scispace - formally typeset
Open AccessJournal ArticleDOI

Inhibition of hepatic gluconeogenesis by ethanol

Hans A. Krebs, +3 more
- 01 Mar 1969 - 
- Vol. 112, Iss: 1, pp 117-124
Reads0
Chats0
TLDR
The great majority of the findings support the view that the inhibition of gluconeogensis by ethanol is caused by the alcohol dehydrogenase reaction, which decreases the [free NAD(+)]/[free NADH] ratio.
Abstract
1. Gluconeogenesis from 10mm-lactate in the perfused liver of starved rats is inhibited by ethanol. The degree of inhibition reached a maximum of 66% at 10mm-ethanol under the test conditions and decreased at higher ethanol concentrations. The concentration-dependence of the inhibition is paralleled by the concentration-dependence of the activity of alcohol dehydrogenase. The enzyme is also inhibited by ethanol concentrations above 10mm. 2. Gluconeogenesis from pyruvate is not inhibited by ethanol. 3. The degree of the inhibition of gluconeogenesis from lactate by ethanol depends on the concentration of lactate and other oxidizable substances, e.g. oleate, in the perfusion medium. 4. Ethanol also inhibits, to different degrees, gluconeogenesis from glycerol, dihydroxyacetone, proline, serine, alanine, fructose and galactose. 5. The inhibition of gluconeogenesis from lactate by ethanol is reversed by acetaldehyde. 6. Pyrazole, a specific inhibitor of alcohol dehydrogenase, also reverses the inhibition of gluconeogenesis by ethanol. 7. Gluconeogenesis in kidney cortex, where the activity of alcohol dehydrogenase is very low, is not inhibited by ethanol. 8. Kidney cortex, testis, ovary, uterus and certain tissues of the alimentary tract were the only rat tissues, apart from the liver, that showed measurable alcohol dehydrogenase activity. 9. The concentrations of pyruvate in the liver were decreased to about one-fifth by ethanol. 10. The concentration of lactate in the perfused liver was about 3mm below that of the perfusion medium 30min. after the addition of 10mm-lactate. 11. The great majority of the findings support the view that the inhibition of gluconeogensis by ethanol is caused by the alcohol dehydrogenase reaction, which decreases the [free NAD+]/[free NADH] ratio. The decrease lowers the concentration of pyruvate and this is the immediate cause of the inhibition of gluconeogenesis from lactate, alanine and serine: the fall in the concentration of pyruvate lowers the rate of the pyruvate carboxylase reaction, one of the rate-limiting reactions of gluconeogenesis. The cause of the inhibition of gluconeogenesis from other substrates is discussed.

read more

Citations
More filters
Journal ArticleDOI

Determinants of alcohol use and abuse: Impact of quantity and frequency patterns on liver disease.

TL;DR: Knowing the pattern of drinking will shed light on how severely individuals are alcohol‐dependent and on the extent of liver damage, and a better understanding of these relationships will guide hepatologists in managing alcoholic liver disease.
Journal ArticleDOI

Complementation of mitochondrial electron transport chain by manipulation of the NAD+/NADH ratio.

TL;DR: A water-forming NADH oxidase from Lactobacillus brevis (LbNOX) is used as a genetic tool for inducing a compartment-specific increase of the NAD+/NADH ratio in human cells.
Journal ArticleDOI

The regulation of folate and methionine metabolism.

H A Krebs, +2 more
- 15 Aug 1976 - 
TL;DR: The isolated perfused rat liver and suspensions of isolated rat hepatocytes fail to form glucose from histidine, in contrast with the liver in vivo, and throw light on the biochemical abnormalities associated with cobalamin deficiency (megaloblastic anaemia), especially on the 'methylfolate-trap hypothesis'.
Journal ArticleDOI

The regulation of gluconeogenesis in isolated rat liver cells by glucagon, insulin, dibutyryl cyclic adenosine monophosphate, and fatty acids.

TL;DR: Suspensions of rat liver cells from starved rats converted three carbon precursors to glucose and responded to hormones such as glucagon and insulin, and the effects of insulin and glucagon on liver cells were abolished by short term treatment of cell suspensions with trypsin.
References
More filters
Journal ArticleDOI

The Redox State of Free Nicotinamide-Adenine Dinucleotide in the Cytoplasm and Mitochondria of Rat Liver

TL;DR: The bearing of these findings on various problems, including the number of NAD(+)-NADH pools in liver cells; the applicability of the method to tissues other than liver; the transhydrogenase activity of glutamate dehydrogenase; the physiological significance of the difference of the redox states of mitochondria and cytoplasm; aspects of the regulation of theredox state of cell compartments; the steady-state concentration of mitochondrial oxaloacetate.
Journal ArticleDOI

Gluconeogenesis in the perfused rat liver.

TL;DR: Addition of lactate, and especially ammonium salts, increased the uptake of oxygen more than expected on the basis of the ATP requirements of the gluconeogenesis and urea synthesis.
Journal ArticleDOI

The rate of gluconeogenesis from various precursors in the perfused rat liver.

TL;DR: Two sites of action of glucagon must therefore be postulated: one concerned with mobilization of liver glycogen, the other with the promotion of gluconeogenesis.
Journal ArticleDOI

The kinetics and mechanism of liver alcohol dehydrogenase with primary and secondary alcohols as substrates.

K Dalziel, +1 more
- 01 Jul 1966 - 
TL;DR: A mechanism that provides for dissociation of either coenzyme or substrate from the reactive ternary complex is described, and shown to account for the initial-rate data for both primary and secondary alcohols, and for isotope-exchange results for the former.
Related Papers (5)