Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1973 Jan;132(1):19-25.
doi: 10.1042/bj1320019.

Hepatic redox state and gluconeogenesis from lactate in vivo in the rat

Hepatic redox state and gluconeogenesis from lactate in vivo in the rat

R A Hawkins et al. Biochem J. 1973 Jan.

Abstract

1. To examine the role of the hepatic redox state on the rate of gluconeogenesis the effects of sodium crotonate injection (6mmol/kg body wt.) on rat liver metabolite concentrations and gluconeogenesis from lactate were studied in vivo. 2. Crotonate caused a marked oxidation of cytoplasmic and mitochondrial redox couples; decreases were observed in the ratios of [lactate]/[pyruvate], [glycerol 3-phosphate]/[dihydroxyacetone phosphate], [hydroxybutyrate]/[acetoacetate] and measured [NAD(+)]/[NADH]. 3. Increases occurred in the liver concentrations of all gluconeogenic intermediates from pyruvate through to glucose 6-phosphate, but there was no change in lactate concentration. 4. To determine whether gluconeogenesis from lactate was altered by the more-oxidized hepatic redox state l-[2-(14)C]lactic acid was infused into the inferior vena cava (50mumol/min per kg body wt.) and the incorporation of radioactivity into blood glucose was measured. 5. Administration of crotonate transiently decreased the rate of lactate incorporation into glucose but within a few minutes the rate of incorporation returned to that of the controls. 6. The results indicate that in these experiments alteration of the NAD(+)-NADH systems of cytoplasm and mitochondria to a more-oxidized state did not change the rate of gluconeogenesis.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Can J Biochem Physiol. 1959 Feb;37(2):285-95 - PubMed
    1. Eur J Biochem. 1969 Oct;10(3):484-93 - PubMed
    1. Proc Natl Acad Sci U S A. 1966 Jul;56(1):247-54 - PubMed
    1. Biochem J. 1967 May;103(2):514-27 - PubMed
    1. J Physiol. 1965 Jul;179(2):193-237 - PubMed

MeSH terms