Exercise In A Pill: Compounds That Reproduce The Effects Of Exercise On Muscle Metabolism And Growth

Tech ID: 30362 / UC Case 2019-355-0

Summary

UCLA researchers in the Department of Neurology have identified and synthesized small molecule analogs that activate skeletal muscle growth, mediated by calcium calmodulin kinase II signaling.

Background

Skeletal muscle has a remarkable ability to alter its metabolic and contractile phenotype in response to changes in functional demands.  Increased load bearing and extended duration of activation leads to muscle adaptation by triggering target genes to induce muscle hypertrophy, fiber type transitions, or mitochondrial biogenesis.  Similarly, decreased mechanical loading due to inactivity or injury activates signaling pathways that induce muscle atrophy.  In skeletal muscle, calcium-mediated signaling plays an essential role in the muscle contraction relaxation cycle, as well as contractile activity-dependent and fiber type-specific gene expression.  Calcium calmodulin-dependent kinases (CaMKs) have been shown to promote mitochondrial biogenesis, and expression of fiber type-specific myofibrillar proteins for fiber type transition, as well as to sense altered functional demands and activate adaptation responses.

Innovation

Researchers at UCLA have identified a small molecule activator of calcium calmodulin kinase II (CaMKIIβ).  Activation of CaMKIIβ increases muscle size, mitochondrial bioenergetics, and improves the performance of mouse with limb girdle muscular dystrophy.  Small molecule activator analogs are synthesized with increased solubility and reduced toxicity to develop therapeutics for individuals suffering from a variety of muscle conditions.

Applications

  • Reverse muscle wasting and metabolic deficiencies in limb girdle muscular dystrophy, sarcopenia (from aging or extended bed rest), cachexia, and triadopathies.

Advantages

  • Identified mechanism of action
  • Validated in animal disease models

State Of Development

The benefit effect has been demonstrated in limb girdle muscular dystrophy type 2A (LGMD2A) mouse model.

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Inventors

  • John, Varghese

Other Information

Keywords

musculoskeletal disease, skeletal muscle, muscle growth, muscle metabolism, muscle adaptation, limb girdle muscular dystrophy, sarcopenia, cachexia, triadopathy

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