TY - JOUR
T1 - Consumption of conjugated linoleic acid (CLA)-supplemented diet during colitis development ameliorates gut inflammation without causing steatosis in mice
AU - Moreira, Thais Garcias
AU - Gomes-Santos, Ana Cristina
AU - Horta, Laila Sampaio
AU - Goncalves, Mariana Camila
AU - Santiago, Andrezza Fernanda
AU - Lauar, Juliana Gonçalves
AU - dos Reis, Daniela Silva
AU - Castro-Junior, Archimedes Barbosa
AU - Lemos, Luisa
AU - Guimarães, Mauro
AU - Aguilar, Edenil Costa
AU - Pap, Attila
AU - Amaral, Joana Ferreira
AU - Alvarez-Leite, Jacqueline I.
AU - Cara, Denise Carmona
AU - Rezende, Rafael Machado
AU - Nagy, Laszlo
AU - Faria, Ana Maria Caetano
AU - Maioli, Tatiani Uceli
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/7
Y1 - 2018/7
N2 - Dietary supplementation with conjugated linoleic acid (CLA) has been proposed for weight management and to prevent gut inflammation. However, some animal studies suggest that supplementation with CLA leads to the development of nonalcoholic fatty liver disease. The aims of this study were to test the efficiency of CLA in preventing dextran sulfate sodium (DSS)-induced colitis, to analyze the effects of CLA in the liver function, and to access putative liver alterations upon CLA supplementation during colitis. So, C57BL/6 mice were supplemented for 3 weeks with either control diet (AIN-G) or 1% CLA-supplemented diet. CLA content in the diet and in the liver of mice fed CLA containing diet were accessed by gas chromatography. On the first day of the third week of dietary treatment, mice received ad libitum a 1.5%–2.5% DSS solution for 7 days. Disease activity index score was evaluated; colon and liver samples were stained by hematoxylin and eosin for histopathology analysis and lamina propria cells were extracted to access the profile of innate cell infiltrate. Metabolic alterations before and after colitis induction were accessed by an open calorimetric circuit. Serum glucose, cholesterol, triglycerides and alanine aminotransaminase were measured; the content of fat in liver and feces was also accessed. CLA prevented weight loss, histopathologic and macroscopic signs of colitis, and inflammatory infiltration. Mice fed CLA-supplemented without colitis induction diet developed steatosis, which was prevented in mice with colitis probably due to the higher lipid consumption as energy during gut inflammation. This result suggests that CLA is safe for use during gut inflammation but not at steady-state conditions.
AB - Dietary supplementation with conjugated linoleic acid (CLA) has been proposed for weight management and to prevent gut inflammation. However, some animal studies suggest that supplementation with CLA leads to the development of nonalcoholic fatty liver disease. The aims of this study were to test the efficiency of CLA in preventing dextran sulfate sodium (DSS)-induced colitis, to analyze the effects of CLA in the liver function, and to access putative liver alterations upon CLA supplementation during colitis. So, C57BL/6 mice were supplemented for 3 weeks with either control diet (AIN-G) or 1% CLA-supplemented diet. CLA content in the diet and in the liver of mice fed CLA containing diet were accessed by gas chromatography. On the first day of the third week of dietary treatment, mice received ad libitum a 1.5%–2.5% DSS solution for 7 days. Disease activity index score was evaluated; colon and liver samples were stained by hematoxylin and eosin for histopathology analysis and lamina propria cells were extracted to access the profile of innate cell infiltrate. Metabolic alterations before and after colitis induction were accessed by an open calorimetric circuit. Serum glucose, cholesterol, triglycerides and alanine aminotransaminase were measured; the content of fat in liver and feces was also accessed. CLA prevented weight loss, histopathologic and macroscopic signs of colitis, and inflammatory infiltration. Mice fed CLA-supplemented without colitis induction diet developed steatosis, which was prevented in mice with colitis probably due to the higher lipid consumption as energy during gut inflammation. This result suggests that CLA is safe for use during gut inflammation but not at steady-state conditions.
KW - Colitis
KW - Conjugated Linoleic Acid
KW - DSS
KW - Inflammation
KW - Metabolism
KW - Steatosis
UR - http://www.scopus.com/inward/record.url?scp=85048709505&partnerID=8YFLogxK
U2 - 10.1016/j.jnutbio.2018.04.003
DO - 10.1016/j.jnutbio.2018.04.003
M3 - Article
C2 - 29800810
AN - SCOPUS:85048709505
SN - 0955-2863
VL - 57
SP - 238
EP - 245
JO - Journal of Nutritional Biochemistry
JF - Journal of Nutritional Biochemistry
ER -