Abstract

Sarcopenia and impaired cardiorespiratory fitness are commonly observed in older individuals and patients with chronic kidney disease (CKD). Declines in skeletal muscle function and aerobic capacity can progress into impaired physical function and inability to perform activities of daily living. Physical function is highly associated with important clinical outcomes such as hospitalization, functional independence, quality of life, and mortality. While lifestyle modifications such as exercise and dietary interventions have been shown to prevent and reverse declines in physical function, the utility of these treatment strategies is limited by poor widespread adoption and adherence due to a wide variety of both perceived and actual barriers to exercise. Therefore, identifying novel treatment targets to manage physical function decline is critically important. Klotho, a remarkable protein with powerful anti-aging properties has recently been investigated for its role in musculoskeletal health and physical function. Klotho is involved in several key processes that regulate skeletal muscle function, such as muscle regeneration, mitochondrial biogenesis, endothelial function, oxidative stress, and inflammation. This is particularly important for older adults and patients with CKD, which are known states of Klotho deficiency. Emerging data support the existence of Klotho-related benefits to exercise and for potential Klotho-based therapeutic interventions for the treatment of sarcopenia and its progression to physical disability. However, significant gaps in our understanding of Klotho must first be overcome before we can consider its potential ergogenic benefits. These advances will be critical to establish the optimal approach to future Klotho-based interventional trials and to determine if Klotho can regulate physical dysfunction.

Highlights

  • In 1997, Kuro-o and colleagues [1] identified a novel gene that encodes a transmembrane protein with powerful anti-aging properties

  • In EFmKL46 mice, Klotho gene expression was elevated over the entire regeneration period, and muscle fiber size significantly increased by 139% between 7 and 21 days post-injury, while wild-type mice showed only a 60% increase size during the same period of muscle repair [82]. These findings suggest that upregulation of locally expressed Klotho in skeletal muscle following injury is critical for effective muscle regeneration and this process is blunted in aged muscle

  • Limited evidence suggests that the gangliosides GM1 and GM3 present in lipid rafts may serve as membrane receptors for soluble isoform of Klotho (sKlotho) [205]

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Summary

INTRODUCTION

In 1997, Kuro-o and colleagues [1] identified a novel gene that encodes a transmembrane protein with powerful anti-aging properties. Research in animal models suggests that enhancing Klotho levels may improve skeletal muscle strength, quality, and recovery following injury and may represent a novel ergogenic agent [5, 33, 34] This comprehensive review considers the biological mechanisms of Klotho, detrimental effects imposed by its deficiency on physical function in aging and CKD, and explores contemporary evidence supporting the potential ergogenic benefits of therapeutic targeting of Klotho. Studies in Klotho deficient mice [3] and older adults [7,8,9,10,11] have revealed a strong association between Klotho levels and skeletal muscle strength and physical function. Welc et Frontiers in Rehabilitation Sciences | www.frontiersin.org

Key findings
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CONCLUSIONS AND FUTURE DIRECTIONS
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