Plasticity changes in iron homeostasis in hibernating Daurian ground squirrels (Spermophilus dauricus) may counteract chronically inactive skeletal muscle atrophy

J Comp Physiol B. 2024 Apr;194(2):191-202. doi: 10.1007/s00360-024-01543-7. Epub 2024 Mar 24.

Abstract

Disuse-induced muscular atrophy is frequently accompanied by iron overload. Hibernating animals are a natural animal model for resistance to disuse muscle atrophy. In this paper, we explored changes in skeletal muscle iron content of Daurian ground squirrels (Spermophilus dauricus) during different periods of hibernation as well as the regulatory mechanisms involved. The results revealed that compared with the summer active group (SA), iron content in the soleus muscle (SOL) decreased (- 65%) in the torpor group (TOR), but returned to normal levels in the inter-bout arousal (IBA); splenic iron content increased in the TOR group (vs. SA, + 67%), decreased in the IBA group (vs. TOR, - 37%). Expression of serum hepcidin decreased in the TOR group (vs. SA, - 22%) and returned to normal levels in the IBA groups; serum ferritin increased in the TOR group (vs. SA, + 31%), then recovered in the IBA groups. Soleus muscle transferrin receptor 1 (TfR1) expression increased in the TOR group (vs. SA, + 83%), decreased in the IBA group (vs. TOR, - 30%); ferroportin 1 increased in the IBA group (vs. SA, + 55%); ferritin increased in the IBA group (vs. SA, + 42%). No significant differences in extensor digitorum longus in iron content or iron metabolism-related protein expression were observed among the groups. Significantly, all increased or decreased indicators in this study returned to normal levels after the post-hibernation group, showing remarkable plasticity. In summary, avoiding iron overload may be a potential mechanism for hibernating Daurian ground squirrels to avoid disuse induced muscular atrophy. In addition, the different skeletal muscle types exhibited unique strategies for regulating iron homeostasis.

Keywords: Hepcidin; Hibernation; Iron metabolism; Skeletal muscle; Spleen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD*
  • Cation Transport Proteins / metabolism
  • Ferritins* / metabolism
  • Hepcidins* / metabolism
  • Hibernation* / physiology
  • Homeostasis*
  • Iron* / metabolism
  • Male
  • Muscle, Skeletal* / metabolism
  • Muscular Atrophy* / metabolism
  • Muscular Atrophy* / pathology
  • Receptors, Transferrin* / metabolism
  • Sciuridae* / physiology
  • Spleen / metabolism

Substances

  • Iron
  • Hepcidins
  • Receptors, Transferrin
  • Ferritins
  • metal transporting protein 1
  • CD71 antigen
  • Cation Transport Proteins
  • Antigens, CD