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Thrifty: Advancing Muscle Fiber Type Identification through High−Speed Precision Analysis
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Journal of Molecular Histology & Medical Physiology

ISSN: 2684-494X

Open Access

Brief Report - (2023) Volume 8, Issue 3

Thrifty: Advancing Muscle Fiber Type Identification through High−Speed Precision Analysis

William Edman*
*Correspondence: William Edman, Department of Physiology, Nutrition and Biomechanics, Swedish School of Sport and Health Sciences, Stockholm, Sweden, Email:
Department of Physiology, Nutrition and Biomechanics, Swedish School of Sport and Health Sciences, Stockholm, Sweden

Received: 02-May-2023, Manuscript No. jmhmp-23-110623; Editor assigned: 04-May-2023, Pre QC No. P-110623; Reviewed: 16-May-2023, QC No. Q-110623; Revised: 22-May-2023, Manuscript No. R-110623; Published: 29-May-2023 , DOI: 10.37421/2684-494X.2023.8.75
Citation: Edman, William. “Thrifty: Advancing Muscle Fiber Type Identification through High-Speed Precision Analysis.” J Mol Hist Med Phys 8 (2023): 75.
Copyright: © 2023 Edman W. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Comprehensive insights into muscle physiology necessitate in-depth analyses of fiber types, yet the laborious nature of dissecting and typing individual fibers has posed significant challenges. This often limits investigations to a scant number of fibers from a handful of participants, casting doubts on the representativeness of both the fiber and participant populations. To surmount these obstacles and enable large-scale, fiber-specific studies, an innovative and rapid technique for high-throughput fiber typing of individually dissected fibers has been developed and named Thrifty (High-Throughput Immunofluorescence Fiber Typing). In the Thrifty approach, 400 fiber segments are affixed to microscope slides with a pre-printed grid system, subjected to antibody probing against myosin heavy chain (MyHC)-I and MyHC-II, and classified under a fluorescence microscope. The effectiveness and expediency of Thrifty are benchmarked against a previously established protocol (dot blot) on a fiber-by-fiber basis, while the purity of fiber pools is verified using the gold standard SDS-PAGE and silver staining. Additionally, a modified Thrifty protocol utilizing fluorescence western blot equipment has been successfully validated. Thrifty exhibits exceptional concurrence with the dot blot protocol, yielding a K value of 0.955 (95% CI: 0.928, 0.982), P<0.001. Both the original and modified Thrifty methods consistently yield type I and type II fiber pools of absolute purity. Impressively, the Thrifty procedure accomplishes the typing of 400 fibers in just under 11 hours, nearly three times faster than the dot blot method. Notably, Thrifty emerges as an inventive and dependable approach, boasting remarkable versatility for swift fiber typing of individual fibers. Consequently, Thrifty stands poised to streamline the generation of extensive fiber pools, thereby paving the way for more comprehensive explorations into the intricate mechanisms governing skeletal muscle physiology.

Keywords

Skeletal muscle • Muscle physiology • Fibers

Introduction

Skeletal muscles play a vital role in the human body, enabling movement, maintaining posture, and supporting metabolic functions. These muscles are composed of various fiber types, each with distinct properties that influence muscle performance and adaptability. Fiber type identification is crucial for understanding muscle physiology, exercise responses, and even diagnosing certain muscle-related disorders. Traditional methods of identifying muscle fiber types have been laborious and time-consuming, limiting their applicability in research and clinical settings. However, a groundbreaking innovation known as Thrifty (Rapid Fiber Type Identification of Isolated Skeletal Muscle Fibers) is changing the landscape of muscle fiber analysis. This novel high-throughput method allows for swift and accurate identification of muscle fiber types, opening new avenues for research and medical diagnostics [1].

Muscle fibers are categorized into different types based on their contractile and metabolic properties. The two main types are Type I (slow-twitch) and Type II (fast-twitch), each further divided into subtypes. These distinctions have substantial implications for an individual's athletic performance, endurance, and overall health. For instance, elite endurance athletes tend to have a higher proportion of Type I fibers, while power athletes often possess a greater number of Type II fibers. Additionally, certain medical conditions, such as muscular dystrophy, are associated with specific alterations in fiber type composition. Accurate and efficient fiber type identification is therefore essential for optimizing training regimens, assessing muscle-related pathologies, and advancing our understanding of muscle biology [2].

Description

Challenges of traditional fiber typing methods

Historically, fiber type identification has relied on histochemical staining techniques. These methods involve labor-intensive processes, including tissue fixation, sectioning, staining, and microscopic analysis. While effective, they are time-consuming and often subject to variability and subjectivity in interpretation. As a result, researchers and clinicians have sought a more efficient and precise method for characterizing muscle fiber types [3].

THRIFTY is a revolutionary approach that combines cutting-edge technology and advanced computational algorithms to rapidly and accurately identify muscle fiber types. The method involves the isolation of individual muscle fibers, followed by real-time analysis using specialized imaging equipment. The key features of Thrifty include:

High-throughput analysis: Thrifty can process a large number of fibers simultaneously, enabling researchers to analyze hundreds to thousands of fibers in a fraction of the time required by traditional methods.

Automated image processing: The imaging equipment used in Thrifty captures detailed information about fiber morphology, contractile properties, and metabolic markers. Advanced algorithms then analyze these images, categorizing fibers into different types with a high degree of accuracy.

Objective and reproducible results: By minimizing human intervention and subjectivity, Thrifty provides consistent and reliable fiber type classifications, reducing the potential for experimental bias.

Adaptability: Thrifty can be customized to analyze additional features, such as fiber size, capillary density, and mitochondrial content, further enhancing the depth of analysis.

Potential clinical applications: Thrifty's speed and precision make it a promising tool for diagnosing muscle-related disorders and tracking therapeutic interventions over time [4].

Future implications and advancements

The development of Thrifty represents a significant leap forward in muscle fiber type identification, but ongoing research is likely to refine and expand its capabilities. As technology continues to evolve, we can anticipate improvements in imaging resolution, data processing, and integration with other analytical techniques. Additionally, THRIFTY's potential for clinical applications could lead to enhanced diagnostics and personalized treatment strategies for individuals with muscle-related conditions [5,6].

Conclusion

Thrifty has emerged as a game-changing innovation in the field of muscle physiology and research. Its ability to swiftly and accurately identify muscle fiber types has the potential to reshape our understanding of muscle biology, exercise responses, and disease mechanisms. By eliminating the limitations of traditional methods, Thrifty opens new avenues for scientific discovery and clinical translation, ultimately contributing to advancements in human health and performance.

Acknowledgement

None.

Conflict of Interest

None.

References

  1. Alp, PR., EA Newsholme and VA Zammit. "Activities of citrate synthase and NAD+-linked and NADP+-linked isocitrate dehydrogenase in muscle from vertebrates and invertebrates." Biochem J 154 (1976): 689-700.
  2. Google Scholar, Crossref, Indexed at

  3. Andersen, Jesper L and Per Aagaard. "Myosin heavy chain IIX overshoot in human skeletal muscle." Muscle Nerve: Off J Amer Asst Electrodiag Med 23 (2000): 1095-1104.
  4. Google Scholar, Crossref, Indexed at

  5. Andersen, Jesper Løvind, T Mohr, F Biering-Sørensen and H Galbo, et al. "Myosin heavy chain isoform transformation in single fibres from m. vastus lateralis in spinal cord injured individuals: Effects of long-term Functional Electrical Stimulation (FES)." Pflüg Arch 431 (1996): 513-518.
  6. Google Scholar, Crossref, Indexed at

  7. Apró, William, Marcus Moberg, D Lee Hamilton and Björn Ekblom, et al. "Leucine does not affect mechanistic target of rapamycin complex 1 assembly but is required for maximal ribosomal protein s6 kinase 1 activity in human skeletal muscle following resistance exercise." FASEB J 29 (2015): 4358-4373.
  8. Google Scholar, Crossref, Indexed at

  9. Bloemberg, Darin and Joe Quadrilatero. "Rapid determination of myosin heavy chain expression in rat, mouse, and human skeletal muscle using multicolor immunofluorescence analysis." PloS One 7 (2012): e35273.
  10. Google Scholar, Crossref, Indexed at

  11. Cardinale, Daniele A., Kasper D Gejl, Niels Ortenblad and Bjorn Ekblom, et al. "Reliability of maximal mitochondrial oxidative phosphorylation in permeabilized fibers from the vastus lateralis employing high‐resolution respirometry." Phys Rep 6 (2018): e13611.
  12. Google Scholar, Crossref, Indexed at

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