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Métodos Terapéuticos y Terapias MTCI
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1.
Bratisl Lek Listy ; 115(6): 345-51, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25023424

RESUMEN

OBJECTIVE: The incidence of urinary bladder disturbances and renal structural changes and functional decline are found to increase with age. METHODS: We investigated the effect of melatonin treatment in addition to estrogen replacement therapy in pinealectomized (Px) and ovariectomized (Ovx) rats. 56 female Wistar rats were divided into seven groups, each containing eight animals: Sham, (Ovx), (Px), Px+Ovx, Px+Ovx receiving estrogen (Px+Ovx+E), Px+Ovx receiving melatonin (Px+Ovx+M) and Px+Ovx estrogen and melatonin supplemented (Px+Ovx+EM) group (EM group). We evaluated reduced glutathione (GSH) levels and malondialdehyde (MDA) levels. The mean collagen fiber (CF)/smooth muscle (SM) ratio in the bladder wall and structure of the kidney were examined histolologically. We also recorded response of the bladder contractility to acetylcholine (Ach). RESULTS: Px and Ovx groups showed statistically significant reductions of antioxidant defenses, impaired Ach-evoked contraction, histological changes compared with the control group. Also, these changes were prominent in Px+Ovx group compared with all other groups. Both estrogen and melatonin reversed these changes however best restoration was observed in the EM group. CONCLUSIONS: Px performed in addition to Ovx led to a distinct increase in oxidative damage in bladder and renal tissue and deteriorate of the detrussor function. Either estradiol or melatonin replacement alone or in combination prevents significant alterations of tissue histology and bladder contractility following Ovx and Px. Thus, combination treatment appears to be the best method to restore both contractility and histomorphology of bladder and kidney tissues after Ovx and Px (Tab. 3, Fig. 4, Ref. 44).


Asunto(s)
Terapia de Reemplazo de Estrógeno , Riñón/efectos de los fármacos , Melatonina/farmacología , Ovariectomía , Glándula Pineal/cirugía , Vejiga Urinaria/efectos de los fármacos , Animales , Antioxidantes/farmacología , Femenino , Riñón/patología , Contracción Muscular/efectos de los fármacos , Contracción Muscular/fisiología , Ratas , Ratas Wistar , Vejiga Urinaria/patología , Vejiga Urinaria/fisiopatología
2.
Ir J Med Sci ; 182(4): 557-63, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23456133

RESUMEN

OBJECTIVES: The aim of the study was to investigate the effect of ozone on oxidative/nitrosative stress and bladder injury caused by Escherichia coli in rat bladder. METHODS: Twenty-one Wistar-Albino-type female rats included in the study were divided into three groups of equal number: (1) sham operation (control), (2) E. coli-only (EC), (3) EC + ozone. After ozone therapy for 3 days, urine and tissue samples were obtained for biochemical, microbiological, and histopathological analysis. RESULTS: Tissue malondialdehyde (MDA), myeloperoxidase (MPO), and nitric oxide (NO) level were increased, whereas superoxide dismutase (SOD) and glutathione peroxidase (GPx) activity was decreased in the EC group. MDA, MPO, and NO levels were decreased, whereas SOD, GPx activity was increased in the ozone-treated group. Also, there was no bacterial translocation in this group. CONCLUSION: The results of the present study suggest that ozone may be used as an agent to protect the bladder from oxidative/nitrosative stress occurring in cystitis.


Asunto(s)
Antibacterianos/farmacología , Cistitis/tratamiento farmacológico , Infecciones por Escherichia coli/tratamiento farmacológico , Ozono/farmacología , Vejiga Urinaria/efectos de los fármacos , Infecciones Urinarias/tratamiento farmacológico , Animales , Traslocación Bacteriana/efectos de los fármacos , Cistitis/microbiología , Modelos Animales de Enfermedad , Escherichia coli/efectos de los fármacos , Infecciones por Escherichia coli/microbiología , Femenino , Glutatión Peroxidasa/metabolismo , Malondialdehído/metabolismo , Óxido Nítrico/metabolismo , Estrés Oxidativo/efectos de los fármacos , Peroxidasa/metabolismo , Ratas , Ratas Wistar , Superóxido Dismutasa/metabolismo , Vejiga Urinaria/microbiología , Infecciones Urinarias/microbiología
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