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      Role of vitamin D on the expression of glucose transporters in L6 myotubes

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          Abstract

          Altered expression of glucose transporters is a major characteristic of diabetes. Vitamin D has evolved widespread interest in the pathogenesis and prevention of diabetes. The present study was designed to investigate the effect of vitamin D in the overall regulation of muscle cell glucose transporter expression. L6 cells were exposed to type 1 and type 2 diabetic conditions and the effect of calcitriol (1,25, dihydroxy cholicalciferol) on the expression of glucose transporters was studied by real time polymerase chain reaction (RT-PCR). There was a significant decrease in glucose transporter type 1 (GLUT1), GLUT4, vitamin D receptor (VDR), and IR expression in type 1 and 2 diabetic model compared to control group. Treatment of myoblasts with 10-7 M calcitriol for 24 h showed a significant increase in GLUT1, GLUT4, VDR, and insulin receptor (IR) expression. The results indicate a potential antidiabetic function of vitamin D on GLUT1, GLUT4, VDR, and IR by improving receptor gene expression suggesting a role for vitamin D in regulation of expression of the glucose transporters in muscle cells.

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          Facilitative glucose transporters: regulatory mechanisms and dysregulation in diabetes.

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            Regulation of Glucose Transporters in Diabetes

            It is now widely accepted that insulin stimulates glucose metabolism in its target tissues via recruitment of transporters from a large intracellular pool to the plasma membrane. Recent studies, however, suggest a two-step model for insulin action, of transporter translocation and transporter activation. Data confirming this hypothesis for the first time are presented. It is shown that insulin significantly enhances the intrinsic activity of glucose transporters in human and rat adipose cells, in physiological as well as in diabetic state. The functional activity of transporters is impaired in the diabetic state, but surprisingly, ‘diabetic’ transporters exhibit normal or even enhanced intrinsic activity. In both noninsulin-dependent diabetes mellitus and streptozotocin-diabetic rats, insulin resistance is associated with 50% transporter depletion in the intracellular pool, thus leading to a decreased number of transporters appearing in the plasma membrane in response to insulin. It is concluded that impaired glucose transport in diabetes is secondary (1) to intracellular transporter depletion, and (2) to the presence of inhibitory factors interfering with the full expression of glucose transporters at the plasma membrane, thus contributing to postreceptor insulin resistance.
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              Author and article information

              Journal
              Indian J Endocrinol Metab
              Indian J Endocrinol Metab
              IJEM
              Indian Journal of Endocrinology and Metabolism
              Medknow Publications & Media Pvt Ltd (India )
              2230-8210
              2230-9500
              October 2013
              : 17
              : Suppl1
              : S326-S328
              Affiliations
              [1] Department of Endocrinology, Diabetes and Metabolism, Sri Ramachandra University, Chennai, Tamil Nadu, India
              [1 ] Department of Human Genetics, Sri Ramachandra University, Chennai, Tamil Nadu, India
              Author notes
              Corresponding Author: Dr. Krishna G. Seshadri, Department of Endocrinology, Diabetes and Metabolism, Sri Ramachandra University, Chennai - 600 116, Tamil Nadu, India. E-mail: krishnagseshadri@ 123456gmail.com
              Article
              IJEM-17-326
              10.4103/2230-8210.119642
              3830349
              24251203
              80793274-8792-41fe-9bd1-513fc98daa5a
              Copyright: © Indian Journal of Endocrinology and Metabolism

              This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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              Endocrinology & Diabetes
              diabetes,glucose transporters,vitamin d
              Endocrinology & Diabetes
              diabetes, glucose transporters, vitamin d

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