Beta-blockade with propranolol and hepatic artery blood flow in patients with cirrhosis. 1989

R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
Liver Unit, Hospital Clínic i Provincial, University of Barcelona, Spain.

In patients with cirrhosis and portal hypertension, propranolol administration reduces heart rate and cardiac output and diminishes portal pressure and collateral blood flow. However, there is little information on the possible effects of propranolol on hepatic artery blood flow. The present study addressed this question in 12 cirrhotic patients with end-to-side portacaval shunt, in whom all of the liver blood flow represents the hepatic artery blood flow. Hepatic artery blood flow (continuous infusion of indocyanine green), cardiac output (thermal dilution), heart rate and mean arterial pressure were measured before and 20 min after the intravenous infusion of 10 to 15 mg of propranolol. beta-Adrenergic blockade caused a significant reduction of cardiac output (from 9.1 +/- 2.1 to 7.1 +/- 1.4 liters per min, p less than 0.001) (mean +/- S.D.) and heart rate (from 85 +/- 10 to 71 +/- 7 beats per min, p less than 0.001), and a significant increase of systemic vascular resistance (from 9.0 +/- 2.1 to 11.7 +/- 2.7 mmHg per liter per min, p less than 0.001), whereas mean arterial pressure did not change (77 vs. 78 mmHg). Propranolol significantly reduced hepatic artery blood flow (from 0.65 +/- 0.20 to 0.55 +/- 0.14 liters per min, p less than 0.01). However, reduction of hepatic artery blood flow (-12.9 +/- 7.3%) was significantly less than reduction of cardiac output (-21.1 +/- 5.2%, p less than 0.01). As a result, the fraction of the cardiac output delivered to the liver was significantly greater after propranolol (8.0 +/- 1.7%) than before (7.3 +/- 1.7%, p less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

UI MeSH Term Description Entries
D008102 Liver Circulation The circulation of BLOOD through the LIVER. Hepatic Circulation,Circulation, Liver,Circulation, Hepatic
D008103 Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. Cirrhosis, Liver,Fibrosis, Liver,Hepatic Cirrhosis,Liver Fibrosis,Cirrhosis, Hepatic
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D011167 Portacaval Shunt, Surgical Surgical portasystemic shunt between the portal vein and inferior vena cava. Eck Fistula,Portacaval Anastomosis,Portacaval Shunt,Shunt, Surgical Portacaval,Surgical Portacaval Shunt,Anastomoses, Portacaval,Anastomosis, Portacaval,Fistula, Eck,Portacaval Anastomoses,Portacaval Shunts,Portacaval Shunts, Surgical,Shunt, Portacaval,Shunts, Portacaval,Shunts, Surgical Portacaval,Surgical Portacaval Shunts
D011433 Propranolol A widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse effects instigate replacement by newer drugs. Dexpropranolol,AY-20694,Anaprilin,Anapriline,Avlocardyl,Betadren,Dociton,Inderal,Obsidan,Obzidan,Propanolol,Propranolol Hydrochloride,Rexigen,AY 20694,AY20694,Hydrochloride, Propranolol
D005260 Female Females
D006439 Hemodynamics The movement and the forces involved in the movement of the blood through the CARDIOVASCULAR SYSTEM. Hemodynamic
D006499 Hepatic Artery A branch of the celiac artery that distributes to the stomach, pancreas, duodenum, liver, gallbladder, and greater omentum. Arteries, Hepatic,Artery, Hepatic,Hepatic Arteries
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
April 1985, Clinical pharmacology and therapeutics,
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
January 1984, Hepatology (Baltimore, Md.),
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
October 1988, Scandinavian journal of gastroenterology,
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
December 1998, Cardiovascular drugs and therapy,
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
January 1968, Acta physiologica Academiae Scientiarum Hungaricae,
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
January 1976, Stroke,
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
August 1971, Lancet (London, England),
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
January 1987, Minerva dietologica e gastroenterologica,
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
January 1984, Hepatology (Baltimore, Md.),
R Mastai, and J Bosch, and J Bruix, and M Navasa, and D Kravetz, and J Rodés
January 1984, Gastroenterology,
Copied contents to your clipboard!