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1.
Cytobios ; 105(408): 27-34, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11368265

RESUMEN

Experimental autoimmune vitiligo was induced by intradermal injection of mushroom tyrosinase emulsified in complete Freund's adjuvant in female C57BL/6 mice. The onset of vitiligo was characterized by hair hypopigmentation and total melanocyte depletion in the basal layer of the epidermis. Oral administration of mushroom tyrosinase prevented the expression of mushroom tyrosinase induced experimental autoimmune vitiligo. Based on the results it is likely that oral administration of mushroom tyrosinase may have practical implications in vitiligo.


Asunto(s)
Agaricus/enzimología , Enfermedades Autoinmunes/tratamiento farmacológico , Monofenol Monooxigenasa/inmunología , Monofenol Monooxigenasa/uso terapéutico , Vitíligo/tratamiento farmacológico , Administración Oral , Animales , Enfermedades Autoinmunes/inmunología , Enfermedades Autoinmunes/patología , Modelos Animales de Enfermedad , Femenino , Hipersensibilidad Tardía , Ratones , Ratones Endogámicos C57BL , Monofenol Monooxigenasa/administración & dosificación , Monofenol Monooxigenasa/metabolismo , Piel/patología , Vitíligo/inmunología , Vitíligo/patología
2.
Microbios ; 102(403): 135-45, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-10955827

RESUMEN

The extent of destruction of insulin-secreting beta cells of the Islets of Langerhans was investigated in an animal model using oral administration of glutamic acid decarboxylase (GAD) isolated from Escherichia coli. The extent of lymphocytic infiltration of the pancreatic Islet cells and the severity of diabetes were significantly reduced by oral administration of GAD to rats 14 days before intraperitoneal injections of streptozotocin (STZ, 40 mg/kg body wt on 5 consecutive days). In addition, oral administration of GAD to rats 14 days before or 3 days after STZ treatment significantly (p <0.05) reduced the levels of GAD-specific antibodies and improved the in vitro proliferative response of splenocytes to concanavalin A (Con A). These data demonstrate that oral GAD administration probably generates active cellular mechanisms which suppress the disease and therefore raise the possibility of using E. coli GAD as a new means for the immunomodulation of autoimmune diabetes.


Asunto(s)
Diabetes Mellitus Experimental/inmunología , Diabetes Mellitus Experimental/fisiopatología , Escherichia coli/enzimología , Glutamato Descarboxilasa/administración & dosificación , Linfocitos/fisiología , Animales , Anticuerpos/sangre , Concanavalina A/farmacología , Diabetes Mellitus Experimental/terapia , Glutamato Descarboxilasa/inmunología , Glutamato Descarboxilasa/metabolismo , Activación de Linfocitos/inmunología , Ratas , Ratas Sprague-Dawley , Bazo/citología , Bazo/inmunología , Estreptozocina
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