Source:http://linkedlifedata.com/resource/pubmed/id/12665667
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-3-31
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pubmed:abstractText |
Previous in vivo studies in dogs suggest that the 9,10-monoepoxide of linoleic acid (9,10-cis-epoxyoctadecenoic acid [9,10-EOA]) has toxic cardiovascular effects that result in death at higher doses. More recent work with rabbit renal proximal tubule cells suggests that the 12,13-metabolites of linoleic acid are more toxic than the 9,10-isomers. Thus, in the current study, we tested the hypothesis that 12,13-EOA and 12,13-dihydroxyoctadecadienoic acid (12,13-DHOA) have direct adverse effects on the heart. Langendorff-perfused rat hearts were exposed to 30 microM linoleic acid, 30 microM 12,13-EOA, or 30 microM 12,13-DHOA for 60 min followed by a 30-min recovery period. As indicated by peak left intraventricular pressure and/or +dP/dt(max), all three of the agents elicited moderate increases in contractile function that peaked within 10 20 min. The effects of linoleic acid and 12,13-EOA returned to control values during the remainder of the 60-min exposure, whereas the positive inotropic response to 12,13-DHOA was maintained until washout. Sustained arrhythmias and negative inotropic actions were not observed with any of the three compounds. Subsequently, the monoepoxides were infused into conscious rats (35 mg/kg/h) while blood pressure, heart rate, and EKG were monitored for 24 h using biotelemetry techniques. The only effect observed was a slight decline in blood pressure. Thus, current data suggest that linoleic acid and its oxidative metabolites do not have direct cardiotoxic effects during acute exposure.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
1530-7905
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
219-30
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12665667-Animals,
pubmed-meshheading:12665667-Blood Pressure,
pubmed-meshheading:12665667-Heart,
pubmed-meshheading:12665667-Heart Rate,
pubmed-meshheading:12665667-Linoleic Acid,
pubmed-meshheading:12665667-Male,
pubmed-meshheading:12665667-Myocardial Contraction,
pubmed-meshheading:12665667-Oleic Acids,
pubmed-meshheading:12665667-Rats,
pubmed-meshheading:12665667-Rats, Sprague-Dawley
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pubmed:year |
2002
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pubmed:articleTitle |
Linoleic acid metabolites act to increase contractility in isolated rat heart.
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pubmed:affiliation |
Department of Pharmaceutical Sciences, University of Kansas for Medical Sciences, Little Rock, AR 72205-7199, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro
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