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Skeletal muscle mitochondrial fragmentation and impaired bioenergetics from nutrient overload are prevented by carbon monoxide.

Publication ,  Journal Article
Gasier, HG; Dohl, J; Suliman, HB; Piantadosi, CA; Yu, T
Published in: Am J Physiol Cell Physiol
October 1, 2020

Nutrient excess increases skeletal muscle oxidant production and mitochondrial fragmentation that may result in impaired mitochondrial function, a hallmark of skeletal muscle insulin resistance. This led us to explore whether an endogenous gas molecule, carbon monoxide (CO), which is thought to prevent weight gain and metabolic dysfunction in mice consuming high-fat diets, alters mitochondrial morphology and respiration in C2C12 myoblasts exposed to high glucose (15.6 mM) and high fat (250 µM BSA-palmitate) (HGHF). Also, skeletal muscle mitochondrial morphology, distribution, respiration, and energy expenditure were examined in obese resistant (OR) and obese prone (OP) rats that consumed a high-fat and high-sucrose diet for 10 wk with or without intermittent low-dose inhaled CO and/or exercise training. In cells exposed to HGHF, superoxide production, mitochondrial membrane potential (ΔΨm), mitochondrial fission regulatory protein dynamin-related protein 1 (Drp1) and mitochondrial fragmentation increased, while mitochondrial respiratory capacity was reduced. CO decreased HGHF-induced superoxide production, Drp1 protein levels and mitochondrial fragmentation, maintained ΔΨm, and increased mitochondrial respiratory capacity. In comparison with lean OR rats, OP rats had smaller skeletal muscle mitochondria that contained disorganized cristae, a normal mitochondrial distribution, but reduced citrate synthase protein expression, normal respiratory responses, and a lower energy expenditure. The combination of inhaled CO and exercise produced the greatest effect on mitochondrial morphology, increasing ADP-stimulated respiration in the presence of pyruvate, and preventing a decline in resting energy expenditure. These data support a therapeutic role for CO and exercise in preserving mitochondrial morphology and respiration during metabolic overload.

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Published In

Am J Physiol Cell Physiol

DOI

EISSN

1522-1563

Publication Date

October 1, 2020

Volume

319

Issue

4

Start / End Page

C746 / C756

Location

United States

Related Subject Headings

  • Weight Gain
  • Sucrose
  • Reactive Oxygen Species
  • Rats
  • Physiology
  • Physical Conditioning, Animal
  • Obesity
  • Myoblasts
  • Muscle, Skeletal
  • Mitochondrial Dynamics
 

Citation

APA
Chicago
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Gasier, H. G., Dohl, J., Suliman, H. B., Piantadosi, C. A., & Yu, T. (2020). Skeletal muscle mitochondrial fragmentation and impaired bioenergetics from nutrient overload are prevented by carbon monoxide. Am J Physiol Cell Physiol, 319(4), C746–C756. https://doi.org/10.1152/ajpcell.00016.2020
Gasier, Heath G., Jacob Dohl, Hagir B. Suliman, Claude A. Piantadosi, and Tianzheng Yu. “Skeletal muscle mitochondrial fragmentation and impaired bioenergetics from nutrient overload are prevented by carbon monoxide.Am J Physiol Cell Physiol 319, no. 4 (October 1, 2020): C746–56. https://doi.org/10.1152/ajpcell.00016.2020.
Gasier HG, Dohl J, Suliman HB, Piantadosi CA, Yu T. Skeletal muscle mitochondrial fragmentation and impaired bioenergetics from nutrient overload are prevented by carbon monoxide. Am J Physiol Cell Physiol. 2020 Oct 1;319(4):C746–56.
Gasier, Heath G., et al. “Skeletal muscle mitochondrial fragmentation and impaired bioenergetics from nutrient overload are prevented by carbon monoxide.Am J Physiol Cell Physiol, vol. 319, no. 4, Oct. 2020, pp. C746–56. Pubmed, doi:10.1152/ajpcell.00016.2020.
Gasier HG, Dohl J, Suliman HB, Piantadosi CA, Yu T. Skeletal muscle mitochondrial fragmentation and impaired bioenergetics from nutrient overload are prevented by carbon monoxide. Am J Physiol Cell Physiol. 2020 Oct 1;319(4):C746–C756.

Published In

Am J Physiol Cell Physiol

DOI

EISSN

1522-1563

Publication Date

October 1, 2020

Volume

319

Issue

4

Start / End Page

C746 / C756

Location

United States

Related Subject Headings

  • Weight Gain
  • Sucrose
  • Reactive Oxygen Species
  • Rats
  • Physiology
  • Physical Conditioning, Animal
  • Obesity
  • Myoblasts
  • Muscle, Skeletal
  • Mitochondrial Dynamics