2019
DOI: 10.1002/mus.26714
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Altered muscle electrical tissue properties in a mouse model of premature aging

Abstract: Introduction Improved methods are needed to detect and quantify age‐related muscle change. In this study we assessed the electrical properties of muscle impacted by acquired mitochondrial DNA mutations via the PolG mouse, which exhibits typical age‐associated features, and the impact of a potential therapy, nicotinamide mononucleotide (NMN). Methods The gastrocnemii of 24 PolG and 30 wild‐type (WT) mice (8 PolG and 17 WT treated with NMN) were studied in an electrical impedance‐measuring cell. Conductivity and… Show more

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Cited by 10 publications
(17 citation statements)
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“…Following ex vivo impedance measurements, GA muscles were fixed, sectioned, stained to identify myocyte cell membranes and nuclei, and the stained sections imaged and myofiber cross‐sectional area (CSA) determined as previously described 15 . On average, 300 myofibers (per WT muscle) and 375 myofibers (per db/db muscle) were counted per animal, for an average total number of 1487 myofibers for WT mice and 1867 myofibers for db/db mice at each timepoint.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Following ex vivo impedance measurements, GA muscles were fixed, sectioned, stained to identify myocyte cell membranes and nuclei, and the stained sections imaged and myofiber cross‐sectional area (CSA) determined as previously described 15 . On average, 300 myofibers (per WT muscle) and 375 myofibers (per db/db muscle) were counted per animal, for an average total number of 1487 myofibers for WT mice and 1867 myofibers for db/db mice at each timepoint.…”
Section: Methodsmentioning
confidence: 99%
“…Following ex vivo impedance measurements, GA muscles were fixed, sectioned, stained to identify myocyte cell membranes and nuclei, and the stained sections imaged and myofiber cross-sectional area (CSA) determined as previously described. 15 On average, 300 myofibers (per WT muscle) and 375 myofibers (per db/db muscle) were counted per animal, for an average total number of 1487 myofibers for WT mice and 1867 myofibers for db/db mice at each timepoint. We built separate models for predicting CSA and TG content for each EIM modality by implementing our previously adopted statistical approach 27,28 using the least absolute shrinkage and selection operator (LASSO) to perform a penalized regression procedure, coupled with a variable tuning parameter to avoid over-fitting 39 and select the most influential predictors.…”
Section: Histologymentioning
confidence: 99%
“…The success of obtaining information about the impedance characteristics of muscle using EIM has been demonstrated in rodent models of injury, [36][37][38] inflammation, 39 aging, 27,30,40 and neuromuscular conditions, 41,42 and clinically during therapy trials in a variety of neuromuscular diseases (NMDs). 2,8,[43][44][45] Previous studies have also investigated relationships between impedance values and cell size and connective tissue deposition.…”
Section: Discussionmentioning
confidence: 99%
“…Samples were then embedded in paraffin blocks, sectioned into 10‐μm slices, and stained with anti–collagen VI antibody (Abcam ab6588) to identify the myocyte cell membranes and 4′,6‐diamidino‐2‐phenylindole (DAPI) to detect nuclei. The myofiber CSA was determined as described elsewhere 30 . Sections were imaged at 20× with an epifluorescence microscope (AxioImager M1; Carl Zeiss, Oberkochen, Germany) and myofiber area was measured using the muscle morphometry plug‐in (developed by A. Sinadinos using Eclipse IDE) in FIJI, the open source image processing software (ImageJ version 2.0.0‐rc‐68/1.52d; W.S.…”
Section: Methodsmentioning
confidence: 99%
“…Clearly there is a need for small, non-invasive diagnostic tools that will allow monitoring of muscle health and condition during all upcoming missions. Electrical impedance myography (EIM) is a technology that has been used in both pre-clinical (Li et al, 2016;Kapur et al, 2018b;Nagy et al, 2018;Clark-Matott et al, 2019;Mortreux et al, 2019d) and clinical studies (Spieker et al, 2013;Mcilduff et al, 2017;Rutkove et al, 2017;Sanchez and Rutkove, 2017a;Shefner et al, 2018). By applying a high-frequency, low-amplitude electrical current in the muscle and recording the resulting voltages, muscle quality can be assessed non-invasively (Sanchez and Rutkove, 2017b).…”
Section: Introductionmentioning
confidence: 99%