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Changes in signalling from faecal neuroactive metabolites following dietary modulation of IBS pain.
Tuck, Caroline J; Abu Omar, Amal; De Palma, Giada; Osman, Samira; Jiménez-Vargas, Nestor N; Yu, Yang; Bennet, Sean Mp; Lopez-Lopez, Cintya; Jaramillo-Polanco, Josue O; Baker, Corey C; Bennett, Aidan Sw; Guzman-Rodriguez, Mabel; Tsang, Quentin; Alward, Taylor; Rolland, Sebastien; Morissette, Celine; Verdu, Elena F; Bercik, Premysl; Vanner, Stephen J; Lomax, Alan E; Reed, David E.
Affiliation
  • Tuck CJ; Department of Sport, Exercise and Nutrition Sciences, La Trobe University, Melbourne, Victoria, Australia.
  • Abu Omar A; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • De Palma G; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Osman S; Department of Physiology, Jordan University of Science and Technology, Irbid, Jordan.
  • Jiménez-Vargas NN; Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Yu Y; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Bennet SM; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Lopez-Lopez C; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Jaramillo-Polanco JO; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Baker CC; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Bennett AS; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Guzman-Rodriguez M; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Tsang Q; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Alward T; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Rolland S; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Morissette C; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Verdu EF; Department of Medicine, Hopital Maisonneuve-Rosemont, Montreal, Québec, Canada.
  • Bercik P; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
  • Vanner SJ; Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Lomax AE; Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Reed DE; Gastrointestinal Diseases Research Unit, Queen's University, Kingston, Ontario, Canada.
Gut ; 2022 Dec 13.
Article in En | MEDLINE | ID: mdl-36591617
OBJECTIVE: Dietary therapies for irritable bowel syndrome (IBS) have received increasing interest but predicting which patients will benefit remains a challenge due to a lack of mechanistic insight. We recently found evidence of a role for the microbiota in dietary modulation of pain signalling in a humanised mouse model of IBS. This randomised cross-over study aimed to test the hypothesis that pain relief following reduced consumption of fermentable carbohydrates is the result of changes in luminal neuroactive metabolites. DESIGN: IBS (Rome IV) participants underwent four trial periods: two non-intervention periods, followed by a diet low (LFD) and high in fermentable carbohydrates for 3 weeks each. At the end of each period, participants completed questionnaires and provided stool. The effects of faecal supernatants (FS) collected before (IBS FS) and after a LFD (LFD FS) on nociceptive afferent neurons were assessed in mice using patch-clamp and ex vivo colonic afferent nerve recording techniques. RESULTS: Total IBS symptom severity score and abdominal pain were reduced by the LFD (N=25; p<0.01). Excitability of neurons was increased in response to IBS FS, but this effect was reduced (p<0.01) with LFD FS from pain-responders. IBS FS from pain-responders increased mechanosensitivity of nociceptive afferent nerve axons (p<0.001), an effect lost following LFD FS administration (p=NS) or when IBS FS was administered in the presence of antagonists of histamine receptors or protease inhibitors. CONCLUSIONS: In a subset of IBS patients with improvement in abdominal pain following a LFD, there is a decrease in pronociceptive signalling from FS, suggesting that changes in luminal mediators may contribute to symptom response.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Gut Year: 2022 Document type: Article Affiliation country: Australia Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: Gut Year: 2022 Document type: Article Affiliation country: Australia Country of publication: United kingdom