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Métodos Terapéuticos y Terapias MTCI
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1.
Hum Exp Toxicol ; 33(4): 383-95, 2014 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-24107454

RESUMEN

The aim of this study was to evaluate the acute effect of high-dose acetylsalicylic acid (ASA) on kidney and testis, and the potential protective and therapeutic effects of melatonin on ASA-related pathology. A total of 40 rats were randomly divided into the following 5 groups (n = 8): group 1: control, not given any drug; group 2: only 200 mg/kg ASA was given; group 3: 5 mg/kg melatonin was given 45 min before administering 200 mg/kg ASA; group 4: 5 mg/kg melatonin was given 45 min after administering 200 mg/kg ASA; and group 5: only 5 mg/kg melatonin was given. The histopathological changes and the biochemical findings; such as malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), reduced glutathione (GSH), and blood urea nitrogen (BUN) as well as serum creatinine (Cr) levels were evaluated. ASA significantly increased MDA levels in both kidney and testis, whereas it significantly decreased the values of SOD, CAT, GPX, and GSH in kidney and CAT levels in testis. Melatonin significantly decreased MDA levels in kidney and ameliorated it in testis, whereas it caused elevation in the levels of antioxidants. BUN and Cr levels were higher after ASA, whereas these levels were diminished after melatonin administration. The improvement obtained by melatonin on ASA-induced histological alterations was more prominent when it was used after ASA in kidney and before ASA in testis. In this study, we demonstrated the beneficial effect of melatonin on high-dose ASA-related pathology of kidney and testis for the first time.


Asunto(s)
Aspirina/farmacología , Riñón/efectos de los fármacos , Melatonina/farmacología , Testículo/efectos de los fármacos , Animales , Nitrógeno de la Urea Sanguínea , Peso Corporal/efectos de los fármacos , Catalasa/metabolismo , Creatina/sangre , Glutatión/metabolismo , Glutatión Peroxidasa/metabolismo , Riñón/enzimología , Riñón/metabolismo , Riñón/patología , Masculino , Malondialdehído/metabolismo , Tamaño de los Órganos/efectos de los fármacos , Ratas , Ratas Wistar , Superóxido Dismutasa/metabolismo , Testículo/enzimología , Testículo/metabolismo , Testículo/patología
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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