Cargando…
The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue
Diabetes mellitus is a public health concern, affecting 10.5% of the population. Protocatechuic acid (PCA), a polyphenol, exerts beneficial effects on insulin resistance and diabetes. This study investigated the role of PCA in improving insulin resistance and the crosstalk between muscle with liver...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253324/ https://www.ncbi.nlm.nih.gov/pubmed/37298440 http://dx.doi.org/10.3390/ijms24119490 |
_version_ | 1785056378644070400 |
---|---|
author | Shakoor, Hira Hussein, Haneen Al-Hassan, Nour Alketbi, Mouza Kizhakkayil, Jaleel Platat, Carine |
author_facet | Shakoor, Hira Hussein, Haneen Al-Hassan, Nour Alketbi, Mouza Kizhakkayil, Jaleel Platat, Carine |
author_sort | Shakoor, Hira |
collection | PubMed |
description | Diabetes mellitus is a public health concern, affecting 10.5% of the population. Protocatechuic acid (PCA), a polyphenol, exerts beneficial effects on insulin resistance and diabetes. This study investigated the role of PCA in improving insulin resistance and the crosstalk between muscle with liver and adipose tissue. C2C12 myotubes received four treatments: Control, PCA, insulin resistance (IR), and IR-PCA. Conditioned media from C2C12 was used to incubate HepG2 and 3T3-L1 adipocytes. The impact of PCA was analyzed on glucose uptake and signaling pathways. PCA (80 µM) significantly enhanced glucose uptake in C2C12, HepG2, and 3T3-L1 adipocytes (p < 0.05). In C2C12, PCA significantly elevated GLUT-4, IRS-1, IRS-2, PPAR-γ, P-AMPK, and P-Akt vs. Control (p ≤ 0.05), and modulated pathways in IR-PCA. In HepG2, PPAR-γ and P-Akt increased significantly in Control (CM) vs. No CM, and PCA dose upregulated PPAR-γ, P-AMPK, and P-AKT (p < 0.05). In the 3T3-L1 adipocytes, PI3K and GLUT-4 expression was elevated in PCA (CM) vs. No CM. A significant elevation of IRS-1, GLUT-4, and P-AMPK was observed in IR-PCA vs. IR (p ≤ 0.001). Herein, PCA strengthens insulin signaling by activating key proteins of that pathway and regulating glucose uptake. Further, conditioned media modulated crosstalk between muscle with liver and adipose tissue, thus regulating glucose metabolism. |
format | Online Article Text |
id | pubmed-10253324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102533242023-06-10 The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue Shakoor, Hira Hussein, Haneen Al-Hassan, Nour Alketbi, Mouza Kizhakkayil, Jaleel Platat, Carine Int J Mol Sci Article Diabetes mellitus is a public health concern, affecting 10.5% of the population. Protocatechuic acid (PCA), a polyphenol, exerts beneficial effects on insulin resistance and diabetes. This study investigated the role of PCA in improving insulin resistance and the crosstalk between muscle with liver and adipose tissue. C2C12 myotubes received four treatments: Control, PCA, insulin resistance (IR), and IR-PCA. Conditioned media from C2C12 was used to incubate HepG2 and 3T3-L1 adipocytes. The impact of PCA was analyzed on glucose uptake and signaling pathways. PCA (80 µM) significantly enhanced glucose uptake in C2C12, HepG2, and 3T3-L1 adipocytes (p < 0.05). In C2C12, PCA significantly elevated GLUT-4, IRS-1, IRS-2, PPAR-γ, P-AMPK, and P-Akt vs. Control (p ≤ 0.05), and modulated pathways in IR-PCA. In HepG2, PPAR-γ and P-Akt increased significantly in Control (CM) vs. No CM, and PCA dose upregulated PPAR-γ, P-AMPK, and P-AKT (p < 0.05). In the 3T3-L1 adipocytes, PI3K and GLUT-4 expression was elevated in PCA (CM) vs. No CM. A significant elevation of IRS-1, GLUT-4, and P-AMPK was observed in IR-PCA vs. IR (p ≤ 0.001). Herein, PCA strengthens insulin signaling by activating key proteins of that pathway and regulating glucose uptake. Further, conditioned media modulated crosstalk between muscle with liver and adipose tissue, thus regulating glucose metabolism. MDPI 2023-05-30 /pmc/articles/PMC10253324/ /pubmed/37298440 http://dx.doi.org/10.3390/ijms24119490 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shakoor, Hira Hussein, Haneen Al-Hassan, Nour Alketbi, Mouza Kizhakkayil, Jaleel Platat, Carine The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue |
title | The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue |
title_full | The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue |
title_fullStr | The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue |
title_full_unstemmed | The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue |
title_short | The Muscle-Conditioned Medium Containing Protocatechuic Acid Improves Insulin Resistance by Modulating Muscle Communication with Liver and Adipose Tissue |
title_sort | muscle-conditioned medium containing protocatechuic acid improves insulin resistance by modulating muscle communication with liver and adipose tissue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10253324/ https://www.ncbi.nlm.nih.gov/pubmed/37298440 http://dx.doi.org/10.3390/ijms24119490 |
work_keys_str_mv | AT shakoorhira themuscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT husseinhaneen themuscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT alhassannour themuscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT alketbimouza themuscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT kizhakkayiljaleel themuscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT platatcarine themuscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT shakoorhira muscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT husseinhaneen muscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT alhassannour muscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT alketbimouza muscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT kizhakkayiljaleel muscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue AT platatcarine muscleconditionedmediumcontainingprotocatechuicacidimprovesinsulinresistancebymodulatingmusclecommunicationwithliverandadiposetissue |