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1.
Clin Sci (Lond) ; 132(18): 2071-2085, 2018 09 28.
Artigo em Inglês | MEDLINE | ID: mdl-29959186

RESUMO

Congenital urinary tract obstruction is one of the most frequent malformations in fetuses or neonates, which usually causes profound impairment of renal function including reductions in both glomerular filtration rate (GFR) and tubular handling of water and solutes. Although obstruction can be released by surgical operation, the child will suffer from diuresis for sometime. It has been reported that erythropoietin (EPO) could prevent the down-regulation of aquaporin-2 (AQP2) and urinary-concentrating defects induced by renal ischemia/reperfusion (I/R) injury. However, whether EPO could promote the recovery of renal function and AQP2 expression after releasing of ureteral obstruction has not been reported yet. The purposes of the present study were to investigate the effects of EPO on renal function and AQP2 expression after release of bilateral ureteral obstruction (BUO-R) in rats. The results showed that EPO could promote interleukin (IL) 10 (IL-10) expression; inhibit tumor necrosis factor-α (TNF-α), IL-6, and inducible nitric oxide synthase (iNOS) expressions; reduce the fractional excretion of sodium (FENa) and plasma creatinine (CREA) and urea; and promote the recovery of water and salt handling and AQP2 expression in BUO-R rats, especially in the high dose of EPO-treated group rats. In conclusion, EPO could promote the recovery of renal function and AQP2 expression in BUO-R rats, which may partially associate with its anti-inflammation effect.


Assuntos
Modelos Animais de Doenças , Eritropoetina/farmacologia , Rim/efeitos dos fármacos , Obstrução Ureteral/fisiopatologia , Animais , Aquaporina 2/genética , Aquaporina 2/metabolismo , Taxa de Filtração Glomerular/efeitos dos fármacos , Humanos , Rim/metabolismo , Rim/fisiopatologia , Masculino , Substâncias Protetoras/farmacologia , Ratos Sprague-Dawley , Traumatismo por Reperfusão/metabolismo , Traumatismo por Reperfusão/fisiopatologia , Obstrução Ureteral/genética , Obstrução Ureteral/metabolismo
2.
Urol Int ; 87(4): 429-33, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22057293

RESUMO

OBJECTIVE: To summarize the clinical features and follow-up, the effects of melamine-tainted milk powder (MMP) consumption on kidney and body growth in children who suffered from melamine-related urinary stones (MUS) 2 years earlier were checked. MEASUREMENTS: Body height and weight, kidney and bladder morphology monitored by ultrasound, urinalysis and renal function were recorded. Plain abdominal radiography was performed for differential diagnosis. The first follow-up was carried out at 15 months and the second 2 years later for patients who showed any abnormality at the first follow-up. Two hundred age- and gender-matched cohorts were included. RESULTS: All cases received conservative treatment in hospital. Fifteen months of follow-up was successfully carried out in 167 cases. 91 children had residual MUS at the time of discharge, 58 MUS disappeared completely, 25 dissolved partially, 1 increased in size, and 7 did not change. At 2 years of follow-up, the residual stones all disappeared except for 1 case; the patient who showed a delayed development with regard to height caught up at 24 months of follow-up. CONCLUSIONS: Conservative treatment shows a high effectiveness in cases with residual MUS. Consumption of MMP with timely treatment did not demonstrate an evident impact on kidney and bladder although body height is slightly affected in a few cases.


Assuntos
Contaminação de Alimentos , Fórmulas Infantis , Triazinas/efeitos adversos , Cálculos Urinários/induzido quimicamente , Estatura , Estudos de Casos e Controles , Distribuição de Qui-Quadrado , Desenvolvimento Infantil , Pré-Escolar , China , Feminino , Seguimentos , Humanos , Lactente , Rim/crescimento & desenvolvimento , Masculino , Prognóstico , Radiografia , Indução de Remissão , Fatores de Tempo , Bexiga Urinária/crescimento & desenvolvimento , Cálculos Urinários/diagnóstico por imagem , Cálculos Urinários/fisiopatologia , Cálculos Urinários/terapia
4.
Neurourol Urodyn ; 28(5): 423-6, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19012298

RESUMO

OBJECTIVE: To evaluate the effect of familial aggregation on the children with PNE by evaluating nocturnal urine output, bladder, and arouse function. PATIENTS AND METHODS: According to whether relatives of family of probands over three generations were affected by PNE, forty-five children with familial aggregation PNE (FPNE), seventy children with sporadic PNE (SPNE) and ten children with normal lower urinary tract function but waiting for operation (control group) were included. Questionnaire of arousal from sleep (AS scores), bladder diary and daytime urodynamic studies were performed in all patients. RESULTS: The incidences of severe PNE and nonmonosymptomatic PNE in FPNE group were significantly higher than those in SPNE group. The nocturnal urine output and AS scores in both PNE groups was significantly higher, maximal voided volume significantly smaller than those in control group. Moreover, the incidences of small bladder in FPNE group was 44%, significantly higher than that in SPNE group (21%), but no significantly difference was found in nocturnal polyuria and arousal AS scores between two PNE groups. There were 53% patents with daytime detrusor overactivity and 60% patents with urodynamic functional bladder outflow obstruction in FPNE group, significantly higher than those in SPNE group (19% and 37%). Maximum cystometric capacity significantly decreased from control group to FPNE group. CONCLUSION: Familial aggregation has significant effects on the children with PNE, and FPNE are more likely to be severe symptoms and bladder dysfunction. It would be beneficial to have an urodynamic study for their diagnosis and treatment. Neurourol. Urodynam. 28:423-426, 2009. (c) 2008 Wiley-Liss, Inc.


Assuntos
Nível de Alerta , Enurese Noturna/genética , Sono , Bexiga Urinária/fisiopatologia , Urodinâmica , Adolescente , Estudos de Casos e Controles , Criança , Feminino , Predisposição Genética para Doença , Humanos , Masculino , Enurese Noturna/diagnóstico , Enurese Noturna/fisiopatologia , Linhagem , Fatores de Risco , Índice de Gravidade de Doença , Inquéritos e Questionários
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