Effect of Long-term Administration of Oral Magnesium Sulfate and Insulin to Reduce Streptozotocin-Induced Hyperglycemia in Rats: the Role of Akt2 and IRS1 Gene Expressions

(2019) Effect of Long-term Administration of Oral Magnesium Sulfate and Insulin to Reduce Streptozotocin-Induced Hyperglycemia in Rats: the Role of Akt2 and IRS1 Gene Expressions. Biological Trace Element Research. pp. 396-404. ISSN 0163-4984

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Official URL: WOS:000473414000013

Abstract

The effects of long-term oral administration of magnesium sulfate and insulin on hyperglycemia were investigated using Akt2 and IRS1 gene expression methods in streptozotocin-induced diabetic rats. Fifty rats were randomly divided into five experimental groups: 1, non-diabetic control (NDC); 2, Mg2+-treated non-diabetic control (Mg-NDC); 3, chronic diabetic (CD); 4, Mg2+-treated chronic diabetic (Mg-CD); and 5, insulin-treated chronic diabetic (Ins-CD). Streptozotocin was used to induce diabetes. The Mg-CD and Mg-NDC groups received 10g/l of MgSO4 added to drinking water. The Ins-CD group received 2.5U/kg of insulin twice a day. Blood glucose level and body weight were measured every week. The intraperitoneal glucose tolerance test (IPGTT) was performed after 16weeks. MgSO4 administration improved the blood glucose level and IPGTT. It also increased Akt2 and IRS1 genes as well as protein expression. Insulin lowered the blood glucose level and increased IRS1 gene and protein expression, but did not affect Akt2 gene and protein expression. Glucose reduction after Mg therapy may be mediated, at least partially, via IRS1 and Akt2 genes and protein stimulation. In insulin-treated rats, insulin resistance was not significant due to the absence of Akt2 gene expression.

Item Type: Article
Keywords: Diabetes Magnesium Insulin Akt2 IRS1 akt/protein-kinase-b diabetes-mellitus glut4 expression glucose-uptake up-regulation mice lacking double-blind resistance muscle sensitivity Biochemistry & Molecular Biology Endocrinology & Metabolism
Subjects: WD Disorders of Systemic, Metabolic or Environmental Origin, etc.
Divisions: Faculty of Medicine > Department of Basic Science > Department of Physiology
Faculty of Medicine > Departments of Clinical Sciences > Department of Pathology
Page Range: pp. 396-404
Journal or Publication Title: Biological Trace Element Research
Journal Index: ISI
Volume: 190
Number: 2
Identification Number: https://doi.org/10.1007/s12011-018-1555-z
ISSN: 0163-4984
Depositing User: Zahra Otroj
URI: http://eprints.mui.ac.ir/id/eprint/11147

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