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1.
Chinese Medical Journal ; (24): 562-569, 2016.
Artigo em Inglês | WPRIM | ID: wpr-328199

RESUMO

<p><b>BACKGROUND</b>Renin-angiotensin system inhibitor and calcium channel blocker (CCB) are widely used in controlling blood pressure (BP) in patients with chronic kidney disease (CKD). We carried out a meta-analysis to compare the renoprotective effect of the combination of angiotensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) and CCB (i.e., ACEI/ARB + CCB) with ACEI/ARB monotherapy in patients with hypertension and CKD.</p><p><b>METHODS</b>Publications were identified from PubMed, Embase, Medline, and Cochrane databases. Only randomized controlled trials (RCTs) of BP lowering treatment for patients with hypertension and CKD were considered. The outcomes of end-stage renal disease (ESRD), cardiovascular events, BP, urinary protein measures, estimated glomerular filtration rate (GFR), and adverse events were extracted.</p><p><b>RESULTS</b>Based on seven RCTs with 628 patients, ACEI/ARB + CCB did not show additional benefit for the incidence of ESRD (risk ratio [RR] = 0.84; 95% confidence interval [CI]: 0.52-1.33) and cardiovascular events (RR = 0.58; 95% CI: 0.21-1.63) significantly, compared with ACEI/ARB monotherapy. There were no significant differences in change from baseline to the end points in diastolic BP (weighted mean difference [WMD] = -1.28 mmHg; 95% CI: -3.18 to -0.62), proteinuria (standard mean difference = -0.55; 95% CI: -1.41 to -0.30), GFR (WMD = -0.32 ml/min; 95% CI: -1.53 to -0.89), and occurrence of adverse events (RR = 1.05; 95% CI: 0.72-1.53). However, ACEI/ARB + CCB showed a greater reduction in systolic BP (WMD = -4.46 mmHg; 95% CI: -6.95 to -1.97), compared with ACEI/ARB monotherapy.</p><p><b>CONCLUSION</b>ACEI/ARB + CCB had no additional renoprotective benefit beyond than what could be achieved with ACEI/ARB monotherapy.</p>


Assuntos
Humanos , Antagonistas de Receptores de Angiotensina , Farmacologia , Usos Terapêuticos , Inibidores da Enzima Conversora de Angiotensina , Farmacologia , Usos Terapêuticos , Bloqueadores dos Canais de Cálcio , Farmacologia , Usos Terapêuticos , Quimioterapia Combinada , Taxa de Filtração Glomerular , Hipertensão , Tratamento Farmacológico , Rim , Insuficiência Renal Crônica , Tratamento Farmacológico
2.
National Journal of Andrology ; (12): 755-760, 2005.
Artigo em Chinês | WPRIM | ID: wpr-339433

RESUMO

<p><b>OBJECTIVE</b>To screen the stage-specific expression proteins during rats spermatogenesis, and to investigate the beta-actin expression and localization in the tissues of rat testicular.</p><p><b>METHODS</b>Highly enriched type A spermatogonia, pachytene spermatocytes and round spermatids were isolated by STAPUT method (sedimentation velocity at unit gravity, with 2% - 4% BSA gradient in DMEM/F12 medium) respectively to get the total proteins. The difference of protein expression between the three kinds of cells was analyzed by two-dimensional electrophoresis. Then the distribution of beta-actin in rat testicular tissues was investigated using specific anti-beta-actin antibodies by immunohistochemical method.</p><p><b>RESULTS</b>beta-actin was identified as a stage-specific expression protein by two-dimensional electrophoresis. beta-actin protein was more strongly expressed in type A spermatogonia and pachytene spermatocytes, but not in round spermatids. The immunohistochemical results showed that beta-actin was mainly located in the cytoplasm of type A spermatogonia and pachytene spermatocytes and in the nuclei of nearly mature spermatids.</p><p><b>CONCLUSION</b>beta-actin protein is a stage-specific expressed protein and may play an important role in spermatogenesis.</p>


Assuntos
Animais , Masculino , Ratos , Actinas , Eletroforese em Gel Bidimensional , Espectrometria de Massas , Ratos Sprague-Dawley , Espermatogênese , Fisiologia , Testículo , Biologia Celular , Metabolismo
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