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Related Experiment Videos

Endotoxin increases hepatic glutamine transport activity

Y Inoue1, A J Pacitti, W W Souba

  • 1Department of Surgery, University of Florida, Gainesville 32610-0286.

The Journal of Surgical Research
|May 1, 1993
PubMed
Summary

Sepsis accelerates liver glutamine uptake by increasing the activity of the Na(+)-dependent System N transporter in hepatocytes. This enhanced transport mechanism is crucial for managing elevated hepatic glutamine during severe infections.

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Area of Science:

  • Hepatology
  • Molecular Physiology
  • Sepsis Pathophysiology

Background:

  • Liver glutamine uptake increases during endotoxemia (a model of sepsis).
  • The specific plasma membrane transport systems responsible for this altered uptake remain largely uncharacterized.
  • Understanding these transporters is key to comprehending hepatic metabolic responses during sepsis.

Purpose of the Study:

  • To investigate the impact of sepsis on hepatic glutamine transport systems.
  • To determine if increased hepatocyte plasma membrane transport activity underlies accelerated liver glutamine uptake during endotoxemia.
  • To characterize the roles of Na(+)-dependent System N and Na(+)-independent System n transporters.

Main Methods:

  • Preparation of rat hepatocyte plasma membrane vesicles (HPMVs) from control and lipopolysaccharide (LPS)-treated rats.

Related Experiment Videos

  • Assay of [3H]glutamine transport in HPMVs using a rapid mixing/filtration technique.
  • Measurement of Na(+)-dependent (System N) and Na(+)-independent (System n) transport activities, Vmax, and Km.
  • Main Results:

    • Na(+)-independent glutamine transport (System n) activity remained unchanged after LPS administration.
    • A time- and dose-dependent 2- to 3-fold increase in Na(+)-dependent glutamine transport (System N) was observed in HPMVs from endotoxemic rats.
    • This increase was attributed to a higher Vmax, indicating more transporter proteins, while glutamine affinity (Km) was unaffected.

    Conclusions:

    • Endotoxemia significantly enhances the activity of the Na(+)-dependent glutamine transporter (System N) in the hepatocyte plasma membrane.
    • This upregulation of System N activity is a primary mechanism driving accelerated hepatic glutamine uptake during severe infection.
    • The findings provide critical insights into the metabolic adaptations of the liver during sepsis.