HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Phytosterols promote liver injury and Kupffer cell activation in parenteral nutrition-associated liver disease.

Abstract
Parenteral nutrition-associated liver disease (PNALD) is a serious complication of PN in infants who do not tolerate enteral feedings, especially those with acquired or congenital intestinal diseases. Yet, the mechanisms underlying PNALD are poorly understood. It has been suggested that a component of soy oil (SO) lipid emulsions in PN solutions, such as plant sterols (phytosterols), may be responsible for PNALD, and that use of fish oil (FO)-based lipid emulsions may be protective. We used a mouse model of PNALD combining PN infusion with intestinal injury to demonstrate that SO-based PN solution causes liver damage and hepatic macrophage activation and that PN solutions that are FO-based or devoid of all lipids prevent these processes. We have furthermore demonstrated that a factor in the SO lipid emulsions, stigmasterol, promotes cholestasis, liver injury, and liver macrophage activation in this model and that this effect may be mediated through suppression of canalicular bile transporter expression (Abcb11/BSEP, Abcc2/MRP2) via antagonism of the nuclear receptors Fxr and Lxr, and failure of up-regulation of the hepatic sterol exporters (Abcg5/g8/ABCG5/8). This study provides experimental evidence that plant sterols in lipid emulsions are a major factor responsible for PNALD and that the absence or reduction of plant sterols is one of the mechanisms for hepatic protection in infants receiving FO-based PN or lipid minimization PN treatment. Modification of lipid constituents in PN solutions is thus a promising strategy to reduce incidence and severity of PNALD.
AuthorsKarim C El Kasmi, Aimee L Anderson, Michael W Devereaux, Padade M Vue, Wujuan Zhang, Kenneth D R Setchell, Saul J Karpen, Ronald J Sokol
JournalScience translational medicine (Sci Transl Med) Vol. 5 Issue 206 Pg. 206ra137 (Oct 09 2013) ISSN: 1946-6242 [Electronic] United States
PMID24107776 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Emulsions
  • Fish Oils
  • Lipids
  • Membrane Transport Proteins
  • Phytosterols
  • Solutions
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Stigmasterol
Topics
  • Animals
  • Bile (metabolism)
  • Bile Canaliculi (drug effects, metabolism, pathology)
  • Bone Marrow Cells (drug effects, metabolism, pathology)
  • Disease Models, Animal
  • Emulsions
  • Fish Oils (pharmacology)
  • Gastrointestinal Tract (drug effects, microbiology)
  • Gene Expression Regulation (drug effects)
  • Kupffer Cells (drug effects, metabolism, pathology)
  • Lipids (chemistry)
  • Liver (metabolism, pathology)
  • Liver Diseases (genetics, pathology, prevention & control)
  • Macrophage Activation (drug effects)
  • Membrane Transport Proteins (metabolism)
  • Mice
  • Mice, Inbred C57BL
  • Microbiota (drug effects)
  • Parenteral Nutrition (adverse effects)
  • Phytosterols (toxicity)
  • Signal Transduction
  • Solutions
  • Stigmasterol (blood)
  • Toll-Like Receptor 4 (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: