Digestive Diseases and Sciences

, Volume 40, Issue 9, pp 1913–1921 | Cite as

Influence of bradykinin in gastrointestinal disorders and visceral pain induced by acute or chronic inflammation in rats

  • Véronique Julia
  • Théodora Mezzasalma
  • Lionel Buéno
Intestinal Disorders, Inflammatory Bowel Disease, Immunology, and Microbiology


This work investigated the role of bradykinin in viscerosensitivity before and during inflammation in two models of visceral pain induced by rectal distension (RD) or “abdominal distension” (AD) in rats. RD induced both inhibition of colonic motility and an increase of abdominal spike bursts. Bradykinin receptor antagonist, Hoe 140 did not affect any of the RD-induced responses. After TNB-induced rectal inflammation, colonic inhibition and the number of abdominal contractions were enhanced. Hoe 140 selectively reduced the abdominal response to the highest distension volume, without affecting the colonic response. In AD group, acetic acid inhibited gastric emptying and increased the number of abdominal ontractions, whereas the same volume of saline did not affect any of the responses. Before inflammation, Hoe 140 (1–5 mg/kg, intraperitoneally) did not affectper se abdominal and gastric emptying responses; in contrast, at 5 mg/kg, intraperitoneally, it reduced significantly (P<0.05) both acetic acid-induced responses. We conclude that bradykinin is involved in viscerosensitivity changes related to abdominal and rectal distension in inflammatory conditions.

Key Words

rectal distension motility gastric emptying rat inflammation visceral pain 


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Copyright information

© Plenum Publishing Corporation 1995

Authors and Affiliations

  • Véronique Julia
    • 1
  • Théodora Mezzasalma
    • 1
  • Lionel Buéno
    • 1
  1. 1.Department of PharmacologyINRAToulouse cedexFrance

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