Chronic ethanol inhibits receptor-stimulated phosphoinositide hydrolysis in rat liver slices
Creators
- 1. Department of Pharmacology, University of Texas, Austin (USA)
Description
The effects of chronic ethanol feeding on norepinephrine (NE)- and arginine-vasopressin (AVP)-stimulated phosphoinositide (PI) hydrolysis in rat liver slices was determined. The maximum NE-stimulated PI response was significantly reduced by 40% in liver slices from 8-month-old rats which had been treated for 5 months with a liquid diet containing ethanol compared to pair-fed controls. The maximum AVP-stimulated PI response was decreased by 39% in liver slices from the ethanol-fed rats compared to control. EC50 values for NE- and AVP-stimulated PI hydrolysis in liver slices were not affected by the chronic ethanol treatment. Similar reductions in the maximal NE- and AVP-stimulated PI hydrolysis (28% and 27%, respectively) were found in 22-month-old rats which had been maintained on an ethanol containing diet for 5 months compared to pair-fed controls. The binding of [3H]prazosin and [3H]AVP to liver plasma membranes from 8-month-old ethanol-fed rats was not significantly different from binding to liver membranes from sucrose-fed controls. Our data suggest that chronic ethanol ingestion may lead to a reduction in PI-linked signal transduction in liver
Additional details
Publishing Information
- Journal Title
- Alcohol
- Journal Volume
- 8
- Journal Issue
- 2
- Series
- Alcohol.
- Journal Page Range
- 131-136
- ISSN
- 0741-8329
- CODEN
- ALCOE
INIS
- Country of Publication
- United States
- Country of Input or Organization
- United States
- INIS RN
- 22090062
- Subject category
- S61: RADIATION PROTECTION AND DOSIMETRY; S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- BIOLOGICAL EFFECTS; CHRONIC EXPOSURE; ETHANOL; HYDROLYSIS; IN VITRO; LIVER; METABOLISM; NORADRENALINE; PHOSPHOLIPIDS; RADIOASSAY; RATS; TRACER TECHNIQUES; TRITIUM COMPOUNDS
- Descriptors DEC
- ADRENAL HORMONES; ALCOHOLS; ANIMALS; AUTONOMIC NERVOUS SYSTEM AGENT; BODY; CARDIOTONICS; CARDIOVASCULAR AGENTS; CHEMICAL REACTIONS; DECOMPOSITION; DIGESTIVE SYSTEM; DRUGS; ESTERS; GLANDS; HORMONES; HYDROGEN COMPOUNDS; HYDROXY COMPOUNDS; ISOTOPE APPLICATIONS; LIPIDS; MAMMALS; NEUROREGULATORS; ORGANIC COMPOUNDS; ORGANIC PHOSPHORUS COMPOUNDS; ORGANS; RODENTS; SOLVOLYSIS; SYMPATHOMIMETICS; VERTEBRATES