Animal assays for anti-psoriatic, retinoid and sun protective agents
- PMID: 6378247
- DOI: 10.1111/j.1365-2133.1984.tb15587.x
Animal assays for anti-psoriatic, retinoid and sun protective agents
Abstract
It is possible to evaluate different dermatological therapeutic agents intended for human use in a variety of animal assays. This review will discuss some of these assays, and attempt to correlate animal and human skin responses. Psoriasis is a disease where changes in epidermal proliferation may be an important factor. It is possible to assay potential anti-psoriatic agents by measuring their ability to suppress DNA synthesis in the epidermis of hairless mice. This assay is predictive of the anti-psoriatic effectiveness of numerous agents including a variety of anti-proliferative drugs and anthralin, and has been used to evaluate the potential efficacy of purified coal tar shampoos and body preparations. The activity of the polyamine biosynthesis enzyme ornithine decarboxylase (ODC) is elevated in psoriatic skin, and it is induced in mouse epidermis by tape stripping. Retinoids can inhibit the induction of ODC activity, and this inhibition may be used to evaluate novel synthetic retinoids. Retinoids have beneficial effects on the abnormal keratinization found in various diseases. Rhino mice have multiple keratin-filled epidermal utricles, and the size of these is reduced by retinoid treatment. Observing the changes in the size of the utricles can be utilized to evaluate the effects of retinoids on keratinization. Sunscreen agents are tested on human volunteers by observing their ability to inhibit the erythema induced by exposure to solar-simulated light, to obtain a sun protection factor (SPF). It is possible to utilize the ability of sunscreens to inhibit other actinic-induced changes in the skin using animals. Parameters that may be measured include changes in DNA synthesis and ODC activity in the epidermis following ultraviolet irradiation. Some of these assays correlate well with human SPF determinations.
Similar articles
-
Induction of ornithine decarboxylase activity and DNA synthesis in hairless mouse epidermis by retinoids.Cancer Res. 1983 Nov;43(11):5174-7. Cancer Res. 1983. PMID: 6616453
-
The potential of the essential fatty acid-deficient hairless rat as a psoriasis screening model for topical anti-proliferative drugs.Skin Pharmacol Appl Skin Physiol. 2002 Nov-Dec;15(6):401-13. doi: 10.1159/000066453. Skin Pharmacol Appl Skin Physiol. 2002. PMID: 12476014
-
Etretinate treatment for psoriasis inhibits epidermal ornithine decarboxylase.J Am Acad Dermatol. 1982 Apr;6(4 Pt 2 Suppl):697-8. doi: 10.1016/s0190-9622(82)70059-3. J Am Acad Dermatol. 1982. PMID: 7068977
-
Sunscreens containing the broad-spectrum UVA absorber, Mexoryl SX, prevent the cutaneous detrimental effects of UV exposure: a review of clinical study results.Photodermatol Photoimmunol Photomed. 2008 Aug;24(4):164-74. doi: 10.1111/j.1600-0781.2008.00365.x. Photodermatol Photoimmunol Photomed. 2008. PMID: 18717957 Review.
-
Broad-spectrum sunscreens provide better protection from solar ultraviolet-simulated radiation and natural sunlight-induced immunosuppression in human beings.J Am Acad Dermatol. 2008 May;58(5 Suppl 2):S149-54. doi: 10.1016/j.jaad.2007.04.035. J Am Acad Dermatol. 2008. PMID: 18410801 Review.
Cited by
-
Evaluation of retinoids as therapeutic agents in dermatology.Pharm Res. 1994 Feb;11(2):192-200. doi: 10.1023/a:1018938920796. Pharm Res. 1994. PMID: 8165176
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials