Remodeling of lung interstitium but not resistance vessels in canine pacing-induced heart failure

Departments of 1  Physiology and 2  Pathology, University of South Alabama, Mobile, Alabama 36688; 3  Department of Physiology, University of Bergen, Bergen, Norway; and 4  Department of Medicine, University of California, San Diego, La Jolla, California 92103 We previously showed that pacing-induce...

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Veröffentlicht in:Journal of applied physiology (1985) 1999-11, Vol.87 (5), p.1823-1830
Hauptverfasser: Townsley, Mary I, Snell, Kenneth S, Ivey, Claire L, Culberson, Donald E, Liu, Da Chang, Reed, Rolf K, Mathieu-Costello, Odile
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container_end_page 1830
container_issue 5
container_start_page 1823
container_title Journal of applied physiology (1985)
container_volume 87
creator Townsley, Mary I
Snell, Kenneth S
Ivey, Claire L
Culberson, Donald E
Liu, Da Chang
Reed, Rolf K
Mathieu-Costello, Odile
description Departments of 1  Physiology and 2  Pathology, University of South Alabama, Mobile, Alabama 36688; 3  Department of Physiology, University of Bergen, Bergen, Norway; and 4  Department of Medicine, University of California, San Diego, La Jolla, California 92103 We previously showed that pacing-induced heart failure in dogs results in an enhancement of pulmonary vascular reactivity. In the present study we hypothesized that enhanced matrix deposition and structural remodeling of lung resistance microvessels would underlie these functional changes. Using biochemical measures, we found no difference in the normalized lung content of hyaluronan, uronic acid, and collagen between control dogs and dogs paced for 1 mo, although lung dry weight and noncollagen protein content increased significantly in the paced group ( P  
doi_str_mv 10.1152/jappl.1999.87.5.1823
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In the present study we hypothesized that enhanced matrix deposition and structural remodeling of lung resistance microvessels would underlie these functional changes. Using biochemical measures, we found no difference in the normalized lung content of hyaluronan, uronic acid, and collagen between control dogs and dogs paced for 1 mo, although lung dry weight and noncollagen protein content increased significantly in the paced group ( P  &lt; 0.05). From separate Formalin-fixed lung lobes, 5-µm frozen sections were prepared and stained with Masson's trichrome, and vascular structure was evaluated using standard morphometric techniques. When perivascular fluid cuffs were excluded from the measure of wall thickness, collagen and media volume fractions in any size range did not differ between paced and control groups. Similarly, in the paced group, medial thickness in &lt;400-µm arterial or venular microvessels did not vary significantly from that in the controls. In contrast, the relationship of interstitial fluid pressure to lung water was significantly shifted to the right in the paced group, such that normal tissue pressures were observed, despite the increased water content. We conclude that although 1 mo of pacing-induced heart failure results in altered interstitial function, the attendant pulmonary hypertension and/or hormonal responses are insufficient to induce medial hypertrophy or other remodeling of the extra-alveolar microvasculature. interstitial fluid pressure; interstitial matrix; morphometry; pulmonary venous hypertension</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/jappl.1999.87.5.1823</identifier><identifier>PMID: 10562627</identifier><identifier>CODEN: JAPHEV</identifier><language>eng</language><publisher>Bethesda, MD: Am Physiological Soc</publisher><subject>Anatomy &amp; physiology ; Animals ; Biological and medical sciences ; Blood Vessels - pathology ; Cardiac Pacing, Artificial ; Cardiology. 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In the present study we hypothesized that enhanced matrix deposition and structural remodeling of lung resistance microvessels would underlie these functional changes. Using biochemical measures, we found no difference in the normalized lung content of hyaluronan, uronic acid, and collagen between control dogs and dogs paced for 1 mo, although lung dry weight and noncollagen protein content increased significantly in the paced group ( P  &lt; 0.05). From separate Formalin-fixed lung lobes, 5-µm frozen sections were prepared and stained with Masson's trichrome, and vascular structure was evaluated using standard morphometric techniques. When perivascular fluid cuffs were excluded from the measure of wall thickness, collagen and media volume fractions in any size range did not differ between paced and control groups. Similarly, in the paced group, medial thickness in &lt;400-µm arterial or venular microvessels did not vary significantly from that in the controls. 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Vascular system</subject><subject>Collagen - metabolism</subject><subject>Dogs</subject><subject>Extracellular Space - metabolism</subject><subject>Extravascular Lung Water - metabolism</subject><subject>Glycosaminoglycans - metabolism</subject><subject>Heart</subject><subject>Heart failure</subject><subject>Heart Failure - pathology</subject><subject>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</subject><subject>In Vitro Techniques</subject><subject>Lung - pathology</subject><subject>Lungs</subject><subject>Medical sciences</subject><subject>Microcirculation - pathology</subject><subject>Microcirculation - physiopathology</subject><subject>Models, Biological</subject><subject>Pulmonary Alveoli - pathology</subject><subject>Pulmonary Alveoli - physiology</subject><subject>Pulmonary Circulation - physiology</subject><subject>Space life sciences</subject><subject>Vascular Resistance - physiology</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kF2L1DAUhoMo7rj6D0SCiHjTmqRJk1zK4qqwIMjchzQ9ncmQaWuSrs6_N3UGv8Crc5HnfU_Og9BzSmpKBXt7sPMcaqq1rpWsRU0Vax6gTXliFW0JfYg2SgpSSaHkFXqS0oEQyrmgj9EVJaJlLZMbZL_Aceoh-HGHpwGHpUw_Zogp--yXI-6WjMcp4wjJp2xHB_geUoKQCoedHf0IeLauFFR-7BcHPd6DjRkP1oclwlP0aLAhwbPLvEbb2_fbm4_V3ecPn27e3VWONzJXkpJey6ZVhDs16EF3jCuum56prmsYUbqXroNykuVSU9E423ZCiMFJ2TnXXKPX59o5Tl8XSNkcfXIQgh1hWpJpNVMtFbqAL_8BD9MSx_I1wxgrRNuqAvEz5OKUUoTBzNEfbTwZSsyq3_zUb1b9RkkjzKq_xF5cupfuCP0fobPvAry6ADY5G4ZYhPr0m2OUU7pib87Y3u_233wEM-9PyU9h2p3WzX-t5P9Hb5cQtvA9r5lfETP3Q_MDTMSwig</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>Townsley, Mary I</creator><creator>Snell, Kenneth S</creator><creator>Ivey, Claire L</creator><creator>Culberson, Donald E</creator><creator>Liu, Da Chang</creator><creator>Reed, Rolf K</creator><creator>Mathieu-Costello, Odile</creator><general>Am Physiological Soc</general><general>American Physiological Society</general><scope>IQODW</scope><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>7TK</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>19991101</creationdate><title>Remodeling of lung interstitium but not resistance vessels in canine pacing-induced heart failure</title><author>Townsley, Mary I ; Snell, Kenneth S ; Ivey, Claire L ; Culberson, Donald E ; Liu, Da Chang ; Reed, Rolf K ; Mathieu-Costello, Odile</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-710d9736804c8f9f9b248493d28bb32089d7cbe875a479153ca6b555fc77bcc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Anatomy &amp; physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Vessels - pathology</topic><topic>Cardiac Pacing, Artificial</topic><topic>Cardiology. 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In the present study we hypothesized that enhanced matrix deposition and structural remodeling of lung resistance microvessels would underlie these functional changes. Using biochemical measures, we found no difference in the normalized lung content of hyaluronan, uronic acid, and collagen between control dogs and dogs paced for 1 mo, although lung dry weight and noncollagen protein content increased significantly in the paced group ( P  &lt; 0.05). From separate Formalin-fixed lung lobes, 5-µm frozen sections were prepared and stained with Masson's trichrome, and vascular structure was evaluated using standard morphometric techniques. When perivascular fluid cuffs were excluded from the measure of wall thickness, collagen and media volume fractions in any size range did not differ between paced and control groups. Similarly, in the paced group, medial thickness in &lt;400-µm arterial or venular microvessels did not vary significantly from that in the controls. In contrast, the relationship of interstitial fluid pressure to lung water was significantly shifted to the right in the paced group, such that normal tissue pressures were observed, despite the increased water content. We conclude that although 1 mo of pacing-induced heart failure results in altered interstitial function, the attendant pulmonary hypertension and/or hormonal responses are insufficient to induce medial hypertrophy or other remodeling of the extra-alveolar microvasculature. interstitial fluid pressure; interstitial matrix; morphometry; pulmonary venous hypertension</abstract><cop>Bethesda, MD</cop><pub>Am Physiological Soc</pub><pmid>10562627</pmid><doi>10.1152/jappl.1999.87.5.1823</doi><tpages>8</tpages></addata></record>
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source MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Anatomy & physiology
Animals
Biological and medical sciences
Blood Vessels - pathology
Cardiac Pacing, Artificial
Cardiology. Vascular system
Collagen - metabolism
Dogs
Extracellular Space - metabolism
Extravascular Lung Water - metabolism
Glycosaminoglycans - metabolism
Heart
Heart failure
Heart Failure - pathology
Heart failure, cardiogenic pulmonary edema, cardiac enlargement
In Vitro Techniques
Lung - pathology
Lungs
Medical sciences
Microcirculation - pathology
Microcirculation - physiopathology
Models, Biological
Pulmonary Alveoli - pathology
Pulmonary Alveoli - physiology
Pulmonary Circulation - physiology
Space life sciences
Vascular Resistance - physiology
title Remodeling of lung interstitium but not resistance vessels in canine pacing-induced heart failure
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