Abstract
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Journal of Cardiovascular Pharmacology |
| Vol/bind | 47 |
| Udgave nummer | 2 |
| Sider (fra-til) | 236-42 |
| Antal sider | 6 |
| ISSN | 0160-2446 |
| DOI | |
| Status | Udgivet - 2006 |
Bibliografisk note
Keywords: Animals; Anti-Arrhythmia Agents; Body Weight; Chronic Disease; Gap Junctions; Heart Ventricles; Hemodynamics; Male; Myocardial Infarction; Oligopeptides; Organ Size; Rats; Rats, Inbred Lew; Time FactorsAdgang til dokumentet
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I: Journal of Cardiovascular Pharmacology, Bind 47, Nr. 2, 2006, s. 236-42.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
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TY - JOUR
T1 - Treatment with the gap junction modifier rotigaptide (ZP123) reduces infarct size in rats with chronic myocardial infarction.
AU - Haugan, Ketil
AU - Marcussen, Niels
AU - Kjølbye, Anne Louise
AU - Nielsen, Morten Schak
AU - Hennan, James K
AU - Petersen, Jørgen Søberg
N1 - Keywords: Animals; Anti-Arrhythmia Agents; Body Weight; Chronic Disease; Gap Junctions; Heart Ventricles; Hemodynamics; Male; Myocardial Infarction; Oligopeptides; Organ Size; Rats; Rats, Inbred Lew; Time Factors
PY - 2006
Y1 - 2006
N2 - Treatment with non-selective drugs (eg, long-chain alcohols, halothane) that reduce gap junction intercellular communication (GJIC) is associated with reduced infarct size after myocardial infarction (MI). Therefore, it has been suggested that gap junction intercellular communication stimulating compounds may increase infarct size. The antiarrhythmic peptide analogue rotigaptide (ZP123) increases cardiac gap junction intercellular communication and the purpose of the present study was to examine the effects of rotigaptide treatment on infarct size. Myocardial infarction was induced in male rats by ligation of the left anterior descending artery (LAD). Rats (n = 156) were treated with rotigaptide at three dose levels or vehicle from the onset of ischemia and for 3 weeks following LAD occlusion. Infarct size was determined using histomorphometry after 3 weeks treatment. Rotigaptide treatment producing steady state plasma levels of 0.8 +/- 0.1, 5.5 +/- 0.5, and 86 +/- 8 nmol/L had no effect on mortality, but reduced infarct size to 90 +/- 10% (P = 0.41), 67 +/- 7% (P = 0.005), and 82 +/- 7% (P = 0.13), respectively relative to vehicle-treated myocardial infarction rats (100 +/- 12%). In contrast to what was predicted, our data demonstrates that rotigaptide treatment was associated with a significant infarct size reduction. We conclude that whereas treatment with non-selective inhibitors of gap junction intercellular communication cause a reduction in infarct size, this information cannot be extrapolated to the effects of compounds that selectively increase gap junction intercellular communication.
AB - Treatment with non-selective drugs (eg, long-chain alcohols, halothane) that reduce gap junction intercellular communication (GJIC) is associated with reduced infarct size after myocardial infarction (MI). Therefore, it has been suggested that gap junction intercellular communication stimulating compounds may increase infarct size. The antiarrhythmic peptide analogue rotigaptide (ZP123) increases cardiac gap junction intercellular communication and the purpose of the present study was to examine the effects of rotigaptide treatment on infarct size. Myocardial infarction was induced in male rats by ligation of the left anterior descending artery (LAD). Rats (n = 156) were treated with rotigaptide at three dose levels or vehicle from the onset of ischemia and for 3 weeks following LAD occlusion. Infarct size was determined using histomorphometry after 3 weeks treatment. Rotigaptide treatment producing steady state plasma levels of 0.8 +/- 0.1, 5.5 +/- 0.5, and 86 +/- 8 nmol/L had no effect on mortality, but reduced infarct size to 90 +/- 10% (P = 0.41), 67 +/- 7% (P = 0.005), and 82 +/- 7% (P = 0.13), respectively relative to vehicle-treated myocardial infarction rats (100 +/- 12%). In contrast to what was predicted, our data demonstrates that rotigaptide treatment was associated with a significant infarct size reduction. We conclude that whereas treatment with non-selective inhibitors of gap junction intercellular communication cause a reduction in infarct size, this information cannot be extrapolated to the effects of compounds that selectively increase gap junction intercellular communication.
U2 - 10.1097/01.fjc.0000200990.31611.6e
DO - 10.1097/01.fjc.0000200990.31611.6e
M3 - Journal article
C2 - 16495761
SN - 0160-2446
VL - 47
SP - 236
EP - 242
JO - Journal of Cardiovascular Pharmacology
JF - Journal of Cardiovascular Pharmacology
IS - 2
ER -