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1.
Int. braz. j. urol ; 38(4): 552-560, July-Aug. 2012. ilus, tab
Artículo en Inglés | LILACS | ID: lil-649450

RESUMEN

OBJECTIVE: This study was developed to determine whether the generation of free radicals, induced by ischemia followed by reperfusion in a model of chronic intravesical obstruction in rats, would lead to damage in the detrusor. It also investigates the possible protective action of the flavonoid galangin on the tissue lesion induced by lipid peroxidation. MATERIALS AND METHODS: Twenty-one male rats were divided into three groups of seven animals each. Group A was subjected to a sham procedure; group B to partial obstruction of the bladder neck; and group C to partial obstruction of the bladder neck, but also received a diet rich in the flavonoid galangin. All the animals were subjected to urodynamic evaluation and then sacrificed. The bladders were sent for enzymatic tests. RESULTS: The urodynamic showed that group B developed significantly greater numbers of involuntary contractions of the detrusor, greater post-micturition residue and lower compliance. The group A presented TEAC levels greater than to the group B. Comparative analysis of group A, B and C demonstrated significantly greater malondialdehyde levels in group B in relation to groups A and C. The group B presented smaller contraction amplitudes than did groups A and C, in electrically stimulated contractions. CONCLUSIONS: That oxidative stress is implicated in the damage to the detrusor musculature following a period of chronic intravesical obstruction. We show, for the first time, that administration of an antioxidant prior to and following the start of chronic obstruction makes it possible to avoid the cellular lesions that cause detrusor dysfunction.


Asunto(s)
Animales , Masculino , Ratas , Antioxidantes/uso terapéutico , Estrés Oxidativo/fisiología , Obstrucción del Cuello de la Vejiga Urinaria/etiología , Trastornos Urinarios/etiología , Antioxidantes/farmacología , Modelos Animales de Enfermedad , Fenómenos Electrofisiológicos , Flavonoides/administración & dosificación , Contracción Muscular , Malondialdehído/análisis , Mutágenos/administración & dosificación , Urodinámica , Obstrucción del Cuello de la Vejiga Urinaria/fisiopatología , Vejiga Urinaria/enzimología
2.
Int. braz. j. urol ; 36(6): 749-758, Dec. 2010. graf
Artículo en Inglés | LILACS | ID: lil-572403

RESUMEN

PURPOSE: The etiology of obstructive bladder dysfunction includes free radical damage to mitochondria. Feeding rabbits a standardized grape suspension protects the ability of the bladder to contract and empty in part by preventing mitochondrial damage, thus maintaining smooth muscle and mucosal metabolism. The objective of the current study is to determine the direct effect of this grape suspension on the response of mitochondria to the oxidative effects of hydrogen peroxide. MATERIALS AND METHODS: Six male rabbits were anesthetized with sodium pentobarbital and the bladders excised. Four full thickness strips were obtained for contractile studies and the balance separated into smooth muscle and mucosa compartments by blunt dissection. The effect of hydrogen peroxide on the contractile response to field stimulation was quantitated. Each tissue was homogenized and the effects of increasing concentrations of hydrogen peroxide in the presence and absence of grape suspension on citrate synthase activity was determined. RESULTS: Citrate synthase activity was significantly higher in the mucosa than in the muscle. The grape suspension had no effect on control citrate synthase activity. However, the grape suspension provided significant protection of both smooth muscle and mucosal citrate synthase activity. CONCLUSIONS: These studies support the conclusion that the grape suspension provides direct protection of mitochondrial function.


Asunto(s)
Animales , Masculino , Conejos , Citrato (si)-Sintasa/metabolismo , Peróxido de Hidrógeno/farmacología , Mitocondrias/metabolismo , Vejiga Urinaria/efectos de los fármacos , Vitis , Antioxidantes/farmacología , Peróxido de Hidrógeno/efectos adversos , Membrana Mucosa/efectos de los fármacos , Membrana Mucosa/enzimología , Contracción Muscular/efectos de los fármacos , Músculo Liso/efectos de los fármacos , Músculo Liso/enzimología , Obstrucción del Cuello de la Vejiga Urinaria/enzimología , Vejiga Urinaria/enzimología
3.
Journal of Korean Medical Science ; : 1652-1656, 2010.
Artículo en Inglés | WPRIM | ID: wpr-44275

RESUMEN

Ischemia/reperfusion (I/R) injury-induced oxidative stress plays an important role in the functional impairment of the bladder following acute bladder outlet obstruction (BOO) via induction of apoptosis. The purpose of this study was to investigate the time course of the bladder apoptosis, and apoptosis related molecular changes in the early stage of acute BOO. Twelve-week-old male Sprague Dawley rats were divided into control, acute BOO only (I), and acute BOO plus subsequent emptying (I/R) for 30, 60, 120 min, 3 days and 2 weeks. We examined the extent of bladder apoptosis, expression of Mn-superoxide dismutase (Mn-SOD), Bcl-2, Bax, caspase 3 and poly (ADP-ribose) (PAR) in the bladder. Bladder apoptosis was significantly increased in the I/R group at 30, 60, and 120 min following bladder emptying. BOO plus subsequent emptying for 30, 60, 120 min showed significant decrease in MnSOD and Bcl-2 expression, and significant increase in caspase 3, Bax expression, and amounts of PAR. These results indicate that bladder apoptosis, induced by acute BOO and subsequent emptying, is associated with decreased MnSOD expression, increased PARP activity and imbalance in apoptosis pathways.


Asunto(s)
Animales , Masculino , Ratas , Apoptosis , Caspasa 3/metabolismo , Estrés Oxidativo , Poli(ADP-Ribosa) Polimerasas/metabolismo , Proteínas Proto-Oncogénicas c-bcl-2/metabolismo , Ratas Sprague-Dawley , Superóxido Dismutasa/metabolismo , Factores de Tiempo , Vejiga Urinaria/enzimología , Obstrucción del Cuello de la Vejiga Urinaria/enzimología , Proteína X Asociada a bcl-2/metabolismo
4.
P. R. health sci. j ; 13(1): 19-23, mar. 1994.
Artículo en Inglés | LILACS | ID: lil-176771

RESUMEN

Thymidine kinase is a key enzyme responsible for the activation of several anticancer and antiviral drugs. As the first enzyme in the salvage pathway of thymidine, it is regulated by the feedback inhibition exerted by the end-product of the pathway, namely thymidine 5'-triphosphate. 5'-Aminothymidine is a non-toxic analogue of thymidine capable of interfering with this regulatory mechanism. In fact, it has been shown that 5'-aminothymidine increases the cytotoxicity and metabolism of various thymidine analogues currently in use of the clinic as antineoplastic agents. This mini-review article focuses in the evidence supporting the role of 5'-aminothymidine as a potential prototype drug for a new class of anticancer agents: drugs which affect the regulation of key metabolic pathways that determine the efficacy of agents with cytotoxic activity. The mechanism of action, antineoplastic activities and basis for selectivity in tissue culture models are also described


Asunto(s)
Animales , Humanos , Antineoplásicos/farmacología , Timidina Quinasa/metabolismo , Timidina/análogos & derivados , Antineoplásicos/farmacocinética , Antivirales/farmacocinética , Biotransformación/efectos de los fármacos , Células HeLa/efectos de los fármacos , Células HeLa/enzimología , Daño del ADN/efectos de la radiación , Floxuridina/farmacocinética , Idoxuridina/farmacocinética , Idoxuridina/toxicidad , Nucleótidos/antagonistas & inhibidores , Proteínas de Neoplasias/metabolismo , Retroalimentación/efectos de los fármacos , Neoplasias de la Vejiga Urinaria/enzimología , Neoplasias de la Vejiga Urinaria/patología , Vejiga Urinaria/enzimología
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