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Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice

Atherosclerosis (AS) is recognized as the original cause of most cardiovascular and cerebrovascular diseases. The dual-protein (DP) nutrition that consists of soy protein and whey protein is reported to be associated with a reduction in AS; however, the relationship between DP and AS remains ambiguo...

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Autores principales: Huang, Yingchun, Zhang, Kun, Zhang, Li, Qiu, Juhui, Fu, Lin, Yin, Tieying, Wang, Jing, Qin, Rui, Zhang, Jingjie, Dong, Xianwen, Wang, Guixue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879330/
https://www.ncbi.nlm.nih.gov/pubmed/35215505
http://dx.doi.org/10.3390/nu14040855
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author Huang, Yingchun
Zhang, Kun
Zhang, Li
Qiu, Juhui
Fu, Lin
Yin, Tieying
Wang, Jing
Qin, Rui
Zhang, Jingjie
Dong, Xianwen
Wang, Guixue
author_facet Huang, Yingchun
Zhang, Kun
Zhang, Li
Qiu, Juhui
Fu, Lin
Yin, Tieying
Wang, Jing
Qin, Rui
Zhang, Jingjie
Dong, Xianwen
Wang, Guixue
author_sort Huang, Yingchun
collection PubMed
description Atherosclerosis (AS) is recognized as the original cause of most cardiovascular and cerebrovascular diseases. The dual-protein (DP) nutrition that consists of soy protein and whey protein is reported to be associated with a reduction in AS; however, the relationship between DP and AS remains ambiguous. Therefore, this study aimed to verify the effect of DP on AS and explore the optimal DP intake to improve AS. ApoE(−/−) mice were administrated with low- (LDP), middle- (MDP), and high-dose (HDP) DP. The MDP group exhibited significant improvements in AS. In terms of lipid metabolism, the levels of plasma total triglyceride and LDL-C and the mRNA expression levels of Cyp7a1 and PCSK9 were markedly tuned in the MDP group. In addition, the MDP treatment group had a substantially lower inflammatory response and better intestinal barrier function than LDP and HDP groups. The species richness demonstrated by the Chao1 index was distinctly increased in the MDP group, and the relative abundance of intestinal-permeability-protective microbes Blautia and Akkermansia was significantly elevated. In summary, an adequate intake of DP was able to counteract atherosclerosis development in ApoE(−/−) mice, and this study provides a scientific theoretical basis for the application of DP in the food and pharmaceutical fields.
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spelling pubmed-88793302022-02-26 Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice Huang, Yingchun Zhang, Kun Zhang, Li Qiu, Juhui Fu, Lin Yin, Tieying Wang, Jing Qin, Rui Zhang, Jingjie Dong, Xianwen Wang, Guixue Nutrients Article Atherosclerosis (AS) is recognized as the original cause of most cardiovascular and cerebrovascular diseases. The dual-protein (DP) nutrition that consists of soy protein and whey protein is reported to be associated with a reduction in AS; however, the relationship between DP and AS remains ambiguous. Therefore, this study aimed to verify the effect of DP on AS and explore the optimal DP intake to improve AS. ApoE(−/−) mice were administrated with low- (LDP), middle- (MDP), and high-dose (HDP) DP. The MDP group exhibited significant improvements in AS. In terms of lipid metabolism, the levels of plasma total triglyceride and LDL-C and the mRNA expression levels of Cyp7a1 and PCSK9 were markedly tuned in the MDP group. In addition, the MDP treatment group had a substantially lower inflammatory response and better intestinal barrier function than LDP and HDP groups. The species richness demonstrated by the Chao1 index was distinctly increased in the MDP group, and the relative abundance of intestinal-permeability-protective microbes Blautia and Akkermansia was significantly elevated. In summary, an adequate intake of DP was able to counteract atherosclerosis development in ApoE(−/−) mice, and this study provides a scientific theoretical basis for the application of DP in the food and pharmaceutical fields. MDPI 2022-02-18 /pmc/articles/PMC8879330/ /pubmed/35215505 http://dx.doi.org/10.3390/nu14040855 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Huang, Yingchun
Zhang, Kun
Zhang, Li
Qiu, Juhui
Fu, Lin
Yin, Tieying
Wang, Jing
Qin, Rui
Zhang, Jingjie
Dong, Xianwen
Wang, Guixue
Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice
title Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice
title_full Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice
title_fullStr Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice
title_full_unstemmed Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice
title_short Dosage of Dual-Protein Nutrition Differentially Impacts the Formation of Atherosclerosis in ApoE(−/−) Mice
title_sort dosage of dual-protein nutrition differentially impacts the formation of atherosclerosis in apoe(−/−) mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879330/
https://www.ncbi.nlm.nih.gov/pubmed/35215505
http://dx.doi.org/10.3390/nu14040855
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