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©2006 Baishideng Publishing Group Co.
World J Gastroenterol. May 14, 2006; 12(18): 2806-2817
Published online May 14, 2006. doi: 10.3748/wjg.v12.i18.2806
Published online May 14, 2006. doi: 10.3748/wjg.v12.i18.2806
Stimulationmodality | Stimulatedstructures | Advantages | Limitations |
Electrical | Nerve fibers primarily in mucosa and muscle layers dependent of the stimulation intensity (not a specific activation of the nociceptors) | Excellent for repeated stimulation, suitable for neurophysiologic assessments of the pain | The electrical threshold depends on the fiber diameter, i.e. small-diameter nerves cannot be excited without exciting others. May induce arrhythmias in areas near the heart |
Mechanical | Mechanoreceptors located in different layers | Imitates a bolus, reproducible stimulus | Problems with estimating the transmural pressure and change in circumference |
Thermal | Thermal sensitive receptors preferentially in the luminal layers | Activation of unmyelinated afferents in the mucosa selectively | Temperature stimuli in the range that can be felt are normally only relevant for sensation in the upper GI tract. |
Chemical | Chemo-sensitive receptors, primarily in the mucosa | Resembles clinical inflammation, chemical stimuli activate predominantly unmyelinated C-fibres | Require a relative long latency time to the onset of effects, and that they are often not reproducible when repeated |
- Citation: Drewes AM, Arendt-Nielsen L, Funch-Jensen P, Gregersen H. Experimental human pain models in gastro-esophageal reflux disease and unexplained chest pain. World J Gastroenterol 2006; 12(18): 2806-2817
- URL: https://www.wjgnet.com/1007-9327/full/v12/i18/2806.htm
- DOI: https://dx.doi.org/10.3748/wjg.v12.i18.2806