Effect of robotic gait training on muscle and bone characteristics in spinal cord transected rats

Author:

LeBlanc Michele1ORCID,Soucy Michael1,Moustafa‐Bayoumi Moustafa2,Soto Dalziel3,Nessler Jeff3

Affiliation:

1. Exercise Science Department California Lutheran University Thousand Oaks California USA

2. Exercise Science Department Helwan University Cairo Egypt

3. Department of Kinesiology California State University San Marcos USA

Abstract

AbstractOsteoporosis and loss of muscle mass are secondary issues with spinal cord injury. Robotic gait training has provided evidence of increasing bone density and muscle mass, but its effect on bone strength is undetermined. The purpose of this study was to determine the effect of a 6‐week robotic locomotion training program on skeletal muscle mass and bone characteristics. Twelve female Sprague‐Dawley rats received a mid‐thoracic spinal cord transection at 5 days old and at 3 weeks old were assigned to a Control or Trained Group. The Trained Group performed 5‐min sessions on the Rat Stepper 5 days a week for 6 weeks with 90% of body weight supported. At the end of the 6 weeks, body mass was obtained and right femurs and four lower extremity muscles were harvested. Femur bone mineral density was measured with DXA and mechanical characteristics of the femur were determined via 3‐point bending testing. Independent t‐tests, effects sizes and percent differences were computed between the two groups (p < 0.05). The Trained Group had significantly larger normalized femur mass (p = 0.007) and normalized soleus muscle mass (p = 0.033) when compared to the Control Group. There was a medium or large effect size with the Trained Groups' femurs having larger mass, bone mineral density, rupture loads, cortical wall thickness, shaft cross sectional area, soleus mass, normalized gastrocnemius mass, and smaller shaft inner diameters compared to the Control Group. These changes may contribute to decreasing osteoporosis and fracture risk in those with spinal cord injuries.

Publisher

Wiley

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