Prevention of Mast Cell Degranulation by Disodium Cromoglycate Attenuates the Development of Hypoxic Pulmonary Hypertension in Rats Exposed to Chronic Hypoxia
Background: Chronic hypoxia induces lung vascular remodeling, which results in pulmonary hypertension. Vascular remodeling is associated with collagenolysis and activation of matrix metalloproteinases (MMPs). One of the possible sources of MMPs in hypoxic lung are mast cells. Objective: The role of...
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creator | Baňasová, Alena Maxová, Hana Hampl, Václav Vízek, Martin Povýšilová, Viera Novotná, Jana Vajnerová, Olga Hniličková, Olga Herget, Jan |
description | Background: Chronic hypoxia induces lung vascular remodeling, which results in pulmonary hypertension. Vascular remodeling is associated with collagenolysis and activation of matrix metalloproteinases (MMPs). One of the possible sources of MMPs in hypoxic lung are mast cells. Objective: The role of lung mast cell collagenolytic activity in hypoxic pulmonary hypertension was tested by the inhibitor of mast cell degranulation disodium cromoglycate (DSCG). Methods: Rats were treated with DSCG in an early or later phase of isobaric hypoxia. Control groups were exposed to hypoxia only or to normoxia. Lung hemodynamics, muscularization and collagen metabolism in the walls of peripheral pulmonary vessels in the lungs were measured. Results: DSCG applied at an early phase of exposure to hypoxia reduced the development of pulmonary hypertension, inhibited muscularization in peripheral pulmonary arteries and decreased the amount of collagen cleavage fragments in prealveolar vessels. Conclusions: Mast cell degranulation plays a role in the initiation of hypoxic pulmonary vascular remodeling. |
doi_str_mv | 10.1159/000121410 |
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Vascular remodeling is associated with collagenolysis and activation of matrix metalloproteinases (MMPs). One of the possible sources of MMPs in hypoxic lung are mast cells. Objective: The role of lung mast cell collagenolytic activity in hypoxic pulmonary hypertension was tested by the inhibitor of mast cell degranulation disodium cromoglycate (DSCG). Methods: Rats were treated with DSCG in an early or later phase of isobaric hypoxia. Control groups were exposed to hypoxia only or to normoxia. Lung hemodynamics, muscularization and collagen metabolism in the walls of peripheral pulmonary vessels in the lungs were measured. Results: DSCG applied at an early phase of exposure to hypoxia reduced the development of pulmonary hypertension, inhibited muscularization in peripheral pulmonary arteries and decreased the amount of collagen cleavage fragments in prealveolar vessels. Conclusions: Mast cell degranulation plays a role in the initiation of hypoxic pulmonary vascular remodeling.</description><identifier>ISSN: 0025-7931</identifier><identifier>EISSN: 1423-0356</identifier><identifier>DOI: 10.1159/000121410</identifier><identifier>PMID: 18349522</identifier><identifier>CODEN: RESPBD</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Animals ; Basic Science Investigations ; Biological and medical sciences ; Blood vessels ; Cell Degranulation - drug effects ; Cellular biology ; Collagen - metabolism ; Cromolyn Sodium - pharmacology ; Hypertension, Pulmonary - etiology ; Hypertension, Pulmonary - metabolism ; Hypertension, Pulmonary - physiopathology ; Hypertension, Pulmonary - prevention & control ; Hypoxia ; Hypoxia - complications ; Lungs ; Male ; Mast Cells - drug effects ; Mast Cells - physiology ; Medical sciences ; Pathology ; Pneumology ; Proteins ; Pulmonary Artery - metabolism ; Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases ; Rats ; Rats, Wistar ; Respiratory diseases</subject><ispartof>Respiration, 2008-01, Vol.76 (1), p.102-107</ispartof><rights>2008 S. Karger AG, Basel</rights><rights>2008 INIST-CNRS</rights><rights>2008 S. Karger AG, Basel.</rights><rights>Copyright (c) 2008 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c458t-7252ae1ab91f31434401de91547243377b1b3701c44f380bae143b8199b2168f3</citedby><cites>FETCH-LOGICAL-c458t-7252ae1ab91f31434401de91547243377b1b3701c44f380bae143b8199b2168f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20457522$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18349522$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baňasová, Alena</creatorcontrib><creatorcontrib>Maxová, Hana</creatorcontrib><creatorcontrib>Hampl, Václav</creatorcontrib><creatorcontrib>Vízek, Martin</creatorcontrib><creatorcontrib>Povýšilová, Viera</creatorcontrib><creatorcontrib>Novotná, Jana</creatorcontrib><creatorcontrib>Vajnerová, Olga</creatorcontrib><creatorcontrib>Hniličková, Olga</creatorcontrib><creatorcontrib>Herget, Jan</creatorcontrib><title>Prevention of Mast Cell Degranulation by Disodium Cromoglycate Attenuates the Development of Hypoxic Pulmonary Hypertension in Rats Exposed to Chronic Hypoxia</title><title>Respiration</title><addtitle>Respiration</addtitle><description>Background: Chronic hypoxia induces lung vascular remodeling, which results in pulmonary hypertension. Vascular remodeling is associated with collagenolysis and activation of matrix metalloproteinases (MMPs). One of the possible sources of MMPs in hypoxic lung are mast cells. Objective: The role of lung mast cell collagenolytic activity in hypoxic pulmonary hypertension was tested by the inhibitor of mast cell degranulation disodium cromoglycate (DSCG). Methods: Rats were treated with DSCG in an early or later phase of isobaric hypoxia. Control groups were exposed to hypoxia only or to normoxia. Lung hemodynamics, muscularization and collagen metabolism in the walls of peripheral pulmonary vessels in the lungs were measured. Results: DSCG applied at an early phase of exposure to hypoxia reduced the development of pulmonary hypertension, inhibited muscularization in peripheral pulmonary arteries and decreased the amount of collagen cleavage fragments in prealveolar vessels. Conclusions: Mast cell degranulation plays a role in the initiation of hypoxic pulmonary vascular remodeling.</description><subject>Animals</subject><subject>Basic Science Investigations</subject><subject>Biological and medical sciences</subject><subject>Blood vessels</subject><subject>Cell Degranulation - drug effects</subject><subject>Cellular biology</subject><subject>Collagen - metabolism</subject><subject>Cromolyn Sodium - pharmacology</subject><subject>Hypertension, Pulmonary - etiology</subject><subject>Hypertension, Pulmonary - metabolism</subject><subject>Hypertension, Pulmonary - physiopathology</subject><subject>Hypertension, Pulmonary - prevention & control</subject><subject>Hypoxia</subject><subject>Hypoxia - complications</subject><subject>Lungs</subject><subject>Male</subject><subject>Mast Cells - drug effects</subject><subject>Mast Cells - physiology</subject><subject>Medical sciences</subject><subject>Pathology</subject><subject>Pneumology</subject><subject>Proteins</subject><subject>Pulmonary Artery - metabolism</subject><subject>Pulmonary hypertension. 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Karger AG</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>3V.</scope><scope>7RQ</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>U9A</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20080101</creationdate><title>Prevention of Mast Cell Degranulation by Disodium Cromoglycate Attenuates the Development of Hypoxic Pulmonary Hypertension in Rats Exposed to Chronic Hypoxia</title><author>Baňasová, Alena ; Maxová, Hana ; Hampl, Václav ; Vízek, Martin ; Povýšilová, Viera ; Novotná, Jana ; Vajnerová, Olga ; Hniličková, Olga ; Herget, Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c458t-7252ae1ab91f31434401de91547243377b1b3701c44f380bae143b8199b2168f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Basic Science Investigations</topic><topic>Biological and medical sciences</topic><topic>Blood vessels</topic><topic>Cell Degranulation - drug effects</topic><topic>Cellular biology</topic><topic>Collagen - metabolism</topic><topic>Cromolyn Sodium - pharmacology</topic><topic>Hypertension, Pulmonary - etiology</topic><topic>Hypertension, Pulmonary - metabolism</topic><topic>Hypertension, Pulmonary - physiopathology</topic><topic>Hypertension, Pulmonary - prevention & control</topic><topic>Hypoxia</topic><topic>Hypoxia - complications</topic><topic>Lungs</topic><topic>Male</topic><topic>Mast Cells - drug effects</topic><topic>Mast Cells - physiology</topic><topic>Medical sciences</topic><topic>Pathology</topic><topic>Pneumology</topic><topic>Proteins</topic><topic>Pulmonary Artery - metabolism</topic><topic>Pulmonary hypertension. 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Pulmonary vascular diseases</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Respiratory diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baňasová, Alena</creatorcontrib><creatorcontrib>Maxová, Hana</creatorcontrib><creatorcontrib>Hampl, Václav</creatorcontrib><creatorcontrib>Vízek, Martin</creatorcontrib><creatorcontrib>Povýšilová, Viera</creatorcontrib><creatorcontrib>Novotná, Jana</creatorcontrib><creatorcontrib>Vajnerová, Olga</creatorcontrib><creatorcontrib>Hniličková, Olga</creatorcontrib><creatorcontrib>Herget, Jan</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>ProQuest Central (Corporate)</collection><collection>Career & Technical Education Database</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Respiration</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baňasová, Alena</au><au>Maxová, Hana</au><au>Hampl, Václav</au><au>Vízek, Martin</au><au>Povýšilová, Viera</au><au>Novotná, Jana</au><au>Vajnerová, Olga</au><au>Hniličková, Olga</au><au>Herget, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevention of Mast Cell Degranulation by Disodium Cromoglycate Attenuates the Development of Hypoxic Pulmonary Hypertension in Rats Exposed to Chronic Hypoxia</atitle><jtitle>Respiration</jtitle><addtitle>Respiration</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>76</volume><issue>1</issue><spage>102</spage><epage>107</epage><pages>102-107</pages><issn>0025-7931</issn><eissn>1423-0356</eissn><coden>RESPBD</coden><abstract>Background: Chronic hypoxia induces lung vascular remodeling, which results in pulmonary hypertension. Vascular remodeling is associated with collagenolysis and activation of matrix metalloproteinases (MMPs). One of the possible sources of MMPs in hypoxic lung are mast cells. Objective: The role of lung mast cell collagenolytic activity in hypoxic pulmonary hypertension was tested by the inhibitor of mast cell degranulation disodium cromoglycate (DSCG). Methods: Rats were treated with DSCG in an early or later phase of isobaric hypoxia. Control groups were exposed to hypoxia only or to normoxia. Lung hemodynamics, muscularization and collagen metabolism in the walls of peripheral pulmonary vessels in the lungs were measured. Results: DSCG applied at an early phase of exposure to hypoxia reduced the development of pulmonary hypertension, inhibited muscularization in peripheral pulmonary arteries and decreased the amount of collagen cleavage fragments in prealveolar vessels. Conclusions: Mast cell degranulation plays a role in the initiation of hypoxic pulmonary vascular remodeling.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>18349522</pmid><doi>10.1159/000121410</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Basic Science Investigations Biological and medical sciences Blood vessels Cell Degranulation - drug effects Cellular biology Collagen - metabolism Cromolyn Sodium - pharmacology Hypertension, Pulmonary - etiology Hypertension, Pulmonary - metabolism Hypertension, Pulmonary - physiopathology Hypertension, Pulmonary - prevention & control Hypoxia Hypoxia - complications Lungs Male Mast Cells - drug effects Mast Cells - physiology Medical sciences Pathology Pneumology Proteins Pulmonary Artery - metabolism Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases Rats Rats, Wistar Respiratory diseases |
title | Prevention of Mast Cell Degranulation by Disodium Cromoglycate Attenuates the Development of Hypoxic Pulmonary Hypertension in Rats Exposed to Chronic Hypoxia |
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