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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1993-6-1
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pubmed:abstractText |
Superoxide dismutase (SOD) has an important role in the protection against O2 toxicity. Conjugation of Cu,Zn-SOD to polyethylene glycol (PEG-SOD) prolongs its plasma half-life and facilitates its cellular uptake. However, prior studies have shown that intravenous injection of PEG-SOD does not protect animals against O2 toxicity. In this study, we demonstrated that tracheal insufflation of PEG-SOD resulted in a dose-dependent protection against O2 toxicity. Nine of 15 rats (60%) insufflated with 25,000 U PEG-SOD survived continuous 100% O2 exposure for more than 7 days compared with control rats (n = 45), all of which died within 3 days of O2 exposure (P < 0.025). In contrast, insufflation of 25,000 U SOD, 9.7 mg methoxy-PEG (equivalent to the amount of methoxy-PEG present in 25,000 U PEG-SOD), or a combination of SOD and methoxy-PEG had no protective effect. Furthermore, intravenous or intraperitoneal injection of PEG-SOD did not afford significant protection. Protection against O2 toxicity by PEG-SOD insufflation was associated with attenuated O2-induced pulmonary injury as evidenced by a reduced volume of pleural effusion. Insufflation of PEG-SOD markedly increased pulmonary SOD activity (to 300 and 370% of controls at 24 and 50 h, respectively) without affecting pulmonary catalase activity. We conclude that insufflation of PEG-SOD protects rats against O2 toxicity, possibly by enhancing pulmonary SOD activity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antioxidants,
http://linkedlifedata.com/resource/pubmed/chemical/Oxygen,
http://linkedlifedata.com/resource/pubmed/chemical/Polyethylene Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Superoxide Dismutase,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
8750-7587
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
74
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1425-31
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:8482686-Administration, Inhalation,
pubmed-meshheading:8482686-Animals,
pubmed-meshheading:8482686-Antioxidants,
pubmed-meshheading:8482686-Injections, Intraperitoneal,
pubmed-meshheading:8482686-Injections, Intravenous,
pubmed-meshheading:8482686-Lung Injury,
pubmed-meshheading:8482686-Male,
pubmed-meshheading:8482686-Oxygen,
pubmed-meshheading:8482686-Polyethylene Glycols,
pubmed-meshheading:8482686-Pulmonary Alveoli,
pubmed-meshheading:8482686-Rats,
pubmed-meshheading:8482686-Rats, Sprague-Dawley,
pubmed-meshheading:8482686-Superoxide Dismutase,
pubmed-meshheading:8482686-Therapeutic Irrigation,
pubmed-meshheading:8482686-Trachea,
pubmed-meshheading:8482686-Tumor Necrosis Factor-alpha
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pubmed:year |
1993
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pubmed:articleTitle |
Polyethylene glycol-conjugated superoxide dismutase protects rats against oxygen toxicity.
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pubmed:affiliation |
Research Service, Samuel S. Stratton Department of Veterans Affairs Medical Center, Albany, New York.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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