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High-intensity interval training alleviates STZ-induced muscle atrophy by restoration of nuclear positioning defects in C57BL/6 male mice
by
Rahmati, Masoud
, Nikooie, Rohollah
in
631/443
/ 631/80
/ Animals
/ Apoptosis
/ Atrophy
/ Cell Nucleus - metabolism
/ Cell Nucleus - pathology
/ Diabetes
/ Diabetes mellitus
/ Diabetes Mellitus, Experimental - complications
/ Diabetes Mellitus, Experimental - pathology
/ Diabetic myopathy
/ Dynein
/ High-Intensity Interval Training
/ Humanities and Social Sciences
/ Hypertrophy
/ Hypothesis testing
/ Interval training
/ Kinesin-1
/ Kinesins - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Morphology
/ Morphometry
/ multidisciplinary
/ Muscle Fibers, Skeletal - metabolism
/ Muscle Fibers, Skeletal - pathology
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscular Atrophy - chemically induced
/ Muscular Atrophy - etiology
/ Muscular Atrophy - metabolism
/ Muscular Atrophy - pathology
/ Muscular Atrophy - therapy
/ Musculoskeletal system
/ Nuclear movement
/ Physical Conditioning, Animal
/ Satellite cells
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Streptozocin
/ Training
2025
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High-intensity interval training alleviates STZ-induced muscle atrophy by restoration of nuclear positioning defects in C57BL/6 male mice
by
Rahmati, Masoud
, Nikooie, Rohollah
in
631/443
/ 631/80
/ Animals
/ Apoptosis
/ Atrophy
/ Cell Nucleus - metabolism
/ Cell Nucleus - pathology
/ Diabetes
/ Diabetes mellitus
/ Diabetes Mellitus, Experimental - complications
/ Diabetes Mellitus, Experimental - pathology
/ Diabetic myopathy
/ Dynein
/ High-Intensity Interval Training
/ Humanities and Social Sciences
/ Hypertrophy
/ Hypothesis testing
/ Interval training
/ Kinesin-1
/ Kinesins - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Morphology
/ Morphometry
/ multidisciplinary
/ Muscle Fibers, Skeletal - metabolism
/ Muscle Fibers, Skeletal - pathology
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscular Atrophy - chemically induced
/ Muscular Atrophy - etiology
/ Muscular Atrophy - metabolism
/ Muscular Atrophy - pathology
/ Muscular Atrophy - therapy
/ Musculoskeletal system
/ Nuclear movement
/ Physical Conditioning, Animal
/ Satellite cells
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Streptozocin
/ Training
2025
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High-intensity interval training alleviates STZ-induced muscle atrophy by restoration of nuclear positioning defects in C57BL/6 male mice
by
Rahmati, Masoud
, Nikooie, Rohollah
in
631/443
/ 631/80
/ Animals
/ Apoptosis
/ Atrophy
/ Cell Nucleus - metabolism
/ Cell Nucleus - pathology
/ Diabetes
/ Diabetes mellitus
/ Diabetes Mellitus, Experimental - complications
/ Diabetes Mellitus, Experimental - pathology
/ Diabetic myopathy
/ Dynein
/ High-Intensity Interval Training
/ Humanities and Social Sciences
/ Hypertrophy
/ Hypothesis testing
/ Interval training
/ Kinesin-1
/ Kinesins - metabolism
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Morphology
/ Morphometry
/ multidisciplinary
/ Muscle Fibers, Skeletal - metabolism
/ Muscle Fibers, Skeletal - pathology
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscular Atrophy - chemically induced
/ Muscular Atrophy - etiology
/ Muscular Atrophy - metabolism
/ Muscular Atrophy - pathology
/ Muscular Atrophy - therapy
/ Musculoskeletal system
/ Nuclear movement
/ Physical Conditioning, Animal
/ Satellite cells
/ Science
/ Science (multidisciplinary)
/ Skeletal muscle
/ Streptozocin
/ Training
2025
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High-intensity interval training alleviates STZ-induced muscle atrophy by restoration of nuclear positioning defects in C57BL/6 male mice
Journal Article
High-intensity interval training alleviates STZ-induced muscle atrophy by restoration of nuclear positioning defects in C57BL/6 male mice
2025
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Overview
We tested the hypothesis that improper myonuclei arrangement and morphology are involved in diabetes-induced myofiber atrophy and whether and how high-intensity interval training (HIIT) affects these impairments in isolated skeletal muscle myofibers. STZ-induced diabetes decreased muscle fiber cross-sectional area (CSA) mediated by reduced myonuclear number, enhanced nuclear apoptotic, and failed nuclear accretion from satellite cells. STZ-induced muscle atrophy was accompanied by improper nuclear positioning (sinus of the maximum diameter angles and distance between adjacent myonuclei) and morphology (maximum diameter, area, and volume of the nuclei), which was mediated by suppressed expression of proteins involved in nuclear positioning including KIF5B, dynein, and Nesprin1. Disturbing nuclear positioning by inhibition of Kinsein1 activity reduced CSA to a greater extent than in diabetes alone, suggesting STZ-induced muscle atrophy is mediated by changes in nuclear positioning. HIIT alleviated the STZ-induced decline in muscle CSA and myonuclei per fiber by restoring myonuclear morphometry impairments and improper nuclear positioning to the normal level. HIIT-induced increase in muscle CSA deterred by inhibition of Kinesin1 activity, suggesting its effect is mediated by proper nuclear positioning. These findings suggest that normal nuclear positioning are required for the changes in fiber size properties associated with HIIT in diabetic skeletal muscle fibers.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 631/80
/ Animals
/ Atrophy
/ Diabetes
/ Diabetes Mellitus, Experimental - complications
/ Diabetes Mellitus, Experimental - pathology
/ Dynein
/ High-Intensity Interval Training
/ Humanities and Social Sciences
/ Male
/ Mice
/ Muscle Fibers, Skeletal - metabolism
/ Muscle Fibers, Skeletal - pathology
/ Muscle, Skeletal - metabolism
/ Muscle, Skeletal - pathology
/ Muscular Atrophy - chemically induced
/ Muscular Atrophy - metabolism
/ Muscular Atrophy - pathology
/ Physical Conditioning, Animal
/ Science
/ Training
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