首页> 美国卫生研究院文献>Frontiers in Physiology >Caloric restriction induces energy-sparing alterations in skeletal muscle contraction fiber composition and local thyroid hormone metabolism that persist during catch-up fat upon refeeding
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Caloric restriction induces energy-sparing alterations in skeletal muscle contraction fiber composition and local thyroid hormone metabolism that persist during catch-up fat upon refeeding

机译:热量限制会导致骨骼肌收缩纤维成分和局部甲状腺激素代谢中的能量节省改变这些能量在补充脂肪的追赶脂肪期间持续存在

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摘要

Weight regain after caloric restriction results in accelerated fat storage in adipose tissue. This catch-up fat phenomenon is postulated to result partly from suppressed skeletal muscle thermogenesis, but the underlying mechanisms are elusive. We investigated whether the reduced rate of skeletal muscle contraction-relaxation cycle that occurs after caloric restriction persists during weight recovery and could contribute to catch-up fat. Using a rat model of semistarvation-refeeding, in which fat recovery is driven by suppressed thermogenesis, we show that contraction and relaxation of leg muscles are slower after both semistarvation and refeeding. These effects are associated with (i) higher expression of muscle deiodinase type 3 (DIO3), which inactivates tri-iodothyronine (T3), and lower expression of T3-activating enzyme, deiodinase type 2 (DIO2), (ii) slower net formation of T3 from its T4 precursor in muscles, and (iii) accumulation of slow fibers at the expense of fast fibers. These semistarvation-induced changes persisted during recovery and correlated with impaired expression of transcription factors involved in slow-twitch muscle development. We conclude that diminished muscle thermogenesis following caloric restriction results from reduced muscle T3 levels, alteration in muscle-specific transcription factors, and fast-to-slow fiber shift causing slower contractility. These energy-sparing effects persist during weight recovery and contribute to catch-up fat.
机译:热量限制后体重的重新增加导致脂肪在脂肪组织中的储存加速。据推测,这种追赶脂肪现象部分是由于抑制了骨骼肌的生热作用所致,但其潜在机制尚不清楚。我们研究了热量限制后骨骼肌收缩松弛松弛周期的减少率是否在体重恢复期间持续存在,并且是否有助于追赶脂肪。使用半饥饿-再喂养的大鼠模型,其中脂肪的恢复由抑制的生热作用驱动,我们显示半饥饿和再喂养后腿部肌肉的收缩和松弛较慢。这些作用与(i)3型肌脱碘酶(DIO3)的较高表达(其使三碘甲状腺素(T3)失活)以及T3活化酶2型脱碘酶(DIO2)的较低表达有关(ii)较慢的网形成T3的T4前体在肌肉中的含量;(iii)慢纤维的积累以快纤维为代价。这些半饥饿引起的变化在恢复过程中持续存在,并与慢肌发展相关的转录因子表达受损有关。我们得出的结论是,热量限制后,肌肉生热的减弱是由于肌肉T3水平降低,肌肉特异性转录因子的改变以及快速至缓慢的纤维移位导致收缩力降低所致。这些节省能量的作用在体重恢复期间持续存在,并有助于追赶脂肪。

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