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Nutrition ; 27(7-8): 809-15, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21167680

RESUMO

OBJECTIVE: Patients who have had pelvic radiotherapy as part of their cancer therapy may develop subsequent urinary bladder effects such as hyperactive bladder, incontinence, and dysuria. Therefore, the goal of this study was to evaluate whether glutamine supplementation could prevent collagen expression damage in healthy urinary bladder caused by radiotherapy. METHODS: Fifteen adult Wistar rats were separated into a control group that received food and water ad libitum (C group), an irradiated group that received a single pelvic radiation dose of 1164 cGy (I group), and an irradiated group supplemented with l-glutamine every day during the entire experimental period (0.65 g/kg of body weight; I+G group). All animals were sacrificed 15 d after irradiation. The extracellular matrix and muscle were quantified by a morphometric method. Picro Sirius Red was used to visualize the different collagen types. Reverse transcription-polymerase chain reaction and immunohistochemistry were used to determine collagen type I and III expressions. RESULTS: The extracellular matrix (C group 36.84±4.37, I group 31.64±5.00, I+G group 35.53±2.60, P=0.0001), muscle (C group 36.43±6.15, I group 29.39±7.08, I+G group 31.38±3.14, P=0.0001), and gene expressions of collagen type I (C group 1.067±0.31, I group 0.579±0.17, I+G group 1.816±0.66, P=0.0009) and type III (C group 0.99±0.28, I group 0.54±0.13, I+G group 1.07±0.28, P=0.0080) were decreased in the I group. Apart from muscle, glutamine supplementation prevented these alterations. Immunohistochemistry and Picro Sirius Red showed similar results. CONCLUSION: Supplementation with l-glutamine seems to prevent bladder wall damage in relation to extracellular matrix volumetric density and collagen expression. These results suggest that glutamine supplementation could be efficient in protecting healthy tissues from the adverse effects of radiotherapy.


Assuntos
Colágeno/metabolismo , Suplementos Nutricionais , Glutamina/uso terapêutico , Músculo Liso , Lesões por Radiação/prevenção & controle , Doenças da Bexiga Urinária/prevenção & controle , Bexiga Urinária/efeitos dos fármacos , Animais , Colágeno/genética , Colágeno/efeitos da radiação , Colágeno Tipo I/genética , Colágeno Tipo I/metabolismo , Colágeno Tipo I/efeitos da radiação , Colágeno Tipo III/sangue , Colágeno Tipo III/genética , Colágeno Tipo III/metabolismo , Colágeno Tipo III/efeitos da radiação , Matriz Extracelular/metabolismo , Matriz Extracelular/efeitos da radiação , Expressão Gênica/efeitos dos fármacos , Glutamina/farmacologia , Músculo Liso/efeitos dos fármacos , Músculo Liso/metabolismo , Músculo Liso/efeitos da radiação , Neoplasias/radioterapia , Lesões por Radiação/etiologia , Lesões por Radiação/metabolismo , Ratos , Ratos Wistar , Valores de Referência , Bexiga Urinária/metabolismo , Bexiga Urinária/efeitos da radiação , Doenças da Bexiga Urinária/etiologia , Doenças da Bexiga Urinária/metabolismo
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