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Systemic and splanchnic haemodynamic effects of pentifylline in rats with portal hypertension.

Abstract
1. The systemic and splanchnic haemodynamic effects of pentifylline (40 mg/kg body weight intravenously) were assessed in rats with portal hypertension associated either with CCl4-induced cirrhosis (n = 13) or portal vein ligation (n = 13). 2. Heparinized catheters were placed into the portal vein, inferior vena cava, aorta and left ventricle with exits from the neck. Haemodynamic studies were performed 4 h after consciousness was regained. Cardiac output and regional blood flows were measured using radiolabelled microspheres and the reference sample method in seven rats in each group; portal-systemic shunting was measured using microsphere injection in the ileo-colic vein in six rats in each group. 3. Forty-five minutes after injection, pentifylline had no effect on mean arterial pressure, cardiac output, peripheral resistance, portal venous flow, hepatic artery flow or portal-systemic shunting in either group of rats with portal hypertension. The drug lowered portal pressure (-18%) in cirrhotic rats, but not in portal-vein-ligated rats. 4. These data demonstrate that pentifylline lowers portal pressure in cirrhotic rats without affecting portal venous flow and portal-systemic shunting; this effect is possibly mediated by changes in intrahepatic resistance related to the effects of pentifylline on blood viscosity and/or on intrahepatic vasomotor tone.
AuthorsM Dagenais, G Pomier-Layrargues, B Rocheleau, L Giroux, P M Huet
JournalClinical science (London, England : 1979) (Clin Sci (Lond)) Vol. 83 Issue 1 Pg. 41-5 (Jul 1992) ISSN: 0143-5221 [Print] England
PMID1325320 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • pentifylline
  • Theobromine
Topics
  • Animals
  • Cardiac Output (drug effects)
  • Disease Models, Animal
  • Hemodynamics (drug effects)
  • Hypertension, Portal (blood)
  • Male
  • Rats
  • Rats, Inbred Strains
  • Regional Blood Flow (drug effects)
  • Splanchnic Circulation (drug effects)
  • Theobromine (analogs & derivatives, pharmacology)

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