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   Fluoxetin Upregulates Connexin 43 Expression in Astrocyte  
   
نویسنده Mostafavi Hossein ,Khaksarian Mojtaba ,Joghataei Mohammad Taghi ,Hassanzadeh Gholamreza ,Soleimani Masoud ,Eftekhari Sanaz ,Soleimani Mansooreh ,Mousavizadeh Kazem ,Hadjighassem Mahmoud Reza
منبع Basic And Clinical Neuroscience - 2014 - دوره : 5 - شماره : 1 - صفحه:74 -79
چکیده    Introduction: recent studies have shown that astrocytes play major roles in normal and disease condition of the central nervous system including multiple sclerosis (ms). molecular target therapy studies in ms have revealed that connexin-43 (cx43) and aquaporin-4 (aqp4) contents of astrocytes undergo expression alteration. fluoxetine had some effects in ms patients unrelated to its known antidepressant effects. some of fluoxetine effects were attributed to its capability of camp signaling pathway stimulation. this study aimed to investigate possible acute effects of fluoxetine on cx43 and aqp4 expression in astrocyte. methods: astrocytoma cells were treated for 24 hours with fluoxetine (10 and 20 μg/ml) with or without adenyl cyclase (ac) and protein kinase a (pka) inhibition. cx43 expression at both mrna and protein levels and aqp4 expression at mrna level were evaluated. results: acquired results showed that fluoxetine with and without ac and pka inhibition resulted in cx43 up-regulation both in mrna and protein levels,whereas aqp4 expression have not changed. discussion: in conclusion,data showed that fluoxetine alone and in the absence of serotonin acutely up-regulated cx43 expression in astrocytes that can be assumed in molecular target therapy of ms patients. it seems that camp involvement in fluoxetine effects need more researches.
کلیدواژه Aquaporin-4; Astrocyte; Camp; Connexin-43; Fluoxetine
آدرس Tehran University Of Medical Sciences Tums, School Of Advanced Medical Technologies, Department Of Neuroscience, ایران. Iran University Of Medical Sciences, Cellular And Molecular Research Center, Division Of Neuroscience, ایران. Stem Cell Technology Research Center, Molecular Biology And Genetic Engineering Department, ایران. Zanjan University Of Medical Sciences, Department Of Physiology And Pharmacology, ایران, Tehran University Of Medical Sciences Tums, School Of Advanced Medical Technologies, Department Of Neuroscience, ایران. Stem Cell Technology Research Center, Molecular Biology And Genetic Engineering Department, ایران. Lorestan University Of Medical Sciences, Department Of Physiology, ایران, Tehran University Of Medical Sciences Tums, School Of Advanced Medical Technologies, Department Of Neuroscience, ایران. Iran University Of Medical Sciences, Cellular And Molecular Research Center, Division Of Neuroscience, ایران, Tehran University Of Medical Sciences Tums, School Of Medicine, Department Of Anatomy, ایران, Tarbiat Modares University, Department Of Hematology, ایران, Tehran University Of Medical Sciences Tums, School Of Advanced Medical Technologies, Department Of Neuroscience, ایران. Iran University Of Medical Sciences, Cellular And Molecular Research Center, Division Of Neuroscience, ایران, Iran University Of Medical Sciences, Cellular And Molecular Research Center, Division Of Neuroscience, ایران, Iran University Of Medical Sciences, Cellular And Molecular Research Center, Division Of Neuroscience, Department Of Basic Medical Sciences, ایران, Tehran University Of Medical Sciences Tums, School Of Advanced Medical Technologies, Brain And Spinal Cord Injury Research Center, Neuroscience Institute, Department Of Neuroscience, ایران. Iran University Of Medical Sciences, Cellular And Molecular Research Center, Division Of Neuroscience, ایران
پست الکترونیکی mhadjighassem@tums.ac.ir
 
     
   
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