Astaxanthin from Haematococcus pluvialis alleviates obesity by modulating lipid metabolism and gut microbiota in mice fed a high-fat diet

Obesity is a global chronic disease epidemic that is attributed to the abnormal accumulation of lipids in adipose tissue. Astaxanthin (AST) from , a natural carotenoid, exhibits antioxidant, anti-lipogenic, anti-diabetic and other potent effects. Herein, we evaluated the effect of AST to illuminate...

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Veröffentlicht in:Food & function 2021-10, Vol.12 (20), p.9719-9738
Hauptverfasser: Wang, Meng, Ma, Haotian, Guan, Siyu, Luo, Tao, Zhao, Chunchao, Cai, Guiping, Zheng, Yubin, Jia, Xiaoyun, Di, Jianbing, Li, Runzhi, Cui, Hongli
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container_issue 20
container_start_page 9719
container_title Food & function
container_volume 12
creator Wang, Meng
Ma, Haotian
Guan, Siyu
Luo, Tao
Zhao, Chunchao
Cai, Guiping
Zheng, Yubin
Jia, Xiaoyun
Di, Jianbing
Li, Runzhi
Cui, Hongli
description Obesity is a global chronic disease epidemic that is attributed to the abnormal accumulation of lipids in adipose tissue. Astaxanthin (AST) from , a natural carotenoid, exhibits antioxidant, anti-lipogenic, anti-diabetic and other potent effects. Herein, we evaluated the effect of AST to illuminate its efficacy and mechanisms in high-fat diet-fed mice. AST supplementation not only significantly decreased body weight and lipid droplet accumulation in the liver but also modulated liver function and serum lipid levels. Lipidomic analysis revealed that 13 lipids might be potential biomarkers responsible for the effects of AST in lipid reduction, such as total free fatty acids (FFAs), triacylglycerols (TGs) and cholesterol esters (CEs). The gut microbiota sequencing results indicated that AST alleviated HFD-induced gut microbiota dysbiosis by optimizing the ratio of Firmicutes to Bacteroides and inhibiting the abundance of obesity-related pathogenic microbiota while promoting the abundance of probiotics related to glucose and lipid metabolism. In addition, qRT-PCR demonstrated that AST could regulate the gene expressions of the AMPK/SREBP1c pathway by downregulating lipogenesis correlated-genes and upregulating the lipid oxidant related-gene. The present study revealed the new function of AST in regulating lipid metabolism, which provided a theoretical basis for the development of high-quality AST functional food and the application of diet active substances in obesity, as demonstrated in mice.
doi_str_mv 10.1039/d1fo01495a
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Astaxanthin (AST) from , a natural carotenoid, exhibits antioxidant, anti-lipogenic, anti-diabetic and other potent effects. Herein, we evaluated the effect of AST to illuminate its efficacy and mechanisms in high-fat diet-fed mice. AST supplementation not only significantly decreased body weight and lipid droplet accumulation in the liver but also modulated liver function and serum lipid levels. Lipidomic analysis revealed that 13 lipids might be potential biomarkers responsible for the effects of AST in lipid reduction, such as total free fatty acids (FFAs), triacylglycerols (TGs) and cholesterol esters (CEs). The gut microbiota sequencing results indicated that AST alleviated HFD-induced gut microbiota dysbiosis by optimizing the ratio of Firmicutes to Bacteroides and inhibiting the abundance of obesity-related pathogenic microbiota while promoting the abundance of probiotics related to glucose and lipid metabolism. In addition, qRT-PCR demonstrated that AST could regulate the gene expressions of the AMPK/SREBP1c pathway by downregulating lipogenesis correlated-genes and upregulating the lipid oxidant related-gene. 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Astaxanthin (AST) from , a natural carotenoid, exhibits antioxidant, anti-lipogenic, anti-diabetic and other potent effects. Herein, we evaluated the effect of AST to illuminate its efficacy and mechanisms in high-fat diet-fed mice. AST supplementation not only significantly decreased body weight and lipid droplet accumulation in the liver but also modulated liver function and serum lipid levels. Lipidomic analysis revealed that 13 lipids might be potential biomarkers responsible for the effects of AST in lipid reduction, such as total free fatty acids (FFAs), triacylglycerols (TGs) and cholesterol esters (CEs). The gut microbiota sequencing results indicated that AST alleviated HFD-induced gut microbiota dysbiosis by optimizing the ratio of Firmicutes to Bacteroides and inhibiting the abundance of obesity-related pathogenic microbiota while promoting the abundance of probiotics related to glucose and lipid metabolism. 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nutraceuticals</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>Glucose metabolism</topic><topic>Haematococcus pluvialis</topic><topic>High fat diet</topic><topic>Intestinal microflora</topic><topic>Lipid metabolism</topic><topic>Lipid Metabolism - drug effects</topic><topic>Lipids</topic><topic>Lipogenesis</topic><topic>Liver</topic><topic>Male</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microbiota</topic><topic>Obesity</topic><topic>Obesity - prevention &amp; control</topic><topic>Oxidants</topic><topic>Oxidizing agents</topic><topic>Probiotics</topic><topic>Triglycerides</topic><topic>Xanthophylls - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Meng</creatorcontrib><creatorcontrib>Ma, Haotian</creatorcontrib><creatorcontrib>Guan, Siyu</creatorcontrib><creatorcontrib>Luo, Tao</creatorcontrib><creatorcontrib>Zhao, Chunchao</creatorcontrib><creatorcontrib>Cai, Guiping</creatorcontrib><creatorcontrib>Zheng, Yubin</creatorcontrib><creatorcontrib>Jia, Xiaoyun</creatorcontrib><creatorcontrib>Di, Jianbing</creatorcontrib><creatorcontrib>Li, Runzhi</creatorcontrib><creatorcontrib>Cui, Hongli</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Food &amp; 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Astaxanthin (AST) from , a natural carotenoid, exhibits antioxidant, anti-lipogenic, anti-diabetic and other potent effects. Herein, we evaluated the effect of AST to illuminate its efficacy and mechanisms in high-fat diet-fed mice. AST supplementation not only significantly decreased body weight and lipid droplet accumulation in the liver but also modulated liver function and serum lipid levels. Lipidomic analysis revealed that 13 lipids might be potential biomarkers responsible for the effects of AST in lipid reduction, such as total free fatty acids (FFAs), triacylglycerols (TGs) and cholesterol esters (CEs). The gut microbiota sequencing results indicated that AST alleviated HFD-induced gut microbiota dysbiosis by optimizing the ratio of Firmicutes to Bacteroides and inhibiting the abundance of obesity-related pathogenic microbiota while promoting the abundance of probiotics related to glucose and lipid metabolism. In addition, qRT-PCR demonstrated that AST could regulate the gene expressions of the AMPK/SREBP1c pathway by downregulating lipogenesis correlated-genes and upregulating the lipid oxidant related-gene. The present study revealed the new function of AST in regulating lipid metabolism, which provided a theoretical basis for the development of high-quality AST functional food and the application of diet active substances in obesity, as demonstrated in mice.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>34664590</pmid><doi>10.1039/d1fo01495a</doi><tpages>20</tpages><orcidid>https://orcid.org/0000-0001-7785-8222</orcidid><orcidid>https://orcid.org/0000-0002-9933-5024</orcidid></addata></record>
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subjects Abundance
Accumulation
Adipose tissue
Algae
Animals
Antioxidants
Astaxanthin
Biomarkers
Body weight
Chlorophyta
Cholesterol
Chronic illnesses
Diabetes mellitus
Diet
Diet, High-Fat
Dietary supplements
Dysbacteriosis
Dysbiosis - prevention & control
Epidemics
Esters
Fatty acids
Food quality
Functional foods & nutraceuticals
Gastrointestinal Microbiome - drug effects
Glucose metabolism
Haematococcus pluvialis
High fat diet
Intestinal microflora
Lipid metabolism
Lipid Metabolism - drug effects
Lipids
Lipogenesis
Liver
Male
Metabolism
Mice
Mice, Inbred C57BL
Microbiota
Obesity
Obesity - prevention & control
Oxidants
Oxidizing agents
Probiotics
Triglycerides
Xanthophylls - pharmacology
title Astaxanthin from Haematococcus pluvialis alleviates obesity by modulating lipid metabolism and gut microbiota in mice fed a high-fat diet
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