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Métodos Terapéuticos y Terapias MTCI
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1.
Acta Cir Bras ; 31(4): 256-63, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-27168538

RESUMEN

PURPOSE: To investigate the effect of medical ozone treatment on the experimental acute distal colitis in rats. METHODS: Eighteen rats were randomly distributed into three equal groups; control, acute distal colitis (ADC) without and with medical ozone treatment. Rats in the control group were taken saline. ADC was performed by rectal way with 4% acetic acid in groups 2 and 3, and the group 3 was treated with medical ozone for three weeks both rectally and intraperitoneally. At the twenty second day the distal colons samples were obtained for malondialdehyde and myeloperoxidase, blood samples were obtained to measure the levels of TNF-α and IL-1ß levels. Histolopatological examination was evaluated with Ki-67, IL-1ß and VEGF immunostaining densities. RESULTS: There was significant increase in tissue MDA, MPO activity, TNF-α and IL-1ß after ozone administration. There was also a significant difference at immunostaining densities of histopathological examination. CONCLUSIONS: Medical ozone treatment ameliorated the experimental acute distal colitis induced by acetic acid in rats. Its possible effect is by means of decreasing inflammation, edema, and affecting the proliferation and the vascularization.


Asunto(s)
Colitis Ulcerosa/tratamiento farmacológico , Oxidantes Fotoquímicos/uso terapéutico , Ozono/uso terapéutico , Ácido Acético , Enfermedad Aguda , Animales , Colitis Ulcerosa/patología , Colon/patología , Modelos Animales de Enfermedad , Inmunohistoquímica , Interleucina-1beta/sangre , Masculino , Malondialdehído/análisis , Peroxidasa/análisis , Distribución Aleatoria , Ratas Wistar , Reproducibilidad de los Resultados , Factores de Tiempo , Resultado del Tratamiento , Factor de Necrosis Tumoral alfa/sangre , Factor A de Crecimiento Endotelial Vascular/análisis
2.
Acta Cir Bras ; 31(3): 183-9, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-27050789

RESUMEN

PURPOSE: To determine the effect of grape-seed extract against ischemia/reperfusion injury in cholestatic liver. METHODS: Eighteen Wistar albino rats were divided into three groups. In control and study groups, cholestasis was provided by bile duct ligation. Seven days later, the rats were subjected to 30 min hepatic ischemia, followed by 60 min of reperfusion. Oral administration of 50 mg/kg/day grape-seed extract was started 15 days before bile duct ligation and continued to the second operation in the study group. Serum, plasma and liver samples were taken. Laboratory analysis, tissue gluthation, malondialdehyde, myeloperoxidase levels and histopathological examination were performed. RESULTS: Significant decrease in liver gluthation level and significant increase in malondialdehyde level and myeloperoxidase activity were observed after ischemia/reperfusion in cholestatic rats. Serum and plasma levels for laboratory analysis were also significantly higher in cholestatic I/R group. Hepatic necrosis and fibrosis were detected in histopathological examination. Oral grape-seed extract administiration reversed all these parameters and histopathological findings except serum bilirubin levels. CONCLUSION: Oral grape-seed extract treatment can improve liver functions and attenuate the inflammation and oxidative stress in cholestatic ischemia/reperfusion injury.


Asunto(s)
Antioxidantes/farmacología , Colestasis/complicaciones , Extracto de Semillas de Uva/farmacología , Daño por Reperfusión/prevención & control , Alanina Transaminasa/efectos de los fármacos , Alanina Transaminasa/metabolismo , Animales , Aspartato Aminotransferasas/efectos de los fármacos , Aspartato Aminotransferasas/metabolismo , Bilirrubina/metabolismo , Colestasis/metabolismo , Colestasis/patología , Modelos Animales de Enfermedad , Inflamación/metabolismo , Lactato Deshidrogenasas/efectos de los fármacos , Lactato Deshidrogenasas/metabolismo , Hígado/efectos de los fármacos , Hígado/patología , Masculino , Estrés Oxidativo/efectos de los fármacos , Ratas Wistar , Daño por Reperfusión/metabolismo
3.
Acta cir. bras ; 31(4): 256-263, Apr. 2016. graf
Artículo en Inglés | LILACS | ID: lil-781329

RESUMEN

PURPOSE: To investigate the effect of medical ozone treatment on the experimental acute distal colitis in rats. METHODS: Eighteen rats were randomly distributed into three equal groups; control, acute distal colitis (ADC) without and with medical ozone treatment. Rats in the control group were taken saline. ADC was performed by rectal way with 4% acetic acid in groups 2 and 3, and the group 3 was treated with medical ozone for three weeks both rectally and intraperitoneally. At the twenty second day the distal colons samples were obtained for malondialdehyde and myeloperoxidase, blood samples were obtained to measure the levels of TNF-α and IL-1β levels. Histolopatological examination was evaluated with Ki-67, IL-1β and VEGF immunostaining densities. RESULTS: There was significant increase in tissue MDA, MPO activity, TNF-α and IL-1β after ozone administration. There was also a significant difference at immunostaining densities of histopathological examination. CONCLUSIONS: Medical ozone treatment ameliorated the experimental acute distal colitis induced by acetic acid in rats. Its possible effect is by means of decreasing inflammation, edema, and affecting the proliferation and the vascularization.


Asunto(s)
Animales , Masculino , Oxidantes Fotoquímicos/uso terapéutico , Ozono/uso terapéutico , Colitis Ulcerosa/tratamiento farmacológico , Factores de Tiempo , Inmunohistoquímica , Colitis Ulcerosa/patología , Distribución Aleatoria , Enfermedad Aguda , Reproducibilidad de los Resultados , Factor de Necrosis Tumoral alfa/sangre , Resultado del Tratamiento , Ratas Wistar , Colon/patología , Peroxidasa/análisis , Ácido Acético , Factor A de Crecimiento Endotelial Vascular/análisis , Modelos Animales de Enfermedad , Interleucina-1beta/sangre , Malondialdehído/análisis
4.
Acta cir. bras ; 31(3): 183-189, Mar. 2016. tab, graf
Artículo en Inglés | LILACS | ID: lil-777096

RESUMEN

ABSTRACT PURPOSE: To determine the effect of grape-seed extract against ischemia/reperfusion injury in cholestatic liver. METHODS: Eighteen Wistar albino rats were divided into three groups. In control and study groups, cholestasis was provided by bile duct ligation. Seven days later, the rats were subjected to 30 min hepatic ischemia, followed by 60 min of reperfusion. Oral administration of 50 mg/kg/day grape-seed extract was started 15 days before bile duct ligation and continued to the second operation in the study group. Serum, plasma and liver samples were taken. Laboratory analysis, tissue gluthation, malondialdehyde, myeloperoxidase levels and histopathological examination were performed. RESULTS: Significant decrease in liver gluthation level and significant increase in malondialdehyde level and myeloperoxidase activity were observed after ischemia/reperfusion in cholestatic rats. Serum and plasma levels for laboratory analysis were also significantly higher in cholestatic I/R group. Hepatic necrosis and fibrosis were detected in histopathological examination. Oral grape-seed extract administiration reversed all these parameters and histopathological findings except serum bilirubin levels. CONCLUSION: Oral grape-seed extract treatment can improve liver functions and attenuate the inflammation and oxidative stress in cholestatic ischemia/reperfusion injury.


Asunto(s)
Animales , Masculino , Daño por Reperfusión/prevención & control , Colestasis/complicaciones , Extracto de Semillas de Uva/farmacología , Antioxidantes/farmacología , Aspartato Aminotransferasas/efectos de los fármacos , Aspartato Aminotransferasas/metabolismo , Bilirrubina/metabolismo , Daño por Reperfusión/metabolismo , Colestasis/metabolismo , Colestasis/patología , Ratas Wistar , Estrés Oxidativo/efectos de los fármacos , Lactato Deshidrogenasas/efectos de los fármacos , Lactato Deshidrogenasas/metabolismo , Alanina Transaminasa/efectos de los fármacos , Alanina Transaminasa/metabolismo , Modelos Animales de Enfermedad , Inflamación/metabolismo , Hígado/efectos de los fármacos , Hígado/patología
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