Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2002-1-28
pubmed:abstractText
Carbon monoxide (CO) formation was studied in the process of lipid peroxidation in phenobarbital-induced rabbit liver microsomes. The reaction was NADPH-dependent and required Fe(2+), which occurs in microsomes as being protein bound and is not a consequence of heme destruction. Zn-protoporphyrin IX, an inhibitor of the heme oxygenase activity, proved to have no effect on CO production, suggesting that heme oxygenase is not involved into the CO generation reaction. At the same time, the addition of cytochrome P450 typical inhibitors SKF 525A and metyrapone to the reaction mixture had an inhibitory effect on the CO formation rate. Antioxidants such as alpha-tocopherol and desferal inhibited lipid peroxidation in phenobarbital-induced rabbit liver microsomes, and in this case the CO production was not registered. Thus, on the basis of the results presented here it is possible to assert that the process of NADPH, Fe(2+)-dependent carbon monoxide formation in microsomes is a result of lipid peroxidation with cytochrome P450 2B4 participation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aryl Hydrocarbon Hydroxylases, http://linkedlifedata.com/resource/pubmed/chemical/Carbon Monoxide, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System, http://linkedlifedata.com/resource/pubmed/chemical/Deferoxamine, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Heme Oxygenase (Decyclizing), http://linkedlifedata.com/resource/pubmed/chemical/Iron, http://linkedlifedata.com/resource/pubmed/chemical/Metyrapone, http://linkedlifedata.com/resource/pubmed/chemical/Phenobarbital, http://linkedlifedata.com/resource/pubmed/chemical/Proadifen, http://linkedlifedata.com/resource/pubmed/chemical/Protoporphyrins, http://linkedlifedata.com/resource/pubmed/chemical/Steroid Hydroxylases, http://linkedlifedata.com/resource/pubmed/chemical/alpha-Tocopherol, http://linkedlifedata.com/resource/pubmed/chemical/steroid 15-alpha-hydroxylase, http://linkedlifedata.com/resource/pubmed/chemical/zinc protoporphyrin
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0887-2333
pubmed:author
pubmed:issnType
Print
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1-10
pubmed:dateRevised
2009-4-10
pubmed:meshHeading
pubmed-meshheading:11812634-Animals, pubmed-meshheading:11812634-Aryl Hydrocarbon Hydroxylases, pubmed-meshheading:11812634-Carbon Monoxide, pubmed-meshheading:11812634-Cytochrome P-450 Enzyme System, pubmed-meshheading:11812634-Deferoxamine, pubmed-meshheading:11812634-Enzyme Induction, pubmed-meshheading:11812634-Enzyme Inhibitors, pubmed-meshheading:11812634-Heme Oxygenase (Decyclizing), pubmed-meshheading:11812634-Iron, pubmed-meshheading:11812634-Lipid Peroxidation, pubmed-meshheading:11812634-Metyrapone, pubmed-meshheading:11812634-Microsomes, Liver, pubmed-meshheading:11812634-Phenobarbital, pubmed-meshheading:11812634-Proadifen, pubmed-meshheading:11812634-Protoporphyrins, pubmed-meshheading:11812634-Rabbits, pubmed-meshheading:11812634-Steroid Hydroxylases, pubmed-meshheading:11812634-alpha-Tocopherol
pubmed:year
2002
pubmed:articleTitle
Production of carbon monoxide by cytochrome P450 during iron-dependent lipid peroxidation.
pubmed:affiliation
Institute of Biomedical Chemistry RAMS, 119832, Pogodinskaya Street, 10, Moscow, Russia.
pubmed:publicationType
Journal Article, In Vitro, Research Support, Non-U.S. Gov't