Literature DB >> 20564752

Simulated reflux decreases vocal fold epithelial barrier resistance.

Elizabeth Erickson1, Mahalakshmi Sivasankar.   

Abstract

OBJECTIVES/HYPOTHESIS: The vocal fold epithelium provides a barrier to the entry of inhaled and systemic challenges. However, the location of the epithelium makes it vulnerable to damage. Past research suggests, but does not directly demonstrate, that exposure to gastric reflux adversely affects the function of the epithelial barrier. Understanding the nature of reflux-induced epithelial barrier dysfunction is necessary to better recognize the mechanisms for vocal fold susceptibility to this disease. Therefore, we examined the effects of physiologically relevant reflux challenges on vocal fold transepithelial resistance and gross epithelial and subepithelial appearance. STUDY
DESIGN: Ex vivo, mixed design with between-group and repeated-measures analyses.
METHODS: Healthy, native porcine vocal folds (N = 52) were exposed to physiologically relevant acidic pepsin, acid-only, or pepsin-only challenges and examined with electrophysiology and light microscopy. For all challenges, vocal folds exposed to a neutral pH served as control.
RESULTS: Acidic pepsin and acid-only challenges, but not pepsin-only or control challenges significantly reduced transepithelial resistance within 30 minutes. Reductions in transepithelial resistance were irreversible. Challenge exposure produced minimal gross changes in vocal fold epithelial or subepithelial appearance as evidenced by light microscopy.
CONCLUSIONS: These findings demonstrate that acidic environments characteristic of gastric reflux compromise epithelial barrier function without gross structural changes. In healthy, native vocal folds, reductions in transepithelial resistance could reflect reflux-related epithelial disruption. These results might guide the development of pharmacologic and therapeutic recommendations for patients with reflux, such as continued acid-suppression therapy and patient antireflux behavioral education.

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Year:  2010        PMID: 20564752      PMCID: PMC2927501          DOI: 10.1002/lary.20983

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  25 in total

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2.  Relationship between time of exposure of laryngopharyngeal reflux and gene expression in laryngeal fibroblasts.

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3.  Regulation of vocal fold transepithelial water fluxes.

Authors:  K V Fisher; A Telser; J E Phillips; D B Yeates
Journal:  J Appl Physiol (1985)       Date:  2001-09

4.  Dilation of intercellular spaces is associated with laryngo-pharyngeal reflux: an ultrastructural morphometric analysis of laryngeal epithelium.

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Journal:  Eur Arch Otorhinolaryngol       Date:  2007-04-14       Impact factor: 2.503

5.  Pepsin and carbonic anhydrase isoenzyme III as diagnostic markers for laryngopharyngeal reflux disease.

Authors:  Nikki Johnston; John Knight; Peter W Dettmar; Mark O Lively; Jamie Koufman
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6.  Characterisation of adherens and tight junctional molecules in normal animal larynx; determining a suitable model for studying molecular abnormalities in human laryngopharyngeal reflux.

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Review 8.  The otolaryngologic manifestations of gastroesophageal reflux disease (GERD): a clinical investigation of 225 patients using ambulatory 24-hour pH monitoring and an experimental investigation of the role of acid and pepsin in the development of laryngeal injury.

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9.  Pepsin in nonacidic refluxate can damage hypopharyngeal epithelial cells.

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10.  Symptoms of extraesophageal reflux in a community-dwelling sample.

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  19 in total

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4.  Role for ion transport in porcine vocal fold epithelial defense to acid challenge.

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5.  Acute Nanoparticle Exposure to Vocal Folds: A Laboratory Study.

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7.  Bicarbonate availability for vocal fold epithelial defense to acidic challenge.

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8.  Human embryonic stem cell-derived epithelial cells in a novel in vitro model of vocal mucosa.

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9.  In vivo measurement of vocal fold surface resistance.

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10.  Effects of phonation time and magnitude dose on vocal fold epithelial genes, barrier integrity, and function.

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