Correlation Engine 2.0
Clear Search sequence regions


  • calcineurin (6)
  • control group (1)
  • factors (4)
  • fast (1)
  • fiber (8)
  • isoforms (4)
  • male (2)
  • Myosin (2)
  • new york (1)
  • NFAT isoforms (2)
  • NFATC (2)
  • nfatc1 protein (1)
  • NFATc4 (1)
  • protein rat (1)
  • random (1)
  • rats (1)
  • twitch (2)
  • wistar rats (2)
  • Sizes of these terms reflect their relevance to your search.

    The purpose of this study was to determine whether the aerobic training-induced fiber-type transition in different muscles is associated with alterations in NFAT isoforms gene expression. We hypothesized that the aerobic training-induced fiber-type transition would be mediated by NFATc1-c3 isoforms without altering the CaN expression. Male Wistar rats (80 days old) were divided into a trained group (T; n=8) that underwent an 8-wk swimming endurance training program (5 days/week) and a control group (C; n=8). After the experimental period, the animals were sacrificed, and the soleus (SOL) and plantaris (PL) muscles were collected for morphometrical, histochemical and molecular analyses. Aerobic training induced a type I-to-type IIA fiber transition in the SOL muscle and a type IIB-to-type IIA fiber transition in the PL muscle, which were concomitant with a significant (p<0.05) increase in NFATc1-c3 gene expression in both the SOL and PL muscles. In contrast, the expression levels of calcineurin (CaN) and NFATc4 remained unchanged. Therefore, our results showed that fiber type switching induced by aerobic training is mediated by NFATc1-c3 isoforms without altering the CaN expression. © Georg Thieme Verlag KG Stuttgart · New York.

    Citation

    I J Vechetti, A F Aguiar, R W A de Souza, F L A Almeida, H B de Almeida Dias, M A de Aguiar Silva, F R Carani, R L P Ferraresso, R F Carvalho, M Dal-Pai-Silva. NFAT isoforms regulate muscle fiber type transition without altering CaN during aerobic training. International journal of sports medicine. 2013 Oct;34(10):861-7

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 23549689

    View Full Text