Crural and costal diaphragm function during emesis

Together, the costal and crural diaphragm constitute the primary respiratory muscle in mammals, but functionally, they are distinct. The crural segment has additional gastrointestinal function, wrapped around the esophagus at the esophagogastric junction, contributing to the esophageal sphincter. Emesis is an expulsive process that requires the coordinated action of multiple muscles to rapidly force out gastric contents. The simultaneous mechanical action and neural activation of the diaphragm segments during the process of emesis, especially expulsion, is uncertain. Detailed divergence of the crural diaphragm to sphincter function during emesis has not been studied. In six awake, spontaneously breathing canines, electrical activity and corresponding muscle shortening of the costal and crural diaphragm were measured at five phases of emesis (rest, early prodrome, mid prodrome, late prodrome, and expulsion) induced by apomorphine. Overall, baseline muscle length decreased and baseline EMG increased progressively from rest through prodrome for both costal and crural, but at expulsion, the crural segment diverged, lengthening abruptly. Shortening and EMG activity per breath for costal changed slightly throughout emesis; crural shortening and EMG activity increased abruptly at expulsion. The divergent action of crural during expulsion developed sequentially through each breath. Also, neuromechanical coupling of the segments reversed at expulsion, with contractility of the crural surpassing that of the costal. These measurements confirm a disparate action of crural diaphragm, compared with costal, to facilitate expulsion. During the process of emesis, although the costal persists as an obligatory respiratory muscle, the crural converts from respiratory muscle to opening sphincter.<b>NEW & NOTEWORTHY</b> Although the diaphragm is known as a primary respiratory muscle, the two diaphragm sections, the costal and crural, have notably different functions. This study elucidates the essential role of the crural diaphragm during emesis, a gastrointestinal process. During emesis, the crural diaphragm abandons respiratory function and transmutes to act as an esophageal sphincter. Meanwhile, the costal diaphragm continues ventilatory function.

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Publication Details

Journal
American Journal of Physiology-Gastrointestinal and Liver Physiology
Published
2025-05-17
DOI
https://doi.org/10.1152/ajpgi.00354.2024
Primary Topic
Infant Health and Development
Type
article
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article

Crural and costal diaphragm function during emesis

Ravinder K. Mittal, Paul A. Easton, Michael Ji, J. Park et al.
American Journal of Physiology-Gastrointestinal and Liver Physiology
Infant Health and Development
article

Crural and costal diaphragm function during emesis

Ravinder K. Mittal, Paul A. Easton, Michael Ji, J. Park, Giovanni Tagliabue
article en

Abstract

Together, the costal and crural diaphragm constitute the primary respiratory muscle in mammals, but functionally, they are distinct. The crural segment has additional gastrointestinal function, wrapped around the esophagus at the esophagogastric junction, contributing to the esophageal sphincter. Emesis is an expulsive process that requires the coordinated action of multiple muscles to rapidly force out gastric contents. The simultaneous mechanical action and neural activation of the diaphragm segments during the process of emesis, especially expulsion, is uncertain. Detailed divergence of the crural diaphragm to sphincter function during emesis has not been studied. In six awake, spontaneously breathing canines, electrical activity and corresponding muscle shortening of the costal and crural diaphragm were measured at five phases of emesis (rest, early prodrome, mid prodrome, late prodrome, and expulsion) induced by apomorphine. Overall, baseline muscle length decreased and baseline EMG increased progressively from rest through prodrome for both costal and crural, but at expulsion, the crural segment diverged, lengthening abruptly. Shortening and EMG activity per breath for costal changed slightly throughout emesis; crural shortening and EMG activity increased abruptly at expulsion. The divergent action of crural during expulsion developed sequentially through each breath. Also, neuromechanical coupling of the segments reversed at expulsion, with contractility of the crural surpassing that of the costal. These measurements confirm a disparate action of crural diaphragm, compared with costal, to facilitate expulsion. During the process of emesis, although the costal persists as an obligatory respiratory muscle, the crural converts from respiratory muscle to opening sphincter.<b>NEW & NOTEWORTHY</b> Although the diaphragm is known as a primary respiratory muscle, the two diaphragm sections, the costal and crural, have notably different functions. This study elucidates the essential role of the crural diaphragm during emesis, a gastrointestinal process. During emesis, the crural diaphragm abandons respiratory function and transmutes to act as an esophageal sphincter. Meanwhile, the costal diaphragm continues ventilatory function.

American Journal of Physiology-Gastrointestinal and Liver PhysiologyVol. 329(1)
University of Alberta (CA), University of Calgary (CA), University of California San Diego (US)
Openalex Percentile: Top 83%
Infant Health and Development
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