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Energy Metabolism in Skeletal Muscle: From Physiology to Pharmacology

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Endocrinology and Metabolism".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 2270

Special Issue Editor


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Guest Editor
Division of Physiology, Pharmacology and Neuroscience, School of Life Sciences, Queen’s Medical Centre, University of Nottingham Medical School, Nottingham NG7 2UH, UK
Interests: type 2 diabetes; muscle insulin resistance; sepsis; inflammation; energy metabolism; ageing; inactivity
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Special Issue Information

Dear Colleagues,

Energy metabolism is the process of generating energy (ATP) from nutrients, mainly in the form of sugars and fatty acids. The process comprises a series of interrelated pathways that can function with or without oxygen. The capacity of a cell to perform vital functions such as metabolism, growth, reproduction, some form of responsiveness, and adaptability all require energy in the form of ATP. Skeletal muscles represent the largest insulin-sensitive tissue in the body (40%) and are the primary site for insulin-stimulated glucose usage at rest and glucose and fatty acids utilisation during muscle contraction. The disruption of myocardial and skeletal muscle energy metabolism in metabolic syndromes such as obesity and diabetes are associated with various health problems along with decreased muscle mass and strength, impaired mobility, and fatigue symptoms. There is also a financial burden on the national health services as, on average, people with diagnosed type 2 diabetes (T2DM) have medical expenditures several times higher than what expenditures would be in the absence of diabetes.

In this background, the ability to address the presence of impaired energy metabolism in various pathological conditions would represent not only an ethical act but would also provide better management of the country's finances.

Being physically active and consuming a diet lower in saturated fats and refined sugars (non-pharmacological interventions) is good for T2DM as they improve blood glucose control, reduce cardiovascular risk factors, contribute to weight loss, and improve well-being.

Along with insulin therapy that helps maintain glucose homeostasis, numerous pharmacological approaches for treating T2DM have also become available in recent years. For instance, metformin is the most common medicine for T2DM.

Contributions to the field of restoring muscle energy metabolism in pathological conditions are welcome, which can be extended beyond T2DM such as sepsis, inflammation, ageing, or immobilisation through physiological and pharmacological interventions.

Dr. Dumitru Constantin-Teodosiu
Guest Editor

Manuscript Submission Information

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Keywords

  • skeletal muscle
  • energy
  • impaired metabolism
  • diseases
  • interventions

Published Papers (1 paper)

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Research

14 pages, 2287 KiB  
Article
A Cell-Based Assessment of the Muscle Anabolic Potential of Blue Whiting (Micromesistius poutassou) Protein Hydrolysates
by Niloofar Shekoohi, Miryam Amigo-Benavent, Guilherme Wesley Peixoto da Fonseca, Pádraigín A. Harnedy-Rothwell, Richard J. FitzGerald and Brian P. Carson
Int. J. Mol. Sci. 2023, 24(3), 2001; https://doi.org/10.3390/ijms24032001 - 19 Jan 2023
Cited by 3 | Viewed by 1705
Abstract
Blue whiting (BW) represents an underutilised fish species containing a high-quality protein and amino acid (AA) profile with numerous potentially bioactive peptide sequences, making BW an economic and sustainable alternative source of protein. This study investigated the impact of three different BW protein [...] Read more.
Blue whiting (BW) represents an underutilised fish species containing a high-quality protein and amino acid (AA) profile with numerous potentially bioactive peptide sequences, making BW an economic and sustainable alternative source of protein. This study investigated the impact of three different BW protein hydrolysates (BWPH-X, Y and Z) on growth, proliferation and muscle protein synthesis (MPS) in skeletal muscle (C2C12) myotubes. BWPHs were hydrolysed using different enzymatic and heat exposures and underwent simulated gastrointestinal digestion (SGID), each resulting in a high degree of hydrolysis (33.41–37.29%) and high quantities of low molecular mass peptides (86.17–97.12% <1 kDa). C2C12 myotubes were treated with 1 mg protein equivalent/mL of SGID-BWPHs for 4 h. Muscle growth and myotube thickness were analysed using an xCelligence™ platform. Anabolic signalling (phosphorylation of mTOR, rpS6 and 4E-BP1) and MPS measured by puromycin incorporation were assessed using immunoblotting. BWPH-X significantly increased muscle growth (p < 0.01) and myotube thickness (p < 0.0001) compared to the negative control (amino acid and serum free media). Muscle protein synthesis (MPS), as measured by puromycin incorporation, was significantly higher after incubation with BWPH-X compared with the negative control, but did not significantly change in response to BWPH-Y and Z treatments. Taken together, these preliminary findings demonstrate the anabolic potential of some but not all BWPHs on muscle enhancement, thus providing justification for human dietary intervention studies to confirm and translate the results of such investigations to dietary recommendations and practices. Full article
(This article belongs to the Special Issue Energy Metabolism in Skeletal Muscle: From Physiology to Pharmacology)
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