University of Hertfordshire

  • Yang Yu
  • Egina Villalobos- Hernandez
  • Sabindra Pradhananga
  • Corey Baker
  • Christopher Keating
  • David Grundy
  • Allan Lomax
  • David Reed
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Original languageEnglish
JournalAmerican Journal of Physiology - Gastrointestinal and Liver Physiology
Journal publication date19 Jun 2019
Early online date19 Jun 2019
DOIs
Publication statusE-pub ahead of print - 19 Jun 2019

Abstract

Increasedbile acids in the colon can evoke increased epithelial secretion resulting in diarrhea but little is known whether colonic bile acids contribute to abdominal pain. This study aimed to investigate the mechanisms underlying activation of colonic extrinsic afferent nerves and their neuronal cell bodies by a major secondary bile acid, deoxycholic acid (DCA). All experiments were performed on male C57BL/6 mice. Afferent sensitivity was evaluated using in vitroextracellular recordings from mesenteric nerves in the proximal colon (innervated by vagal and spinal afferents) and distal colon (spinal afferents only). Neuronal excitability of cultured dorsal root ganglion (DRG) and nodose ganglion (NG) neurons was examined with perforated patch clamp. Colonic 5-HT release was assessed using ELISA, and 5-HT immunoreactive enterochromaffin (EC) cells were quantified.Intraluminal DCA increased afferent nerve firing rate concentration-dependently in both proximal and distal colon. This DCA-elicited increase was significantly inhibited by a 5-HT3antagonist in the proximal colon but not in the distal colon, which may be in part due to lower 5-HT immunoreactive EC cell density and lower 5-HT levels in the distal colon following DCA stimulation. DCA increased the excitability of DRG neurons, whereas it decreased the excitability of NG neurons. DCA potentiated mechanosensitivity of high threshold spinal afferents independent of 5-HT release. Together, this study suggests that DCA can excite colonic afferents via direct and indirect mechanisms but the predominant mechanism may differ between vagal and spinal afferents. Furthermore,DCA increased mechanosensitivity of high threshold spinal afferents and may be a mechanism of visceral hypersensitivity.

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