Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2005-2-2
pubmed:abstractText
Hypothyroid heart displays a phenotype of cardioprotection against ischemia and this study investigated whether administration of dronedarone, an amiodarone-like compound that has been shown to preferentially antagonize thyroid hormone binding to thyroid hormone receptor alpha1 (TRalpha1), results in a similar effect. Dronedarone was given in Wistar rats (90 mg/kg, once daily (od) for 2 weeks) (DRON), while untreated animals served as controls (CONT). Hypothyroidism (HYPO) was induced by propylthiouracil administration. Isolated rat hearts were perfused in Langendorff mode and subjected to 20 minutes of zero-flow global ischemia (I) followed by 45 minutes of reperfusion (R). 3,5,3' Triiodothyronine remained unchanged while body weight and food intake were reduced. alpha-Myosin heavy chain (alpha-MHC) decreased in DRON while beta-myosin heavy chain (beta-MHC) and sarcoplasmic reticulum Ca2+ adenosine triphosphatase (ATPase) expression (SERCA) was similar to CONT. In HYPO, alpha-MHC and SERCA were decreased while beta-MHC was increased. Myocardial glycogen content was increased in both DRON and HYPO. In DRON, resting heart rate and contractility were reduced and ischemic contracture was significantly suppressed while postischemic left ventricular end-diastolic pressure and lactate dehydrogenase release (IU/L min) after I/R were significantly decreased. In conclusion, dronedarone treatment results in cardioprotection by selectively mimicking hypothyroidism. This is accompanied by a reduction in body weight because of the suppression of food intake. TRs might prove novel pharmacologic targets for the treatment of cardiovascular illnesses.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1050-7256
pubmed:author
pubmed:issnType
Print
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
16-23
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:15687816-Adaptation, Physiological, pubmed-meshheading:15687816-Amiodarone, pubmed-meshheading:15687816-Animals, pubmed-meshheading:15687816-Calcium-Transporting ATPases, pubmed-meshheading:15687816-Eating, pubmed-meshheading:15687816-Glycogen, pubmed-meshheading:15687816-Heart, pubmed-meshheading:15687816-Heart Rate, pubmed-meshheading:15687816-Hypothyroidism, pubmed-meshheading:15687816-Isomerism, pubmed-meshheading:15687816-L-Lactate Dehydrogenase, pubmed-meshheading:15687816-Male, pubmed-meshheading:15687816-Myocardial Contraction, pubmed-meshheading:15687816-Myocardial Ischemia, pubmed-meshheading:15687816-Myocardial Reperfusion Injury, pubmed-meshheading:15687816-Myocardium, pubmed-meshheading:15687816-Myosins, pubmed-meshheading:15687816-Rats, pubmed-meshheading:15687816-Rats, Wistar, pubmed-meshheading:15687816-Sarcoplasmic Reticulum, pubmed-meshheading:15687816-Thyroid Hormone Receptors alpha, pubmed-meshheading:15687816-Thyroid Hormones, pubmed-meshheading:15687816-Weight Gain
pubmed:year
2005
pubmed:articleTitle
Dronedarone administration prevents body weight gain and increases tolerance of the heart to ischemic stress: a possible involvement of thyroid hormone receptor alpha1.
pubmed:affiliation
Department of Pharmacology, University of Athens, Athens, Greece. cpantos@cc.uoa.gr
pubmed:publicationType
Journal Article, In Vitro