Document Detail


Effects of glucose or fat calories in total parenteral nutrition on fat metabolism and systemic inflammation in rats.
MedLine Citation:
PMID:  20096898     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
This study compared the effects of total parenteral nutrition (TPN) by central vein with or without fat provided at maintenance energy requirement on fatty acid metabolism, de novo lipogenesis, and the risk of hepatic and systemic inflammation in rats. Study 1 was conducted in 2 groups: high glucose (HG), where fat-free TPN was given at maintenance levels of 180 kcal/(kg d), and low glucose (LG), where fat-free TPN containing 30% fewer calories at 126 kcal/(kg d) was provided by reducing 54 kcal/(kg d) from parenteral glucose. Study 2 contained 3 TPN groups: 1 LG group at 126 kcal/(kg d) and 2 groups at 180 kcal/(kg d) with 30% of total calories (54 kcal/[kg d]) either from soybean or fish oil emulsion. In both studies, animals fed a chow diet ad libitum were included. Plasma and hepatic triglyceride and phospholipid fatty acid profiles, enzymes indicating hepatic injury, and C-reactive protein levels (CRP) reflecting systemic injury were measured. In study 1, evidence of de novo lipogenesis was noted in LG and was more prominent in HG with elevation of CRP in HG. In study 2, de novo lipogenesis was reduced by adding either fat to LG to achieve maintenance energy levels. Moreover, adding fat as soybean oil but not fish oil significantly increased plasma and hepatic triglyceride and also elevated aspartate aminotransferase and CRP levels, reflecting inflammation. Thus, in rats, either hypocaloric feeding as glucose-based TPN or TPN provided at maintenance energy levels with the addition of fish oil limits hepatic lipid accumulation and prevents the evidence of hepatic and systemic injury found with maintenance level TPN as glucose only or glucose plus soybean oil.
Authors:
Pei-Ra Ling; Charlotte Andersson; Robert Strijbosch; Sang Lee; Anthony Silvestri; Kathleen M Gura; Mark Puder; Bruce R Bistrian
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Publication Detail:
Type:  Journal Article     Date:  2010-01-25
Journal Detail:
Title:  Metabolism: clinical and experimental     Volume:  60     ISSN:  1532-8600     ISO Abbreviation:  Metab. Clin. Exp.     Publication Date:  2011 Feb 
Date Detail:
Created Date:  2011-01-24     Completed Date:  2011-03-04     Revised Date:  2011-11-01    
Medline Journal Info:
Nlm Unique ID:  0375267     Medline TA:  Metabolism     Country:  United States    
Other Details:
Languages:  eng     Pagination:  195-205     Citation Subset:  IM    
Copyright Information:
© 2011 Elsevier Inc. All rights reserved.
Affiliation:
Laboratory of Nutrition/Infection, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Aspartate Aminotransferases / analysis
C-Reactive Protein / analysis
Caloric Restriction
Dietary Fats / administration & dosage*,  metabolism*
Fatty Acids / blood
Fish Oils / administration & dosage,  metabolism
Glucose / administration & dosage*,  metabolism*
Inflammation / metabolism*
Lipogenesis / physiology
Liver / chemistry,  enzymology
Male
Parenteral Nutrition, Total*
Phospholipids / blood
Rats
Rats, Sprague-Dawley
Soybean Oil / administration & dosage,  metabolism
Triglycerides / blood
Grant Support
ID/Acronym/Agency:
P30 DK040561-15/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Dietary Fats; 0/Fatty Acids; 0/Fish Oils; 0/Phospholipids; 0/Triglycerides; 50-99-7/Glucose; 8001-22-7/Soybean Oil; 9007-41-4/C-Reactive Protein; EC 2.6.1.1/Aspartate Aminotransferases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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