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
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