Differential neutrophil activation before and after endotoxin infusion in enterally versus parenterally fed

J Meyer1, R W Yurt, R Duhaney

  • 1Department of Surgery, Cornell University Medical College, New York, New York.

Surgery, Gynecology & Obstetrics
|December 1, 1988
PubMed

Insights

Enteral nutrition enhances neutrophil function, unlike parenteral nutrition, which may impair immune response. This study investigated how feeding routes affect neutrophil responsiveness and infection susceptibility in patients.

Area of Science:

  • Immunology
  • Nutrition Science
  • Gastroenterology

Background:

  • Increased infection susceptibility is observed in enterally versus parenterally fed patients.
  • Neutrophil (PMN) responsiveness is a key factor in host defense against infection.

Purpose of the Study:

  • To determine if altered neutrophil responsiveness explains increased infection susceptibility in enterally fed patients.
  • To investigate the differential effects of enteral versus parenteral nutrition on human neutrophil activation and function.

Main Methods:

  • Assayed plasma C3a levels, circulating PMN counts, PMN migration (chemotaxis), and leukotriene B4 (LTB4) generation.
  • Measured these parameters before and after endotoxin infusion in normal volunteers receiving either enteral or parenteral nutrition for seven days.
  • Utilized chemotaxis assays with LTB4, N-formyl-methionyl-leucyl-phenylalanine (FMLP), and zymosan activated serum (ZAS).

Main Results:

  • Prior to endotoxin, enterally fed group showed elevated plasma C3a, circulating PMN counts, and LTB4 chemotaxis (p < 0.02).
  • Baseline LTB4 generation was higher in parenterally fed individuals (p < 0.05).
  • Post-endotoxin, neutrophil counts increased more significantly in the enterally fed group; plasma C3a rose in enterally fed but not parenterally fed individuals.

Conclusions:

  • Route of feeding significantly impacts neutrophil function.
  • Parenteral nutrition may impair host immune responsiveness compared to enteral nutrition.
  • Altered neutrophil responsiveness could contribute to differential infection susceptibility based on feeding route.

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