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Photoaging: A Daily Care Introduction


European Journal of Dermatology. Volume 11, Number 2, 164, March - April 2001, Compte-rendu de réunion


Summary  

Author(s) : André ROUGIER, International Scientific Manager, La Roche-Posay Pharmaceutical Laboratories, Asnières, France.

Summary : There is increasing awareness that exposure of skin to UVA radiation cannot be considered to be without risk. The amount of UVA reaching the surface of the earth is approximately 20 times greater than that of UVB. Moreover, unlike UVB rays, UVA rays are not attenuated by the ozone layer, they pass through clouds and glass and are emitted at a constant rate throughout the day from the sunrise to the sunset. Finally while 90% of UVB radiation is blocked by the stratum corneum, over 50% of UVA radiation is capable of penetrating deep into the cutaneous structures as far as the papillary and reticular dermis.

ARTICLE

There is increasing awareness that exposure of skin to UVA radiation cannot be considered to be without risk.

The amount of UVA reaching the surface of the earth is approximately 20 times greater than that of UVB. Moreover, unlike UVB rays, UVA rays are not attenuated by the ozone layer, they pass through clouds and glass and are emitted at a constant rate throughout the day from the sunrise to the sunset. Finally while 90% of UVB radiation is blocked by the stratum corneum, over 50% of UVA radiation is capable of penetrating deep into the cutaneous structures as far as the papillary and reticular dermis.

It has been shown that UVA induces damage in cellular DNA, which is clearly different from that induced by UVB. Thus, although the UVB radiations are directly absorbed by DNA, the UVA require photodynamic reactions in which endogenous chromophores contribute to the formation of reactive oxygen species liable to induce DNA alterations. In addition to these effects there is more and more evidence that chronic exposure to UVA can induce immunosuppression at the skin site.

Besides possible tumor induction, photoaging may be involved with UVA exposure. UVA transmission to the dermal tissue is much greater than that of UVB. Thus the connective tissue and cells that synthesize dermal matrix proteins are targets for UVA radiation. The UVA generated reactive oxygen species can cause cross links of proteins, inactivation of enzymes, cell membrane alterations and release of proteases, collagenase and elastase which clinically results in wrinkling, furrowing and sagging of the skin. Moreover, as Pr. Kligman mentioned in one of his numerous papers on the mechanisms involved in photoaging, "Predicting chronic effects of UV based only on acute exposures is completely misleading. Even small amounts of UVA received chronically is damaging".

As you will see during this symposium, recent studies have clearly demonstrated that even small suberythemogenic amounts of UVA radiation can cause significant chronic photodamage to human skin both at the epidermal and dermal level.

Whether the use of low concentration sunscreen in daily care products can prevent all or part of these deleterious effects is a question we will try to answer during this symposium.


 

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