Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid Administration

Although exerting valuable functions in living organisms, nonesterified fatty acids (NEFAs) can be toxic to cells. Increased blood concentration of oleic acid (OLA) and other fatty acids is detected in many pathological conditions. In sepsis and leptospirosis, high plasma levels of NEFA and low albu...

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Main Authors: Cassiano Felippe Gonçalves de Albuquerque, Patrícia Burth, Mauricio Younes Ibrahim, Diogo Gomes Garcia, Patrícia Torres Bozza, Hugo Caire Castro Faria Neto, Mauro Velho Castro Faria
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2012/601032
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author Cassiano Felippe Gonçalves de Albuquerque
Patrícia Burth
Mauricio Younes Ibrahim
Diogo Gomes Garcia
Patrícia Torres Bozza
Hugo Caire Castro Faria Neto
Mauro Velho Castro Faria
author_facet Cassiano Felippe Gonçalves de Albuquerque
Patrícia Burth
Mauricio Younes Ibrahim
Diogo Gomes Garcia
Patrícia Torres Bozza
Hugo Caire Castro Faria Neto
Mauro Velho Castro Faria
author_sort Cassiano Felippe Gonçalves de Albuquerque
collection DOAJ
description Although exerting valuable functions in living organisms, nonesterified fatty acids (NEFAs) can be toxic to cells. Increased blood concentration of oleic acid (OLA) and other fatty acids is detected in many pathological conditions. In sepsis and leptospirosis, high plasma levels of NEFA and low albumin concentrations are correlated to the disease severity. Surprisingly, 24 h after intravenous or intragastric administration of OLA, main NEFA levels (OLA inclusive) were dose dependently decreased. However, lung injury was detected in intravenously treated mice, and highest dose killed all mice. When administered by the enteral route, OLA was not toxic in any tested conditions. Results indicate that OLA has important regulatory properties on fatty acid metabolism, possibly lowering circulating fatty acid through activation of peroxisome proliferator-activated receptors. The significant reduction in blood NEFA levels detected after OLA enteral administration can contribute to the already known health benefits brought about by unsaturated-fatty-acid-enriched diets.
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institution Kabale University
issn 0962-9351
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publishDate 2012-01-01
publisher Wiley
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series Mediators of Inflammation
spelling doaj-art-560865dea4f049aab0bd560d674871012025-02-03T06:07:20ZengWileyMediators of Inflammation0962-93511466-18612012-01-01201210.1155/2012/601032601032Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid AdministrationCassiano Felippe Gonçalves de Albuquerque0Patrícia Burth1Mauricio Younes Ibrahim2Diogo Gomes Garcia3Patrícia Torres Bozza4Hugo Caire Castro Faria Neto5Mauro Velho Castro Faria6Laboratório de Imunofarmacologia, Fundação Oswaldo Cruz, FIOCRUZ, Rio de Janeiro 21040-900, BrazilDepartamento de Biologia Celular e Molecular, Instituto de Biologia, Universidade Federal Fluminense, Niteroi 24020-150, BrazilDepartamento de Medicina Interna, Faculdade de Ciências Medicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro 20550-900, BrazilLaboratório de Imunofarmacologia, Fundação Oswaldo Cruz, FIOCRUZ, Rio de Janeiro 21040-900, BrazilLaboratório de Imunofarmacologia, Fundação Oswaldo Cruz, FIOCRUZ, Rio de Janeiro 21040-900, BrazilLaboratório de Imunofarmacologia, Fundação Oswaldo Cruz, FIOCRUZ, Rio de Janeiro 21040-900, BrazilDepartamento de Medicina Interna, Faculdade de Ciências Medicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro 20550-900, BrazilAlthough exerting valuable functions in living organisms, nonesterified fatty acids (NEFAs) can be toxic to cells. Increased blood concentration of oleic acid (OLA) and other fatty acids is detected in many pathological conditions. In sepsis and leptospirosis, high plasma levels of NEFA and low albumin concentrations are correlated to the disease severity. Surprisingly, 24 h after intravenous or intragastric administration of OLA, main NEFA levels (OLA inclusive) were dose dependently decreased. However, lung injury was detected in intravenously treated mice, and highest dose killed all mice. When administered by the enteral route, OLA was not toxic in any tested conditions. Results indicate that OLA has important regulatory properties on fatty acid metabolism, possibly lowering circulating fatty acid through activation of peroxisome proliferator-activated receptors. The significant reduction in blood NEFA levels detected after OLA enteral administration can contribute to the already known health benefits brought about by unsaturated-fatty-acid-enriched diets.http://dx.doi.org/10.1155/2012/601032
spellingShingle Cassiano Felippe Gonçalves de Albuquerque
Patrícia Burth
Mauricio Younes Ibrahim
Diogo Gomes Garcia
Patrícia Torres Bozza
Hugo Caire Castro Faria Neto
Mauro Velho Castro Faria
Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid Administration
Mediators of Inflammation
title Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid Administration
title_full Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid Administration
title_fullStr Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid Administration
title_full_unstemmed Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid Administration
title_short Reduced Plasma Nonesterified Fatty Acid Levels and the Advent of an Acute Lung Injury in Mice after Intravenous or Enteral Oleic Acid Administration
title_sort reduced plasma nonesterified fatty acid levels and the advent of an acute lung injury in mice after intravenous or enteral oleic acid administration
url http://dx.doi.org/10.1155/2012/601032
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