Chitosan Oligosaccharides Attenuate Atherosclerosis and Decrease Non-HDL in ApoE-/- Mice

Aim: Chitosan-oligosaccharides (COS) treatment showed lipid lowering effects in rats and reverse cholesterol transport (RCT) promotion in mice, suggested that COS might be a potential atheroprotective material. In this study, we investigated the effects of COS treatment on atherosclerosis (AS) in ap...

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Veröffentlicht in:Journal of Atherosclerosis and Thrombosis 2015/09/16, Vol.22(9), pp.926-941
Hauptverfasser: Yu, Yang, Luo, Tian, Liu, Shuai, Song, Guohua, Han, Jiju, Wang, Yun, Yao, Shutong, Feng, Lei, Qin, Shucun
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container_end_page 941
container_issue 9
container_start_page 926
container_title Journal of Atherosclerosis and Thrombosis
container_volume 22
creator Yu, Yang
Luo, Tian
Liu, Shuai
Song, Guohua
Han, Jiju
Wang, Yun
Yao, Shutong
Feng, Lei
Qin, Shucun
description Aim: Chitosan-oligosaccharides (COS) treatment showed lipid lowering effects in rats and reverse cholesterol transport (RCT) promotion in mice, suggested that COS might be a potential atheroprotective material. In this study, we investigated the effects of COS treatment on atherosclerosis (AS) in apolipoprotein E deficient mice (apoE-/-). Methods: After feeding high fat (HF) diet for 12 weeks with the gastric gavages administration of COS or vehicle, respectively, the mice were sacrificed for the assessment of atherosclerosis, plaque stability, and the mechanism investigation. Results: Cholesterol and TG in non-high density lipoprotein (non-HDL) fractions were reduced dramatically in COS groups. The COS treatment decreased the lesion areas of aortic enface, plaque areas in aortic root, and increased plaque stability in apoE-/-. Furthermore, the COS treatment significantly enhanced the expression of liver low density lipoprotein receptor (LDL-R), scavenger receptor BI (SR-BI) as well as the expression of macrophage SR-BI and ATP binding cassette transporter A1(ABCA1). We also found that the COS treatment did not affect the plasma lipid level in LDL-R deficient mice and cholesterol absorption in wild type mice. Conclusions: COS treatment attenuated AS and decreased plasma non-HDL level in apoE-/-, and the potential mechanism might be involved with enhanced expression of hepatic LDL-R and SR-BI, and macrophage ABCA1.
doi_str_mv 10.5551/jat.22939
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In this study, we investigated the effects of COS treatment on atherosclerosis (AS) in apolipoprotein E deficient mice (apoE-/-). Methods: After feeding high fat (HF) diet for 12 weeks with the gastric gavages administration of COS or vehicle, respectively, the mice were sacrificed for the assessment of atherosclerosis, plaque stability, and the mechanism investigation. Results: Cholesterol and TG in non-high density lipoprotein (non-HDL) fractions were reduced dramatically in COS groups. The COS treatment decreased the lesion areas of aortic enface, plaque areas in aortic root, and increased plaque stability in apoE-/-. Furthermore, the COS treatment significantly enhanced the expression of liver low density lipoprotein receptor (LDL-R), scavenger receptor BI (SR-BI) as well as the expression of macrophage SR-BI and ATP binding cassette transporter A1(ABCA1). We also found that the COS treatment did not affect the plasma lipid level in LDL-R deficient mice and cholesterol absorption in wild type mice. Conclusions: COS treatment attenuated AS and decreased plasma non-HDL level in apoE-/-, and the potential mechanism might be involved with enhanced expression of hepatic LDL-R and SR-BI, and macrophage ABCA1.</description><identifier>ISSN: 1340-3478</identifier><identifier>EISSN: 1880-3873</identifier><identifier>DOI: 10.5551/jat.22939</identifier><identifier>PMID: 25843117</identifier><language>eng</language><publisher>Japan: Japan Atherosclerosis Society</publisher><subject>Animals ; Aorta - pathology ; Apolipoproteins E - genetics ; Atherosclerosis ; Atherosclerosis - metabolism ; Atherosclerosis - therapy ; ATP Binding Cassette Transporter 1 - metabolism ; ATP binding cassette transporter A1 ; ATP Binding Cassette Transporter, Sub-Family G, Member 5 ; ATP-Binding Cassette Transporters - metabolism ; Biological Transport ; Cell Line ; Chitosan - chemistry ; Chitosan - therapeutic use ; Chitosan oligosaccharides ; Cholesterol - blood ; Cholesterol - genetics ; Cholesterol, HDL - blood ; Cholesterol, HDL - genetics ; Disease Models, Animal ; Hep G2 Cells ; Humans ; Lipids - blood ; Lipoproteins - metabolism ; Low density lipoprotein receptor ; Macrophages - metabolism ; Male ; Matrix Metalloproteinase 9 - metabolism ; Mice ; Mice, Knockout ; Oligosaccharides - chemistry ; Oligosaccharides - therapeutic use ; Receptors, LDL - metabolism ; Scavenger receptor BI ; Scavenger Receptors, Class B - metabolism ; Triglycerides - blood</subject><ispartof>Journal of Atherosclerosis and Thrombosis, 2015/09/16, Vol.22(9), pp.926-941</ispartof><rights>2015 Japan Atherosclerosis Society</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-f4e3418974af87aa7f22a2834b37b3d63d0ff6ee8f68ac917f566995237045a93</citedby><cites>FETCH-LOGICAL-c598t-f4e3418974af87aa7f22a2834b37b3d63d0ff6ee8f68ac917f566995237045a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,1879,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25843117$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Yang</creatorcontrib><creatorcontrib>Luo, Tian</creatorcontrib><creatorcontrib>Liu, Shuai</creatorcontrib><creatorcontrib>Song, Guohua</creatorcontrib><creatorcontrib>Han, Jiju</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><creatorcontrib>Yao, Shutong</creatorcontrib><creatorcontrib>Feng, Lei</creatorcontrib><creatorcontrib>Qin, Shucun</creatorcontrib><creatorcontrib>Key Laboratory of Atherosclerosis in Universities of Shandong ; Institute of Atherosclerosis</creatorcontrib><creatorcontrib>Taishan Medical University</creatorcontrib><title>Chitosan Oligosaccharides Attenuate Atherosclerosis and Decrease Non-HDL in ApoE-/- Mice</title><title>Journal of Atherosclerosis and Thrombosis</title><addtitle>JAT</addtitle><description>Aim: Chitosan-oligosaccharides (COS) treatment showed lipid lowering effects in rats and reverse cholesterol transport (RCT) promotion in mice, suggested that COS might be a potential atheroprotective material. In this study, we investigated the effects of COS treatment on atherosclerosis (AS) in apolipoprotein E deficient mice (apoE-/-). Methods: After feeding high fat (HF) diet for 12 weeks with the gastric gavages administration of COS or vehicle, respectively, the mice were sacrificed for the assessment of atherosclerosis, plaque stability, and the mechanism investigation. Results: Cholesterol and TG in non-high density lipoprotein (non-HDL) fractions were reduced dramatically in COS groups. The COS treatment decreased the lesion areas of aortic enface, plaque areas in aortic root, and increased plaque stability in apoE-/-. Furthermore, the COS treatment significantly enhanced the expression of liver low density lipoprotein receptor (LDL-R), scavenger receptor BI (SR-BI) as well as the expression of macrophage SR-BI and ATP binding cassette transporter A1(ABCA1). We also found that the COS treatment did not affect the plasma lipid level in LDL-R deficient mice and cholesterol absorption in wild type mice. Conclusions: COS treatment attenuated AS and decreased plasma non-HDL level in apoE-/-, and the potential mechanism might be involved with enhanced expression of hepatic LDL-R and SR-BI, and macrophage ABCA1.</description><subject>Animals</subject><subject>Aorta - pathology</subject><subject>Apolipoproteins E - genetics</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - metabolism</subject><subject>Atherosclerosis - therapy</subject><subject>ATP Binding Cassette Transporter 1 - metabolism</subject><subject>ATP binding cassette transporter A1</subject><subject>ATP Binding Cassette Transporter, Sub-Family G, Member 5</subject><subject>ATP-Binding Cassette Transporters - metabolism</subject><subject>Biological Transport</subject><subject>Cell Line</subject><subject>Chitosan - chemistry</subject><subject>Chitosan - therapeutic use</subject><subject>Chitosan oligosaccharides</subject><subject>Cholesterol - blood</subject><subject>Cholesterol - genetics</subject><subject>Cholesterol, HDL - blood</subject><subject>Cholesterol, HDL - genetics</subject><subject>Disease Models, Animal</subject><subject>Hep G2 Cells</subject><subject>Humans</subject><subject>Lipids - blood</subject><subject>Lipoproteins - metabolism</subject><subject>Low density lipoprotein receptor</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Oligosaccharides - chemistry</subject><subject>Oligosaccharides - therapeutic use</subject><subject>Receptors, LDL - metabolism</subject><subject>Scavenger receptor BI</subject><subject>Scavenger Receptors, Class B - metabolism</subject><subject>Triglycerides - blood</subject><issn>1340-3478</issn><issn>1880-3873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE9PGzEQxS1EBTTlwBdAe-Ww4L9r-4SiQKFSWi6t1Js18Y6Jo403Wm8k-Pb1EprLmyfN0_j5R8gVo7dKKXa3gfGWcyvsCblgxtBaGC1OixeyeKnNOfma84ZSIZTiZ-ScKyMFY_qC_F2s49hnSNVLF1-L8X4NQ2wxV_NxxLSHEYtb49Bn300acwWprR7QDwgZq199qp8fllVM1XzXP9Z3dfUzevxGvgToMl5-zhn58_3x9-K5Xr48_VjMl7VX1ox1kCgkM1ZLCEYD6MA5cCPkSuiVaBvR0hAaRBMaA94yHVTTWKu40FQqsGJGbg53femWBwxuN8QtDO-OUTfRcYWO-6BTsteH7G6_2mJ7TP7HUQJPh0DZRg9dn7qY0G36_ZDKJxy-6bbfvoPjlClHKefUlqEdtbwpItlU3ZR2M3J_uLTJI7zi8SkYxlg4fpZydpKPcsfNxN9hEv8AkZaL_g</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Yu, Yang</creator><creator>Luo, Tian</creator><creator>Liu, Shuai</creator><creator>Song, Guohua</creator><creator>Han, Jiju</creator><creator>Wang, Yun</creator><creator>Yao, Shutong</creator><creator>Feng, Lei</creator><creator>Qin, Shucun</creator><general>Japan Atherosclerosis Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20150101</creationdate><title>Chitosan Oligosaccharides Attenuate Atherosclerosis and Decrease Non-HDL in ApoE-/- Mice</title><author>Yu, Yang ; 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Institute of Atherosclerosis</creatorcontrib><creatorcontrib>Taishan Medical University</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Yang</au><au>Luo, Tian</au><au>Liu, Shuai</au><au>Song, Guohua</au><au>Han, Jiju</au><au>Wang, Yun</au><au>Yao, Shutong</au><au>Feng, Lei</au><au>Qin, Shucun</au><aucorp>Key Laboratory of Atherosclerosis in Universities of Shandong ; Institute of Atherosclerosis</aucorp><aucorp>Taishan Medical University</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chitosan Oligosaccharides Attenuate Atherosclerosis and Decrease Non-HDL in ApoE-/- Mice</atitle><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle><addtitle>JAT</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>22</volume><issue>9</issue><spage>926</spage><epage>941</epage><pages>926-941</pages><issn>1340-3478</issn><eissn>1880-3873</eissn><abstract>Aim: Chitosan-oligosaccharides (COS) treatment showed lipid lowering effects in rats and reverse cholesterol transport (RCT) promotion in mice, suggested that COS might be a potential atheroprotective material. In this study, we investigated the effects of COS treatment on atherosclerosis (AS) in apolipoprotein E deficient mice (apoE-/-). Methods: After feeding high fat (HF) diet for 12 weeks with the gastric gavages administration of COS or vehicle, respectively, the mice were sacrificed for the assessment of atherosclerosis, plaque stability, and the mechanism investigation. Results: Cholesterol and TG in non-high density lipoprotein (non-HDL) fractions were reduced dramatically in COS groups. The COS treatment decreased the lesion areas of aortic enface, plaque areas in aortic root, and increased plaque stability in apoE-/-. Furthermore, the COS treatment significantly enhanced the expression of liver low density lipoprotein receptor (LDL-R), scavenger receptor BI (SR-BI) as well as the expression of macrophage SR-BI and ATP binding cassette transporter A1(ABCA1). We also found that the COS treatment did not affect the plasma lipid level in LDL-R deficient mice and cholesterol absorption in wild type mice. Conclusions: COS treatment attenuated AS and decreased plasma non-HDL level in apoE-/-, and the potential mechanism might be involved with enhanced expression of hepatic LDL-R and SR-BI, and macrophage ABCA1.</abstract><cop>Japan</cop><pub>Japan Atherosclerosis Society</pub><pmid>25843117</pmid><doi>10.5551/jat.22939</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Aorta - pathology
Apolipoproteins E - genetics
Atherosclerosis
Atherosclerosis - metabolism
Atherosclerosis - therapy
ATP Binding Cassette Transporter 1 - metabolism
ATP binding cassette transporter A1
ATP Binding Cassette Transporter, Sub-Family G, Member 5
ATP-Binding Cassette Transporters - metabolism
Biological Transport
Cell Line
Chitosan - chemistry
Chitosan - therapeutic use
Chitosan oligosaccharides
Cholesterol - blood
Cholesterol - genetics
Cholesterol, HDL - blood
Cholesterol, HDL - genetics
Disease Models, Animal
Hep G2 Cells
Humans
Lipids - blood
Lipoproteins - metabolism
Low density lipoprotein receptor
Macrophages - metabolism
Male
Matrix Metalloproteinase 9 - metabolism
Mice
Mice, Knockout
Oligosaccharides - chemistry
Oligosaccharides - therapeutic use
Receptors, LDL - metabolism
Scavenger receptor BI
Scavenger Receptors, Class B - metabolism
Triglycerides - blood
title Chitosan Oligosaccharides Attenuate Atherosclerosis and Decrease Non-HDL in ApoE-/- Mice
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