Protective effects of erythropoietin against cuprizone-induced oxidative stress and demyelination in the mouse corpus callosum

  • سال انتشار: 1396
  • محل انتشار: مجله علوم پایه پزشکی ایران، دوره: 20، شماره: 8
  • کد COI اختصاصی: JR_IJBMS-20-8_007
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 377
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نویسندگان

Iraj Ragerdi Kashani

Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Hossein Chavoshi

Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Parichehr Pasbakhsh

Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Mahmoud Hassani

Department of Medical Nanotechnologies, School of Advanced Technologies, Tehran University of Medical Sciences, Tehran, Iran

Ameneh Omidi

Department of Anatomical Sciences, Medical Sciences Faculty, Tarbiat Modares University, Tehran, Iran

Reza Mahmoudi

Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran

Cordian Beyer

Faculty of Medicine, Institute of Neuroanatomy, RWth Aachen University, Aachen, Germany

Adib Zendedel

Faculty of Medicine, Institute of Neuroanatomy, RWth Aachen University, Aachen, Germany

چکیده

Objective(s): Increasing evidence in both experimental and clinical studies suggests that oxidative stress plays a major role in the pathogenesis of multiple sclerosis. The aim of the present work is to investigate the protective effects of erythropoietin against cuprizone-induced oxidative stress. Materials and Methods: Adult male C۵۷BL/۶J mice were fed a chow containing ۰.۲ % cuprizone for ۶ weeks. After ۳ weeks, mice were simultaneously treated with erythropoietin (۵,۰۰۰ IU/ kg body weight) by daily intraperitoneal injections. Results: Our results showed that cuprizone induced oxidative stress accompanied with down-regulation of subunits of the respiratory chain complex and demyelination of corpus callosum. Erythropoietin antagonized these effects. Biochemical analysis showed that oxidative stress induced by cuprizone was regulated by erythropoietin. Similarly, erythropoietin induced the expression of subunits of the respiratory chain complex over normal control values reflecting a mechanism to compensate cuprizone-mediated down-regulation of these genes. Conclusion: The data implicate that erythropoietin abolishes destructive cuprizone effects in the corpus callosum by decreasing oxidative stress and restoring mitochondrial respiratory enzyme activity.

کلیدواژه ها

Cuprizone, Demyelination, Erythropoietin, Multiple Sclerosis, Oxidative stress

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