Improvement of Physical Decline Through Combined Effects of Muscle Enhancement and Mitochondrial Activation by a Gastric Hormone Ghrelin in Male 5/6Nx CKD Model Mice

Endocrinology. 2015 Oct;156(10):3638-48. doi: 10.1210/en.2015-1353. Epub 2015 Aug 4.

Abstract

Because a physical decline correlates with an increased risk of a wide range of disease and morbidity, an improvement of physical performance is expected to bring significant clinical benefits. The primary cause of physical decline in 5/6 nephrectomized (5/6Nx) chronic kidney disease model mice has been regarded as a decrease in muscle mass; however, our recent study showed that a decrease in muscle mitochondria plays a critical role. In the present study, we examined the effects of a gastric hormone ghrelin, which has been reported to promote muscle mitochondrial oxidation, on the physical decline in the chronic kidney disease model mice, focusing on the epigenetic modulations of a mitochondrial activator gene, peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α). Ghrelin treatment improved a decline in exercise endurance of 5/6Nx mice, associated with an increase in both of the muscle mass and mitochondrial amount. The expression level of PGC-1α was decreased in the skeletal muscle of 5/6Nx mice, which was associated with an increase in the methylation ratio of the cytosine residue at 260 base pairs upstream of the initiation point. Conversely, ghrelin treatment de-methylated the cytosine residue and increased the expression of PGC-1α. A representative muscle anabolic factor, IGF-1, did not affect the expression of PGC-1α and muscle mitochondrial amount, although it increased muscle mass. As a result, IGF-1 treatment in 5/6Nx mice did not increase the decreased exercise endurance as effectively as ghrelin treatment did. These findings indicate an advantage of ghrelin treatment for a recovery of physical decline.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Blotting, Western
  • Cell Line
  • DNA Methylation / drug effects
  • Disease Models, Animal
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism
  • Gene Expression / drug effects
  • Ghrelin / blood
  • Ghrelin / genetics
  • Ghrelin / pharmacology*
  • Male
  • Mice, Inbred C57BL
  • Mitochondria, Muscle / drug effects*
  • Mitochondria, Muscle / genetics
  • Mitochondria, Muscle / metabolism
  • Motor Activity / drug effects
  • Muscle Weakness / drug therapy*
  • Muscle Weakness / genetics
  • Muscle Weakness / metabolism
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Myoblasts / drug effects
  • Myoblasts / metabolism
  • Nephrectomy
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RNA Interference
  • Receptors, Ghrelin / genetics
  • Receptors, Ghrelin / metabolism
  • Renal Insufficiency, Chronic / complications*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Ghrelin
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, mouse
  • Receptors, Ghrelin
  • Transcription Factors
  • Electron Transport Complex IV
  • AMP-Activated Protein Kinases