Influence of acclimation temperature on mitochondrial DNA, RNA, and enzymes in skeletal muscle

1998 ◽  
Vol 275 (3) ◽  
pp. R905-R912 ◽  
Author(s):  
Brendan James Battersby ◽  
Christopher D. Moyes

Skeletal muscle fibers typically undergo modifications in their mitochondrial content, concomitant with alterations in oxidative metabolism that occur during the development of muscle fiber and in response to physiological stimuli. We examined how cold acclimation affects the mitochondrial properties of two fish skeletal muscle fiber types and how the regulators of mitochondrial content differed between tissues. After 2 mo of acclimation to either 4 or 18°C, mitochondrial enzyme activities in both red and white muscle were higher in cold-acclimated fish. No significant differences were detected between acclimation temperatures in the abundance of steady-state mitochondrial mRNA (cytochrome- c oxidase 1, subunit 6 of F0F1-ATPase), rRNA (16S), or DNA copy number. Steady-state mRNA for nuclear-encoded respiratory (adenine nucleotide translocase 1) and glycolytic genes showed high interindividual variability, particularly in the cold-acclimated fish. Although mitochondrial enzymes were 10-fold different between the two muscle types, mitochondrial DNA copy number differed only 4-fold. The relative abundance of mitochondrial mRNA and nuclear mRNA in red and white muscle reflected the differences in copy number of their respective genes. These data suggest that the response to physiological stimuli and determination of tissue-specific mitochondrial properties likely result from the regulation of nuclear-encoded genes.

2000 ◽  
Vol 6 (S2) ◽  
pp. 852-853
Author(s):  
Glenn M. Cohen ◽  
Margaret F. Scott

Striated skeletal muscle has been considered radioresistant because it is highly differentiated and post-mitotic. Striated muscle does, however, respond to irradiation with morphological and biochemical changes after short and long latency periods; vascular and/or neurological impairments might contribute to the delayed responses to irradiation.The objective of the present study was to determine the susceptibility of three amphibian muscle fiber types to Co60 irradiation. In amphibians, the three major fiber types are 1) large twitch fibers, which contain low levels of mitochondrial enzymes and lipids, but intermediate levels of glycogen; 2) small twitch fibers, which contain high levels of both glycolytic and mitochondrial enzymes (FIG. 1); and tonic fibers, which contain low levels of all three histochemical markers. Thus, the determination of susceptibility of different amphibian fiber types to irradiation might indicate whether the metabolic characteristics of the fibers, rather than morphological or electrical properties, could serve as an early indicator of radiation damage.


2021 ◽  
pp. 2101507
Author(s):  
Lorna E. Latimer ◽  
Dumitru Constantin-Teodosiu ◽  
Bhavesh Popat ◽  
Despina Constantin ◽  
Linzy Houchen-Wolloff ◽  
...  

COPD patients exhibit lower peak oxygen consumption (V̇O2PEAK), altered muscle metabolism and impaired exercise tolerance compared with age-matched controls. Whether these traits reflect muscle level deconditioning (impacted by ventilatory constraints) and/or dysfunction in mitochondrial ATP production capacity is debated. By studying aerobic exercise training (AET) at a matched relative intensity and subsequent exercise withdrawal period (EW) we aimed to elucidate the whole-body and muscle mitochondrial responsiveness of healthy-young (HY), healthy-older (HO) and COPD volunteers to whole-body exercise.The HY (n=10), HO (n=10) and COPD (n=20) volunteers were studied before, after eight-weeks AET (65% V̇O2PEAK) and after four-weeks EW. V̇O2PEAK, muscle maximal mitochondrial ATP production rates (MAPR), mitochondrial content, mitochondrial DNA copy number and abundance of 59 targeted fuel metabolism mRNAs were determined at all time-points.Muscle MAPR (normalised for mitochondrial content) was not different for any substrate combination in HO, HY and COPD at baseline, but mitochondrial DNA copy number relative to a nuclear-encoded house-keeping gene was greater in HY (mean±sd) (804±67) than in HO (631±69), p=0.041. AET increased V̇O2PEAK in HO (17%, p=0.002) and HY (21%, p<0.001) but not COPD (p=0.603). Muscle MAPR for palmitate increased with training in HO (57%, p=0.041) and HY (56%, p=0.003) and decreased with EW in HO (−45%, p=0.036) and HY (−30%, p=0.016), but was unchanged in COPD (p=0.594). Mitochondrial DNA copy number increased with AET in HY (66%, p=0.001) but not HO (p=0.081) or COPD (p=0.132). The observed changes in muscle mRNA abundance were similar in all groups after AET and EW.Intrinsic mitochondrial function was not impaired by ageing or COPD in the untrained state. Whole-body and muscle mitochondrial responses to AET were robust in HY, evident in HO, but deficient in COPD. All showed robust muscle mRNA responses. Higher relative exercise intensities during whole-body training may be needed to maximise whole-body and muscle mitochondrial adaptation in COPD.


Cells ◽  
2019 ◽  
Vol 8 (3) ◽  
pp. 247 ◽  
Author(s):  
Ji Baek ◽  
Hyeonwi Son ◽  
Young-Hoon Jeong ◽  
Sang Park ◽  
Hyun Kim

The changes in telomere length and mitochondrial DNA copy number (mtDNAcn) are considered to be aging markers. However, many studies have provided contradictory or only fragmentary information about changes of these markers in animal models, due to inaccurate analysis methods and a lack of objective aging standards. To establish chronological aging standards for these two markers, we analyzed telomere length and mtDNAcn in 12 tissues—leukocytes, prefrontal cortex, hippocampus, pituitary gland, adrenal gland, retina, aorta, liver, kidney, spleen, skeletal muscle, and skin—from a commonly used rodent model, C57BL/6 male mice aged 2–24 months. It was found that at least one of the markers changed age-dependently in all tissues. In the leukocytes, hippocampus, retina, and skeletal muscle, both markers changed age-dependently. As a practical application, the aging marker changes were analyzed after chronic immobilization stress (CIS) to see whether CIS accelerated aging or not. The degree of tissue-aging was calculated using each standard curve and found that CIS accelerated aging in a tissue-specific manner. Therefore, it is expected that researchers can use our standard curves to objectively estimate tissue-specific aging accelerating effects of experimental conditions for least 12 tissues in C57BL/6 male mice.


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