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Nephron ; 129(2): 137-42, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25634142

RESUMO

BACKGROUND/AIMS: Long-term kidney affections after sepsis are poorly understood. Animal models for investigating kidney damage in the late phase of disease progression are limited. The aim of this study was to investigate the impact of two antibiotic regimes on persistence of kidney injury after peritonitis. METHODS: Kidney damage was investigated 65 days after polymicrobial peritoneal contamination and infection (PCI) sepsis induction in C57BL/6 mice. Short-term antibiotic therapy (STA, 4 days) was compared to long-term (LTA, 10 days) treatment using plasma creatinine, plasma and urine neutrophil gelatinase-associated lipocalin (NGAL), urine albumin/creatinine ratio and renal histology. RESULTS: Sepsis resulted in mortality rates of 68.2% (STA) and 61.0% (LTA). Surviving STA animals showed the most pronounced kidney damage indicated by significantly elevated levels of creatinine and acute tubular damage (ATD), whereas NGAL was significantly increased in LTA survivors only. A creatinine level above 0.3 mg/dl was used to define kidney injury, found in 21.4% of STA animals and 7.8% of LTA animals. While animals with kidney injury demonstrated significantly higher ATD scores and persistent tubular damage, no significant differences were found for plasma or urine NGAL levels or urine albumin/creatinine ratios. CONCLUSION: Prolonged antibiotic treatment reduced the rate of ongoing peritonitis-induced kidney injury in a C57BL/6 mouse model. Plasma or urine NGAL levels were not able to identify animals with or without persistent kidney injury. The kidney injury after the PCI mouse model represents prototypic clinical findings and should be used for further studies investigating disease mechanisms.


Assuntos
Injúria Renal Aguda/etiologia , Antibacterianos/uso terapêutico , Coinfecção/complicações , Coinfecção/tratamento farmacológico , Cavidade Peritoneal/microbiologia , Sepse/complicações , Sepse/tratamento farmacológico , Injúria Renal Aguda/microbiologia , Injúria Renal Aguda/patologia , Proteínas de Fase Aguda/metabolismo , Animais , Infecções Bacterianas/complicações , Infecções Bacterianas/tratamento farmacológico , Infecções Bacterianas/microbiologia , Biomarcadores/metabolismo , Coinfecção/microbiologia , Rim/patologia , Rim/fisiopatologia , Testes de Função Renal , Túbulos Renais/patologia , Lipocalina-2 , Lipocalinas/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Modelos Animais , Proteínas Oncogênicas/metabolismo , Sepse/microbiologia
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