A quantitative approach to recording peristaltic activity from segments of rat small intestine in vivo

Neurogastroenterol Motil. 2005 Apr;17(2):262-72. doi: 10.1111/j.1365-2982.2004.00605.x.

Abstract

We have developed methods that allow correlation of propulsive reflexes of the intestine with measurements of intraluminal pressure, fluid movement and spatio-temporal maps of intestinal wall movements for the first time in vivo. A segment of jejunum was cannulated and set up in a Trendelenburg recording system while remaining connected to the vascular and nerve supply of the anaesthetized rat. The resting intraluminal pressure in intact intestine was 2-4 mmHg. Hydrostatic pressures of 2, 4, 8 and 16 mmHg were imposed. At a baseline pressure of 4 mmHg, propulsive waves generated pressures of 9 +/- 1 mmHg, that progressed oral to anal at 2-5 mm s(-1). Individual propulsive waves propelled 0.8 +/- 0.4 mL of fluid. The frequency of propulsive waves increased with pressure, but peristaltic efficiency (mL per contraction) decreased with pressure increase between 4 and 16 mmHg. Atropine, as a bolus, transiently blocked peristalsis, but caused maintained block when infused. Hexamethonium blocked propulsive contractions. Inhibition of nitrergic transmission converted regular peristalsis to non-propulsive contractions. These studies demonstrate the utility of an adapted Trendelenburg method for quantitative investigation of motility and pharmacology of enteric reflexes in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atropine / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Ganglionic Blockers / pharmacology
  • Hexamethonium / pharmacology
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / physiology
  • Intestine, Small / physiology*
  • Male
  • Muscarinic Antagonists / pharmacology
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nitric Oxide Synthase / metabolism
  • Peristalsis / drug effects
  • Peristalsis / physiology*
  • Pressure
  • Rats
  • Videotape Recording

Substances

  • Enzyme Inhibitors
  • Ganglionic Blockers
  • Muscarinic Antagonists
  • Hexamethonium
  • Atropine
  • Nitric Oxide Synthase
  • NG-Nitroarginine Methyl Ester