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1.
Exp Dermatol ; 29(3): 341-348, 2020 03.
Artículo en Inglés | MEDLINE | ID: mdl-31638285

RESUMEN

Hair growth, a complex process, has long been the subject of intense research. Recent developments in material technology have revealed boehmite as a new therapeutic modality for use in wound healing and scar reduction, indicating its beneficial effects. Nonetheless, the biological bases of the beneficial effects of boehmite remain unknown. We investigated the hair growth properties of boehmite in vitro and in vivo and observed dose-dependent proliferation of human dermal papilla cells (hDPCs) in vitro and hair regrowth in a mouse model. To investigate the effects of boehmite on the promotion of cell transition to the anagen phase, we evaluated hDPC viability, alkaline phosphatase (ALP) activity, protein expression and vascular endothelial growth factor (VEGF) secretion in vitro and assessed the anagen-promoting effects of boehmite via gross observation and histological analysis in a mouse model. Boehmite increased hDPC viability, ALP activity, AKT/GSK3ß/ß-catenin pathway activity, anagen-related gene expression and VEGF secretion; moreover, it accelerated hair regrowth in a catagen-anagen transition model via upregulation of ß-catenin signalling and follicular cell proliferation. Collectively, our results indicate that boehmite accelerates hair growth, partly via its effects on critical events in the active phase of the hair follicle cycle, including the promotion of the proliferation of hDPCs and their immediate progeny to the follicle base.


Asunto(s)
Hidróxido de Aluminio/farmacología , Óxido de Aluminio/farmacología , Folículo Piloso/efectos de los fármacos , Piel/metabolismo , beta Catenina/metabolismo , Animales , Proliferación Celular , Dermis/citología , Modelos Animales de Enfermedad , Femenino , Cabello/fisiología , Humanos , Ratones , Ratones Endogámicos C3H , Transducción de Señal , Factor A de Crecimiento Endotelial Vascular/metabolismo , Vía de Señalización Wnt , Cicatrización de Heridas , Difracción de Rayos X
2.
Exp Dermatol ; 28(2): 169-176, 2019 02.
Artículo en Inglés | MEDLINE | ID: mdl-30566262

RESUMEN

Boehmite (γ-AlOOH) has a wide range of applications in a variety of industrial and biological fields. However, little is known about its potential roles in skin diseases. The current study investigated its effect on atopic dermatitis (AD). Following characterization, cytotoxicity, pro-inflammatory response and oxidative stress associated with boehmite were assessed, using TNF-α-induced keratinocytes and mast cells. In addition, therapeutic effects of boehmite, topically administered to Balb/c mice induced by 2,4-dinitrochlorobenzene (DNCB), were evaluated. Expression of cytokines (TLSP, IL-25 and IL-33) and the generation of ROS from keratinocytes induced by TNF-α were significantly inhibited by boehmite without affecting cell viability. MAPKs (ERK, JNK and p38) required for cytokine expression were suppressed by boehmite treatment. Up-regulation of cytokines (TSLP, IL-4, IL-5, IL-13, RANTES) in human mast cells treated with phorbol 12-myristate 13-acetate and calcium ionophore was also suppressed by boehmite. Boehmite improved the AD severity score, epidermal hyperplasia and transepidermal water loss in DNCB-induced AD-like lesions. Moreover, Th2-mediated cytokine expression, mast cell hyperplasia and destruction of the skin barrier were improved by boehmite treatment. Overall, we demonstrated that boehmite may potentially protect against AD.


Asunto(s)
Hidróxido de Aluminio/uso terapéutico , Óxido de Aluminio/uso terapéutico , Dermatitis Atópica/tratamiento farmacológico , Enfermedades de la Piel/tratamiento farmacológico , Piel/efectos de los fármacos , Administración Tópica , Animales , Antiinflamatorios/uso terapéutico , Línea Celular Tumoral , Supervivencia Celular , Dinitroclorobenceno , Epidermis/metabolismo , Humanos , Inflamación , Interleucina-33/metabolismo , Interleucinas/metabolismo , Queratinocitos/citología , Mastocitos/metabolismo , Ratones , Ratones Endogámicos BALB C , Estrés Oxidativo , Serina Endopeptidasas/metabolismo , Acetato de Tetradecanoilforbol , Factor de Necrosis Tumoral alfa/metabolismo
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