Title of article :
Pre-Treatment with Erythropoietin Attenuates Bilateral Renal Ischemia- Induced Cognitive Impairments
Author/Authors :
Tahamtan, Mahshid Intracellular Recording Lab, Kerman Neuroscience Research Center - Neuropharmacology Institute - Kerman University of Medical Sciences, Kerman, Iran , Sheibani, Vahid Intracellular Recording Lab, Kerman Neuroscience Research Center - Neuropharmacology Institute - Kerman University of Medical Sciences, Kerman, Iran , Shid Moosavi, Mostafa Physiology Department - Shiraz University of Medical Sciences, Shiraz, Iran , Asadi-Shekaari, Majid Intracellular Recording Lab, Kerman Neuroscience Research Center - Neuropharmacology Institute - Kerman University of Medical Sciences, Kerman, Iran , Esmaeili-Mahani, Saeed Intracellular Recording Lab, Kerman Neuroscience Research Center - Neuropharmacology Institute - Kerman University of Medical Sciences, Kerman, Iran , Aghaei, Iraj Department of Neuroscience - Neuroscience Research Center - Poursina Hospital - Guilan University of Medical Sciences, Rasht, Iran , Shabani, Mohammad Intracellular Recording Lab, Kerman Neuroscience Research Center - Neuropharmacology Institute - Kerman University of Medical Sciences, Kerman, Iran
Pages :
12
From page :
601
To page :
612
Abstract :
One of the most common causes of mortality in acute kidney injury is brain dysfunction. Here we investigated the possible protective effect of erythropoietin (EPO) on cognitive impairments induced by bilateral renal ischemia (BRI). Eighty male Wistar rats were allocated into 8 groups: 1, 2) Sham +V (Vehicle), 3, 4) Sham+EPO, 5, 6) BRI+V, 7, 8) BRI+EPO. The groups followed by the reperfusion periods of 24hours (24 h) and 1week (1w). EPO or saline was administrated 30 min before surgery (1000 IU/kg, i.p). The cognitive function was assessed by passive avoidance learning and Morris water maze tests. Hippocampal brain-derived neurotrophic factor (BDNF) protein expression was assessed by western blotting. BUN (blood urea nitrogen) and creatinine (Cr) concentrations were significantly increased in BRI+V group 24 h after reperfusion. BRI+V rats had just an increased level of BUN but not Cr 1w after reperfusion. EPO reversed passive avoidance learning impairments observed in BRI+V group 24 h after reperfusion. There were no significant differences in spatial and passive avoidance learning between experimental groups 1w after reperfusion and histological evaluation confirmed the behavioral data. BRI significantly decreased the BDNF protein expression in the hippocampus and EPO increased that 24 h after operation. These observations showed protective effect of EPO against cognitive dysfunctions following BRI 24 h after reperfusion through increase in BDNF protein expression.
Keywords :
Memory , Cognitive Impairments , Erythropoietin , Bilateral Renal Ischemia , Acute Kidney Injury
Journal title :
Astroparticle Physics
Serial Year :
2018
Record number :
2416826
Link To Document :
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