Inhaled Aerosolized Insulin: A “Topical” Anti-inflammatory Treatment for Acute Lung Injury and Respiratory Distress Syndrome?
Acute lung injury (ALI) and the more severe acute respiratory distress syndrome (ARDS) are forms of pulmonary edema that result from robust local and systemic inflammatory states, such as sepsis. The morbidity and mortality associated with ALI and ARDS are significant and the treatment of these cond...
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Veröffentlicht in: | Inflammation 2010-10, Vol.33 (5), p.315-319 |
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creator | Shapiro, Haim Kagan, Ilya Shalita-Chesner, Michal Singer, Joelle Singer, Pierre |
description | Acute lung injury (ALI) and the more severe acute respiratory distress syndrome (ARDS) are forms of pulmonary edema that result from robust local and systemic inflammatory states, such as sepsis. The morbidity and mortality associated with ALI and ARDS are significant and the treatment of these conditions presents a formidable challenge. Controlling hyperglycemia with insulin is a core component of patient management in the critically ill. Insulin treatment also exerts beneficial metabolic effects beyond glucose control, as well as non-metabolic effects, in insulin-resistant states. For instance, insulin inhibits NF-κB—dependent synthesis of pro-inflammatory factors and attenuates production of ROS. Indeed, intravenous administration of insulin ameliorates pulmonary injury and dysfunction in the LPS model of ALI. Most recently, an inhalable insulin formulation was shown to effectively reduce glucose concentrations with minimal impact on long-term pulmonary function. We propose that administering inhalable insulin to hyperglycemic ALI/ARDS patients could directly reduce alveolar inflammation while reducing circulating glucose levels. |
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The morbidity and mortality associated with ALI and ARDS are significant and the treatment of these conditions presents a formidable challenge. Controlling hyperglycemia with insulin is a core component of patient management in the critically ill. Insulin treatment also exerts beneficial metabolic effects beyond glucose control, as well as non-metabolic effects, in insulin-resistant states. For instance, insulin inhibits NF-κB—dependent synthesis of pro-inflammatory factors and attenuates production of ROS. Indeed, intravenous administration of insulin ameliorates pulmonary injury and dysfunction in the LPS model of ALI. Most recently, an inhalable insulin formulation was shown to effectively reduce glucose concentrations with minimal impact on long-term pulmonary function. We propose that administering inhalable insulin to hyperglycemic ALI/ARDS patients could directly reduce alveolar inflammation while reducing circulating glucose levels.</description><identifier>ISSN: 0360-3997</identifier><identifier>EISSN: 1573-2576</identifier><identifier>DOI: 10.1007/s10753-010-9187-2</identifier><identifier>PMID: 20186475</identifier><identifier>CODEN: INFLD4</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Acute Lung Injury - complications ; Acute Lung Injury - drug therapy ; Administration, Inhalation ; Aerosols ; Animals ; Anti-Inflammatory Agents - administration & dosage ; Biomedical and Life Sciences ; Biomedicine ; Blood Glucose - drug effects ; Humans ; Hyperglycemia - blood ; Hyperglycemia - complications ; Hyperglycemia - drug therapy ; Hypoglycemic Agents - administration & dosage ; Immunology ; Insulin - administration & dosage ; Internal Medicine ; Pathology ; Pharmacology/Toxicology ; Respiratory Distress Syndrome, Adult - complications ; Respiratory Distress Syndrome, Adult - drug therapy ; Rheumatology</subject><ispartof>Inflammation, 2010-10, Vol.33 (5), p.315-319</ispartof><rights>Springer Science+Business Media, LLC 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-d4f96824f543b1cfee63f4e333b6e393f178d36b0ae654ad97a54203452a07ee3</citedby><cites>FETCH-LOGICAL-c469t-d4f96824f543b1cfee63f4e333b6e393f178d36b0ae654ad97a54203452a07ee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10753-010-9187-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10753-010-9187-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20186475$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shapiro, Haim</creatorcontrib><creatorcontrib>Kagan, Ilya</creatorcontrib><creatorcontrib>Shalita-Chesner, Michal</creatorcontrib><creatorcontrib>Singer, Joelle</creatorcontrib><creatorcontrib>Singer, Pierre</creatorcontrib><title>Inhaled Aerosolized Insulin: A “Topical” Anti-inflammatory Treatment for Acute Lung Injury and Respiratory Distress Syndrome?</title><title>Inflammation</title><addtitle>Inflammation</addtitle><addtitle>Inflammation</addtitle><description>Acute lung injury (ALI) and the more severe acute respiratory distress syndrome (ARDS) are forms of pulmonary edema that result from robust local and systemic inflammatory states, such as sepsis. The morbidity and mortality associated with ALI and ARDS are significant and the treatment of these conditions presents a formidable challenge. Controlling hyperglycemia with insulin is a core component of patient management in the critically ill. Insulin treatment also exerts beneficial metabolic effects beyond glucose control, as well as non-metabolic effects, in insulin-resistant states. For instance, insulin inhibits NF-κB—dependent synthesis of pro-inflammatory factors and attenuates production of ROS. Indeed, intravenous administration of insulin ameliorates pulmonary injury and dysfunction in the LPS model of ALI. Most recently, an inhalable insulin formulation was shown to effectively reduce glucose concentrations with minimal impact on long-term pulmonary function. We propose that administering inhalable insulin to hyperglycemic ALI/ARDS patients could directly reduce alveolar inflammation while reducing circulating glucose levels.</description><subject>Acute Lung Injury - complications</subject><subject>Acute Lung Injury - drug therapy</subject><subject>Administration, Inhalation</subject><subject>Aerosols</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents - administration & dosage</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Blood Glucose - drug effects</subject><subject>Humans</subject><subject>Hyperglycemia - blood</subject><subject>Hyperglycemia - complications</subject><subject>Hyperglycemia - drug therapy</subject><subject>Hypoglycemic Agents - administration & dosage</subject><subject>Immunology</subject><subject>Insulin - administration & dosage</subject><subject>Internal Medicine</subject><subject>Pathology</subject><subject>Pharmacology/Toxicology</subject><subject>Respiratory Distress Syndrome, Adult - complications</subject><subject>Respiratory Distress Syndrome, Adult - drug therapy</subject><subject>Rheumatology</subject><issn>0360-3997</issn><issn>1573-2576</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc2KFDEQx4Mo7jj6AF4keNFLNN_peJFm_RoYEHQ8N5nuypqhOz0m3YfxtL6Hvtw-iVl6VRD0VIH61a-o_BF6yOgzRql5nhk1ShDKKLGsMoTfQiumjCBcGX0brajQlAhrzRm6l_OBUlrZStxFZ5yySkujVujbJn52PXS4hjTmsQ9fy3sT89yH-ALX-Ory-248htb1V5c_cB2nQEL0vRsGN43phHcJ3DRAnLAfE67beQK8neNFcRzm0nexwx8gH0Na-FchTwlyxh9PsUvjAC_vozve9Rke3NQ1-vTm9e78Hdm-f7s5r7ekldpOpJPe6opLr6TYs9YDaOElCCH2GoQVnpmqE3pPHWglXWeNU5JTIRV31ACINXqyeI9p_DJDnpoh5Bb63kUY59wYWVlhhKkK-fS_JJOMK1VZaQr6-C_0MM4pljuKTwtOTZGuEVugtnxxTuCbYwqDS6eG0eY6yGYJsilBNtdBNrzMPLoRz_sBut8Tv5IrAF-AXFrxAtKfzf-2_gR8wKrM</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Shapiro, Haim</creator><creator>Kagan, Ilya</creator><creator>Shalita-Chesner, Michal</creator><creator>Singer, Joelle</creator><creator>Singer, Pierre</creator><general>Springer US</general><general>Springer Nature B.V</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>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20101001</creationdate><title>Inhaled Aerosolized Insulin: A “Topical” Anti-inflammatory Treatment for Acute Lung Injury and Respiratory Distress Syndrome?</title><author>Shapiro, Haim ; 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subjects | Acute Lung Injury - complications Acute Lung Injury - drug therapy Administration, Inhalation Aerosols Animals Anti-Inflammatory Agents - administration & dosage Biomedical and Life Sciences Biomedicine Blood Glucose - drug effects Humans Hyperglycemia - blood Hyperglycemia - complications Hyperglycemia - drug therapy Hypoglycemic Agents - administration & dosage Immunology Insulin - administration & dosage Internal Medicine Pathology Pharmacology/Toxicology Respiratory Distress Syndrome, Adult - complications Respiratory Distress Syndrome, Adult - drug therapy Rheumatology |
title | Inhaled Aerosolized Insulin: A “Topical” Anti-inflammatory Treatment for Acute Lung Injury and Respiratory Distress Syndrome? |
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