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Pathogenesis of hepatic steatosis in the parenterally fed rat.

Publication ,  Journal Article
Hall, RI; Grant, JP; Ross, LH; Coleman, RA; Bozovic, MG; Quarfordt, SH
Published in: J Clin Invest
November 1984

Hepatic steatosis frequently complicates total parenteral nutrition (TPN). Some of the mechanisms responsible were examined in rats receiving calories as dextrose (CHO-TPN) or dextrose plus lipid emulsion (Lipid-TPN). Hepatic triglyceride content increased approximately threefold after CHO-TPN and twofold after Lipid-TPN (P less than 0.02). Hepatic triglyceride fatty acid composition reflected endogenous synthesis. Hepatic acetyl-Coenzyme A carboxylase specific activity increased fourfold after CHO-TPN and twofold after Lipid-TPN, and it correlated positively with hepatic lipid content (r = 0.82). The activities of the microsomal enzymes of complex lipid synthesis were unchanged in the TPN groups. Both TPN regimens suppressed hepatic triglyceride secretion, measured by the rise in plasma triglyceride and the incorporation of [14C]palmitic acid into plasma triglyceride after intravenous Triton. Hepatic triglyceride secretion correlated negatively with total hepatic lipid content (r = -0.89). CHO-TPN increased the uptake of a radiolabeled triglyceride emulsion and increased hepatic lipase activity, whereas Lipid-TPN decreased both. Both adipose and cardiac lipase were higher for Lipid-TPN animals than for CHO-TPN or control animals. Hepatic 14C-triglyceride content was increased in both TPN groups as compared with controls after the injection of 1-[14C]-palmitic acid. This increment was proportional to the decreased hepatic secretion. Triglyceride fatty acid oxidation was significantly suppressed by CHO-TPN, less so by Lipid-TPN. Free fatty acid oxidation was suppressed only by CHO-TPN. The results suggest that the steatosis induced by TPN in rats was due to enhanced hepatic synthesis of fatty acid and reduced triglyceride secretion. Reduced hepatic triglyceride uptake, enhanced fatty acid oxidation, and enhanced peripheral tissue plasma triglyceride lipolysis when CHO-TPN is supplemented with lipid may modulate the accumulation of hepatic triglyceride and, along with reduced synthesis of fatty acid, lead to a lower hepatic triglyceride content.

Duke Scholars

Published In

J Clin Invest

DOI

ISSN

0021-9738

Publication Date

November 1984

Volume

74

Issue

5

Start / End Page

1658 / 1668

Location

United States

Related Subject Headings

  • Triglycerides
  • Rats
  • Polyethylene Glycols
  • Phosphatidylcholines
  • Parenteral Nutrition, Total
  • Parenteral Nutrition
  • Nitrogen
  • Male
  • Liver
  • Lipids
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Hall, R. I., Grant, J. P., Ross, L. H., Coleman, R. A., Bozovic, M. G., & Quarfordt, S. H. (1984). Pathogenesis of hepatic steatosis in the parenterally fed rat. J Clin Invest, 74(5), 1658–1668. https://doi.org/10.1172/JCI111582
Hall, R. I., J. P. Grant, L. H. Ross, R. A. Coleman, M. G. Bozovic, and S. H. Quarfordt. “Pathogenesis of hepatic steatosis in the parenterally fed rat.J Clin Invest 74, no. 5 (November 1984): 1658–68. https://doi.org/10.1172/JCI111582.
Hall RI, Grant JP, Ross LH, Coleman RA, Bozovic MG, Quarfordt SH. Pathogenesis of hepatic steatosis in the parenterally fed rat. J Clin Invest. 1984 Nov;74(5):1658–68.
Hall, R. I., et al. “Pathogenesis of hepatic steatosis in the parenterally fed rat.J Clin Invest, vol. 74, no. 5, Nov. 1984, pp. 1658–68. Pubmed, doi:10.1172/JCI111582.
Hall RI, Grant JP, Ross LH, Coleman RA, Bozovic MG, Quarfordt SH. Pathogenesis of hepatic steatosis in the parenterally fed rat. J Clin Invest. 1984 Nov;74(5):1658–1668.

Published In

J Clin Invest

DOI

ISSN

0021-9738

Publication Date

November 1984

Volume

74

Issue

5

Start / End Page

1658 / 1668

Location

United States

Related Subject Headings

  • Triglycerides
  • Rats
  • Polyethylene Glycols
  • Phosphatidylcholines
  • Parenteral Nutrition, Total
  • Parenteral Nutrition
  • Nitrogen
  • Male
  • Liver
  • Lipids