Abstract |
We treated Skh:HR1 hairless albino mice, NSA mice and hairless albino guinea pigs topically with N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide ( W7) or trifluoperazine (TFP) before or after ultraviolet (UV) irradiation. When applied before irradiation, W7 and TFP prevented edema in Skh-1 mice and W7 prevented UV-induced edema in NSA mice in a dose-dependent manner. Preirradiation treatment with 2% W7 reduced erythema in guinea pigs by 50%. Epidermal histology of UVR-treated Skh-1 mice pretreated with W7 before UVR was similar to unirradiated mice. W7 did not reverse or prevent these UV-induced effects when applied after irradiation. Neither TFP nor W7 absorbed UV based on forward scattering absorbance spectra; we conclude that neither are physical or chemical sunscreens. These results suggest that calmodulin and/or protein kinase C-dependent events are involved in manifesting some of the effects of UV irradiation on skin.
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Authors | F A Anthony, J C Dowdy, M E Costlow |
Journal | Photodermatology, photoimmunology & photomedicine
(Photodermatol Photoimmunol Photomed)
Vol. 10
Issue 6
Pg. 227-34
(Dec 1994)
ISSN: 0905-4383 [Print] England |
PMID | 7727278
(Publication Type: Journal Article)
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Chemical References |
- Calmodulin
- Sulfonamides
- Sunscreening Agents
- Trifluoperazine
- W 7
- Protein Kinase C
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Topics |
- Absorption
- Administration, Cutaneous
- Animals
- Calmodulin
(antagonists & inhibitors)
- Dose-Response Relationship, Drug
- Edema
(pathology, prevention & control)
- Erythema
(pathology, prevention & control)
- Female
- Guinea Pigs
- Mice
- Mice, Hairless
- Mice, Inbred Strains
- Protein Kinase C
(antagonists & inhibitors)
- Skin
(drug effects, pathology, radiation effects)
- Skin Diseases
(pathology, prevention & control)
- Skinfold Thickness
- Sulfonamides
(administration & dosage, therapeutic use)
- Sunscreening Agents
(therapeutic use)
- Trifluoperazine
(administration & dosage, therapeutic use)
- Ultraviolet Rays
(adverse effects)
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