Periadventitial Adipose Tissue Plays a Critical Role in Vascular Remodeling

RATIONALE:Obesity is associated with a high incidence of cardiovascular complications. However, the molecular link between obesity and vascular disease is not fully understood. Most previous studies have focused on the association between cardiovascular disease and accumulation of visceral fat. Peri...

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Veröffentlicht in:Circulation research 2009-10, Vol.105 (9), p.906-911
Hauptverfasser: Takaoka, Minoru, Nagata, Daisuke, Kihara, Shinji, Shimomura, Iichiro, Kimura, Yu, Tabata, Yasuhiko, Saito, Yoshihiko, Nagai, Ryozo, Sata, Masataka
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container_end_page 911
container_issue 9
container_start_page 906
container_title Circulation research
container_volume 105
creator Takaoka, Minoru
Nagata, Daisuke
Kihara, Shinji
Shimomura, Iichiro
Kimura, Yu
Tabata, Yasuhiko
Saito, Yoshihiko
Nagai, Ryozo
Sata, Masataka
description RATIONALE:Obesity is associated with a high incidence of cardiovascular complications. However, the molecular link between obesity and vascular disease is not fully understood. Most previous studies have focused on the association between cardiovascular disease and accumulation of visceral fat. Periadventitial fat is distributed ubiquitously around arteries throughout the body. OBJECTIVE:Here, we investigated the impact of obesity on inflammation in the periadventitial adipose tissue and on lesion formation after vascular injury. METHODS AND RESULTS:High-fat, high-sucrose feeding induced inflammatory changes and decreased adiponectin expression in the periadventitial adipose tissue, which was associated with enhanced neointima formation after endovascular injury. Removal of periadventitial fat markedly enhanced neointima formation after injury, which was attenuated by transplantation of subcutaneous adipose tissue from mice fed on regular chow. Adiponectin-deficient mice showed markedly enhanced lesion formation, which was reversed by local delivery, but not systemic administration, of recombinant adiponectin to the periadventitial area. The conditioned medium from subcutaneous fat attenuated increased cell number of smooth muscle cells in response to platelet derived growth factor-BB. CONCLUSIONS:Our findings suggest that periadventitial fat may protect against neointimal formation after angioplasty under physiological conditions and that inflammatory changes in the periadventitial fat may have a direct role in the pathogenesis of vascular disease accelerated by obesity.
doi_str_mv 10.1161/CIRCRESAHA.109.199653
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However, the molecular link between obesity and vascular disease is not fully understood. Most previous studies have focused on the association between cardiovascular disease and accumulation of visceral fat. Periadventitial fat is distributed ubiquitously around arteries throughout the body. OBJECTIVE:Here, we investigated the impact of obesity on inflammation in the periadventitial adipose tissue and on lesion formation after vascular injury. METHODS AND RESULTS:High-fat, high-sucrose feeding induced inflammatory changes and decreased adiponectin expression in the periadventitial adipose tissue, which was associated with enhanced neointima formation after endovascular injury. Removal of periadventitial fat markedly enhanced neointima formation after injury, which was attenuated by transplantation of subcutaneous adipose tissue from mice fed on regular chow. Adiponectin-deficient mice showed markedly enhanced lesion formation, which was reversed by local delivery, but not systemic administration, of recombinant adiponectin to the periadventitial area. The conditioned medium from subcutaneous fat attenuated increased cell number of smooth muscle cells in response to platelet derived growth factor-BB. CONCLUSIONS:Our findings suggest that periadventitial fat may protect against neointimal formation after angioplasty under physiological conditions and that inflammatory changes in the periadventitial fat may have a direct role in the pathogenesis of vascular disease accelerated by obesity.</description><identifier>ISSN: 0009-7330</identifier><identifier>EISSN: 1524-4571</identifier><identifier>DOI: 10.1161/CIRCRESAHA.109.199653</identifier><identifier>PMID: 19762682</identifier><identifier>CODEN: CIRUAL</identifier><language>eng</language><publisher>Hagerstown, MD: American Heart Association, Inc</publisher><subject>Adiponectin - administration &amp; dosage ; Adiponectin - deficiency ; Adiponectin - genetics ; Adiponectin - metabolism ; Adipose Tissue - metabolism ; Adipose Tissue - pathology ; Adipose Tissue - transplantation ; AMP-Activated Protein Kinases - genetics ; AMP-Activated Protein Kinases - metabolism ; Animals ; Biological and medical sciences ; Cell Proliferation ; Cells, Cultured ; Connective Tissue - metabolism ; Connective Tissue - pathology ; Culture Media, Conditioned - metabolism ; Disease Models, Animal ; Femoral Artery - injuries ; Femoral Artery - metabolism ; Femoral Artery - pathology ; Fundamental and applied biological sciences. Psychology ; Green Fluorescent Proteins - genetics ; Hyperplasia ; Inflammation - etiology ; Inflammation - metabolism ; Inflammation - pathology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Muscle, Smooth, Vascular - metabolism ; Obesity - complications ; Obesity - metabolism ; Obesity - pathology ; Platelet-Derived Growth Factor - metabolism ; Proto-Oncogene Proteins c-sis ; Rats ; Recombinant Proteins - metabolism ; Tissue Culture Techniques ; Transduction, Genetic ; Tunica Intima - metabolism ; Tunica Intima - pathology ; Vascular Diseases - etiology ; Vascular Diseases - metabolism ; Vascular Diseases - pathology ; Vertebrates: cardiovascular system</subject><ispartof>Circulation research, 2009-10, Vol.105 (9), p.906-911</ispartof><rights>2009 American Heart Association, Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6280-7c1e070c0df0da0b5793204c61d7a535d7874730a2ebad8b33b759d403c981673</citedby><cites>FETCH-LOGICAL-c6280-7c1e070c0df0da0b5793204c61d7a535d7874730a2ebad8b33b759d403c981673</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3674,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22063257$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19762682$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takaoka, Minoru</creatorcontrib><creatorcontrib>Nagata, Daisuke</creatorcontrib><creatorcontrib>Kihara, Shinji</creatorcontrib><creatorcontrib>Shimomura, Iichiro</creatorcontrib><creatorcontrib>Kimura, Yu</creatorcontrib><creatorcontrib>Tabata, Yasuhiko</creatorcontrib><creatorcontrib>Saito, Yoshihiko</creatorcontrib><creatorcontrib>Nagai, Ryozo</creatorcontrib><creatorcontrib>Sata, Masataka</creatorcontrib><title>Periadventitial Adipose Tissue Plays a Critical Role in Vascular Remodeling</title><title>Circulation research</title><addtitle>Circ Res</addtitle><description>RATIONALE:Obesity is associated with a high incidence of cardiovascular complications. However, the molecular link between obesity and vascular disease is not fully understood. Most previous studies have focused on the association between cardiovascular disease and accumulation of visceral fat. Periadventitial fat is distributed ubiquitously around arteries throughout the body. OBJECTIVE:Here, we investigated the impact of obesity on inflammation in the periadventitial adipose tissue and on lesion formation after vascular injury. METHODS AND RESULTS:High-fat, high-sucrose feeding induced inflammatory changes and decreased adiponectin expression in the periadventitial adipose tissue, which was associated with enhanced neointima formation after endovascular injury. Removal of periadventitial fat markedly enhanced neointima formation after injury, which was attenuated by transplantation of subcutaneous adipose tissue from mice fed on regular chow. Adiponectin-deficient mice showed markedly enhanced lesion formation, which was reversed by local delivery, but not systemic administration, of recombinant adiponectin to the periadventitial area. The conditioned medium from subcutaneous fat attenuated increased cell number of smooth muscle cells in response to platelet derived growth factor-BB. 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Psychology</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Hyperplasia</topic><topic>Inflammation - etiology</topic><topic>Inflammation - metabolism</topic><topic>Inflammation - pathology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Mice, Transgenic</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Obesity - complications</topic><topic>Obesity - metabolism</topic><topic>Obesity - pathology</topic><topic>Platelet-Derived Growth Factor - metabolism</topic><topic>Proto-Oncogene Proteins c-sis</topic><topic>Rats</topic><topic>Recombinant Proteins - metabolism</topic><topic>Tissue Culture Techniques</topic><topic>Transduction, Genetic</topic><topic>Tunica Intima - metabolism</topic><topic>Tunica Intima - pathology</topic><topic>Vascular Diseases - etiology</topic><topic>Vascular Diseases - metabolism</topic><topic>Vascular Diseases - pathology</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takaoka, Minoru</creatorcontrib><creatorcontrib>Nagata, Daisuke</creatorcontrib><creatorcontrib>Kihara, Shinji</creatorcontrib><creatorcontrib>Shimomura, Iichiro</creatorcontrib><creatorcontrib>Kimura, Yu</creatorcontrib><creatorcontrib>Tabata, Yasuhiko</creatorcontrib><creatorcontrib>Saito, Yoshihiko</creatorcontrib><creatorcontrib>Nagai, Ryozo</creatorcontrib><creatorcontrib>Sata, Masataka</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takaoka, Minoru</au><au>Nagata, Daisuke</au><au>Kihara, Shinji</au><au>Shimomura, Iichiro</au><au>Kimura, Yu</au><au>Tabata, Yasuhiko</au><au>Saito, Yoshihiko</au><au>Nagai, Ryozo</au><au>Sata, Masataka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Periadventitial Adipose Tissue Plays a Critical Role in Vascular Remodeling</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>2009-10-23</date><risdate>2009</risdate><volume>105</volume><issue>9</issue><spage>906</spage><epage>911</epage><pages>906-911</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><coden>CIRUAL</coden><abstract>RATIONALE:Obesity is associated with a high incidence of cardiovascular complications. However, the molecular link between obesity and vascular disease is not fully understood. Most previous studies have focused on the association between cardiovascular disease and accumulation of visceral fat. Periadventitial fat is distributed ubiquitously around arteries throughout the body. OBJECTIVE:Here, we investigated the impact of obesity on inflammation in the periadventitial adipose tissue and on lesion formation after vascular injury. METHODS AND RESULTS:High-fat, high-sucrose feeding induced inflammatory changes and decreased adiponectin expression in the periadventitial adipose tissue, which was associated with enhanced neointima formation after endovascular injury. Removal of periadventitial fat markedly enhanced neointima formation after injury, which was attenuated by transplantation of subcutaneous adipose tissue from mice fed on regular chow. Adiponectin-deficient mice showed markedly enhanced lesion formation, which was reversed by local delivery, but not systemic administration, of recombinant adiponectin to the periadventitial area. The conditioned medium from subcutaneous fat attenuated increased cell number of smooth muscle cells in response to platelet derived growth factor-BB. CONCLUSIONS:Our findings suggest that periadventitial fat may protect against neointimal formation after angioplasty under physiological conditions and that inflammatory changes in the periadventitial fat may have a direct role in the pathogenesis of vascular disease accelerated by obesity.</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>19762682</pmid><doi>10.1161/CIRCRESAHA.109.199653</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adiponectin - administration & dosage
Adiponectin - deficiency
Adiponectin - genetics
Adiponectin - metabolism
Adipose Tissue - metabolism
Adipose Tissue - pathology
Adipose Tissue - transplantation
AMP-Activated Protein Kinases - genetics
AMP-Activated Protein Kinases - metabolism
Animals
Biological and medical sciences
Cell Proliferation
Cells, Cultured
Connective Tissue - metabolism
Connective Tissue - pathology
Culture Media, Conditioned - metabolism
Disease Models, Animal
Femoral Artery - injuries
Femoral Artery - metabolism
Femoral Artery - pathology
Fundamental and applied biological sciences. Psychology
Green Fluorescent Proteins - genetics
Hyperplasia
Inflammation - etiology
Inflammation - metabolism
Inflammation - pathology
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Muscle, Smooth, Vascular - metabolism
Obesity - complications
Obesity - metabolism
Obesity - pathology
Platelet-Derived Growth Factor - metabolism
Proto-Oncogene Proteins c-sis
Rats
Recombinant Proteins - metabolism
Tissue Culture Techniques
Transduction, Genetic
Tunica Intima - metabolism
Tunica Intima - pathology
Vascular Diseases - etiology
Vascular Diseases - metabolism
Vascular Diseases - pathology
Vertebrates: cardiovascular system
title Periadventitial Adipose Tissue Plays a Critical Role in Vascular Remodeling
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