Changes in aortic stiffness related to elastic fiber network anomalies in the Brown Norway rat during maturation and aging
Adult Brown Norway (BN) rats exhibit numerous internal elastic lamina (IEL) ruptures in the abdominal aorta (AA) and a lower aortic elastin-to-collagen ratio (E/C) compared with other strains. We studied here AA mechanical properties in BN compared with control strains. AA stiffness (assessed by plo...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2010-07, Vol.299 (1), p.H144-H152 |
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description | Adult Brown Norway (BN) rats exhibit numerous internal elastic lamina (IEL) ruptures in the abdominal aorta (AA) and a lower aortic elastin-to-collagen ratio (E/C) compared with other strains. We studied here AA mechanical properties in BN compared with control strains. AA stiffness (assessed by plotting elastic modulus/wall-stress curves obtained under anesthesia), thoracic aorta elastin and collagen contents, and IEL ruptures in AA were measured in male BN and LOU rats aged 6, 10, and 15 wk. The Long Evans (LE) control strain was compared with BN at more advanced ages (15, 28, and 64 wk). At all ages, aortic E/C was lower in BN than in control strains. At 6 wk, AA stiffness was greater in BN than in LOU. In both strains, AA stiffness decreased between 6 and 10 wk, more so in BN than in LOU, and then increased, reaching similar values at 15 wk. BN AA stiffness was not different from that of LE at 15 and 28 wk, but was significantly lower at 64 wk. The increased stiffness in young BN rat AA may be due to the decreased E/C. IEL rupture onset in the BN around 7-8 wk, which decreases stiffness, as suggested by its pharmacological modulation, abolished such differences by 15 wk. Thereafter, age-related AA stiffness increased less in BN than in LE, likely due to the numerous IEL ruptures. We conclude that, in the BN rat, the lower E/C and the presence of IEL ruptures have opposing effects on arterial stiffness. |
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We studied here AA mechanical properties in BN compared with control strains. AA stiffness (assessed by plotting elastic modulus/wall-stress curves obtained under anesthesia), thoracic aorta elastin and collagen contents, and IEL ruptures in AA were measured in male BN and LOU rats aged 6, 10, and 15 wk. The Long Evans (LE) control strain was compared with BN at more advanced ages (15, 28, and 64 wk). At all ages, aortic E/C was lower in BN than in control strains. At 6 wk, AA stiffness was greater in BN than in LOU. In both strains, AA stiffness decreased between 6 and 10 wk, more so in BN than in LOU, and then increased, reaching similar values at 15 wk. BN AA stiffness was not different from that of LE at 15 and 28 wk, but was significantly lower at 64 wk. The increased stiffness in young BN rat AA may be due to the decreased E/C. IEL rupture onset in the BN around 7-8 wk, which decreases stiffness, as suggested by its pharmacological modulation, abolished such differences by 15 wk. Thereafter, age-related AA stiffness increased less in BN than in LE, likely due to the numerous IEL ruptures. We conclude that, in the BN rat, the lower E/C and the presence of IEL ruptures have opposing effects on arterial stiffness.</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00040.2010</identifier><identifier>PMID: 20435849</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Age Factors ; Aging ; Aging - pathology ; Animals ; Antihypertensive Agents - pharmacology ; Aorta, Thoracic - drug effects ; Aorta, Thoracic - pathology ; Aorta, Thoracic - physiopathology ; Aortic Rupture - pathology ; Aortic Rupture - physiopathology ; Aortic Rupture - prevention & control ; Biomechanical Phenomena ; Blood Pressure ; Collagen ; Coronary vessels ; Elastic Modulus ; Elastic Tissue - pathology ; Elastic Tissue - physiopathology ; Enalapril - pharmacology ; Male ; Maturation ; Mibefradil - pharmacology ; Physiology ; Pulsatile Flow ; Rats ; Rats, Inbred BN ; Rats, Long-Evans ; Rodents ; Species Specificity ; Stress, Mechanical</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2010-07, Vol.299 (1), p.H144-H152</ispartof><rights>Copyright American Physiological Society Jul 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-bd683eb4b5f479182ef13e1a0f22ccc77364810b3ff31482c291dc0f8124ff743</citedby><cites>FETCH-LOGICAL-c397t-bd683eb4b5f479182ef13e1a0f22ccc77364810b3ff31482c291dc0f8124ff743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20435849$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Osborne-Pellegrin, Mary</creatorcontrib><creatorcontrib>Labat, Carlos</creatorcontrib><creatorcontrib>Mercier, Nathalie</creatorcontrib><creatorcontrib>Challande, Pascal</creatorcontrib><creatorcontrib>Lacolley, Patrick</creatorcontrib><title>Changes in aortic stiffness related to elastic fiber network anomalies in the Brown Norway rat during maturation and aging</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>Adult Brown Norway (BN) rats exhibit numerous internal elastic lamina (IEL) ruptures in the abdominal aorta (AA) and a lower aortic elastin-to-collagen ratio (E/C) compared with other strains. We studied here AA mechanical properties in BN compared with control strains. AA stiffness (assessed by plotting elastic modulus/wall-stress curves obtained under anesthesia), thoracic aorta elastin and collagen contents, and IEL ruptures in AA were measured in male BN and LOU rats aged 6, 10, and 15 wk. The Long Evans (LE) control strain was compared with BN at more advanced ages (15, 28, and 64 wk). At all ages, aortic E/C was lower in BN than in control strains. At 6 wk, AA stiffness was greater in BN than in LOU. In both strains, AA stiffness decreased between 6 and 10 wk, more so in BN than in LOU, and then increased, reaching similar values at 15 wk. BN AA stiffness was not different from that of LE at 15 and 28 wk, but was significantly lower at 64 wk. The increased stiffness in young BN rat AA may be due to the decreased E/C. IEL rupture onset in the BN around 7-8 wk, which decreases stiffness, as suggested by its pharmacological modulation, abolished such differences by 15 wk. Thereafter, age-related AA stiffness increased less in BN than in LE, likely due to the numerous IEL ruptures. We conclude that, in the BN rat, the lower E/C and the presence of IEL ruptures have opposing effects on arterial stiffness.</description><subject>Age Factors</subject><subject>Aging</subject><subject>Aging - pathology</subject><subject>Animals</subject><subject>Antihypertensive Agents - pharmacology</subject><subject>Aorta, Thoracic - drug effects</subject><subject>Aorta, Thoracic - pathology</subject><subject>Aorta, Thoracic - physiopathology</subject><subject>Aortic Rupture - pathology</subject><subject>Aortic Rupture - physiopathology</subject><subject>Aortic Rupture - prevention & control</subject><subject>Biomechanical Phenomena</subject><subject>Blood Pressure</subject><subject>Collagen</subject><subject>Coronary vessels</subject><subject>Elastic Modulus</subject><subject>Elastic Tissue - pathology</subject><subject>Elastic Tissue - physiopathology</subject><subject>Enalapril - pharmacology</subject><subject>Male</subject><subject>Maturation</subject><subject>Mibefradil - pharmacology</subject><subject>Physiology</subject><subject>Pulsatile Flow</subject><subject>Rats</subject><subject>Rats, Inbred BN</subject><subject>Rats, Long-Evans</subject><subject>Rodents</subject><subject>Species Specificity</subject><subject>Stress, Mechanical</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1vGyEQhlHUKnHS_oJKEeqlp3WBgf04JlaTVorSS3JGLAs27i44wMpKfn1xnPTQEzDzvDNID0JfKFlSKth3td1tjIp5SQjhZMkIJSdoUTqsogK6D2hBoIaqpiDO0HlK28KJpoZTdMYIB9HyboFeVhvl1yZh57EKMTuNU3bWepMSjmZU2Qw4B1xu6dC0rjcRe5P3If7ByodJje4YzxuDr2PYe3wf4l4946gyHubo_BpPKs_l6ULZ4ges1qX4CX20akzm89t5gR5vfjysflZ3v29_ra7uKg1dk6t-qFswPe-F5U1HW2YsBUMVsYxprZsGat5S0oO1QHnLNOvooIltKePWNhwu0Lfj3F0MT7NJWU4uaTOOypswJ9kAgGCtEIX8-h-5DXP05XNSMCo6WkNbIDhCOoaUorFyF92k4rOkRB7EyHcx8lWMPIgpqcu30XM_meFf5t0E_AUjLoxu</recordid><startdate>201007</startdate><enddate>201007</enddate><creator>Osborne-Pellegrin, Mary</creator><creator>Labat, Carlos</creator><creator>Mercier, Nathalie</creator><creator>Challande, Pascal</creator><creator>Lacolley, Patrick</creator><general>American Physiological 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><scope>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201007</creationdate><title>Changes in aortic stiffness related to elastic fiber network anomalies in the Brown Norway rat during maturation and aging</title><author>Osborne-Pellegrin, Mary ; Labat, Carlos ; Mercier, Nathalie ; Challande, Pascal ; Lacolley, Patrick</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-bd683eb4b5f479182ef13e1a0f22ccc77364810b3ff31482c291dc0f8124ff743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Age Factors</topic><topic>Aging</topic><topic>Aging - pathology</topic><topic>Animals</topic><topic>Antihypertensive Agents - pharmacology</topic><topic>Aorta, Thoracic - drug effects</topic><topic>Aorta, Thoracic - pathology</topic><topic>Aorta, Thoracic - physiopathology</topic><topic>Aortic Rupture - pathology</topic><topic>Aortic Rupture - physiopathology</topic><topic>Aortic Rupture - prevention & control</topic><topic>Biomechanical Phenomena</topic><topic>Blood Pressure</topic><topic>Collagen</topic><topic>Coronary vessels</topic><topic>Elastic Modulus</topic><topic>Elastic Tissue - pathology</topic><topic>Elastic Tissue - physiopathology</topic><topic>Enalapril - pharmacology</topic><topic>Male</topic><topic>Maturation</topic><topic>Mibefradil - pharmacology</topic><topic>Physiology</topic><topic>Pulsatile Flow</topic><topic>Rats</topic><topic>Rats, Inbred BN</topic><topic>Rats, Long-Evans</topic><topic>Rodents</topic><topic>Species Specificity</topic><topic>Stress, Mechanical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Osborne-Pellegrin, Mary</creatorcontrib><creatorcontrib>Labat, Carlos</creatorcontrib><creatorcontrib>Mercier, Nathalie</creatorcontrib><creatorcontrib>Challande, Pascal</creatorcontrib><creatorcontrib>Lacolley, Patrick</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Osborne-Pellegrin, Mary</au><au>Labat, Carlos</au><au>Mercier, Nathalie</au><au>Challande, Pascal</au><au>Lacolley, Patrick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in aortic stiffness related to elastic fiber network anomalies in the Brown Norway rat during maturation and aging</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2010-07</date><risdate>2010</risdate><volume>299</volume><issue>1</issue><spage>H144</spage><epage>H152</epage><pages>H144-H152</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>Adult Brown Norway (BN) rats exhibit numerous internal elastic lamina (IEL) ruptures in the abdominal aorta (AA) and a lower aortic elastin-to-collagen ratio (E/C) compared with other strains. We studied here AA mechanical properties in BN compared with control strains. AA stiffness (assessed by plotting elastic modulus/wall-stress curves obtained under anesthesia), thoracic aorta elastin and collagen contents, and IEL ruptures in AA were measured in male BN and LOU rats aged 6, 10, and 15 wk. The Long Evans (LE) control strain was compared with BN at more advanced ages (15, 28, and 64 wk). At all ages, aortic E/C was lower in BN than in control strains. At 6 wk, AA stiffness was greater in BN than in LOU. In both strains, AA stiffness decreased between 6 and 10 wk, more so in BN than in LOU, and then increased, reaching similar values at 15 wk. BN AA stiffness was not different from that of LE at 15 and 28 wk, but was significantly lower at 64 wk. The increased stiffness in young BN rat AA may be due to the decreased E/C. IEL rupture onset in the BN around 7-8 wk, which decreases stiffness, as suggested by its pharmacological modulation, abolished such differences by 15 wk. Thereafter, age-related AA stiffness increased less in BN than in LE, likely due to the numerous IEL ruptures. We conclude that, in the BN rat, the lower E/C and the presence of IEL ruptures have opposing effects on arterial stiffness.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>20435849</pmid><doi>10.1152/ajpheart.00040.2010</doi></addata></record> |
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subjects | Age Factors Aging Aging - pathology Animals Antihypertensive Agents - pharmacology Aorta, Thoracic - drug effects Aorta, Thoracic - pathology Aorta, Thoracic - physiopathology Aortic Rupture - pathology Aortic Rupture - physiopathology Aortic Rupture - prevention & control Biomechanical Phenomena Blood Pressure Collagen Coronary vessels Elastic Modulus Elastic Tissue - pathology Elastic Tissue - physiopathology Enalapril - pharmacology Male Maturation Mibefradil - pharmacology Physiology Pulsatile Flow Rats Rats, Inbred BN Rats, Long-Evans Rodents Species Specificity Stress, Mechanical |
title | Changes in aortic stiffness related to elastic fiber network anomalies in the Brown Norway rat during maturation and aging |
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