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 |
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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. |
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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 ; Luo, Tian ; Liu, Shuai ; Song, Guohua ; Han, Jiju ; Wang, Yun ; Yao, Shutong ; Feng, Lei ; Qin, Shucun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c598t-f4e3418974af87aa7f22a2834b37b3d63d0ff6ee8f68ac917f566995237045a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Aorta - pathology</topic><topic>Apolipoproteins E - genetics</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - metabolism</topic><topic>Atherosclerosis - therapy</topic><topic>ATP Binding Cassette Transporter 1 - metabolism</topic><topic>ATP binding cassette transporter A1</topic><topic>ATP Binding Cassette Transporter, Sub-Family G, Member 5</topic><topic>ATP-Binding Cassette Transporters - metabolism</topic><topic>Biological Transport</topic><topic>Cell Line</topic><topic>Chitosan - chemistry</topic><topic>Chitosan - therapeutic use</topic><topic>Chitosan oligosaccharides</topic><topic>Cholesterol - blood</topic><topic>Cholesterol - genetics</topic><topic>Cholesterol, HDL - blood</topic><topic>Cholesterol, HDL - genetics</topic><topic>Disease Models, Animal</topic><topic>Hep G2 Cells</topic><topic>Humans</topic><topic>Lipids - blood</topic><topic>Lipoproteins - metabolism</topic><topic>Low density lipoprotein receptor</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Oligosaccharides - chemistry</topic><topic>Oligosaccharides - therapeutic use</topic><topic>Receptors, LDL - metabolism</topic><topic>Scavenger receptor BI</topic><topic>Scavenger Receptors, Class B - metabolism</topic><topic>Triglycerides - blood</topic><toplevel>online_resources</toplevel><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><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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