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1.
Disabil Rehabil ; 40(2): 192-198, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-27927033

RESUMEN

PURPOSE: To evaluate the effects of lateral electrical surface stimulation (LESS) on scoliosis and trunk balance in children with severe cerebral palsy (CP). METHODS: Children with severe CP (GMFCS level IV or V) and stationary or progressive scoliosis were enrolled. Children were recommended of two sessions of LESS/day, 1 h/session, for 3 months at home: at 40-80 mA intensity, 200 µs pulse width, 25 Hz frequency, on for 6 s and then off for 6 s on the convex side of the trunk curve. Radiologic (Cobb's, kyphotic, and sacral angles) and functional [gross motor function measurement (GMFM)-88 sitting score, and trunk control measurement scale (TCMS)] measurements were evaluated at 4 periods: (a) 3 months before, (b) just before, (c) 1 month after, and (d) 3 months after LESS. RESULTS: The median Cobb's angle of 11 children (median age, 9 years) was 25°, and it showed significant improvements after both 1 and 3 months of LESS. The LESS intensity correlated with the improvement of GMFM-88 siting score. The parents or main caregivers of the children believed LESS had several positive effects without major adverse effects. CONCLUSIONS: LESS is effective in scoliosis in children with severe CP and it may improve trunk balance. Implications for rehabilitation Scoliosis is a very complicated problem for the children with severe CP. They do not have many options for treatments and scoliosis is usually refractory. Lateral electrical surface stimulation (LESS) is effective in scoliosis in children with severe CP and it may improve trunk balance. LESS may be another option of managing stationary or progressive scoliosis in the children with severe CP who are unable to undergo surgery.


Asunto(s)
Parálisis Cerebral , Terapia por Estimulación Eléctrica/métodos , Escoliosis , Cuidadores/psicología , Parálisis Cerebral/complicaciones , Parálisis Cerebral/rehabilitación , Niño , Preescolar , Comportamiento del Consumidor , Femenino , Humanos , Masculino , Proyectos Piloto , Equilibrio Postural , República de Corea , Escoliosis/etiología , Escoliosis/terapia , Índice de Severidad de la Enfermedad , Resultado del Tratamiento
2.
J Endod ; 39(11): 1401-6, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-24139262

RESUMEN

INTRODUCTION: The chronic nature of diabetes mellitus (DM) raises the risk of oral complication diseases. In general, DM causes oxidative stress to organs. This study aimed to evaluate the cellular change of dental pulp cells against glucose oxidative stress by glucose oxidase with a high glucose state. The purpose of this study was to test the antioxidant character of davallialactone and to reduce the pathogenesis of dental pulp cells against glucose oxidative stress. METHODS: The glucose oxidase with a high glucose concentration was tested for hydroxy peroxide (H2O2) production, cellular toxicity, reactive oxygen species (ROS) formation, induction of inflammatory molecules and disturbance of dentin mineralization in human dental pulp cells. The anti-oxidant effect of Davallilactone was investigated to restore dental pulp cells' vitality and dentin mineralization via reduction of H2O2 production, cellular toxicity, ROS formation and inflammatory molecules. RESULTS: The treatment of glucose oxidase with a high glucose concentration increased H2O2 production, cellular toxicity, and inflammatory molecules and disturbed dentin mineralization by reducing pulp cell activity. However, davallialactone reduced H2O2 production, cellular toxicity, ROS formation, inflammatory molecules, and dentin mineralization disturbances even with a long-term glucose oxidative stress state. CONCLUSIONS: The results of this study imply that the development of oral complications is related to the irreversible damage of dental pulp cells by DM-induced oxidative stress. Davallialactone, a natural antioxidant, may be useful to treat complicated oral disease, representing an improvement for pulp vital therapy.


Asunto(s)
Antiinflamatorios/farmacología , Antioxidantes/farmacología , Pulpa Dental/efectos de los fármacos , Dentinogénesis/efectos de los fármacos , Glucosa Oxidasa/efectos de los fármacos , Lactonas/farmacología , Estrés Oxidativo/efectos de los fármacos , Pulpitis/prevención & control , Agaricales , Fosfatasa Alcalina/análisis , Proteínas Angiogénicas/análisis , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Citocinas/efectos de los fármacos , Pulpa Dental/citología , Dentina/efectos de los fármacos , Diabetes Mellitus/metabolismo , Glucosa/metabolismo , Humanos , Peróxido de Hidrógeno/antagonistas & inhibidores , Peróxido de Hidrógeno/metabolismo , Mediadores de Inflamación/análisis , Extractos Vegetales/farmacología , Especies Reactivas de Oxígeno/metabolismo , Calcificación de Dientes/efectos de los fármacos
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