Betulinic acid attenuates lung injury by modulation of inflammatory cytokine response in experimentally-induced polymicrobial sepsis in mice
•Betulinic acid improves survival of mice in septic-lung injury model.•Betulinic acid exerts anti-inflammatory effect in CLP-induced pro-inflammatory lung damage in mice.•Betulinic acid can be a therapeutic modality in treatment of pro-inflammatory lung injury in septic patients. Sepsis commonly pro...
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creator | Lingaraju, Madhu Cholenahalli Pathak, Nitya Nand Begum, Jubeda Balaganur, Venkanna Bhat, Rafia Ahmad Ramachandra, Harish Darasaguppe Ayanur, Anjaneya Ram, Mahendra Singh, Vishakha Kumar, Dhirendra Kumar, Dinesh Tandan, Surendra Kumar |
description | •Betulinic acid improves survival of mice in septic-lung injury model.•Betulinic acid exerts anti-inflammatory effect in CLP-induced pro-inflammatory lung damage in mice.•Betulinic acid can be a therapeutic modality in treatment of pro-inflammatory lung injury in septic patients.
Sepsis commonly progresses to acute lung injury (ALI), an inflammatory lung disease with high morbidity and mortality. Septic ALI is characterized by excessive production of proinflammatory mediators. It remained refractory to present therapies and new therapies need to be developed to improve further clinical outcomes. Betulinic acid (BA), a pentacyclic lupane group triterpenoid has been shown to have anti-inflammatory activities in many studies. However, its therapeutic efficacy in polymicrobial septic ALI is yet unknown. Therefore, we investigated the effects of BA on septic ALI using cecal ligation and puncture (CLP) model in mice. Vehicle or BA (3, 10, and 30mg/kg) was administered intraperitoneally, 3 times (0, 24 and 48h) before CLP and CLP was done on 49thh of the study. Survival rate was observed till 120h post CLP. Lung tissues were collected for analysis by sacrificing mice 18h post CLP. BA at 10 and 30mg/kg dose significantly reduced sepsis-induced mortality and lung injury as implied by attenuated lung histopathological changes, decreased protein and neutrophils infiltration. BA also decreased lung NF-κB expression, cytokine, intercellular adhesion molecule-1, monocyte chemoattractant protein-1 and matrix metalloproteinase-9 levels. These evidences suggest that, the protective effects of BA on lungs are associated with defending action against inflammatory response and BA could be a potential modulatory agent of inflammation in sepsis-induced ALI. |
doi_str_mv | 10.1016/j.cyto.2014.09.004 |
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Sepsis commonly progresses to acute lung injury (ALI), an inflammatory lung disease with high morbidity and mortality. Septic ALI is characterized by excessive production of proinflammatory mediators. It remained refractory to present therapies and new therapies need to be developed to improve further clinical outcomes. Betulinic acid (BA), a pentacyclic lupane group triterpenoid has been shown to have anti-inflammatory activities in many studies. However, its therapeutic efficacy in polymicrobial septic ALI is yet unknown. Therefore, we investigated the effects of BA on septic ALI using cecal ligation and puncture (CLP) model in mice. Vehicle or BA (3, 10, and 30mg/kg) was administered intraperitoneally, 3 times (0, 24 and 48h) before CLP and CLP was done on 49thh of the study. Survival rate was observed till 120h post CLP. Lung tissues were collected for analysis by sacrificing mice 18h post CLP. BA at 10 and 30mg/kg dose significantly reduced sepsis-induced mortality and lung injury as implied by attenuated lung histopathological changes, decreased protein and neutrophils infiltration. BA also decreased lung NF-κB expression, cytokine, intercellular adhesion molecule-1, monocyte chemoattractant protein-1 and matrix metalloproteinase-9 levels. These evidences suggest that, the protective effects of BA on lungs are associated with defending action against inflammatory response and BA could be a potential modulatory agent of inflammation in sepsis-induced ALI.</description><identifier>ISSN: 1043-4666</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1016/j.cyto.2014.09.004</identifier><identifier>PMID: 25277468</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Acute Lung Injury - drug therapy ; Acute Lung Injury - therapy ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Cecal ligation and puncture ; Cecum ; Coinfection - drug therapy ; Coinfection - microbiology ; Cytokines ; Cytokines - genetics ; Cytokines - immunology ; Disease Models, Animal ; Inflammatory pulmonary insult ; Intercellular Adhesion Molecule-1 - genetics ; Intercellular Adhesion Molecule-1 - metabolism ; Lung - drug effects ; Lung - immunology ; Lung - pathology ; Lung - ultrastructure ; Matrix metalloproteinase (MMP)-9 ; Matrix Metalloproteinase 9 - genetics ; Matrix Metalloproteinase 9 - metabolism ; Mice ; NF-kappa B - genetics ; NF-kappa B - metabolism ; Sepsis - drug therapy ; Sepsis - microbiology ; Sepsis - therapy ; Triterpenes - administration & dosage ; Triterpenes - therapeutic use ; Triterpenoid</subject><ispartof>Cytokine (Philadelphia, Pa.), 2015-01, Vol.71 (1), p.101-108</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-c13179e1ba09ae136c6fd8d80ca98794020fe44dca2d5fe77cf6d7c64fcc48723</citedby><cites>FETCH-LOGICAL-c389t-c13179e1ba09ae136c6fd8d80ca98794020fe44dca2d5fe77cf6d7c64fcc48723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cyto.2014.09.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25277468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lingaraju, Madhu Cholenahalli</creatorcontrib><creatorcontrib>Pathak, Nitya Nand</creatorcontrib><creatorcontrib>Begum, Jubeda</creatorcontrib><creatorcontrib>Balaganur, Venkanna</creatorcontrib><creatorcontrib>Bhat, Rafia Ahmad</creatorcontrib><creatorcontrib>Ramachandra, Harish Darasaguppe</creatorcontrib><creatorcontrib>Ayanur, Anjaneya</creatorcontrib><creatorcontrib>Ram, Mahendra</creatorcontrib><creatorcontrib>Singh, Vishakha</creatorcontrib><creatorcontrib>Kumar, Dhirendra</creatorcontrib><creatorcontrib>Kumar, Dinesh</creatorcontrib><creatorcontrib>Tandan, Surendra Kumar</creatorcontrib><title>Betulinic acid attenuates lung injury by modulation of inflammatory cytokine response in experimentally-induced polymicrobial sepsis in mice</title><title>Cytokine (Philadelphia, Pa.)</title><addtitle>Cytokine</addtitle><description>•Betulinic acid improves survival of mice in septic-lung injury model.•Betulinic acid exerts anti-inflammatory effect in CLP-induced pro-inflammatory lung damage in mice.•Betulinic acid can be a therapeutic modality in treatment of pro-inflammatory lung injury in septic patients.
Sepsis commonly progresses to acute lung injury (ALI), an inflammatory lung disease with high morbidity and mortality. Septic ALI is characterized by excessive production of proinflammatory mediators. It remained refractory to present therapies and new therapies need to be developed to improve further clinical outcomes. Betulinic acid (BA), a pentacyclic lupane group triterpenoid has been shown to have anti-inflammatory activities in many studies. However, its therapeutic efficacy in polymicrobial septic ALI is yet unknown. Therefore, we investigated the effects of BA on septic ALI using cecal ligation and puncture (CLP) model in mice. Vehicle or BA (3, 10, and 30mg/kg) was administered intraperitoneally, 3 times (0, 24 and 48h) before CLP and CLP was done on 49thh of the study. Survival rate was observed till 120h post CLP. Lung tissues were collected for analysis by sacrificing mice 18h post CLP. BA at 10 and 30mg/kg dose significantly reduced sepsis-induced mortality and lung injury as implied by attenuated lung histopathological changes, decreased protein and neutrophils infiltration. BA also decreased lung NF-κB expression, cytokine, intercellular adhesion molecule-1, monocyte chemoattractant protein-1 and matrix metalloproteinase-9 levels. These evidences suggest that, the protective effects of BA on lungs are associated with defending action against inflammatory response and BA could be a potential modulatory agent of inflammation in sepsis-induced ALI.</description><subject>Acute Lung Injury - drug therapy</subject><subject>Acute Lung Injury - therapy</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Cecal ligation and puncture</subject><subject>Cecum</subject><subject>Coinfection - drug therapy</subject><subject>Coinfection - microbiology</subject><subject>Cytokines</subject><subject>Cytokines - genetics</subject><subject>Cytokines - immunology</subject><subject>Disease Models, Animal</subject><subject>Inflammatory pulmonary insult</subject><subject>Intercellular Adhesion Molecule-1 - genetics</subject><subject>Intercellular Adhesion Molecule-1 - metabolism</subject><subject>Lung - drug effects</subject><subject>Lung - immunology</subject><subject>Lung - pathology</subject><subject>Lung - ultrastructure</subject><subject>Matrix metalloproteinase (MMP)-9</subject><subject>Matrix Metalloproteinase 9 - genetics</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Mice</subject><subject>NF-kappa B - genetics</subject><subject>NF-kappa B - metabolism</subject><subject>Sepsis - drug therapy</subject><subject>Sepsis - microbiology</subject><subject>Sepsis - therapy</subject><subject>Triterpenes - administration & dosage</subject><subject>Triterpenes - therapeutic use</subject><subject>Triterpenoid</subject><issn>1043-4666</issn><issn>1096-0023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1v1TAQjBCIlpY_wAH5yCXBTvzsWOICVQtIlbjQs-Vnr5Efjh38gch_4Efj6BWOnHa1Ozvamem6VwQPBBP29jTorcRhxIQOWAwY0yfdJcGC9RiP09O9p1NPGWMX3YucTxhjMXH-vLsYDyPnlM2X3e8PUKp3wWmktDNIlQKhqgIZ-Rq-IRdONW3ouKElmupVcTGgaNvcerUsqsS23d_47gKgBHmNIUNbI_i1QnILhKK833oXTNVg0Br9tjid4tEpjzKs2eUd3mZw3T2zymd4-Vivuoe72683n_r7Lx8_37y_7_U0i9JrMhEugBwVFgrIxDSzZjYz1krMXFA8YguUGq1Gc7DAubbMcM2o1ZrOfJyuujdn3jXFHxVykYvLGrxXAWLNkjDKm4OHmTXoeIa2j3NOYOXaRKm0SYLlnoI8yV2-3FOQWMiWQjt6_chfjwuYfyd_bW-Ad2cANJU_HSSZtYPQ_HEJdJEmuv_x_wHqpJ3N</recordid><startdate>201501</startdate><enddate>201501</enddate><creator>Lingaraju, Madhu Cholenahalli</creator><creator>Pathak, Nitya Nand</creator><creator>Begum, Jubeda</creator><creator>Balaganur, Venkanna</creator><creator>Bhat, Rafia Ahmad</creator><creator>Ramachandra, Harish Darasaguppe</creator><creator>Ayanur, Anjaneya</creator><creator>Ram, Mahendra</creator><creator>Singh, Vishakha</creator><creator>Kumar, Dhirendra</creator><creator>Kumar, Dinesh</creator><creator>Tandan, Surendra Kumar</creator><general>Elsevier Ltd</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>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope></search><sort><creationdate>201501</creationdate><title>Betulinic acid attenuates lung injury by modulation of inflammatory cytokine response in experimentally-induced polymicrobial sepsis in mice</title><author>Lingaraju, Madhu Cholenahalli ; Pathak, Nitya Nand ; Begum, Jubeda ; Balaganur, Venkanna ; Bhat, Rafia Ahmad ; Ramachandra, Harish Darasaguppe ; Ayanur, Anjaneya ; Ram, Mahendra ; Singh, Vishakha ; Kumar, Dhirendra ; Kumar, Dinesh ; Tandan, Surendra Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-c13179e1ba09ae136c6fd8d80ca98794020fe44dca2d5fe77cf6d7c64fcc48723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acute Lung Injury - drug therapy</topic><topic>Acute Lung Injury - therapy</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Cecal ligation and puncture</topic><topic>Cecum</topic><topic>Coinfection - drug therapy</topic><topic>Coinfection - microbiology</topic><topic>Cytokines</topic><topic>Cytokines - genetics</topic><topic>Cytokines - immunology</topic><topic>Disease Models, Animal</topic><topic>Inflammatory pulmonary insult</topic><topic>Intercellular Adhesion Molecule-1 - genetics</topic><topic>Intercellular Adhesion Molecule-1 - metabolism</topic><topic>Lung - drug effects</topic><topic>Lung - immunology</topic><topic>Lung - pathology</topic><topic>Lung - ultrastructure</topic><topic>Matrix metalloproteinase (MMP)-9</topic><topic>Matrix Metalloproteinase 9 - genetics</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Mice</topic><topic>NF-kappa B - genetics</topic><topic>NF-kappa B - metabolism</topic><topic>Sepsis - drug therapy</topic><topic>Sepsis - microbiology</topic><topic>Sepsis - therapy</topic><topic>Triterpenes - administration & dosage</topic><topic>Triterpenes - therapeutic use</topic><topic>Triterpenoid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lingaraju, Madhu Cholenahalli</creatorcontrib><creatorcontrib>Pathak, Nitya Nand</creatorcontrib><creatorcontrib>Begum, Jubeda</creatorcontrib><creatorcontrib>Balaganur, Venkanna</creatorcontrib><creatorcontrib>Bhat, Rafia Ahmad</creatorcontrib><creatorcontrib>Ramachandra, Harish Darasaguppe</creatorcontrib><creatorcontrib>Ayanur, Anjaneya</creatorcontrib><creatorcontrib>Ram, Mahendra</creatorcontrib><creatorcontrib>Singh, Vishakha</creatorcontrib><creatorcontrib>Kumar, Dhirendra</creatorcontrib><creatorcontrib>Kumar, Dinesh</creatorcontrib><creatorcontrib>Tandan, Surendra Kumar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lingaraju, Madhu Cholenahalli</au><au>Pathak, Nitya Nand</au><au>Begum, Jubeda</au><au>Balaganur, Venkanna</au><au>Bhat, Rafia Ahmad</au><au>Ramachandra, Harish Darasaguppe</au><au>Ayanur, Anjaneya</au><au>Ram, Mahendra</au><au>Singh, Vishakha</au><au>Kumar, Dhirendra</au><au>Kumar, Dinesh</au><au>Tandan, Surendra Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Betulinic acid attenuates lung injury by modulation of inflammatory cytokine response in experimentally-induced polymicrobial sepsis in mice</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><addtitle>Cytokine</addtitle><date>2015-01</date><risdate>2015</risdate><volume>71</volume><issue>1</issue><spage>101</spage><epage>108</epage><pages>101-108</pages><issn>1043-4666</issn><eissn>1096-0023</eissn><abstract>•Betulinic acid improves survival of mice in septic-lung injury model.•Betulinic acid exerts anti-inflammatory effect in CLP-induced pro-inflammatory lung damage in mice.•Betulinic acid can be a therapeutic modality in treatment of pro-inflammatory lung injury in septic patients.
Sepsis commonly progresses to acute lung injury (ALI), an inflammatory lung disease with high morbidity and mortality. Septic ALI is characterized by excessive production of proinflammatory mediators. It remained refractory to present therapies and new therapies need to be developed to improve further clinical outcomes. Betulinic acid (BA), a pentacyclic lupane group triterpenoid has been shown to have anti-inflammatory activities in many studies. However, its therapeutic efficacy in polymicrobial septic ALI is yet unknown. Therefore, we investigated the effects of BA on septic ALI using cecal ligation and puncture (CLP) model in mice. Vehicle or BA (3, 10, and 30mg/kg) was administered intraperitoneally, 3 times (0, 24 and 48h) before CLP and CLP was done on 49thh of the study. Survival rate was observed till 120h post CLP. Lung tissues were collected for analysis by sacrificing mice 18h post CLP. BA at 10 and 30mg/kg dose significantly reduced sepsis-induced mortality and lung injury as implied by attenuated lung histopathological changes, decreased protein and neutrophils infiltration. BA also decreased lung NF-κB expression, cytokine, intercellular adhesion molecule-1, monocyte chemoattractant protein-1 and matrix metalloproteinase-9 levels. These evidences suggest that, the protective effects of BA on lungs are associated with defending action against inflammatory response and BA could be a potential modulatory agent of inflammation in sepsis-induced ALI.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25277468</pmid><doi>10.1016/j.cyto.2014.09.004</doi><tpages>8</tpages></addata></record> |
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subjects | Acute Lung Injury - drug therapy Acute Lung Injury - therapy Animals Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Cecal ligation and puncture Cecum Coinfection - drug therapy Coinfection - microbiology Cytokines Cytokines - genetics Cytokines - immunology Disease Models, Animal Inflammatory pulmonary insult Intercellular Adhesion Molecule-1 - genetics Intercellular Adhesion Molecule-1 - metabolism Lung - drug effects Lung - immunology Lung - pathology Lung - ultrastructure Matrix metalloproteinase (MMP)-9 Matrix Metalloproteinase 9 - genetics Matrix Metalloproteinase 9 - metabolism Mice NF-kappa B - genetics NF-kappa B - metabolism Sepsis - drug therapy Sepsis - microbiology Sepsis - therapy Triterpenes - administration & dosage Triterpenes - therapeutic use Triterpenoid |
title | Betulinic acid attenuates lung injury by modulation of inflammatory cytokine response in experimentally-induced polymicrobial sepsis in mice |
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