4.0 Article

Iron Supplementation Improves Skeletal Muscle Contractile Properties in Mice with CKD

期刊

KIDNEY360
卷 3, 期 5, 页码 843-858

出版社

AMER SOC NEPHROLOGY
DOI: 10.34067/KID.0004412021

关键词

chronic kidney disease; basic science; frailty; iron; kidney; mice; myosin; physical function

资金

  1. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases [K08 DK114558]
  2. Weill Cornell Medicine Rohr Family Clinical Scholar Award

向作者/读者索取更多资源

Patients with chronic kidney disease (CKD) often have compromised physical performance. In this study, it was found that untreated CKD led to a significant reduction in skeletal muscle force production, which was not solely due to muscle mass loss. Iron supplementation may help improve CKD-induced myopathy.
Background Patients with chronic kidney disease (CKD) frequently have compromised physical performance, which increases their mortality; however, their skeletal muscle dysfunction has not been characterized at the single-fiber and molecular levels. Notably, interventions to mitigate CKD myopathy are scarce. Methods The effect of CKD in the absence and presence of iron supplementation on the contractile function of individual skeletal muscle fibers from the soleus and extensor digitorum longus muscles was evaluated in 16-week-old mice. CKD was induced by the adenine diet, and iron supplementation was by weekly iron dextran injections. Results Maximally activated and fatigued fiber force production was decreased 24%-52% in untreated CKD, independent of size, by reducing strongly bound myosin/actin cross-bridges and/or decreasing myofilament stiffness in myosin heavy chain (MHC) I, IIA, and IIB fibers. Additionally, myosin/actin interactions in untreated CKD were slower for MHC I and IIA fibers and unchanged or faster in MHC IIB fibers. Iron supplementation improved anemia and did not change overall muscle mass in CKD mice. Iron supplementation ameliorated CKD-induced myopathy by increasing strongly bound cross-bridges, leading to improved specific tension, and/or returning the rate of myosin/actin interactions toward or equivalent to control values in MHC IIA and IIB fibers. Conclusions Skeletal muscle force production was significantly reduced in untreated CKD, independent of fiber size, indicating that compromised physical function in patients is not solely due to muscle mass loss. Iron supplementation improved multiple aspects of CKD-induced myopathy, suggesting that timely correction of iron imbalance may aid in ameliorating contractile deficits in CKD patients.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.0
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据