Protective effect and mechanism of hydrogen treatment on lung epithelial barrier dysfunction in rats with sepsis
This study aimed to explore the protective effect of hydrogen and to investigate the underlying mechanism of its preliminary effect on the alveolar epithelial barrier function in septic rats. Forty-five male Sprague-Dawley rats were divided randomly into three groups (N = 15): control [saline inject...
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description | This study aimed to explore the protective effect of hydrogen and to investigate the underlying mechanism of its preliminary effect on the alveolar epithelial barrier function in septic rats. Forty-five male Sprague-Dawley rats were divided randomly into three groups (N = 15): control [saline injection (intraperitoneal, ip), air drawing; SA], acute lung injury group [lipopolysaccharide (LPS) injection (ip, 15 mg/kg), air drawing; LA], and acute lung injury combined with hydrogen drawing group [LPS injection (ip, 15 mg/kg), 2% hydrogen drawing; LH]. The rats were euthanized after 6 h of treatment, and the extravascular lung water (EVLW), pulmonary alveolar-arterial oxygen pressure (A-aDO2), and respiratory index (RI) of each group were measured. The aquaporin-1 (AQP-1) protein expression in the lung tissues was detected using immunohistochemistry and western blotting, and the correlation between the EVLW and AQP-1 was analyzed. The lung morphology was observed with light and electron microscopy. In the LA group, EVLW (0.87 ± 0.17), A-aDO2 (113.21 ± 13.92), RI (0.65 ± 0.26), and AQP-1 expression increased. Additionally, thickened alveolar walls, significant invasion of inflammatory cells around the vessels, capillary ectasia, hyperemia/hemorrhage in the alveolar space, significantly swollen mitochondria, and increased vacuolar degeneration were observed. A significant negative correlation between AQP-1 expression and EVLW was observed (R2 = 0.8806). Compared with the LA group, EVLW (0.71 ± 0.19), A-aDO2 (132.42 ± 17.39), RI (0.75 ± 0.24), and inflammatory reaction decreased and AQP-1 expression increased in the LH group. The damage to pulmonary epithelial cells improved after hydrogen treatment in rats with sepsis; hydrogen could protect the pulmonary epithelial barrier function by acting on AQP-1. |
doi_str_mv | 10.4238/gmr.15016050 |
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Forty-five male Sprague-Dawley rats were divided randomly into three groups (N = 15): control [saline injection (intraperitoneal, ip), air drawing; SA], acute lung injury group [lipopolysaccharide (LPS) injection (ip, 15 mg/kg), air drawing; LA], and acute lung injury combined with hydrogen drawing group [LPS injection (ip, 15 mg/kg), 2% hydrogen drawing; LH]. The rats were euthanized after 6 h of treatment, and the extravascular lung water (EVLW), pulmonary alveolar-arterial oxygen pressure (A-aDO2), and respiratory index (RI) of each group were measured. The aquaporin-1 (AQP-1) protein expression in the lung tissues was detected using immunohistochemistry and western blotting, and the correlation between the EVLW and AQP-1 was analyzed. The lung morphology was observed with light and electron microscopy. In the LA group, EVLW (0.87 ± 0.17), A-aDO2 (113.21 ± 13.92), RI (0.65 ± 0.26), and AQP-1 expression increased. Additionally, thickened alveolar walls, significant invasion of inflammatory cells around the vessels, capillary ectasia, hyperemia/hemorrhage in the alveolar space, significantly swollen mitochondria, and increased vacuolar degeneration were observed. A significant negative correlation between AQP-1 expression and EVLW was observed (R2 = 0.8806). Compared with the LA group, EVLW (0.71 ± 0.19), A-aDO2 (132.42 ± 17.39), RI (0.75 ± 0.24), and inflammatory reaction decreased and AQP-1 expression increased in the LH group. The damage to pulmonary epithelial cells improved after hydrogen treatment in rats with sepsis; hydrogen could protect the pulmonary epithelial barrier function by acting on AQP-1.</description><identifier>ISSN: 1676-5680</identifier><identifier>EISSN: 1676-5680</identifier><identifier>DOI: 10.4238/gmr.15016050</identifier><identifier>PMID: 26909920</identifier><language>eng</language><publisher>Brazil</publisher><subject>Acute Lung Injury - drug therapy ; Acute Lung Injury - etiology ; Acute Lung Injury - metabolism ; Acute Lung Injury - pathology ; Animals ; Aquaporin 1 - drug effects ; Aquaporin 1 - genetics ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Gene Expression Regulation ; Hydrogen - pharmacology ; Hydrogen - therapeutic use ; Male ; Protective Agents - pharmacology ; Pulmonary Alveoli - drug effects ; Pulmonary Alveoli - metabolism ; Pulmonary Alveoli - pathology ; Rats ; Rats, Sprague-Dawley ; Sepsis - complications</subject><ispartof>Genetics and molecular research, 2016-01, Vol.15 (1)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c324t-8bb8574d1364385bf77966179e4036a5a7f283eacab9e415fe4eccab92ed36423</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26909920$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, L-D</creatorcontrib><creatorcontrib>Wu, X-Y</creatorcontrib><creatorcontrib>Tao, B-D</creatorcontrib><creatorcontrib>Wang, N</creatorcontrib><creatorcontrib>Zhang, J</creatorcontrib><title>Protective effect and mechanism of hydrogen treatment on lung epithelial barrier dysfunction in rats with sepsis</title><title>Genetics and molecular research</title><addtitle>Genet Mol Res</addtitle><description>This study aimed to explore the protective effect of hydrogen and to investigate the underlying mechanism of its preliminary effect on the alveolar epithelial barrier function in septic rats. Forty-five male Sprague-Dawley rats were divided randomly into three groups (N = 15): control [saline injection (intraperitoneal, ip), air drawing; SA], acute lung injury group [lipopolysaccharide (LPS) injection (ip, 15 mg/kg), air drawing; LA], and acute lung injury combined with hydrogen drawing group [LPS injection (ip, 15 mg/kg), 2% hydrogen drawing; LH]. The rats were euthanized after 6 h of treatment, and the extravascular lung water (EVLW), pulmonary alveolar-arterial oxygen pressure (A-aDO2), and respiratory index (RI) of each group were measured. The aquaporin-1 (AQP-1) protein expression in the lung tissues was detected using immunohistochemistry and western blotting, and the correlation between the EVLW and AQP-1 was analyzed. The lung morphology was observed with light and electron microscopy. In the LA group, EVLW (0.87 ± 0.17), A-aDO2 (113.21 ± 13.92), RI (0.65 ± 0.26), and AQP-1 expression increased. Additionally, thickened alveolar walls, significant invasion of inflammatory cells around the vessels, capillary ectasia, hyperemia/hemorrhage in the alveolar space, significantly swollen mitochondria, and increased vacuolar degeneration were observed. A significant negative correlation between AQP-1 expression and EVLW was observed (R2 = 0.8806). Compared with the LA group, EVLW (0.71 ± 0.19), A-aDO2 (132.42 ± 17.39), RI (0.75 ± 0.24), and inflammatory reaction decreased and AQP-1 expression increased in the LH group. The damage to pulmonary epithelial cells improved after hydrogen treatment in rats with sepsis; hydrogen could protect the pulmonary epithelial barrier function by acting on AQP-1.</description><subject>Acute Lung Injury - drug therapy</subject><subject>Acute Lung Injury - etiology</subject><subject>Acute Lung Injury - metabolism</subject><subject>Acute Lung Injury - pathology</subject><subject>Animals</subject><subject>Aquaporin 1 - drug effects</subject><subject>Aquaporin 1 - genetics</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Gene Expression Regulation</subject><subject>Hydrogen - pharmacology</subject><subject>Hydrogen - therapeutic use</subject><subject>Male</subject><subject>Protective Agents - pharmacology</subject><subject>Pulmonary Alveoli - drug effects</subject><subject>Pulmonary Alveoli - metabolism</subject><subject>Pulmonary Alveoli - pathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sepsis - complications</subject><issn>1676-5680</issn><issn>1676-5680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTlPxDAQhS0EguXoqJFLChZ8xEdKtOKSVoIC6shJxrtGiRNsB7T_HiMWREc1b0bfvOI9hE4puSwY11erPlxSQagkguygGZVKzoXUZPePPkCHMb4SwkShyT46YLIkZcnIDI1PYUjQJPcOGKzNChvf4h6atfEu9niweL1pw7ACj1MAk3rwCQ8ed5NfYRhdWkPnTIdrE4KDgNtNtJPPjplxHgeTIv7IFI4wRheP0Z41XYST7TxCL7c3z4v7-fLx7mFxvZw3nBVprutaC1W0lMuCa1FbpUopqSqhIFwaYZRlmoNpTJ1PVFgooPlaGLT5hfEjdP7tO4bhbYKYqt7FBrrOeBimWFHNVMkEL8v_USW1EIoomdGLb7QJQ4wBbDUG15uwqSipvuqoch3VTx0ZP9s6T3UP7S_8kz__BOHah2w</recordid><startdate>20160126</startdate><enddate>20160126</enddate><creator>Liu, L-D</creator><creator>Wu, X-Y</creator><creator>Tao, B-D</creator><creator>Wang, N</creator><creator>Zhang, J</creator><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>7X8</scope><scope>7QL</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20160126</creationdate><title>Protective effect and mechanism of hydrogen treatment on lung epithelial barrier dysfunction in rats with sepsis</title><author>Liu, L-D ; Wu, X-Y ; Tao, B-D ; Wang, N ; Zhang, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c324t-8bb8574d1364385bf77966179e4036a5a7f283eacab9e415fe4eccab92ed36423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acute Lung Injury - drug therapy</topic><topic>Acute Lung Injury - etiology</topic><topic>Acute Lung Injury - metabolism</topic><topic>Acute Lung Injury - pathology</topic><topic>Animals</topic><topic>Aquaporin 1 - drug effects</topic><topic>Aquaporin 1 - genetics</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Gene Expression Regulation</topic><topic>Hydrogen - pharmacology</topic><topic>Hydrogen - therapeutic use</topic><topic>Male</topic><topic>Protective Agents - pharmacology</topic><topic>Pulmonary Alveoli - drug effects</topic><topic>Pulmonary Alveoli - metabolism</topic><topic>Pulmonary Alveoli - pathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sepsis - complications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, L-D</creatorcontrib><creatorcontrib>Wu, X-Y</creatorcontrib><creatorcontrib>Tao, B-D</creatorcontrib><creatorcontrib>Wang, N</creatorcontrib><creatorcontrib>Zhang, J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</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>Genetics Abstracts</collection><jtitle>Genetics and molecular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, L-D</au><au>Wu, X-Y</au><au>Tao, B-D</au><au>Wang, N</au><au>Zhang, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective effect and mechanism of hydrogen treatment on lung epithelial barrier dysfunction in rats with sepsis</atitle><jtitle>Genetics and molecular research</jtitle><addtitle>Genet Mol Res</addtitle><date>2016-01-26</date><risdate>2016</risdate><volume>15</volume><issue>1</issue><issn>1676-5680</issn><eissn>1676-5680</eissn><abstract>This study aimed to explore the protective effect of hydrogen and to investigate the underlying mechanism of its preliminary effect on the alveolar epithelial barrier function in septic rats. Forty-five male Sprague-Dawley rats were divided randomly into three groups (N = 15): control [saline injection (intraperitoneal, ip), air drawing; SA], acute lung injury group [lipopolysaccharide (LPS) injection (ip, 15 mg/kg), air drawing; LA], and acute lung injury combined with hydrogen drawing group [LPS injection (ip, 15 mg/kg), 2% hydrogen drawing; LH]. The rats were euthanized after 6 h of treatment, and the extravascular lung water (EVLW), pulmonary alveolar-arterial oxygen pressure (A-aDO2), and respiratory index (RI) of each group were measured. The aquaporin-1 (AQP-1) protein expression in the lung tissues was detected using immunohistochemistry and western blotting, and the correlation between the EVLW and AQP-1 was analyzed. The lung morphology was observed with light and electron microscopy. In the LA group, EVLW (0.87 ± 0.17), A-aDO2 (113.21 ± 13.92), RI (0.65 ± 0.26), and AQP-1 expression increased. Additionally, thickened alveolar walls, significant invasion of inflammatory cells around the vessels, capillary ectasia, hyperemia/hemorrhage in the alveolar space, significantly swollen mitochondria, and increased vacuolar degeneration were observed. A significant negative correlation between AQP-1 expression and EVLW was observed (R2 = 0.8806). Compared with the LA group, EVLW (0.71 ± 0.19), A-aDO2 (132.42 ± 17.39), RI (0.75 ± 0.24), and inflammatory reaction decreased and AQP-1 expression increased in the LH group. The damage to pulmonary epithelial cells improved after hydrogen treatment in rats with sepsis; hydrogen could protect the pulmonary epithelial barrier function by acting on AQP-1.</abstract><cop>Brazil</cop><pmid>26909920</pmid><doi>10.4238/gmr.15016050</doi></addata></record> |
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subjects | Acute Lung Injury - drug therapy Acute Lung Injury - etiology Acute Lung Injury - metabolism Acute Lung Injury - pathology Animals Aquaporin 1 - drug effects Aquaporin 1 - genetics Epithelial Cells - drug effects Epithelial Cells - metabolism Gene Expression Regulation Hydrogen - pharmacology Hydrogen - therapeutic use Male Protective Agents - pharmacology Pulmonary Alveoli - drug effects Pulmonary Alveoli - metabolism Pulmonary Alveoli - pathology Rats Rats, Sprague-Dawley Sepsis - complications |
title | Protective effect and mechanism of hydrogen treatment on lung epithelial barrier dysfunction in rats with sepsis |
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