Title of article
High glucose condition down-regulates the inhibitory G-protein subunit, Gαi, in pheochromocytoma PC12 cells
Author/Authors
اسماعيلي ماهاني، سعيد نويسنده گروه زيست شناسي، دانشگاه شهيد باهنر كرمان , , حاج عليزاده، زهرا نويسنده Laboratory of Molecular Neuroscience, Kerman Neuroscience Research Center, Kerman University of Medical Sciences, Kerman, Iran Hajializadeh, Zahra , تركزاده ماهاني، شيما نويسنده دانشيار، گروه زيستشناسي، دانشگاه پيام نور، واحد تهران، تهران و آزمايشگاه مولكولي، مركز تحقيقات علوم اعصاب، دانشگاه علوم پزشكي كرمان، كرمان، ايران Torkzadeh-Mahani , Shima
Issue Information
فصلنامه با شماره پیاپی 0 سال 2016
Pages
7
From page
239
To page
245
Abstract
Introduction: G-proteins have an important role in the cell signaling of numerous receptors. The situation of G-proteins in health and disease and their critical role in the development of diabetic side effects is an interested scientific field. Here, the changes in the expression of G-protein subunits (G?i, G?s and GB) were evaluated in hyperglycemic situation of PC12 cells as a cellular model for the induction of diabetic side effect.
Methods: Rat pheochromocytoma PC12 cells were grown in normal or high-glucose (4X normal glucose) medium. Cell viability was determined by MTT assay and the generation of intracellular reactive oxygen species (ROS) studied using fluorescence spectrophotometry. RT-PCR and immunobloting were performed to evaluate the expression of specific G-protein subunits in the levels of mRNA and protein, respectively.
Results: In high glucose condition (100 mM glucose for 48h), the cell viability was significantly decreased and intracellular ROS increased. In addition, G?i expression level was significantly decreased in hyperglycemic PC12 cells. However, the levels of G?s and GB mRNAs and their proteins were not altered in high glucose-treated cells.
Conclusion: The results demonstrate that deregulation or disruption in the signaling of Gai coupled receptors can be occurred in hyperglycemic condition.
Journal title
Physiology and Pharmacology
Serial Year
2016
Journal title
Physiology and Pharmacology
Record number
2399028
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