Skeletal muscle denervation investigations: selecting an experimental control wisely

Author:

Liu Haiming1,Thompson LaDora V.2

Affiliation:

1. Division of Gerontology and Geriatric Medicine, Department of Medicine, School of Medicine, University of Washington, and Geriatric Research, Education, and Clinical Center, Veterans Affairs Puget Sound Healthcare System, Seattle, Washington

2. Department of Physical Therapy and Athletic Training, Boston University, Boston, Massachusetts

Abstract

Unilateral denervation is widely used for studies investigating mechanisms of muscle atrophy. The “contralateral-innervated muscle” is a commonly used experimental control in denervation studies. It is not clear whether denervation unilaterally alters the proteolytic system in the contralateral-innervated muscles. Therefore, the objectives of this rapid report are 1) to determine whether unilateral denervation has an effect on the proteolytic system in contralateral-innervated control muscles and 2) to identify the changes in proteasome properties in denervated muscles after 7- and 14-day tibial nerve transection with either the contralateral-innervated muscles or intact muscles from nonsurgical mice used as the experimental control. In the contralateral-innervated muscles after 7 and 14 days of nerve transection, the proteasome activities and content are significantly increased compared with muscles from nonsurgical mice. When the nonsurgical mice are used as the experimental control, a robust increase in proteasome properties is found in the denervated muscles. This robust increase in proteasome properties is eliminated when the contralateral-innervated muscles are the experimental control. In conclusion, there is a crossover effect from unilateral denervation on proteolytic parameters. As a result, the crossover effect on contralateral-innervated muscles must be considered when an experimental control is selected in a denervation study.

Funder

AG/NIA/NIH

Boston University (BU)

University of Minnesota (UM)

U.S. Department of Veterans Affairs (VA)

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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