Transcutaneous vagal nerve stimulation protects against stress‐induced intestinal barrier dysfunction in healthy adults. Issue 10 (28th April 2022)

• Record Type: Journal Article
• Authors: Mogilevski, Tamara; Rosella, Sam; Aziz, Qasim; Gibson, Peter R.
• Is Part Of: Neurogastroenterology & motility. Volume 34:Issue 10(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-04-28
• Subjects: corticotropin releasing hormone (CRH) -- intestinal barrier dysfunction -- intestinal fatty acid binding protein (I‐FABP) -- transcutaneous vagal nerve stimulation -- urine dual sugar test; Gastrointestinal system -- Motility -- Periodicals; Gastrointestinal system -- Innervation -- Periodicals; 616.33
• DOI: 10.1111/nmo.14382
• Languages: English
• ISSNs: 1350-1925

Abstract

Abstract: Background: Intestinal barrier dysfunction is the likely initiating event in multiple human diseases. Currently, there are limited therapeutic strategies to address its dysfunction. Animal studies suggest that vagal nerve stimulation may improve intestinal barrier function, but this has not been evaluated in humans. This study aimed to determine the effect of vagal nerve stimulation on intestinal permeability in adults administered a bolus dose of intravenous corticotropin releasing hormone (CRH) which has been shown to increase small intestinal permeability in healthy human subjects. Methods: In a cross‐over study, 16 volunteers (median age 34 years, 11 female) were randomized to receive auricular transcutaneous vagal nerve or sham stimulation (10 minutes each side) after intravenous administration of 100 µg of CRH. Intestinal barrier function was measured before and 2 h after each intervention with dual‐sugar urine testing (lactulose:mannitol ratio) and intestinal fatty‐acid binding protein (I‐FABP). Key Results: Exposure to CRH increased I‐FABP concentrations by a median of 49 (IQR 4‐71)% ( p = 0.009). Lactulose:mannitol ratios were 0.029 (0.025‐0.050) following vagal stimulation compared with 0.062 (0.032‐0.170) following sham stimulation ( p = 0.0092), representing a fall of 53 (22‐71)%. I‐FABP concentrations did not change ( p = 0.90). Conclusions: Brief non‐invasive vagal nerve stimulation consistently reduces paracellular permeability of the small intestine after CRH administration, but does not entirely mitigate I‐FABP release from the epithelium. Studies of vagal nerve stimulation in disease states are warranted. Abstract : A brief period of transcutaneous vagal stimulation reduced paracellular intestinal permeability by 53% compared with sham stimulation after a single dose of corticotropin releasing hormone. These findings warrant further testing in disease states.