document Type: Article

References (49)

1. Mustafa, M.G. Biochemical basis of ozone toxicity. Free Radic. Biol. Med. 9, 245-265 (1984).
2. Thiele, J., Podda, M. and Packer, L. Tropospheric ozone: an emerging environmental stress to skin. Biol. Chem. 378, 1299-1305 (1997).
3. Kerr, H.D., Kulle, T.J., Mcllhany, M.L. and Swidersky, P. Effects of ozone on pulmonary function in normal subjects. An environmental-chamber study. Am. Rev. Respir. Dis. 111, 763-773 (1975).
4. Calderon-Garciduenas, L., Wen-Wang, L., Zhang, Y.-J. et al. 8-Hydroxy-2′-deoxyguanosine, a major mutagenic oxidative DNA lesion and DNA strand breaks in nasal respiratory epithelium of children exposed to urban pollution. Environ. Health Perspect. 107, 469-474 (1999).
5. Thiele, J.J., Traber, M.G., Tsang, K., Cross, C.E. and Packer, L. In vivo exposure to ozone depletes vitamins C and E and induces lipid peroxidation in epidermal layers of murine skin. Free Radic. Biol. Med. 23, 385-391 (1997).
6. Thiele, J., Traber, M.G., Polefka, T.G., Cross, C.E. and Packer, L. Ozone-exposure depletes vitamin E and induces lipid peroxidation in murine stratum corneum. J. Invest. Dermatol. 108, 753-757 (1997).
7. Thiele, J.J., Traber, M.G., Re, R. et al. Macromolecular carbonyls in human stratum corneum: a biomarker for environmental oxidant exposure. FEBS Lett. 422, 403-406 (1998).
8. Thiele, J.J., Hsieh, S.N., Briviba, K. and Sies, H. Protein oxidation in human stratum corneum: susceptibility of keratins to oxidation in vitro and presence of a keratin oxidation gradient in vivo. J. Invest. Dermatol. 113, 335-339 (1999).
9. Valacchi, G., van der Vliet, A., Schock, B.C. et al. Ozone exposure activates oxidative stress responses in murine skin. Toxicology 179, 163-170 (2002).
10. Valacchi, G., Pagnin, E., Okamoto, T. et al. Induction of stress proteins and MMP-9 by 0.8 ppm of ozone in murine skin. Biochem. Biophys. Res. Commun. 305, 741-746 (2003).
11. Valacchi, G., Pagnin, E., Corbacho, A.M. et al. In vivo ozone exposure induces antioxidant/stress-related responses in murine lung and skin. Free Radic. Biol. Med. 36, 673-681 (2004).
12. Kriwet, K. and Parenteau, N.L. In vitro skin models. Cosmet. Toiletries 111, 93-103 (1996).
13. Ghadially, R., Brown, B.E., Sequeira-Martin, S.M., Feingold, K.R. and Elias, P.M. The aged epidermal permeability barrier. J. Invest. Dermatol. 95, 2281-2290 (1995).
14. Cotovio, J., Onno, L., Justine, P., Lamure, S. and Catroux, P. Generation of oxidative stress in human cutaneous models following in vitro ozone exposure. Toxicol. In Vitro 15, 357-362 (2001).
15. Tavakkol, A., Nabi, Z., Cardona, S., Soliman, N. and Polefka, T. Tropospheric ozone induced lipid hydroperoxides and depletes vitamin E in human skin in vivo with no detectable clinical or biophysical changes. J. Invest. Dermatol. 114, 844 (2000).
16. He, Q., Krone, K., Scherl, D., Kottler, M. and Tavakkol, A. The use of ozone as an oxidizing agent to evaluate antioxidant activities of natural substrates. Skin Pharmacol. Appl. Skin Physiol. 17, 283-289 (2004).
17. Tavakkol, A., Nabi, Z., Soliman, N. and Polefka, T.G. Delivery of vitamin E to the skin by a novel liquid skin cleanser: comparison of topical versus oral supplementation. J. Cosmet. Sci. 55, 177-187 (2004).
18. Nabi, Z., Tavakkol, A., Soliman, N. and Polefka, T. Bioconversion of tocopheryl acetate to tocopherol in human skin: use of human skin organ culture models. J. Invest. Dermatol. 110, 679 (1998).
19. Sharko, P.T., Murhata, R.I., Leyden, J.J. and Grove, G.L. Arm wash evaluation with instrumental evaluation - a sensitive technique for differentiating the irritation potential of personal washing products. J. Derm. Clin. Eval. Soc. 2, 19-29 (1991).
20. Nabi, Z., Hunter, C., Mattai, J. and Polefka, T. A method for measuring stratum corneum lipid hydroperoxides. J. Invest. Dermatol. 100, 600 (1993).
21. Aly, R., Britz, M.B. and Maibach, H.I. Quantitative microbiology of human vulva. Br. J. Dermatol. 101, 445-448 (1979).
22. Redoules, D., Tarroux, R., Assalit, M.F. and Perie, J.J. Characterisation and assay of five enzymatic activities in the stratum corneum using tape-strippings. Skin Pharmacol. Appl. Skin Physiol. 12, 182-192 (1999).
23. Weber, S.U., Oxidants in skin pathophysiology. In: Exercise and Oxygen Toxicity (Sen, C.K., Packer, L. and Hanninen, O. eds), pp. 46-65. Elsevier Science, Amsterdam 1999.
24. Weber, S.U., Han, N. and Packer, L. Ozone: an emerging oxidative stressor to skin. Curr. Probl. Dermatol. 29, 52-61 (2001).
25. Weber, S.U., Thiele, J.J., Cross, C.E. and Packer, L. Vitamin C, uric acid and glutathione gradients in murine stratum corneum and their susceptibility to ozone exposure. J. Invest. Dermatol. 113, 1128-1132 (1999).
26. National Ambient Air Quality Standards for Ozone, Final Rule, from Environmental Protection Agency, Code of Federal Registry 62, 33856-38896 (1997).
27. Thiele, J.J., Traber, M.G., Podda, M., Tsang, K., Cross, C.E. and Packer, L. Ozone depletes tocopherols and tocotrienols topically applied to murine skin. FEBS Lett. 401, 167-170 (1997).
28. Nover, H. and Botzenhart, K. Effects of photochemical smog from a flow reactor on bacteria. I. Determination of the effects of photochemical smog on bacteria. Zentralbl. Bakteriol. Mikrobiol. Hyg. 177, 282-297 (1983).
29. Muraca, P., Stout, J.E. and Yu, V.L. Comparative assessment of chlorine, heat, ozone, and UV light for killing Legionella pneumophila within a model plumbing system. Appl. Environ. Microbiol. 53, 447-453 (1987).
30. Hambidge, A. Reviewing efficacy of alternative water treatment techniques. Health Estate 55, 23-25 (2001).
31. Voss, J.G. Effects of an antibacterial soap on the ecology of aerobic bacterial flora of human skin. Appl. Microbiol. 30, 551-556 (1975).
32. Leyden, J.J., McGinley, K.J., Foglia, A.N., Wahrman, J.E., Gropper, C.N. and Vowels, B.R. A new method for in vivo evaluation of antimicrobial agents by translocation of complex dense populations of cutaneous bacteria. Skin Pharmacol. 9, 60-68 (1996).
33. Del Rio, D., Stewart, A.J. and Pellegrini, N. A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutr. Metab. Cardiovasc. Dis. 15, 316-328 (2005).
34. Valacchi, G., Fortino, V. and Bocci, V. The dual action of ozone on the skin. Br. J. Dermatol. 153, 1096-1100 (2005).
35. Milstone, L.M. Epidermal desquamation. J. Dermatol. Sci. 36, 131-140 (2004).
36. Lundstrom, A., Serre, G., Haftek, M. and Egelrud, T. Evidence for a role of corneodesmosin, a protein which may serve to modify desmosomes during cornification in stratum corneum cell cohesion and desquamation. Arch. Dermatol. Res. 286, 369-375 (1994).
37. Suzuki, Y., Nomura, J., Koyama, J. and Horii, I. The role of proteases in stratum corneum: involvement in stratum corneum desquamation. Arch. Dermatol. Res. 286, 249-253 (1994).
38. Suzuki, Y., Koyama, J., Moro, O. et al. The role of two endogenous proteases of the stratum corneum in degradation of desmoglein-1 and their reduced activity in the skin of ichthyotic patients. Br. J. Dermatol. 134, 460-464 (1996).
39. Sato, J., Denda, M., Nakanishi, J., Nomura, J. and Koyama, J. Cholesterol sulphate inhibits proteases that are involved in desquamation of stratum corneum. J. Invest. Dermatol. 11, 189 (1998).
40. Hirao, T. Involvement of transglutamine in ex vivo maturation of cornified envelopes in the stratum corneum. Int. J. Cosmet. Sci. 25, 245-257 (2003).
41. Harding, C.R., Long, S., Richardson, J. et al. The cornified cell envelop: an important marker of stratum corneum maturation in healthy and dry skin. Int. J. Cosmet. Sci. 25, 1-11 (2003).
42. Folk, J.E. and Chung, S.I. Transglutaminase. Methods Enzymol. 113, 358-375 (1985).
43. Candi, E.M.G., Sette, M., Oddi, S., Guerrieri, P. and Paci, M. Transglutaminase cross-linking properties of the small proline rich 1 family of cornified envelope proteins. J. Biol. Chem. 274, 7226-7237 (1999).
44. Watkinson, A., Harding, C.R. and Rawlings, A.V. The cornified envelope: its role on stratum corneum structure and maturation. In: Skin Moisturization (Leyden, J.J. and Rawling, A.V., eds), pp. 95-117. Marcel Dekker, New York (2002).
45. Thiele, J.J., Dreher, F., Maibach, H.I. and Packer, L. Impact of ultraviolet radiation and ozone on the transepidermal water loss as a function of skin temperature in hairless mice. Skin Pharmacol. Appl. Skin Physiol. 16, 283-290 (2003).
46. Ballinger, C.A., Cueto, R., Squadrito, G. et al. Antioxidant-mediated augmentation of ozone-induced membrane oxidation. Free Radic. Biol. Med. 38, 515-526 (2005).
47. Blank, I.H. Factors which influence the water content of the stratum corneum. J. Invest. Dermatol. 18, 433-440 (1952).
48. Warner, R.R. and Lilly, N.A. Correlation of water content with ultrastructure in the stratum corneum. In: Bioengineering of the Skin: Water and the Stratum Corneum (Elsner, P., Berardesca, E. and Maibach, H.I., eds), pp. 3-12. CRC Press, Boca Raton, FL (1994).
49. Pryor, W.A. Mechanisms of radical formation from reactions of ozone with target molecules in the lung. Free Radic. Biol. Med. 17, 451-465 (1994).