Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1992-8-21
pubmed:abstractText
Methyl-lidocaine is an amphiphilic agent which has been used as an experimental anti-arrhythmic drug. When hamster hearts were perfused with labelled glycerol, the presence of methyl-lidocaine in the perfusate was found to enhance the labelling in phosphatidylserine, phosphatidylinositol, diacylglycerol and triacylglycerol. However, the labelling of phosphatidylcholine and phosphatidylethanolamine was not significantly changed by methyl-lidocaine treatment. Assays in vitro for the enzymes involved in the synthesis of neutral lipids and acidic phospholipids revealed that phosphatidate phosphatase and CTP: phosphatidate cytidylyltransferase activities were stimulated by methyl-lidocaine. The intracellular pool sizes of diacylglycerol and CDP-diacylglycerol were also elevated. We postulate that the enhanced syntheses of the neutral lipids and acidic phospholipids in the methyl-lidocaine-perfused heart were mediated via the direct activation of the key enzymes in the biosynthesis of these lipids de novo.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-1107025, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-1200988, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-13641241, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-14907713, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-173283, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-192211, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-200224, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-213059, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-2158610, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-2222999, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-2550825, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-2663077, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-2822021, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-2822695, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-2890641, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-3029593, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-3032105, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-350877, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-3756197, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-3778529, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-4046045, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-4269073, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-4425092, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-507846, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-5456034, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-5485096, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-560868, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-5660480, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-6089897, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-6263339, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-6267921, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-6331400, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-658442, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-7002922, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-952985, http://linkedlifedata.com/resource/pubmed/commentcorrection/1322123-958324
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/2-acylglycerophosphate..., http://linkedlifedata.com/resource/pubmed/chemical/Acyl Coenzyme A, http://linkedlifedata.com/resource/pubmed/chemical/Acyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/Anti-Arrhythmia Agents, http://linkedlifedata.com/resource/pubmed/chemical/Chlorpromazine, http://linkedlifedata.com/resource/pubmed/chemical/Diacylglycerol O-Acyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/Diglycerides, http://linkedlifedata.com/resource/pubmed/chemical/Glycerol-3-Phosphate..., http://linkedlifedata.com/resource/pubmed/chemical/Lidocaine, http://linkedlifedata.com/resource/pubmed/chemical/N-methyllidocaine, http://linkedlifedata.com/resource/pubmed/chemical/Nucleotidyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidate Phosphatase, http://linkedlifedata.com/resource/pubmed/chemical/Phospholipids, http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides, http://linkedlifedata.com/resource/pubmed/chemical/phosphatidate cytidylyltransferase
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0264-6021
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
285 ( Pt 1)
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
161-6
pubmed:dateRevised
2010-9-7
pubmed:meshHeading
pubmed:year
1992
pubmed:articleTitle
The effect of methyl-lidocaine on the biosynthesis of phospholipids de novo in the isolated hamster heart.
pubmed:affiliation
Department of Biochemistry & Molecular Biology and Pharmacology, Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
pubmed:publicationType
Journal Article, In Vitro
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