Oxidative stress-independent depletion of epidermal vitamin A by UVA

J Invest Dermatol. 2002 Mar;118(3):513-8. doi: 10.1046/j.0022-202x.2002.01674.x.

Abstract

In hairless mice, epidermal vitamin A (retinol and retinyl esters) is strongly decreased following a single exposure to UVB. Here, using the same mouse model, we studied the effects of UVA on epidermal vitamin A content, lipid peroxidation, and CRBP-I expression, as well as the putative prevention of vitamin A depletion or lipid peroxidation by topical alpha-tocopherol. An acute exposure to UVA completely depleted epidermal vitamin A with EC50 of 0.25 and 0.5 J per cm2 for retinyl esters and retinol, respectively; these values were 0.1 J per cm2 for both retinoids under UVB exposure. CRBP-I expression was increased 2-fold 8 h following UVA exposure (10 J per cm2), and this increase persisted for at least 16 h. A single UVA exposure induced a concentration-dependent epidermal lipid peroxidation (EC50 = 3.5 J per cm2) giving rise to 55.4 +/- 4.2 nmol lipid peroxides per g at 20 J per cm2, whereas UVB, up to 1 J per cm2, did not increase the basal concentration of 6.7 +/- 0.9 nmol lipid peroxides per g. On the other hand, topical menadione induced a concentration-dependent lipid peroxidation, but did not affect vitamin A content. Pretreatment with alpha-tocopherol (i) did not inhibit UV-induced vitamin A depletion, (ii) completely inhibited the increased lipid peroxidation induced by UVA or menadione, and (iii) accelerated reconstitution of epidermal vitamin A after UVB but not UVA induced depletion. Thus acute UVA induced both epidermal vitamin A depletion and lipid peroxidation, UVB induced only vitamin A depletion, and menadione induced only a lipid peroxidation; topical alpha-tocopherol prevented lipid peroxidation but not vitamin A depletion. These observations indicate (i) that CRBP-I neither provides protection to UVB- and UVA-induced epidermal vitamin A depletion, nor interferes significantly with reconstitution, and (ii) that the UV-induced vitamin A depletion and lipid peroxidation in mouse epidermis are unrelated processes. UV light does not destroy epidermal vitamin A through an oxidative stress but probably by a photochemical reaction in which UV radiations at about 325 nm give the corresponding activation energy.

MeSH terms

  • Administration, Topical
  • Animals
  • Antioxidants / administration & dosage
  • Antioxidants / pharmacology
  • Epidermis / drug effects
  • Epidermis / metabolism*
  • Epidermis / radiation effects*
  • Lipid Peroxides / antagonists & inhibitors
  • Lipid Peroxides / metabolism
  • Mice
  • Mice, Hairless
  • Oxidative Stress / physiology*
  • Retinoids / antagonists & inhibitors
  • Retinol-Binding Proteins / metabolism
  • Retinol-Binding Proteins, Cellular
  • Tretinoin / metabolism
  • Ultraviolet Rays*
  • Vitamin A / antagonists & inhibitors*
  • Vitamin A / metabolism
  • Vitamin A / radiation effects
  • Vitamin K 3 / pharmacology
  • alpha-Tocopherol / pharmacology

Substances

  • Antioxidants
  • Lipid Peroxides
  • Retinoids
  • Retinol-Binding Proteins
  • Retinol-Binding Proteins, Cellular
  • Vitamin A
  • Tretinoin
  • Vitamin K 3
  • alpha-Tocopherol