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1.
Am J Contact Dermat ; 9(3): 170-5, 1998 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-9744910

RESUMEN

BACKGROUND: Users of cosmetics and skin care products often report adverse reactions ranging from itching and dryness to intense inflammatory responses such as erythema or wheal and rash. Self-assessment is not always an accurate parameter for categorizing skin as sensitive or nonsensitive, although it can be valuable. For this reason, it is important to define sensitive skin by more objective factors. OBJECTIVE: Studies were undertaken to determine if objective biophysical measurements could detect differences in barrier function between those individuals who identified themselves as having sensitive skin and those self-identified as having normal skin. In addition, the effects of treatment on barrier functions of individuals with sensitive skin were determined. METHODS: Three main factors that contribute to cutaneous reactivities were observed for the estimation of skin sensitivity: barrier functions, reactivity to irritants, and neuronal responses manifested as sensory reactions. Barrier functions of the skin was tested by gentle removal of the stratum corneum with simple cellophane tape stripping followed by measurement of transepidermal water loss (TEWL) as a marker of barrier loss. The onset and intensity of skin reaction against an irritant, balsam of Peru, was tested on the same individuals to observe the reactivity of their skin. Using the lactic acid sting test, additional information regarding skin sensitivities was obtained. RESULTS: Sensitive skin individuals exhibiting easy barrier damage possess delicate skin that is also highly reactive to irritants. When these individuals used a regimen of products that contained minimal preservatives and no surfactants for 8 weeks, the skin barrier and reactivity changed such that it was similar to nonsensitive skin. CONCLUSIONS: Skin sensitivity is observed because of a combination of factors, including a disrupted barrier and a tendency to hyperreact to topical agents. Treatment with special topical skin care formulations can reduce overall skin sensitivity.


Asunto(s)
Cuidados de la Piel , Fenómenos Fisiológicos de la Piel , Piel/efectos de los fármacos , Adulto , Bálsamos/efectos adversos , Cosméticos/efectos adversos , Dermatitis por Contacto/etiología , Fármacos Dermatológicos/efectos adversos , Fármacos Dermatológicos/uso terapéutico , Epidermis/efectos de los fármacos , Epidermis/fisiología , Eritema/inducido químicamente , Exantema/inducido químicamente , Femenino , Humanos , Irritantes/efectos adversos , Ácido Láctico/efectos adversos , Persona de Mediana Edad , Neuronas/efectos de los fármacos , Neuronas/fisiología , Conservadores Farmacéuticos/administración & dosificación , Prurito/inducido químicamente , Sensación/efectos de los fármacos , Sensación/fisiología , Piel/inervación , Cuidados de la Piel/efectos adversos , Enfermedades de la Piel/inducido químicamente , Tensoactivos/administración & dosificación , Pérdida Insensible de Agua/efectos de los fármacos , Pérdida Insensible de Agua/fisiología
2.
J Cutan Med Surg ; 2(3): 146-52, 1998 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-9479080

RESUMEN

BACKGROUND: A number of inflammatory and immune diseases are associated with vascular changes. Psoriasis, as an example, is a common inflammatory skin disease with dilation of capillaries as an early histological change. In more developed psoriatic lesions there is proliferation of blood vessels and neovascularization. The use of agents that target these vascular changes represents a novel therapeutic strategy in the treatment of inflammatory diseases. Since cartilage is an avascular tissue, it has been hypothesized that there may be factors found in cartilage that inhibit blood vessel formation. OBJECTIVE: The objectives of this study were 1) to determine whether extracts of cartilage could inhibit angiogenesis, and 2) since altered angiogenesis is associated with certain diseases, including psoriasis, to examine whether inhibition of angiogenesis could potentially contribute to the treatment of psoriasis. METHODS: Extracts of shark cartilage were prepared by homogenization and ultrafiltration to derive the active agent termed AE -941. This agent was tested for antiangiogenesis activity using the embryonic vascularization test, which is a modification of the ex vivo chick embryo culture (CAM). Since one of the first steps in angiogenesis is degradation by metalloproteinases of the basement membrane of capillaries, AE -941 was tested for collagenase activity using a fluorogenic peptide substrate. Anti-inflammatory properties were tested using a cutaneous irritation model in humans. RESULTS: A dose dependent inhibition in embryonic neovascularization as well as in collagenase activity by AE -941 was demonstrated. When test compounds were applied on the forearms of test subjects, AE -941 was shown to have anti-inflammatory properties. Anecdotal data suggested that topical AE -941 had a beneficial effect in psoriasis. CONCLUSION: Our results show that AE -941 has anti-angiogenic and anti-inflammatory properties. Antiangiogenesis agents such as AE -941 provide an entirely new class of agents to treat cutaneous and systemic diseases associated with altered vascularity.


Asunto(s)
Cartílago , Neovascularización Patológica/prevención & control , Psoriasis/tratamiento farmacológico , Extractos de Tejidos/uso terapéutico , Animales , Vasos Sanguíneos/efectos de los fármacos , Células Cultivadas , Embrión de Pollo , Colagenasas/metabolismo , Relación Dosis-Respuesta a Droga , Humanos , Tiburones , Extractos de Tejidos/farmacología
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