Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1976-8-2
pubmed:abstractText
Cobalt ions (Co2+) are potent inducers of haem oxygenase in liver and inhibit microsomal drug oxidation probably by depleting microsomal haem and cytochrome P-450. Complexing of Co2+ ions with cysteine or glutathione (GSH) blocked ability of the former to induce haem oxygenase. When hepatic GSH content was depleted by treatment of animals with diethyl maleate, the inducing effect of Co2+ on haem oxygenase was significantly augmented. Other metal ions such as Cr2+, Mn2+, Fe2+, Fe3+, Ni2+, Cu2+, Zn2+, Cd2+, Hg2+ and Pb2+ were also capable of inducing haem oxygenase and depleting microsomal haem and cytochrome P-450. None of these metal ions had a stimulatory effect on hepatic haem oxidation activity in vitro. It is suggested that the inducing action of Co2+ and other metal ions on microsomal haem oxygenase involves either the covalent binding of the metal ions to some cellular component concerned directly with regulating haem oxygenase or non-specific complex-formation by the metal ions, which depletes some regulatory system in liver cells of an essential component involved in controlling synthesis or activity of the enzyme.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-1117008, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-1126948, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-13105648, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-13295297, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-13890578, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-14007123, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-14209972, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-14907713, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-4146295, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-4370250, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-4530983, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-4854467, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-4957991, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-5160422, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-5513938, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-5543939, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-5761169, http://linkedlifedata.com/resource/pubmed/commentcorrection/819007-805210
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/5-Aminolevulinate Synthetase, http://linkedlifedata.com/resource/pubmed/chemical/Bilirubin, http://linkedlifedata.com/resource/pubmed/chemical/Cations, Divalent, http://linkedlifedata.com/resource/pubmed/chemical/Cobalt, http://linkedlifedata.com/resource/pubmed/chemical/Cysteine, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System, http://linkedlifedata.com/resource/pubmed/chemical/Ethylmorphine-N-Demethylase, http://linkedlifedata.com/resource/pubmed/chemical/Glutathione, http://linkedlifedata.com/resource/pubmed/chemical/Heme, http://linkedlifedata.com/resource/pubmed/chemical/Maleates, http://linkedlifedata.com/resource/pubmed/chemical/Metals, http://linkedlifedata.com/resource/pubmed/chemical/NADPH-Ferrihemoprotein Reductase, http://linkedlifedata.com/resource/pubmed/chemical/Oxygenases, http://linkedlifedata.com/resource/pubmed/chemical/Vitamin E
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0264-6021
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
154
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
125-31
pubmed:dateRevised
2010-9-3
pubmed:meshHeading
pubmed-meshheading:819007-5-Aminolevulinate Synthetase, pubmed-meshheading:819007-Animals, pubmed-meshheading:819007-Bilirubin, pubmed-meshheading:819007-Cations, Divalent, pubmed-meshheading:819007-Cobalt, pubmed-meshheading:819007-Cysteine, pubmed-meshheading:819007-Cytochrome P-450 Enzyme System, pubmed-meshheading:819007-Enzyme Induction, pubmed-meshheading:819007-Ethylmorphine-N-Demethylase, pubmed-meshheading:819007-Glutathione, pubmed-meshheading:819007-Heme, pubmed-meshheading:819007-Liver, pubmed-meshheading:819007-Male, pubmed-meshheading:819007-Maleates, pubmed-meshheading:819007-Metals, pubmed-meshheading:819007-Microsomes, Liver, pubmed-meshheading:819007-NADPH-Ferrihemoprotein Reductase, pubmed-meshheading:819007-Oxygenases, pubmed-meshheading:819007-Rats, pubmed-meshheading:819007-Vitamin E
pubmed:year
1976
pubmed:articleTitle
Studies on the mechanism of induction of haem oxygenase by cobalt and other metal ions.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.