Diagnostics (May 2022)

Feasibility of <sup>18</sup>F-Fluorocholine PET for Evaluating Skeletal Muscle Atrophy in a Starved Rat Model

  • Sun Mi Park,
  • Jisu Kim,
  • Suji Baek,
  • Joo-Yeong Jeon,
  • Sang Ju Lee,
  • Seo Young Kang,
  • Min Young Yoo,
  • Hai-Jeon Yoon,
  • Seung Hae Kwon,
  • Kiwon Lim,
  • Seung Jun Oh,
  • Bom Sahn Kim,
  • Kang Pa Lee,
  • Byung Seok Moon

DOI
https://doi.org/10.3390/diagnostics12051274
Journal volume & issue
Vol. 12, no. 5
p. 1274

Abstract

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Imaging techniques for diagnosing muscle atrophy and sarcopenia remain insufficient, although various advanced diagnostic methods have been established. We explored the feasibility of 18F-fluorocholine (18F-FCH) positron emission tomography/computed tomography (PET/CT) for evaluating skeletal muscle atrophy, as an imaging technique that tracks choline level changes in muscles. Cell uptake in L6 cells by 18F-FCH was performed in a complete medium containing serum (untreated group, UN) and a serum-free medium (starved group, ST). Small-animal-dedicated PET/CT imaging with 18F-FCH was examined in in-vivo models with rats that were starved for 2 days to cause muscle atrophy. After the hind limbs were dissected, starvation-induced in-vivo models were anatomically confirmed by reverse-transcription polymerase chain reaction to evaluate the expression levels of the atrophy markers muscle RING-finger protein-1 (MuRF-1) and atrogin-1. 18F-FCH uptake was lower in the starvation-induced cells than in the untreated group, and in-vivo PET uptake also revealed a similar tendency (the average standardized uptake value (SUVmean) = 0.26 ± 0.06 versus 0.37 ± 0.07, respectively). Furthermore, the expression levels of MuRF-1 and atrogin-1 mRNA were significantly increased in the starvation-induced muscle atrophy of rats compared to the untreated group. 18F-FCH PET/CT may be a promising tool for diagnosing skeletal muscle atrophy.

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