4.7 Article

A Comparative Study on the Effect of Acute Pharyngeal Stimulation with TRP Agonists on the Biomechanics and Neurophysiology of Swallow Response in Patients with Oropharyngeal Dysphagia

期刊

出版社

MDPI
DOI: 10.3390/ijms231810773

关键词

deglutition disorders; gastroenterology; therapeutics; transient receptor potential channels; sensory stimulation; swallowing function

资金

  1. Fondo de Investigaciones Sanitarias, Instituto de Salud Carlos III [PI18/00241]
  2. Proyectos de Investigacion Clinica Independiente, Instituto de Salud Carlos III [ICI20/00117]
  3. CIBERehd, Instituto de Salud Carlos III [EHD16PI02]
  4. Territorial Competitiveness Specialization Project (PECT) of Mataro-Maresme - Government of Catalunya-Generalitat de Catalunya [PRE/161/2019]
  5. Nestle Health Science
  6. Danone Nutricia Research

向作者/读者索取更多资源

This study compared the effects of increasing bolus viscosity and using TRPV1, TRPA1, or TRPM8 agonists on the swallow response in patients with oropharyngeal dysphagia (OD). The results showed that fluid thickening and substances like capsaicin and piperine significantly improved swallow safety and speed, providing potential candidates for the development of new pharmacological strategies.
Fluid thickening is the main compensatory strategy for patients with oropharyngeal dysphagia (OD) associated with aging or neurological diseases, and there is still no pharmacological treatment. We aimed to compare the effects of increasing bolus viscosity with that of acute stimulation with TRPV1, TRPA1 or TRPM8 agonists on the biomechanics and neurophysiology of swallow response in patients with OD. We retrospectively analyzed seven studies from our laboratory on 329 patients with OD. The effect of increasing shear viscosity up to 3682 mPa center dot s was compared by videofluoroscopy and pharyngeal sensory evoked potentials (pSEP) with that of adding to the bolus: capsaicin (TRPV1, 150 mu M/10 mu M), piperine (TRPA1/V1, 1 mM/150 mu M), menthol (TRPM8, 1 mM/10 mM), cinnamaldehyde-zinc (TRPA1, 100 ppm-70 mM), citral (TRPA1, 250 ppm) or citral-isopulegol (TRPA1-TRPM8, 250 ppm-200 ppm). Fluid thickening improved the safety of swallow by 80% (p < 0.0001) by delaying bolus velocity by 20.7 +/- 7.0% and time to laryngeal vestibule closure (LVC) by 23.1 +/- 3.7%. Capsaicin 150 mu M or piperine 1 mM significantly improved safety of swallow by 50% (p < 0.01) and 57.1% (p < 0.01) by speeding time to LVC by 27.6% (p < 0.001) and 19.5% (p < 0.01) and bolus velocity by 24.8% (p < 0.01) and 16.9% (p < 0.05), respectively. Cinnamaldehyde-zinc shortened the P2 latency of pSEPs by 11.0% (p < 0.01) and reduced N2-P2 amplitude by 35% (p < 0.01). In conclusion, TRPV1 and TRPV1/A1 agonists are optimal candidates to develop new pharmacological strategies to promote the recovery of brain and swallow function in patients with chronic OD.

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