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Ren Fail ; 38(7): 1089-98, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27309733

ABSTRACT

Contrast induced nephropathy (CIN) is a major cause of morbidity, and increased costs as well as an increased risk of death. This study was evaluated effects of exogenous sphingosylphosphorylcholine (SPC) administration on CIN in rats. Eight animals were included in each of the following eight groups: control, control phosphate-buffered solution (PBS), control SPC 2, control SPC 10, CIN, CIN PBS, CIN SPC 2 and CIN SPC 10. The induced nephropathy was created by injected with 4 g iodine/kg body weight. SPC was administered 3 d at a daily two different doses of 2 µm/mL and 10 µm/mL intraperitoneally. The severity of renal injury score was determined by the histological and immunohistochemical changes in the kidney. Malondialdehyde (MDA), nitric oxide (NO) and superoxide dismutase (SOD) were determined to evaluate the oxidative status in the renal tissue. Treatment with 2 and 10 µM SPC inhibited the increase in renal MDA, NO levels significantly and also attenuated the depletion of SOD in the renal injuryCIN. These data were supported by histopathological findings. The inducible nitric oxide synthase positive cells and apoptotic cells in the renal tissue were observed to be reduced with the 2 and 10 µM SPC treatment. These findings suggested that 2 and 10 µM doses can attenuate renal damage in contrast nephropathy by prevention of oxidative stress and apoptosis. The low and high dose SPC may be a promising new therapeutic agent for CIN.


Subject(s)
Acute Kidney Injury/chemically induced , Acute Kidney Injury/drug therapy , Antioxidants/therapeutic use , Contrast Media/adverse effects , Kidney/drug effects , Phosphorylcholine/analogs & derivatives , Sphingosine/analogs & derivatives , Animals , Antioxidants/administration & dosage , Apoptosis/drug effects , Creatinine/blood , Humans , Injections, Intraperitoneal , Kidney/metabolism , Kidney/pathology , Malondialdehyde/metabolism , Nitric Oxide/metabolism , Nitric Oxide Synthase Type II/metabolism , Oxidative Stress/drug effects , Phosphorylcholine/administration & dosage , Phosphorylcholine/therapeutic use , Rats , Rats, Wistar , Sphingosine/administration & dosage , Sphingosine/therapeutic use , Superoxide Dismutase/metabolism
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