Skeletal muscle myosin heavy chain expression and 3D capillary network changes in streptozotocin-induced diabetic female mice

Authors

  • Nejc Umek Institute of Anatomy, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia https://orcid.org/0000-0001-5831-2216
  • Luka Pušnik Institute of Anatomy, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia https://orcid.org/0000-0003-3418-0348
  • Chiedozie Kenneth Ugwoke Institute of Anatomy, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia
  • Žiga Šink Institute of Anatomy, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia https://orcid.org/0009-0007-2454-6592
  • Simon Horvat Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia
  • Jiří Janáček Laboratory of Biomathematics, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic
  • Erika Cvetko Institute of Anatomy, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia

DOI:

https://doi.org/10.17305/bb.2023.9843

Keywords:

Type 1 diabetes mellitus (T1DM), skeletal muscle, myosin heavy chain (MyHC) isoforms, capillary network analysis, muscle fiber composition, three-dimensional (3D) image analysis

Abstract

It is not well-understood how type 1 diabetes (T1DM) affects skeletal muscle histological phenotype, particularly capillarisation. This study aimed to analyze skeletal muscle myosin heavy chain (MyHC) fibre type changes and 3D capillary network characteristics in experimental T1DM mice. Female C57BL/6J-OlaHsd mice were categorized into streptozotocin (STZ)-induced diabetic (n = 12) and age-matched non-diabetic controls (n =12). The muscle fibre phenotype of the soleus, gluteus maximus, and gastrocnemius muscles were characterized based on the expression of MyHC isoforms, while capillaries of the gluteus maximus were assessed with immunofluorescence staining, confocal laser microscopy and 3D image analysis. STZ-induced diabetic mice exhibited elevated glucose levels, reduced body weight, and prolonged thermal latency, verifying the T1DM phenotype. In both T1DM and non-diabetic mice, the gluteus maximus and gastrocnemius muscles predominantly expressed fast-twitch type 2b fibers, with no significant differences noted. However, the soleus muscle in non-diabetic mice had a greater proportion of type 2a fibers and comparable type 1 fiber densities (26.2 ± 14.6% vs 21.9 ± 13.5%) relative to diabetic mice. T1DM mice showed reduced fiber diameters (P = 0.026), and the 3D capillary network analysis indicated a higher capillary length per muscle volume in the gluteus maximus of diabetic mice compared to controls (P < 0.05). Overall, T1DM induced significant changes in the skeletal muscle, including shifts in MyHC fibre types, decreased fibre diameters, and increased relative capillarisation, possibly due to muscle fibre atrophy. Our findings emphasize the superior detail provided by the 3D analytical method for characterizing skeletal muscle capillary architecture, highlighting caution in interpreting 2D data for capillary changes in T1DM.

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Skeletal muscle myosin heavy chain expression and 3D capillary network changes in streptozotocin-induced diabetic female mice

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Published

30-10-2023

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Section

Anatomy

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How to Cite

1.
Skeletal muscle myosin heavy chain expression and 3D capillary network changes in streptozotocin-induced diabetic female mice. Biomol Biomed [Internet]. 2023 Oct. 30 [cited 2024 Apr. 21];:582–592. Available from: https://www.bjbms.org/ojs/index.php/bjbms/article/view/9843