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L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats

Apelin is a new adipocytokine that acts as an endogenous hormone in various tissues through its receptor (APJ). This study aimed to investigate the effects of oral administration of L‐carnitine (LC) on the expression of Apelin and APJ in adipose tissue of experimentally induced insulin‐resistant and...

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Autores principales: Ranjbar Kohan, Neda, Tabandeh, Mohammad Reza, Nazifi, Saeed, Soleimani, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718837/
https://www.ncbi.nlm.nih.gov/pubmed/33278072
http://dx.doi.org/10.14814/phy2.14641
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author Ranjbar Kohan, Neda
Tabandeh, Mohammad Reza
Nazifi, Saeed
Soleimani, Zahra
author_facet Ranjbar Kohan, Neda
Tabandeh, Mohammad Reza
Nazifi, Saeed
Soleimani, Zahra
author_sort Ranjbar Kohan, Neda
collection PubMed
description Apelin is a new adipocytokine that acts as an endogenous hormone in various tissues through its receptor (APJ). This study aimed to investigate the effects of oral administration of L‐carnitine (LC) on the expression of Apelin and APJ in adipose tissue of experimentally induced insulin‐resistant and type 2 diabetic rats. In this experimental study, 60 male rats fed with high fat/high carbohydrate (HF/HC) diet. After 50 mg/kg intraperitoneally injection of streptozotocin (STZ) and confirmation of diabetes (FBS higher than 126 mg/dl), the animals were daily treated with 300 mg/kg LC for 28 days. At days 7, 14, and 28 of posttreatment, the expression of apelin and APJ in adipose tissue were determined using qPCR in diabetic, diabetic + LC treated, control, and control + LC treated groups. Apelin, insulin, TNF‐α, and IL1‐β were measured by the ELISA method. Results demonstrated that the rats fed with the HF/HC diet for 5 weeks were hyperinsulinemic and normoglycemic, while after STZ injection, they showed hyperinsulinemia and hyperglycemia with higher levels of HOMA‐IR. Apelin serum level, APJ and apelin gene expression in adipose tissue increased significantly with the development of diabetes compared to the control group. Treatment with LC for 14 days caused a reduction in apelin and APJ expressions in adipose tissue of diabetic rats. TNF‐α and IL1‐β levels were reduced in diabetic rats 14 days after their treatment with LC. The study results show that L‐carnitine could act as a new regulator in apelin gene expression in adipose tissue, improving the metabolic disorders in diabetic patients.
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spelling pubmed-77188372020-12-11 L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats Ranjbar Kohan, Neda Tabandeh, Mohammad Reza Nazifi, Saeed Soleimani, Zahra Physiol Rep Original Articles Apelin is a new adipocytokine that acts as an endogenous hormone in various tissues through its receptor (APJ). This study aimed to investigate the effects of oral administration of L‐carnitine (LC) on the expression of Apelin and APJ in adipose tissue of experimentally induced insulin‐resistant and type 2 diabetic rats. In this experimental study, 60 male rats fed with high fat/high carbohydrate (HF/HC) diet. After 50 mg/kg intraperitoneally injection of streptozotocin (STZ) and confirmation of diabetes (FBS higher than 126 mg/dl), the animals were daily treated with 300 mg/kg LC for 28 days. At days 7, 14, and 28 of posttreatment, the expression of apelin and APJ in adipose tissue were determined using qPCR in diabetic, diabetic + LC treated, control, and control + LC treated groups. Apelin, insulin, TNF‐α, and IL1‐β were measured by the ELISA method. Results demonstrated that the rats fed with the HF/HC diet for 5 weeks were hyperinsulinemic and normoglycemic, while after STZ injection, they showed hyperinsulinemia and hyperglycemia with higher levels of HOMA‐IR. Apelin serum level, APJ and apelin gene expression in adipose tissue increased significantly with the development of diabetes compared to the control group. Treatment with LC for 14 days caused a reduction in apelin and APJ expressions in adipose tissue of diabetic rats. TNF‐α and IL1‐β levels were reduced in diabetic rats 14 days after their treatment with LC. The study results show that L‐carnitine could act as a new regulator in apelin gene expression in adipose tissue, improving the metabolic disorders in diabetic patients. John Wiley and Sons Inc. 2020-12-05 /pmc/articles/PMC7718837/ /pubmed/33278072 http://dx.doi.org/10.14814/phy2.14641 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ranjbar Kohan, Neda
Tabandeh, Mohammad Reza
Nazifi, Saeed
Soleimani, Zahra
L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats
title L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats
title_full L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats
title_fullStr L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats
title_full_unstemmed L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats
title_short L‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats
title_sort l‐carnitine improves metabolic disorders and regulates apelin and apelin receptor genes expression in adipose tissue in diabetic rats
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7718837/
https://www.ncbi.nlm.nih.gov/pubmed/33278072
http://dx.doi.org/10.14814/phy2.14641
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