Passive heat stress induces mitochondrial adaptations in skeletal muscle

被引:7
作者
Marchant, Erik D. [1 ]
Nelson, W. Bradley [2 ]
Hyldahl, Robert D. [2 ]
Gifford, Jayson R. [2 ]
Hancock, Chad R. [1 ,3 ]
机构
[1] Brigham Young Univ, Nutr Dietet & Food Sci, Provo, UT USA
[2] Brigham Young Univ, Exercise Sci, Provo, UT USA
[3] S245 ESC, Provo, UT 84602 USA
关键词
Heat; skeletal muscle; mitochondria; atrophy; thermal; physiological effects of hyperthermia (i.e; perfusion effects; hypoxia; pH; metabolism; microenvironment; redox); heat shock response (i.e; HSP; chaperones; thermotolerance); INDUCED OXIDATIVE STRESS; INSULIN-RESISTANCE; ENERGY-METABOLISM; SHOCK PROTEINS; VITAMIN-E; IN-VIVO; EXERCISE; THERAPY; HEALTH; TEMPERATURE;
D O I
10.1080/02656736.2023.2205066
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mitochondria are central to skeletal muscle metabolic health. Impaired mitochondrial function is associated with various muscle pathologies, including insulin resistance and muscle atrophy. As a result, continuous efforts are made to find ways to improve mitochondrial health in the context of disuse and disease. While exercise is known to cause robust improvements in mitochondrial health, not all individuals are able to exercise. This creates a need for alternate interventions which elicit some of the same benefits as exercise. Passive heating (i.e., application of heat in the absence of muscle contractions) is one potential intervention which has been shown to increase mitochondrial enzyme content and activity, and to improve mitochondrial respiration. Associated with increases in mitochondrial content and/or function, passive heating can also improve insulin sensitivity in the context of type II diabetes and preserve muscle mass in the face of limb disuse. This area of research remains in its infancy, with many questions yet to be answered about how to maximize the benefits of passive heating and elucidate the mechanisms by which heat stress affects muscle mitochondria.
引用
收藏
页数:11
相关论文
共 50 条
  • [41] The heat shock connection: skeletal muscle hypertrophy and atrophy
    Fennel, Zachary J.
    Amorim, Fabiano T.
    Deyhle, Michael R.
    Hafen, Paul S.
    Mermier, Christine M.
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY, INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2022, 323 (01) : R133 - R148
  • [42] Impact of β-adrenergic signaling in PGC-1α-mediated adaptations in mouse skeletal muscle
    Brandt, Nina
    Nielsen, Lene
    Buch, Bjorg Thiellesen
    Gudiksen, Anders
    Ringholm, Stine
    Hellsten, Ylva
    Bangsbo, Jens
    Pilegaard, Henriette
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2018, 314 (01): : E1 - E20
  • [43] The role of weight loss and exercise in correcting skeletal muscle mitochondrial abnormalities in obesity, diabetes and aging
    Toledo, Frederico G. S.
    Goodpaster, Bret H.
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2013, 379 (1-2) : 30 - 34
  • [44] Fructose induces mitochondrial dysfunction and triggers apoptosis in skeletal muscle cells by provoking oxidative stress
    Natasha Jaiswal
    Chandan K. Maurya
    Deepti Arha
    Deepa R. Avisetti
    Ayyappan Prathapan
    Palayyan S. Raj
    Kozhiparambil G. Raghu
    Shasi V. Kalivendi
    Akhilesh Kumar Tamrakar
    Apoptosis, 2015, 20 : 930 - 947
  • [45] Skeletal muscle mitochondrial mass is linked to lipid and metabolic profile in individuals with spinal cord injury
    O'Brien, Laura C.
    Chen, Qun
    Savas, Jeannie
    Lesnefsky, Edward J.
    Gorgey, Ashraf S.
    EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY, 2017, 117 (11) : 2137 - 2147
  • [46] Mitochondrial H+-ATP synthase in human skeletal muscle: contribution to dyslipidaemia and insulin resistance
    Formentini, Laura
    Ryan, Alexander J.
    Galvez-Santisteban, Manuel
    Carter, Leslie
    Taub, Pam
    Lapek, John D., Jr.
    Gonzalez, David J.
    Villarreal, Francisco
    Ciaraldi, Theodore P.
    Cuezva, Jose M.
    Henry, Robert R.
    DIABETOLOGIA, 2017, 60 (10) : 2052 - 2065
  • [47] NOD2 activation induces oxidative stress contributing to mitochondrial dysfunction and insulin resistance in skeletal muscle cells
    Maurya, Chandan K.
    Arha, Deepti
    Rai, Amit K.
    Kumar, Shashi Kant
    Pandey, Jyotsana
    Avisetti, Deepa R.
    Kalivendi, Shasi V.
    Klip, Amira
    Tamrakar, Akhilesh K.
    FREE RADICAL BIOLOGY AND MEDICINE, 2015, 89 : 158 - 169
  • [48] Mitochondrial and performance adaptations to exercise training in mice lacking skeletal muscle LKB1
    Tanner, Colby B.
    Madsen, Steven R.
    Hallowell, David M.
    Goring, Darren M. J.
    Moore, Timothy M.
    Hardman, Shalene E.
    Heninger, Megan R.
    Atwood, Daniel R.
    Thomson, David M.
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2013, 305 (08): : E1018 - E1029
  • [49] Effects of Royal Jelly Administration on Endurance Training-Induced Mitochondrial Adaptations in Skeletal Muscle
    Takahashi, Yumiko
    Hijikata, Kamiyu
    Seike, Kohei
    Nakano, Suguru
    Banjo, Mai
    Sato, Yosuke
    Takahashi, Kenya
    Hatta, Hideo
    NUTRIENTS, 2018, 10 (11)
  • [50] Mitochondrial involvement and impact in aging skeletal muscle
    Hepple, Russell T.
    FRONTIERS IN AGING NEUROSCIENCE, 2014, 6