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
  • [21] Insulin resistance and mitochondrial function in skeletal muscle
    Dela, Flemming
    Helge, Jorn Wulff
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2013, 45 (01) : 11 - 15
  • [22] Acute cold stress induces transient MuRF1 upregulation in the skeletal muscle of zebrafish
    Tamai, Shinsuke
    Fujita, Shin-ichiro
    Komine, Ritsuko
    Kanki, Yasuharu
    Aoki, Kai
    Watanabe, Koichi
    Takekoshi, Kazuhiro
    Sugasawa, Takehito
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2022, 608 : 59 - 65
  • [23] Adaptations to high-intensity interval training in skeletal muscle require NADPH oxidase 2
    Henriquez-Olguin, Carlos
    Renani, Leila Baghersad
    Arab-Ceschia, Lyne
    Raun, Steffen H.
    Bhatia, Aakash
    Li, Zhencheng
    Knudsen, Jonas R.
    Holmdahl, Rikard
    Jensen, Thomas E.
    REDOX BIOLOGY, 2019, 24
  • [24] Azelaic Acid Induces Mitochondrial Biogenesis in Skeletal Muscle by Activation of Olfactory Receptor 544
    Trung Thanh Thach
    Wu, Chunyan
    Hwang, Kwang Yeon
    Lee, Sung-Joon
    FRONTIERS IN PHYSIOLOGY, 2020, 11
  • [25] Daily heat treatment maintains mitochondrial function and attenuates atrophy in human skeletal muscle subjected to immobilization
    Hafen, Paul S.
    Abbott, Kaitlin
    Bowden, Jennifer
    Lopiano, Ryan
    Hancock, Chad R.
    Hyldahl, Robert D.
    JOURNAL OF APPLIED PHYSIOLOGY, 2019, 127 (01) : 47 - 57
  • [26] Mild heat stress induces mitochondrial biogenesis in C2C12 myotubes
    Liu, Chien-Ting
    Brooks, George A.
    JOURNAL OF APPLIED PHYSIOLOGY, 2012, 112 (03) : 354 - 361
  • [27] Passive heat acclimation improves skeletal muscle contractility in humans
    Racinais, S.
    Wilson, M. G.
    Periard, J. D.
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2017, 312 (01) : R101 - R107
  • [28] Impact of capillary and sarcolemmal proximity on mitochondrial structure and energetic function in skeletal muscle
    Parry, Hailey A.
    Willingham, T. Bradley
    Giordano, Kevin A.
    Kim, Yuho
    Qazi, Shureed
    Knutson, Jay R.
    Combs, Christian A.
    Glancy, Brian
    JOURNAL OF PHYSIOLOGY-LONDON, 2024, 602 (09): : 1967 - 1986
  • [29] Twelve hours of heat stress induces inflammatory signaling in porcine skeletal muscle
    Ganesan, Shanthi
    Reynolds, Carmen
    Hollinger, Katrin
    Pearce, Sarah C.
    Gabler, Nicholas K.
    Baumgard, Lance H.
    Rhoads, Robert P.
    Selsby, Joshua T.
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2016, 310 (11) : R1288 - R1296
  • [30] NAD+/NADH and skeletal muscle mitochondrial adaptations to exercise
    White, Amanda T.
    Schenk, Simon
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2012, 303 (03): : E308 - E321