Advances in Chronic Kidney Disease
Volume 16, Issue 6 , Pages 501-510, November 2009

Anabolic and Catabolic Mechanisms in End-Stage Renal Disease

  • Kirsten L. Johansen

      Affiliations

    • Corresponding Author InformationAddress correspondence to Kirsten L. Johansen, MD, Nephrology Section, Box 111J, San Francisco VA Medical Center, 4150 Clement Street, San Francisco, CA 94121.

Nephrology Section, San Francisco VA Medical Center and Division of Nephrology, University of California, San Francisco, San Francisco, CA

Muscle wasting is a prominent feature of end-stage renal disease and is associated with muscle weakness and poor physical functioning. Potential reasons for muscle wasting include advancing age, sedentary behavior, inflammation, poor nutritional intake, androgen deficiency, oxidative stress, metabolic acidosis, and insulin resistance. Each of these conditions can be associated with decreased protein synthesis, increased protein degradation, or both. The primary muscle protein synthesis pathway is the insulin insulin-like growth factor-1/phosphatidyl inositol-3 kinase/Akt pathway, which results in the phosphorylation of the mammalian target of rapamycin and subsequent increased protein synthesis. The major protein degradation pathway is the ubiquitin-proteasome system. This review discusses the ways in which end-stage renal disease tips the balance of protein turnover towards catabolism and the mechanisms by which various interventions may work to mitigate wasting or even cause anabolism.

Key Words: Muscle catabolism, End-Stage Renal Disease (ESRD), Catabolism

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PII: S1548-5595(09)00130-X

doi:10.1053/j.ackd.2009.07.007

Advances in Chronic Kidney Disease
Volume 16, Issue 6 , Pages 501-510, November 2009