Am J Physiol. 1985 Apr;248(4):H468-76. doi: 10.1152/ajpheart.1985.248.4.H468.

Norepinephrine on venous compliance and unstressed volume in cat liver.

The American journal of physiology

C V Greenway, K L Seaman, I R Innes

PMID: 3985172 DOI: 10.1152/ajpheart.1985.248.4.H468

Abstract

Hemodynamic relationships between flows, pressures, and blood volume have been examined in the denervated liver of cats anesthetized with pentobarbital. Portal and hepatic lobar venous pressures, portal and total hepatic flows, and hepatic blood volume were recorded when portal flow was varied from 0 to 240 ml X min-1 X 100 g liver-1 and when hepatic outflow pressure was varied from 0 to 9.5 mmHg, before, during, and after intravenous infusion of norepinephrine (2 micrograms X min-1 X kg body wt-1). Portal pressure was 1-2 mmHg higher than lobar venous pressure and 8-9 mmHg higher than inferior vena caval pressure, showing that the major site of resistance in the portal circuit was in the large hepatic veins. Intrahepatic pressure was linearly related to total hepatic flow, and norepinephrine increased the intercept but not the slope of this relationship. Hepatic blood volume was linearly related to intrahepatic pressure with a calculated compliance of 2.5-3.0 ml X mmHg-1 X 100 g liver-1 and a calculated unstressed volume at zero pressure of 10-15 ml/100 g liver. Norepinephrine did not significantly change vascular compliance but caused a marked reduction of 15-20 ml/100 g liver in calculated unstressed volume. Thus norepinephrine reduced hepatic blood volume by 15-20 ml/100 g liver at any given intrahepatic pressure. It is concluded that venoconstriction in the hepatic bed occurs by a decrease in unstressed volume with little change in compliance. Unstressed volume represents a true blood volume reserve, independent of passive influences, which can be mobilized by the central nervous system.

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Substances

• Norepinephrine

MeSH terms

• Animals
• Blood Pressure / drug effects
• Blood Volume / drug effects
• Cats
• Compliance
• Liver Circulation / drug effects
• Norepinephrine / pharmacology
• Physiology / instrumentation
• Veins / drug effects

Publication Types

• Journal Article
• Research Support, Non-U.S. Gov't

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