Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Aug 28;15(4):512-517.
doi: 10.12965/jer.1938380.190. eCollection 2019 Aug.

Effects of a single bout of exercise on mitochondria-mediated apoptotic signaling in rat cardiac and skeletal muscles

Affiliations

Effects of a single bout of exercise on mitochondria-mediated apoptotic signaling in rat cardiac and skeletal muscles

Su-Zi Yoo et al. J Exerc Rehabil. .

Abstract

This study aimed to determine the effects of a single bout exercise on mitochondria-mediated apoptotic signaling in cardiac and skeletal muscles. Fischer 344 rats (4 months old) were randomly divided into the control or a single bout of exercise group (n=10 each). The rats performed a single bout of treadmill exercise for 60 min. Mitochondria-mediated apoptotic signaling (e.g., Bax, Bcl-2, mitochondrial permeability transition pore [mPTP] opening, cytochrome c, and cleaved caspase-3) was measured in cardiac (e.g., left ventricle) and skeletal (e.g., soleus and white gastrocnemius) muscles. A single bout of exercise significantly decreased mPTP opening sensitivity in all tissues. However, a single bout of exercise did not show any statistical differences in Bax, Bcl-2, cytochrome c, and cleaved caspase-3 in all tissues measured. A single bout of exercise did not show definite results on characteristics of mitochondria-mediated apoptotic signaling. Therefore, further research is necessary to provide a more mechanistic understanding of the apoptosis pathway.

Keywords: Apoptosis; Exercise; Heart; Mitochondria; Skeletal muscle.

PubMed Disclaimer

Conflict of interest statement

CONFLICT OF INTEREST No potential conflict of interest relevant to this article was reported.

Figures

Fig. 1
Fig. 1
Effects of a single bout of exercise on Bax protein level in left ventricle (A), soleus (B), and white gastrocnemius (C). The data are shown as mean±standard error of the mean. CON, control group; EX, exercise group; AU, arbitrary unit; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.
Fig. 2
Fig. 2
Effects of a single bout of exercise on Bcl-2 protein level in left ventricle (A), soleus (B), and white gastrocnemius (C). The data are shown as mean±standard error of the mean. CON, control group; EX, exercise group; AU, arbitrary unit; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.
Fig. 3
Fig. 3
Effects of a single bout of exercise on Bax/Bcl-2 ratio in left ventricle (A), soleus (B), and white gastrocnemius (C). The data are shown as mean±standard error of the mean. CON, control group; EX, exercise group.
Fig. 4
Fig. 4
Effects of a single bout of exercise on mitochondrial permeability transition pore (PTP) opening sensitivity in left ventricle (A), soleus (B), and white gastrocnemius (C). The data are shown as mean±standard error of the mean. CON, control group; EX, exercise group; AU, arbitrary unit; GAPDH, glyceraldehyde-3-phosphate dehydrogenase. *P<0.05 compared to the control group.
Fig. 5
Fig. 5
Effects of a single bout of exercise on cytochrome c protein level in left ventricle (A), soleus (B), and white gastrocnemius (C). The data are shown as mean± standard error of the mean. CON, control group; EX, exercise group; AU, arbitrary unit; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.
Fig. 6
Fig. 6
Effects of a single bout of exercise on cleaved caspase-3 protein level in left ventricle (A), soleus (B), and white gastrocnemius (C). The data are shown as mean±standard error of the mean. CON, control group; EX, exercise group; AU, arbitrary unit; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.

Similar articles

Cited by

References

    1. Boroujerdi SS, Rahimi R. The apoptotic response to resistance exercise with different intensities in athletes. Med Sport. 2011;64:31–44.
    1. Gleeson M, Bishop NC, Stensel DJ, Lindley MR, Mastana SS, Nimmo MA. The anti-inflammatory effects of exercise: mechanisms and implications for the prevention and treatment of disease. Nat Rev Immunol. 2011;11:607–615. - PubMed
    1. Gram M, Vigelsø A, Yokota T, Helge JW, Dela F, Hey-Mogensen M. Skeletal muscle mitochondrial H2O2 emission increases with immobilization and decreases after aerobic training in young and older men. J Physiol. 2015;593:4011–4027. - PMC - PubMed
    1. Heo JW, No MH, Min DH, Kang JH, Kwak HB. Aging-induced sarcopenia and exercise. Asian J Kinesiol. 2017;19:43–59.
    1. Konopka AR, Suer MK, Wolff CA, Harber MP. Markers of human skeletal muscle mitochondrial biogenesis and quality control: effects of age and aerobic exercise training. J Gerontol A Biol Sci Med Sci. 2014;69:371–378. - PMC - PubMed