Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2000-11-1
pubmed:abstractText
Ventilator strategies allowing for increases in carbon dioxide (CO(2)) tensions (hypercapnia) are being emphasized to ameliorate the consequences of inflammatory-mediated lung injury. Inflammatory responses lead to the generation of reactive species including superoxide (O(2)(-)), nitric oxide (.NO), and their product peroxynitrite (ONOO(-)). The reaction of CO(2) and ONOO(-) can yield the nitrosoperoxocarbonate adduct ONOOCO(2)(-), a more potent nitrating species than ONOO(-). Based on these premises, monolayers of fetal rat alveolar epithelial cells were utilized to investigate whether hypercapnia would modify pathways of.NO production and reactivity that impact pulmonary metabolism and function. Stimulated cells exposed to 15% CO(2) (hypercapnia) revealed a significant increase in.NO production and nitric oxide synthase (NOS) activity. Cell 3-nitrotyrosine content as measured by both HPLC and immunofluorescence staining also increased when exposed to these same conditions. Hypercapnia significantly enhanced cell injury as evidenced by impairment of monolayer barrier function and increased induction of apoptosis. These results were attenuated by the NOS inhibitor N-monomethyl-L-arginine. Our studies reveal that hypercapnia modifies.NO-dependent pathways to amplify cell injury. These results affirm the underlying role of.NO in tissue inflammatory reactions and reveal the impact of hypercapnia on inflammatory reactions and its potential detrimental influences.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/3-nitrotyrosine, http://linkedlifedata.com/resource/pubmed/chemical/Carbon Dioxide, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides, http://linkedlifedata.com/resource/pubmed/chemical/Nitrates, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha, http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine, http://linkedlifedata.com/resource/pubmed/chemical/omega-N-Methylarginine, http://linkedlifedata.com/resource/pubmed/chemical/peroxynitric acid
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1040-0605
pubmed:author
pubmed:issnType
Print
pubmed:volume
279
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
L994-1002
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:11053037-Animals, pubmed-meshheading:11053037-Apoptosis, pubmed-meshheading:11053037-Carbon Dioxide, pubmed-meshheading:11053037-Cells, Cultured, pubmed-meshheading:11053037-Cytokines, pubmed-meshheading:11053037-Fetus, pubmed-meshheading:11053037-Hypercapnia, pubmed-meshheading:11053037-Interferon-gamma, pubmed-meshheading:11053037-Interleukin-1, pubmed-meshheading:11053037-Lipopolysaccharides, pubmed-meshheading:11053037-Nitrates, pubmed-meshheading:11053037-Nitric Oxide, pubmed-meshheading:11053037-Nitric Oxide Synthase, pubmed-meshheading:11053037-Pulmonary Alveoli, pubmed-meshheading:11053037-Rats, pubmed-meshheading:11053037-Respiratory Mucosa, pubmed-meshheading:11053037-Tumor Necrosis Factor-alpha, pubmed-meshheading:11053037-Tyrosine, pubmed-meshheading:11053037-omega-N-Methylarginine
pubmed:year
2000
pubmed:articleTitle
Hypercapnia induces injury to alveolar epithelial cells via a nitric oxide-dependent pathway.
pubmed:affiliation
Department of Anesthesiology, The University of Alabama at Birmingham, Birmingham, Alabama 35233-4234, USA. john.lang@ccc.uab.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't