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Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism
BACKGROUND & OBJECTIVES: Amino acids are general nutrients having anti-diabetic property. The present study was undertaken to investigate the mechanism of anti-diabetic effects of amino acids in human visceral adipocyte cells in high glucose environment. METHODS: Experiments were carried out in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507535/ https://www.ncbi.nlm.nih.gov/pubmed/31115373 http://dx.doi.org/10.4103/ijmr.IJMR_1782_16 |
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author | Srinivasan, Vidhya Radhakrishnan, Selvi Angayarkanni, Narayanasamy Sulochana, K.N. |
author_facet | Srinivasan, Vidhya Radhakrishnan, Selvi Angayarkanni, Narayanasamy Sulochana, K.N. |
author_sort | Srinivasan, Vidhya |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: Amino acids are general nutrients having anti-diabetic property. The present study was undertaken to investigate the mechanism of anti-diabetic effects of amino acids in human visceral adipocyte cells in high glucose environment. METHODS: Experiments were carried out in human visceral adipocytes. Adiponectin (APN) siRNAs were designed using Ambion tools. APN mRNA expression was quantified using real-time polymerase chain reaction, and protein level was studied using ELISA. AMP-activated kinase (AMPK) activity was measured and glucose uptake by 2-deoxyglucose uptake method. RESULTS: Amino acids (proline and phenylalanine) exposure to adipocytes significantly (P<0.01) increased APN mRNA by 1.5-folds when compared to control whereas proline increased APN secretion by 10.6-folds (P<0.01), phenylalanine by 12.7-folds (P<0.001) and alanine by 6.3-folds (P<0.01). Free amino acid-induced AMPK activity and glucose uptake were decreased with the transient knockdown of APN. INTERPRETATION & CONCLUSIONS: Antidiabetic effect of the tested amino acids was exhibited by increased glucose uptake through the AMPK pathway by an APN-dependent mechanism in human visceral adipocytes. This should be tested and confirmed in in vivo system. Newer treatment modalities with amino acids which can enhance glucose uptake and APN secretion can be developed as drug for treating both diabetes and obesity. |
format | Online Article Text |
id | pubmed-6507535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65075352019-05-21 Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism Srinivasan, Vidhya Radhakrishnan, Selvi Angayarkanni, Narayanasamy Sulochana, K.N. Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Amino acids are general nutrients having anti-diabetic property. The present study was undertaken to investigate the mechanism of anti-diabetic effects of amino acids in human visceral adipocyte cells in high glucose environment. METHODS: Experiments were carried out in human visceral adipocytes. Adiponectin (APN) siRNAs were designed using Ambion tools. APN mRNA expression was quantified using real-time polymerase chain reaction, and protein level was studied using ELISA. AMP-activated kinase (AMPK) activity was measured and glucose uptake by 2-deoxyglucose uptake method. RESULTS: Amino acids (proline and phenylalanine) exposure to adipocytes significantly (P<0.01) increased APN mRNA by 1.5-folds when compared to control whereas proline increased APN secretion by 10.6-folds (P<0.01), phenylalanine by 12.7-folds (P<0.001) and alanine by 6.3-folds (P<0.01). Free amino acid-induced AMPK activity and glucose uptake were decreased with the transient knockdown of APN. INTERPRETATION & CONCLUSIONS: Antidiabetic effect of the tested amino acids was exhibited by increased glucose uptake through the AMPK pathway by an APN-dependent mechanism in human visceral adipocytes. This should be tested and confirmed in in vivo system. Newer treatment modalities with amino acids which can enhance glucose uptake and APN secretion can be developed as drug for treating both diabetes and obesity. Medknow Publications & Media Pvt Ltd 2019-01 /pmc/articles/PMC6507535/ /pubmed/31115373 http://dx.doi.org/10.4103/ijmr.IJMR_1782_16 Text en Copyright: © 2019 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Srinivasan, Vidhya Radhakrishnan, Selvi Angayarkanni, Narayanasamy Sulochana, K.N. Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism |
title | Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism |
title_full | Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism |
title_fullStr | Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism |
title_full_unstemmed | Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism |
title_short | Antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism |
title_sort | antidiabetic effect of free amino acids supplementation in human visceral adipocytes through adiponectin-dependent mechanism |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507535/ https://www.ncbi.nlm.nih.gov/pubmed/31115373 http://dx.doi.org/10.4103/ijmr.IJMR_1782_16 |
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