RGD Reference Report - Control of glucuronidation during hypoxia. Limitation by UDP-glucose pyrophosphorylase. - Rat Genome Database

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Control of glucuronidation during hypoxia. Limitation by UDP-glucose pyrophosphorylase.

Authors: Aw, TY  Jones, DP 
Citation: Aw TY and Jones DP, Biochem J. 1984 May 1;219(3):707-12.
RGD ID: 2303740
Pubmed: (View Article at PubMed) PMID:6331395

The regulation of glucuronidation during hypoxia was studied in isolated hepatocytes by analysing the dependence of acetaminophen glucuronidation rate on the intracellular concentrations of UTP, glucose 1-phosphate, UDP-glucose and UDP-glucuronic acid. The steady-state concentrations of these metabolites in cells from fed and starved rats were altered by exposure to various hypoxic O2 concentrations and by adding exogenous glucose. Changes in glucuronidation rate under all conditions were explained in terms of the concentrations of the substrates for UDP-glucose pyrophosphorylase, i.e. UTP and glucose 1-phosphate. Steady-state rates for the UDP-glucose pyrophosphorylase reaction, calculated by using published kinetic constants and measured glucose 1-phosphate and UTP concentrations, were in agreement with the measured glucuronidation rates. Thus the UDP-glucose pyrophosphorylase reaction is the key regulatory site for drug glucuronidation during hypoxia. Control at this site indicates that glucuronidation in vivo may be generally depressed in pathological conditions involving hypoxia and energy (calorie) malnutrition.


Gene Ontology Annotations    

Biological Process

Molecular Function

Objects Annotated

Genes (Rattus norvegicus)
Ugp2  (UDP-glucose pyrophosphorylase 2)

Additional Information