Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway

Abstract The mechanisms underlying exercise-induced insulin sensitization are of great interest, as exercise is a clinically critical intervention for diabetic patients. Some microRNAs (miRs) are secreted from skeletal muscle after exercise where they regulate insulin sensitivity, and have potential...

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Main Authors: Sang R. Lee, Kang Joo Jeong, Moeka Mukae, Jinhee Lee, Eui-Ju Hong
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-85174-0
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author Sang R. Lee
Kang Joo Jeong
Moeka Mukae
Jinhee Lee
Eui-Ju Hong
author_facet Sang R. Lee
Kang Joo Jeong
Moeka Mukae
Jinhee Lee
Eui-Ju Hong
author_sort Sang R. Lee
collection DOAJ
description Abstract The mechanisms underlying exercise-induced insulin sensitization are of great interest, as exercise is a clinically critical intervention for diabetic patients. Some microRNAs (miRs) are secreted from skeletal muscle after exercise where they regulate insulin sensitivity, and have potential as diagnostic markers in diabetic patients. miR-204 is well-known for its involvement in development, cancer, and metabolism; however, its role in exercise-induced glycemic control remains unclear. In the present study, endurance exercise in mice increased miR-204 expression levels in skeletal muscle. In a chronic exercise model, miR-204 expression levels were elevated along with glycolytic enzymes in skeletal muscle. When muscular hypoxia was induced after exercise, miR-204 expression also increased with the upregulation of hypoxia-inducible factor 1-alpha (HIF-1α). Furthermore, HIF-1α overexpression led to increased miR-204 expression. Treatment with a miR-204 mimic in C2C12 cells significantly enhanced the glycolysis rate and the mRNA expression of glycolytic enzymes. Notably, intravenous administration of miR-204 in mice increased the glucose clearance rate following refeeding. miR-204 initially elevated blood glucose levels at an early stage of refeeding but later promoted blood glucose reduction as refeeding continued. Additionally, glycolytic enzymes were upregulated in the skeletal muscles of miR-204-injected mice. These findings suggest a novel physiological role for miR-204 in promoting skeletal muscle glycolysis, particularly in situations where insulin action is limited.
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spelling doaj-art-4c9ca8f0c6e24ed4817b1a5c9f010f212025-01-12T12:18:03ZengNature PortfolioScientific Reports2045-23222025-01-0115111110.1038/s41598-025-85174-0Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathwaySang R. Lee0Kang Joo Jeong1Moeka Mukae2Jinhee Lee3Eui-Ju Hong4Laboratory of Biochemistry, College of Veterinary Medicine, Chungnam National UniversityLaboratory of Biochemistry, College of Veterinary Medicine, Chungnam National UniversityLaboratory of Biochemistry, College of Veterinary Medicine, Chungnam National UniversityLaboratory of Biochemistry, College of Veterinary Medicine, Chungnam National UniversityLaboratory of Biochemistry, College of Veterinary Medicine, Chungnam National UniversityAbstract The mechanisms underlying exercise-induced insulin sensitization are of great interest, as exercise is a clinically critical intervention for diabetic patients. Some microRNAs (miRs) are secreted from skeletal muscle after exercise where they regulate insulin sensitivity, and have potential as diagnostic markers in diabetic patients. miR-204 is well-known for its involvement in development, cancer, and metabolism; however, its role in exercise-induced glycemic control remains unclear. In the present study, endurance exercise in mice increased miR-204 expression levels in skeletal muscle. In a chronic exercise model, miR-204 expression levels were elevated along with glycolytic enzymes in skeletal muscle. When muscular hypoxia was induced after exercise, miR-204 expression also increased with the upregulation of hypoxia-inducible factor 1-alpha (HIF-1α). Furthermore, HIF-1α overexpression led to increased miR-204 expression. Treatment with a miR-204 mimic in C2C12 cells significantly enhanced the glycolysis rate and the mRNA expression of glycolytic enzymes. Notably, intravenous administration of miR-204 in mice increased the glucose clearance rate following refeeding. miR-204 initially elevated blood glucose levels at an early stage of refeeding but later promoted blood glucose reduction as refeeding continued. Additionally, glycolytic enzymes were upregulated in the skeletal muscles of miR-204-injected mice. These findings suggest a novel physiological role for miR-204 in promoting skeletal muscle glycolysis, particularly in situations where insulin action is limited.https://doi.org/10.1038/s41598-025-85174-0miRNAmiR-204ExerciseGlycolysisDiabetes
spellingShingle Sang R. Lee
Kang Joo Jeong
Moeka Mukae
Jinhee Lee
Eui-Ju Hong
Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway
Scientific Reports
miRNA
miR-204
Exercise
Glycolysis
Diabetes
title Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway
title_full Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway
title_fullStr Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway
title_full_unstemmed Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway
title_short Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway
title_sort exercise promotes peripheral glycolysis in skeletal muscle through mir 204 induction via the hif 1α pathway
topic miRNA
miR-204
Exercise
Glycolysis
Diabetes
url https://doi.org/10.1038/s41598-025-85174-0
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