Myostatin-deficient mice exhibit reduced insulin resistance through activating the AMP-activated protein kinase signalling pathway
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Aims/hypothesis Myostatin-null mice (Mstn(-/-)) have reduced body fat and increased tolerance to glucose. To date the molecular mechanisms through which myostatin regulates body fat content and insulin sensitivity are not known. Therefore, the aim of the current study was to identify signalling pathways through which myostatin regulates insulin sensitivity.Methods Wild-type (WT) mice and Mstn(-/-) mice were fed either a control chow diet or a high fat diet (HFD) for 12 weeks. Glucose tolerance testing and insulin stimulated glucose uptake by M. extensor digitorum longus (EDL) were used as variables to determine insulin sensitivity. Quantitative PCR, Western blotting and enzyme assays were used to monitor AMP-activated protein kinase (AMPK) levels and activity.Results Mstn(-/-) mice exhibited reduced fat accumulation and peripheral insulin resistance when compared with WT mice, even when they were fed an HFD. Furthermore, treatment with a myostatin antagonist also increased insulin sensitivity during HFD. Consistent with increased insulin sensitivity, we also detected elevated levels of GLUT4, AKT, p-AKT and insulin receptor substrate-1 in Mstn(-/-) muscles. Molecular analysis showed that there is increased expression and activity of AMPK in Mstn(-/-) muscles. Furthermore, we also observed an increase in the AMPK downstream target genes, Sirt1 and Pgc-1α (also known as Ppargc1a), in skeletal muscle of Mstn(-/-) mice.Conclusions/interpretation We conclude that myostatin inactivation leads to increased AMPK levels and activity resulting in increased insulin sensitivity of skeletal muscle. We propose that, by regulating AMPK in skeletal muscle and adipose tissues, myostatin plays a major role in regulating insulin signalling.
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Increased AMPK activity in muscle increases insulin sensitivity and responsiveness.
“Another effect is an increase in AMPK activity in the muscle, which increases insulin sensitivity and responsiveness (Zhang et al., 2011).”
From Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases (2018) · cites this paper as Zhang et al., 2011
Myostatin‐deficient mice also develop insulin resistance via alterations in AMPK activity.
“However, myostatin‐deficient mice also develop insulin resistance via alterations in AMPK activity 148, highlighting the need to determine the exact effects of myostatin signaling, as well as of other myokines correlating with obesity, in whole‐body energy homeostasis 112.”
From Inter‐organ communication: a gatekeeper for metabolic health (2019) · cites this paper as [148]
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Peroxisome Proliferator-activated Receptor β/δ Induces Myogenesis by Modulating Myostatin Activity
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- Authors
- Zhang, C., McFarlane, C., Lokireddy, S., Bonala, S., Ge, X., Masuda, S., Gluckman, P. D., Sharma, M., & Kambadur, R.
- Affiliations
- Singapore Institute for Clinical Sciences (SG)
- Nanyang Technological University (SG)
- National University of Singapore (SG)
- Corresponding author
- Kambadur, R.
- Venue
- Diabetologia
- Published
- 2011-02-24
- Volume
- 54
- Issue
- 6
- Pages
- 1491-1501
- ISSN
- 0012-186X (ISSN-L)
- 1432-0428
- OpenAlex
- W2104321619
- Cited by
- 158
- References
- 47
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 7 · 2023: 9 · 2022: 14 · 2021: 13 · 2020: 13 · 2019: 13 · 2018: 12 · 2017: 12 · 2016: 9 · 2015: 17 · 2014: 12 · 2013: 9 · 2012: 10
- FWCI
- 4.41
- Type
- journal article
- Language
- en
- Update notices
- erratum (2014-12-11)
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Diabetologia (publishedVersion)
- PubMed (publishedVersion)
- ResearchOnline at James Cook University (James Cook University) (submittedVersion)
- ResearchSpace (University of Auckland) (submittedVersion)
- Funders
- Agency for Science, Technology and Research
- Singapore Institute for Clinical Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Keywords
- myostatin, insulin resistance, AMPK, skeletal muscle, high-fat diet, GLUT4, Akt, IRS-1, SIRT1, PGC-1α, adipose tissue, glucose tolerance, insulin signaling
- MeSH terms
- Animals, Dietary Fats, Glucose, Insulin Resistance, Male, Mice, Inbred C57BL, Signal Transduction, Mice, Knockout, Muscle, Skeletal, Models, Animal, Proto-Oncogene Proteins c-akt, Glucose Transporter Type 4, Mice, AMP-Activated Protein Kinases, Myostatin
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