Adrenergic modulation of small bowel haemodynamics in interdigestive motility state of man

Eur J Gastroenterol Hepatol. 1999 Mar;11(3):257-65. doi: 10.1097/00042737-199903000-00009.

Abstract

Objective: We previously reported a new application of semi-invasive laser-Doppler flowmetry (LDF) to record small intestinal haemodynamics in man under basal motor conditions, i.e. during phase I of the migrating motor complex (MMC). In the present study, we evaluated the complete MMC cycle and its haemodynamics in humans; specifically, adrenergic influence on blood flow in all three MMC phases was studied.

Design: Twenty-one fasting healthy male volunteers (21-44 years) were studied during two complete MMC cycles: the first as control period, the second as experimental period with different adrenergic drugs or saline.

Methods: Recording of LDF of intestinal blood flow was performed by attaching two single-fibre microprobes to a small intestinal manometry tube, which simultaneously monitored luminal pressure changes.

Results: Clonidine and oxymetazoline, two alpha2-adrenoceptor agonists, significantly decreased blood flow during all phases of the MMC cycle. In contrast, the non-selective beta-adrenoceptor agonist isoprenaline induced phase II-like activity with a significant increase in blood flow. Propranolol, a beta-adrenoceptor antagonist, did not alter motility but decreased blood flow throughout the MMC cycle.

Conclusions: Both alpha- and beta-adrenergic mechanisms modifying small bowel haemodynamics are in operation throughout phases I, II and III of MMC. Our findings support the use of the semi-invasive LDF technique to measure drug-induced haemodynamic changes in the fasting gut.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Agonists / pharmacology
  • Adrenergic beta-Agonists / pharmacology
  • Adrenergic beta-Antagonists / pharmacology
  • Adult
  • Clonidine / pharmacology
  • Duodenum / blood supply
  • Duodenum / drug effects
  • Duodenum / physiology*
  • Fasting
  • Gastrointestinal Motility / drug effects
  • Gastrointestinal Motility / physiology*
  • Hemodynamics / drug effects
  • Hemodynamics / physiology
  • Humans
  • Isoproterenol / pharmacology
  • Jejunum / blood supply
  • Jejunum / drug effects
  • Jejunum / physiology*
  • Laser-Doppler Flowmetry
  • Male
  • Manometry / instrumentation
  • Myoelectric Complex, Migrating / drug effects
  • Myoelectric Complex, Migrating / physiology*
  • Oxymetazoline / pharmacology
  • Pressure
  • Propranolol / pharmacology
  • Receptors, Adrenergic / drug effects
  • Receptors, Adrenergic / physiology*
  • Regional Blood Flow / drug effects
  • Regional Blood Flow / physiology

Substances

  • Adrenergic alpha-Agonists
  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Receptors, Adrenergic
  • Oxymetazoline
  • Propranolol
  • Isoproterenol
  • Clonidine