Cargando…
A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice
BACKGROUND: Obesity frequently associates with the development of non-alcoholic fatty liver disease (NAFLD) and atherosclerosis. Chronic inflammation in white adipose tissue (WAT) seems to be an important driver of these manifestations. OBJECTIVE: This study investigated a combination of an extensiv...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498059/ https://www.ncbi.nlm.nih.gov/pubmed/28678821 http://dx.doi.org/10.1371/journal.pone.0180648 |
_version_ | 1783248246771023872 |
---|---|
author | Schoemaker, Marieke H. Kleemann, Robert Morrison, Martine C. Verheij, Joanne Salic, Kanita van Tol, Eric A. F. Kooistra, Teake Wielinga, Peter Y. |
author_facet | Schoemaker, Marieke H. Kleemann, Robert Morrison, Martine C. Verheij, Joanne Salic, Kanita van Tol, Eric A. F. Kooistra, Teake Wielinga, Peter Y. |
author_sort | Schoemaker, Marieke H. |
collection | PubMed |
description | BACKGROUND: Obesity frequently associates with the development of non-alcoholic fatty liver disease (NAFLD) and atherosclerosis. Chronic inflammation in white adipose tissue (WAT) seems to be an important driver of these manifestations. OBJECTIVE: This study investigated a combination of an extensively hydrolyzed casein (eHC), docosahexaenoic acid (DHA), arachidonic acid (ARA), and Lactobacillus Rhamnosus GG (LGG) (together referred to as nutritional ingredients, NI) on the development of obesity, metabolic risk factors, WAT inflammation, NAFLD and atherosclerosis in high-fat diet-fed LDLr-/-.Leiden mice, a model that mimics disease development in humans. METHODS: LDLr-/-.Leiden male mice (n = 15/group) received a high-fat diet (HFD, 45 Kcal%) for 21 weeks with or without the NI (23.7% eHC, 0.083% DHA, 0.166% ARA; all w/w and 1x10(9) CFU LGG gavage 3 times/week). HFD and HFD+NI diets were isocaloric. A low fat diet (LFD, 10 Kcal%) was used for reference. Body weight, food intake and metabolic risk factors were assessed over time. At week 21, tissues were analyzed for WAT inflammation (crown-like structures), NAFLD and atherosclerosis. Effects of the individual NI components were explored in a follow-up experiment (n = 7/group). RESULTS: When compared to HFD control, treatment with the NI strongly reduced body weight to levels of the LFD group, and significantly lowered (P<0.01) plasma insulin, cholesterol, triglycerides, leptin and serum amyloid A (P<0.01). NI also reduced WAT mass and inflammation. Strikingly, NI treatment significantly reduced macrovesicular steatosis, lobular inflammation and liver collagen (P<0.05), and attenuated atherosclerosis development (P<0.01). Of the individual components, the effects of eHC were most pronounced but could not explain the entire effects of the NI formulation. CONCLUSIONS: A combination of eHC, ARA, DHA and LGG attenuates obesity and associated cardiometabolic diseases (NAFLD, atherosclerosis) in LDLr-/-.Leiden mice. The observed reduction of inflammation in adipose tissue and in the liver provides a rationale for these comprehensive health effects. |
format | Online Article Text |
id | pubmed-5498059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54980592017-07-25 A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice Schoemaker, Marieke H. Kleemann, Robert Morrison, Martine C. Verheij, Joanne Salic, Kanita van Tol, Eric A. F. Kooistra, Teake Wielinga, Peter Y. PLoS One Research Article BACKGROUND: Obesity frequently associates with the development of non-alcoholic fatty liver disease (NAFLD) and atherosclerosis. Chronic inflammation in white adipose tissue (WAT) seems to be an important driver of these manifestations. OBJECTIVE: This study investigated a combination of an extensively hydrolyzed casein (eHC), docosahexaenoic acid (DHA), arachidonic acid (ARA), and Lactobacillus Rhamnosus GG (LGG) (together referred to as nutritional ingredients, NI) on the development of obesity, metabolic risk factors, WAT inflammation, NAFLD and atherosclerosis in high-fat diet-fed LDLr-/-.Leiden mice, a model that mimics disease development in humans. METHODS: LDLr-/-.Leiden male mice (n = 15/group) received a high-fat diet (HFD, 45 Kcal%) for 21 weeks with or without the NI (23.7% eHC, 0.083% DHA, 0.166% ARA; all w/w and 1x10(9) CFU LGG gavage 3 times/week). HFD and HFD+NI diets were isocaloric. A low fat diet (LFD, 10 Kcal%) was used for reference. Body weight, food intake and metabolic risk factors were assessed over time. At week 21, tissues were analyzed for WAT inflammation (crown-like structures), NAFLD and atherosclerosis. Effects of the individual NI components were explored in a follow-up experiment (n = 7/group). RESULTS: When compared to HFD control, treatment with the NI strongly reduced body weight to levels of the LFD group, and significantly lowered (P<0.01) plasma insulin, cholesterol, triglycerides, leptin and serum amyloid A (P<0.01). NI also reduced WAT mass and inflammation. Strikingly, NI treatment significantly reduced macrovesicular steatosis, lobular inflammation and liver collagen (P<0.05), and attenuated atherosclerosis development (P<0.01). Of the individual components, the effects of eHC were most pronounced but could not explain the entire effects of the NI formulation. CONCLUSIONS: A combination of eHC, ARA, DHA and LGG attenuates obesity and associated cardiometabolic diseases (NAFLD, atherosclerosis) in LDLr-/-.Leiden mice. The observed reduction of inflammation in adipose tissue and in the liver provides a rationale for these comprehensive health effects. Public Library of Science 2017-07-05 /pmc/articles/PMC5498059/ /pubmed/28678821 http://dx.doi.org/10.1371/journal.pone.0180648 Text en © 2017 Schoemaker et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Schoemaker, Marieke H. Kleemann, Robert Morrison, Martine C. Verheij, Joanne Salic, Kanita van Tol, Eric A. F. Kooistra, Teake Wielinga, Peter Y. A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice |
title | A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice |
title_full | A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice |
title_fullStr | A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice |
title_full_unstemmed | A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice |
title_short | A casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in LDLr-/-.Leiden mice |
title_sort | casein hydrolysate based formulation attenuates obesity and associated non-alcoholic fatty liver disease and atherosclerosis in ldlr-/-.leiden mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498059/ https://www.ncbi.nlm.nih.gov/pubmed/28678821 http://dx.doi.org/10.1371/journal.pone.0180648 |
work_keys_str_mv | AT schoemakermariekeh acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT kleemannrobert acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT morrisonmartinec acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT verheijjoanne acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT salickanita acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT vantolericaf acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT kooistrateake acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT wielingapetery acaseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT schoemakermariekeh caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT kleemannrobert caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT morrisonmartinec caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT verheijjoanne caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT salickanita caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT vantolericaf caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT kooistrateake caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice AT wielingapetery caseinhydrolysatebasedformulationattenuatesobesityandassociatednonalcoholicfattyliverdiseaseandatherosclerosisinldlrleidenmice |