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Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet

The impact of casein on atherosclerotic lesion progression remains controversial. In this study, we tested the effect of casein on atherosclerotic development and its potential mechanisms in male apolipoprotein E knockout (apoE(‐/‐)) mice fed with high‐fat diet (HFD). Male apoE(‐/‐) mice fed with HF...

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Autores principales: Hou, Lingbo, Wang, Yuting, Zhang, Mingjing, Yu, Yijun, Gu, Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382161/
https://www.ncbi.nlm.nih.gov/pubmed/32724618
http://dx.doi.org/10.1002/fsn3.1638
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author Hou, Lingbo
Wang, Yuting
Zhang, Mingjing
Yu, Yijun
Gu, Ye
author_facet Hou, Lingbo
Wang, Yuting
Zhang, Mingjing
Yu, Yijun
Gu, Ye
author_sort Hou, Lingbo
collection PubMed
description The impact of casein on atherosclerotic lesion progression remains controversial. In this study, we tested the effect of casein on atherosclerotic development and its potential mechanisms in male apolipoprotein E knockout (apoE(‐/‐)) mice fed with high‐fat diet (HFD). Male apoE(‐/‐) mice fed with HFD were randomized into HFD group (subcutaneous injection with 0.5 ml of 0.9% sodium chloride daily, n = 6) and HFD + Casein group (subcutaneous injection with 0.5 ml of 10% casein daily, n = 6). Body weight was recorded at baseline and once a week thereafter. After 12 weeks of treatment, plasma lipid and inflammatory markers, and histological characterization of atherosclerotic plaques in the aortic arch and aortic sinus were analyzed. There was no significant difference in weight gain between the two groups after 12 weeks of treatment. Plasma levels of total cholesterol (TC), triglyceride (TG), and low‐density lipoprotein cholesterol (LDL‐C) were significantly lower, while high‐density lipoprotein cholesterol (HDL‐C) level tended to be higher in the HFD + Casein group compared with the HFD group. The positive percentages of atherosclerotic lesions in aortic arch and aortic sinus as well as collagen deposition in aortic sinus plaques were significantly lower in the HFD + Casein group compared with the HFD group. Plasma levels of interleukin (IL)‐1β and granulocyte‐macrophage colony‐stimulating factor (GM‐CSF) were also significantly lower in the HFD + Casein group compared with the HFD group. In conclusion, subcutaneous administration of casein attenuates atherosclerotic lesion progression, possibly through decreasing fibrosis and inflammatory responses in male apoE(‐/‐) mice fed with HFD.
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spelling pubmed-73821612020-07-27 Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet Hou, Lingbo Wang, Yuting Zhang, Mingjing Yu, Yijun Gu, Ye Food Sci Nutr Original Research The impact of casein on atherosclerotic lesion progression remains controversial. In this study, we tested the effect of casein on atherosclerotic development and its potential mechanisms in male apolipoprotein E knockout (apoE(‐/‐)) mice fed with high‐fat diet (HFD). Male apoE(‐/‐) mice fed with HFD were randomized into HFD group (subcutaneous injection with 0.5 ml of 0.9% sodium chloride daily, n = 6) and HFD + Casein group (subcutaneous injection with 0.5 ml of 10% casein daily, n = 6). Body weight was recorded at baseline and once a week thereafter. After 12 weeks of treatment, plasma lipid and inflammatory markers, and histological characterization of atherosclerotic plaques in the aortic arch and aortic sinus were analyzed. There was no significant difference in weight gain between the two groups after 12 weeks of treatment. Plasma levels of total cholesterol (TC), triglyceride (TG), and low‐density lipoprotein cholesterol (LDL‐C) were significantly lower, while high‐density lipoprotein cholesterol (HDL‐C) level tended to be higher in the HFD + Casein group compared with the HFD group. The positive percentages of atherosclerotic lesions in aortic arch and aortic sinus as well as collagen deposition in aortic sinus plaques were significantly lower in the HFD + Casein group compared with the HFD group. Plasma levels of interleukin (IL)‐1β and granulocyte‐macrophage colony‐stimulating factor (GM‐CSF) were also significantly lower in the HFD + Casein group compared with the HFD group. In conclusion, subcutaneous administration of casein attenuates atherosclerotic lesion progression, possibly through decreasing fibrosis and inflammatory responses in male apoE(‐/‐) mice fed with HFD. John Wiley and Sons Inc. 2020-06-07 /pmc/articles/PMC7382161/ /pubmed/32724618 http://dx.doi.org/10.1002/fsn3.1638 Text en © 2020 The Authors. Food Science & Nutrition published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Hou, Lingbo
Wang, Yuting
Zhang, Mingjing
Yu, Yijun
Gu, Ye
Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet
title Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet
title_full Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet
title_fullStr Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet
title_full_unstemmed Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet
title_short Subcutaneous administration of casein attenuates atherosclerotic progression in male apoE(‐/‐) mice fed with high‐fat diet
title_sort subcutaneous administration of casein attenuates atherosclerotic progression in male apoe(‐/‐) mice fed with high‐fat diet
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382161/
https://www.ncbi.nlm.nih.gov/pubmed/32724618
http://dx.doi.org/10.1002/fsn3.1638
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