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Improvement of cardiac function with parecoxib, a cyclo-oxygenase-2 inhibitor, in a rat model of ischemic heart failure

Articolo
Data di Pubblicazione:
2007
Abstract:
OBJECTIVE: To assess changes in cardiac function in animals with ischemic congestive heart failure (CHF) treated with a selective cyclo-oxygenase-2 (COX-2) inhibitor. BACKGROUND: In patients with CHF, COX-2 expression was associated with features of worsening failure. However, evidence of beneficial or detrimental functional effects of COX-2 inhibition in ischemic CHF is lacking. METHODS: Thirty male Wistar rats underwent coronary ligation and were allowed to recover for 12 months. Five sham-operated animals were used as controls. After 12 months, six surviving animals underwent baseline echocardiogram to measure end-diastolic diameter (EDD), end-systolic diameters (ESD), fractional shortening (FS), and anterior and posterior diastolic and systolic wall thicknesses. The animals were thereafter treated by daily intraperitoneal parecoxib injections (0.75 mg/kg) for 7 days. On day 7, a repeat echocardiogram was performed. RESULTS: When compared to baseline, repeat echocardiography after 7 days of parecoxib treatment showed no changes in the EDD (9.4 ± 0.4 mm vs. 9.4 ± 0.3 mm, P = 0.9), a significant reduction of ESD (5.5 ± 0.8 mm vs. 6.4 ± 0.3 mm, P = 0.028), and a significant improvement in the FS (43 ± 3% vs. 32 ± 5%, P = 0.027). Improvement of FS was associated with a significant change in systolic thickness in the infarct zone (3.6 ± 0.4 mm vs. 3.0 ± 0.1 mm, P = 0.046), whereas no significant changes in systolic thickness in the remote area were observed. CONCLUSIONS: Administration of parecoxib in ischemic CHF provides functional improvement of the peri-infarct myocardium. This finding may prove useful in improving quality of life and, perhaps, survival in patients with ischemic heart disease. © 2007 Lippincott Williams & Wilkins, Inc.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Cyclo-oxygenase-2; Heart failure; Ischemic heart disease
Elenco autori:
Abbate, A.; Salloum, F. N.; Ockaili, R. A.; Fowler III, A. A.; Biondi-Zoccai, G. G. L.; Straino, S.; Lipinski, M. J.; Baldi, A.; Crea, F.; Biasucci, L. M.; Vetrovec, G. W.; Kukreja, R. C.
Autori di Ateneo:
BALDI ALFONSO
Link alla scheda completa:
https://iris.unilink.it/handle/20.500.14085/24392
Pubblicato in:
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY
Journal
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