scholarly journals Fish oil–based injectable lipid emulsions containing medium-chain triglycerides or added α-tocopherol offer anti-inflammatory benefits in a murine model of parenteral nutrition–induced liver injury

2019 ◽  
Vol 109 (4) ◽  
pp. 1038-1050 ◽  
Author(s):  
Meredith A Baker ◽  
Bennet S Cho ◽  
Lorenzo Anez-Bustillos ◽  
Duy T Dao ◽  
Amy Pan ◽  
...  

ABSTRACT Background Fish oil (FO) intravenous lipid emulsions (ILEs) are used as a monotherapy to treat parenteral nutrition (PN)-associated liver disease and provide essential fatty acids (EFAs) needed to sustain growth and prevent EFA deficiency (EFAD). Studies have suggested that medium-chain triglycerides (MCTs) and α-tocopherol have anti-inflammatory properties. Objective The purpose of this study was to test whether FO-ILEs containing MCTs and/or additional α-tocopherol decrease the inflammatory response to an endotoxin challenge compared with FO-ILE alone and preserve the ability to prevent PN-induced liver injury in mice. Methods A murine model of PN-induced hepatosteatosis was used to compare the effects of ILEs formulated in the laboratory containing varying ratios of FO and MCTs, and subsequently FO- and 50:50 FO:MCT-ILE plus 500 mg/L α-tocopherol (FO + AT and 50:50 + AT, respectively). C57BL/6 mice receiving unpurified diet (UPD), PN-equivalent diet (PN) + saline, and PN + soybean oil (SO)-ILE served as controls. After 19 d, mice received an intraperitoneal saline or endotoxin challenge 4 h before being killed. Serum and livers were harvested for histologic analysis, fatty acid profiling, and measurement of systemic inflammatory markers (tumor necrosis factor-α, interleukin-6). Results All ILEs were well tolerated and prevented biochemical EFAD. Livers of mice that received saline and SO developed steatosis. Mice that received 30:70 FO:MCT developed mild hepatosteatosis. All other FO-containing ILEs preserved normal hepatic architecture. Mice that received FO- or SO-ILE had significantly elevated systemic inflammatory markers after endotoxin challenge compared with UPD-fed controls, whereas 50:50 FO:MCT, 30:70 FO:MCT, FO + AT, and 50:50 + AT groups had significantly lower inflammatory markers similar to those seen in UPD-fed controls. Conclusions Mixed FO/MCT and the addition of α-tocopherol to FO improved the inflammatory response to endotoxin challenge compared with FO-ILE alone while still preventing PN-induced liver injury and EFAD in mice. There was no synergistic relation between α-tocopherol and MCTs.

Nutrients ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 508
Author(s):  
Gregory Guthrie ◽  
Douglas Burrin

Total parenteral nutrition (TPN) is a life-saving intervention for infants that are unable to feed by mouth. Infants that remain on TPN for extended periods of time are at risk for the development of liver injury in the form of parenteral nutrition associated cholestasis (PNAC). Current research suggests the lipid component of TPN is a factor in the development of PNAC. Most notably, the fatty acid composition, vitamin E concentration, and presence of phytosterols are believed key mediators of lipid emulsion driven PNAC development. New emulsions comprised of fish oil and medium chain triglycerides show promise for reducing the incidence of PNAC in infants. In this review we will cover the current clinical studies on the benefit of fish oil and medium chain triglyceride containing lipid emulsions on the development of PNAC, the current constituents of lipid emulsions that may modulate the prevalence of PNAC, and potential new supplements to TPN to further reduce the incidence of PNAC.


2006 ◽  
Vol 136 (11) ◽  
pp. 2766-2772 ◽  
Author(s):  
Kemin Qi ◽  
Toru Seo ◽  
Zaifang Jiang ◽  
Yvon A. Carpentier ◽  
Richard J. Deckelbaum

1999 ◽  
Vol 23 (5) ◽  
pp. 253-259 ◽  
Author(s):  
Erena Treskova ◽  
Yvon A. Carpentier ◽  
Rajasekhar Ramakrishnan ◽  
Maysoon Al-Haideri ◽  
Toru Seo ◽  
...  

2016 ◽  
Vol 41 (2) ◽  
pp. 181-187 ◽  
Author(s):  
Gillian L. Fell ◽  
Bennet S. Cho ◽  
Amy Pan ◽  
Vania Nose ◽  
Lorenzo Anez-Bustillos ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document