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Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat
BACKGROUND: Gamma-aminobutyric acid (GABA) and magnesium sulfate (MgSO(4)) play a crucial role in glycemic control. Therefore, we studied the effect of combination therapy with GABA and MgSO(4) to improve insulin sensitivity in diabetes induced by streptozotocin as well as high-fat diet in a diabeti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863457/ https://www.ncbi.nlm.nih.gov/pubmed/35211170 http://dx.doi.org/10.1155/2022/2144615 |
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author | Sohrabipour, Shahla Sharifi, Mohammad Reza Sharifi, Mohammadreza Talebi, Ardeshir Soltani, Nepton |
author_facet | Sohrabipour, Shahla Sharifi, Mohammad Reza Sharifi, Mohammadreza Talebi, Ardeshir Soltani, Nepton |
author_sort | Sohrabipour, Shahla |
collection | PubMed |
description | BACKGROUND: Gamma-aminobutyric acid (GABA) and magnesium sulfate (MgSO(4)) play a crucial role in glycemic control. Therefore, we studied the effect of combination therapy with GABA and MgSO(4) to improve insulin sensitivity in diabetes induced by streptozotocin as well as high-fat diet in a diabetic rat model. Design and Methods. Forty randomly selected rats were assigned to four groups: nondiabetic control group was fed the normal diet, insulin-resistant diabetic rat model was induced by streptozotocin and high-fat diet, GABA + MgSO(4) group received GABA and MgSO(4), and insulin group was treated with insulin. Body weight, abdominal fat, blood glucose, serum insulin, and glucagon concentration were measured. The glucose clamp technique, glucose tolerance test, and insulin tolerance test were performed to study insulin sensitivity. Also, the expressions of glucose 6 phosphatase, glucagon receptor, and phosphoenolpyruvate carboxykinase genes in liver were assessed for the gluconeogenesis pathway. Protein translocation and glucose transporter 4 (Glut4) genes expression in muscle were also assessed. RESULTS: Combination of GABA + MgSO(4) or insulin therapy enhanced insulin level, glycemic control, glucose and insulin tolerance test, some enzymes expression in the gluconeogenesis pathway, body fat, body weight, and glucagon receptor in diabetic rats. Moreover, an increase was observed in protein and gene expression of Glut4. Insulin sensitivity in combination therapy was more than the insulin group. CONCLUSIONS: GABA and MgSO(4) enhanced insulin sensitivity via increasing Glut4 and reducing the gluconeogenesis enzyme and glucagon receptor gene expressions. |
format | Online Article Text |
id | pubmed-8863457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-88634572022-02-23 Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat Sohrabipour, Shahla Sharifi, Mohammad Reza Sharifi, Mohammadreza Talebi, Ardeshir Soltani, Nepton Int J Endocrinol Research Article BACKGROUND: Gamma-aminobutyric acid (GABA) and magnesium sulfate (MgSO(4)) play a crucial role in glycemic control. Therefore, we studied the effect of combination therapy with GABA and MgSO(4) to improve insulin sensitivity in diabetes induced by streptozotocin as well as high-fat diet in a diabetic rat model. Design and Methods. Forty randomly selected rats were assigned to four groups: nondiabetic control group was fed the normal diet, insulin-resistant diabetic rat model was induced by streptozotocin and high-fat diet, GABA + MgSO(4) group received GABA and MgSO(4), and insulin group was treated with insulin. Body weight, abdominal fat, blood glucose, serum insulin, and glucagon concentration were measured. The glucose clamp technique, glucose tolerance test, and insulin tolerance test were performed to study insulin sensitivity. Also, the expressions of glucose 6 phosphatase, glucagon receptor, and phosphoenolpyruvate carboxykinase genes in liver were assessed for the gluconeogenesis pathway. Protein translocation and glucose transporter 4 (Glut4) genes expression in muscle were also assessed. RESULTS: Combination of GABA + MgSO(4) or insulin therapy enhanced insulin level, glycemic control, glucose and insulin tolerance test, some enzymes expression in the gluconeogenesis pathway, body fat, body weight, and glucagon receptor in diabetic rats. Moreover, an increase was observed in protein and gene expression of Glut4. Insulin sensitivity in combination therapy was more than the insulin group. CONCLUSIONS: GABA and MgSO(4) enhanced insulin sensitivity via increasing Glut4 and reducing the gluconeogenesis enzyme and glucagon receptor gene expressions. Hindawi 2022-02-15 /pmc/articles/PMC8863457/ /pubmed/35211170 http://dx.doi.org/10.1155/2022/2144615 Text en Copyright © 2022 Shahla Sohrabipour et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sohrabipour, Shahla Sharifi, Mohammad Reza Sharifi, Mohammadreza Talebi, Ardeshir Soltani, Nepton Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat |
title | Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat |
title_full | Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat |
title_fullStr | Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat |
title_full_unstemmed | Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat |
title_short | Combination Therapy with GABA and MgSO(4) Improves Insulin Sensitivity in Type 2 Diabetic Rat |
title_sort | combination therapy with gaba and mgso(4) improves insulin sensitivity in type 2 diabetic rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863457/ https://www.ncbi.nlm.nih.gov/pubmed/35211170 http://dx.doi.org/10.1155/2022/2144615 |
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