Glycine receptor subunit-β-deficiency in a mouse model of spasticity results in attenuated physical performance, growth, and muscle strength

Am J Physiol Regul Integr Comp Physiol. 2022 May 1;322(5):R368-R388. doi: 10.1152/ajpregu.00242.2020. Epub 2022 Feb 2.

Abstract

Spasticity is the most common neurological disorder associated with increased muscle contraction causing impaired movement and gait. The aim of this study was to characterize the physical performance, skeletal muscle function, and phenotype of mice with a hereditary spastic mutation (B6.Cg-Glrbspa/J). Motor function, gait, and physical activity of juvenile and adult spastic mice and the morphological, histological, and mechanical characteristics of their soleus and gastrocnemius medialis muscles were compared with those of their wild-type (WT) littermates. Spastic mice showed attenuated growth, impaired motor function, and low physical activity. Gait of spastic mice was characterized by a typical hopping pattern. Spastic mice showed lower muscle forces, which were related to the smaller physiological cross-sectional area of spastic muscles. The muscle-tendon complex length-force relationship of adult gastrocnemius medialis was shifted toward shorter lengths, which was explained by attenuated longitudinal tibia growth. Spastic gastrocnemius medialis was more fatigue resistant than WT gastrocnemius medialis. This was largely explained by a higher mitochondrial content in muscle fibers and relatively higher percentage of slow-type muscle fibers. Muscles of juvenile spastic mice showed similar differences compared with WT juvenile mice, but these were less pronounced than between adult mice. This study shows that in spastic mice, disturbed motor function and gait is likely to be the result of hyperactivity of skeletal muscle and impaired skeletal muscle growth, which progress with age.

Keywords: physiological cross-sectional area; plantar flexor muscles; sarcomeres in series; skeletal muscle; spastic paresis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cerebral Palsy* / pathology
  • Mice
  • Muscle Spasticity* / genetics
  • Muscle Spasticity* / pathology
  • Muscle Strength
  • Muscle, Skeletal / physiology
  • Physical Functional Performance
  • Receptors, Glycine

Substances

  • Receptors, Glycine

Associated data

  • figshare/10.6084/m9.figshare.14838078
  • figshare/10.6084/m9.figshare.17695577
  • figshare/10.6084/m9.figshare.17695619
  • figshare/10.6084/m9.figshare.17695622
  • figshare/10.6084/m9.figshare.17695625