| Literature DB >> 33407830 |
Stephan Kröger1, Bridgette Watkins2.
Abstract
Almost every muscle contains muscle spindles. These delicate sensory receptors inform the central nervous system (CNS) about changes in the length of individual muscles and the speed of stretching. With this information, the CNS computes the position and movement of our extremities in space, which is a requirement for motor control, for maintaining posture and for a stable gait. Many neuromuscular diseases affect muscle spindle function contributing, among others, to an unstable gait, frequent falls and ataxic behavior in the affected patients. Nevertheless, muscle spindles are usually ignored during examination and analysis of muscle function and when designing therapeutic strategies for neuromuscular diseases. This review summarizes the development and function of muscle spindles and the changes observed under pathological conditions, in particular in the various forms of muscular dystrophies.Entities:
Keywords: Intrafusal fibers; Mechanotransduction; Muscular dystrophy; Neuromuscular diseases; Proprioception; Sensory physiology
Mesh:
Year: 2021 PMID: 33407830 PMCID: PMC7788844 DOI: 10.1186/s13395-020-00258-x
Source DB: PubMed Journal: Skelet Muscle ISSN: 2044-5040 Impact factor: 4.912