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Sci Rep ; 9(1): 7090, 2019 05 08.
Article in English | MEDLINE | ID: mdl-31068635

ABSTRACT

Glycerol injection in rats can lead to rhabdomyolysis, with the release of the intracellular muscle content to the extracellular compartment and acute kidney injury (AKI). Oxidative stress and the inflammatory processes contribute to the disturbances in renal function and structure observed in this model. This study evaluated the effect of calcitriol administration in AKI induced by rhabdomyolysis and its relationship with oxidative damage and inflammatory process. Male Wistar Hannover rats were treated with calcitriol (6 ng/day) or vehicle (0.9% NaCl) for 7 days and were injected with 50% glycerol or saline 3 days after the beginning of calcitriol or saline administration. Four days after glycerol or saline injection, urine, plasma and renal tissue samples were collected for renal function and structural analysis. The oxidative stress and the inflammatory processes were also evaluated. Glycerol-injected rats presented increased sodium fractional excretion and decreased glomerular filtration rates. These alterations were associated with tubular injury in the renal cortex. These animals also presented increased oxidative damage, apoptosis, inflammation, higher urinary excretion of vitamin D-binding protein and decreased cubilin expression in renal tissue. All these alterations were less intense in calcitriol-treated animals. This effect was associated with decreases in oxidative damage and inflammation.


Subject(s)
Acute Kidney Injury/drug therapy , Acute Kidney Injury/etiology , Calcitriol/therapeutic use , Glycerol/pharmacology , Protective Agents/therapeutic use , Rhabdomyolysis/chemically induced , Rhabdomyolysis/complications , Acute Kidney Injury/blood , Acute Kidney Injury/urine , Animals , Apoptosis/drug effects , Calcitriol/pharmacology , Calcium/blood , Creatine Kinase/blood , Glomerular Filtration Rate/drug effects , Inflammation/drug therapy , Kidney Function Tests , Male , Oxidative Stress/drug effects , Protective Agents/pharmacology , Rats , Rats, Wistar , Vitamin D-Binding Protein/urine
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