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Erythropoietin attenuates motor impairments induced by bilateral renal ischemia/reperfusion in rats.
Tahamtan, Mahshid; Moosavi, Seyed M S; Sheibani, Vahid; Nayebpour, Mohsen; Esmaeili-Mahani, Saeed; Shabani, Mohammad.
Afiliação
  • Tahamtan M; Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.
  • Moosavi SM; Department of Physiology, The Medical School, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Sheibani V; Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.
  • Nayebpour M; Pouyesh Darou Product Company, Tehran, Iran.
  • Esmaeili-Mahani S; Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran.
  • Shabani M; Department of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran.
Fundam Clin Pharmacol ; 30(6): 502-510, 2016 Dec.
Article em En | MEDLINE | ID: mdl-27473027
Neurologic sequelae remain a common and destructive problem in patients with acute kidney injury. The objective of this study was to evaluate the possible neuroprotective effect of erythropoietin (EPO) on motor impairments following bilateral renal ischemia (BRI) in two time points after reperfusion: short term (24 h) and long term (1 week). Male Wistar rats underwent BRI or sham surgery. EPO or saline administration was performed 30 min before surgery (1000 U/kg, i.p.). Explorative behaviors and motor function of the rats were evaluated by open field, rotarod, and wire grip tests. Plasma concentrations of blood urea nitrogen (BUN) and creatinine (Cr) were significantly enhanced in BRI rats 24 h after reperfusion. BRI group had only an increased level of BUN but not Cr 1 week after reperfusion. Impairment of balance function by BRI was not reversed by EPO 24 h after reperfusion, but counteracted 7 days after renal ischemia. Muscle strength had no significant differences between the groups. BRI group had a decrease in locomotor activity, and EPO could not reverse this reduction in both time points of the experiment. Although EPO could not be offered as a potential neuroprotective agent in the treatment of motor dysfunctions induced by BRI, it could be effective against balance dysfunction 1 week after renal ischemia.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão / Eritropoetina / Fármacos Neuroprotetores / Força Muscular / Transtornos Motores / Locomoção Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão / Eritropoetina / Fármacos Neuroprotetores / Força Muscular / Transtornos Motores / Locomoção Limite: Animals Idioma: En Ano de publicação: 2016 Tipo de documento: Article