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Coordinate Mapping of Hyolaryngeal Mechanics in Swallowing
Published on: May 6, 2014
Neuromuscular specializations within human pharyngeal constrictor muscles
1Department of Otolaryngology, The Mount Sinai School of Medicine, New York, NY 10029-6574, USA.
The Annals of Otology, Rhinology, and Laryngology
|September 13, 2007
Summary
Adult human pharyngeal constrictor muscles have two distinct layers: a slow inner layer (SIL) innervated by nerve IX and a fast outer layer (FOL) innervated by nerve X. This specialization may relate to speech and respiration.
Area of Science:
- Anatomy and Physiology
- Neuroscience
- Muscle Biology
Background:
- Current understanding posits pharyngeal constrictor (PC) muscles are innervated by the vagus (X) nerve and possess homogeneous muscle fiber content.
- This study challenges the homogeneous model, proposing distinct functional layers within the PC muscles.
Purpose of the Study:
- To test the hypothesis that adult human PCs are divided into two distinct, specialized layers: a slow inner layer (SIL) and a fast outer layer (FOL).
- To determine the specific nerve innervating each layer (glossopharyngeal (IX) for SIL, vagus (X) for FOL).
- To characterize the muscle fiber types within each layer.
Main Methods:
- Human pharynges (n=8) were analyzed using Sihler's stain for gross motor innervation, and acetylcholinesterase (AChE) and silver stains for terminal axonal branching.
- Myosin heavy chain (MHC) expression in PC muscle fibers was assessed via immunocytochemical and immunoblotting techniques.
- Developmental, pathological (idiopathic Parkinson's disease), and comparative (macaque monkey) specimens were examined to assess layer specialization.
Main Results:
- Nerve IX innervated the SIL, while nerve X innervated the FOL in adult human PCs.
- The SIL contained slow-tonic and alpha-cardiac MHC isoforms, indicating a slow-contracting muscle.
- The FOL contained developmental MHC isoforms, indicative of fast-contracting muscle; this layer was obscured in elderly individuals and those with idiopathic Parkinson's disease.
Conclusions:
- Human PCs exhibit functional fiber layering with distinct innervation and specialized muscle fibers, with the SIL appearing unique to normal humans.
- The SIL's specialized MHC isoforms suggest a role in sustained contractions for human speech and respiration.
- The FOL's adaptation for rapid movement supports its role in swallowing, and observed fiber shifts in senescence and IPD may explain dysphagia susceptibility.
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