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

被引:15
|
作者
Abbate, Antonio
Salloum, Fadi N.
Ockaili, Ramzi A.
Fowler, Alpha A., II
Biondi-Zoccai, Giuseppe G. L.
Straino, Steania
Lipinski, Michael J.
Baldi, A. Fonso
Crea, Filippo
Biasucci, Luigi M.
Vetrovec, George W.
Kukreja, Rakesh C.
机构
[1] Virginia Commonwealth Univ, Pauley Heart Ctr, Richmond, VA 23233 USA
[2] Univ Turin, Dept Cardiol, Turin, Italy
[3] Ist Dermopat Immacolata, Dept Cardiovasc Sci, Rome, Italy
[4] Univ Naples 2, Dept Biochem & Biophys F Cedrangolo, Sect Pathol Anat, Naples, Italy
[5] Catholic Univ, Inst Cardiol, Rome, Italy
关键词
heart failure; cyclo-oxygenase-2; ischemic heart disease; NITRIC-OXIDE SYNTHASE; MYOCARDIAL-INFARCTION; EXPRESSION; APOPTOSIS;
D O I
10.1097/FJC.0b013e31804a5e50
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:416 / 418
页数:3
相关论文
共 50 条
  • [21] Selective cyclo-oxygenase-2 inhibition with parecoxib acutely impairs endothelium-dependent vasodilatation in patients with essential hypertension
    Bulut, D
    Liaghat, S
    Hanefeld, C
    Koll, R
    Miebach, T
    Mügge, A
    JOURNAL OF HYPERTENSION, 2003, 21 (09) : 1663 - 1667
  • [22] The selective cyclo-oxygenase-2 inhibitor rofecoxib reduces chronic cerebral hypoperfusion-induced apoptosis in the rat hippocampus
    Shim, DS
    Lee, KS
    Choi, YB
    JOURNAL OF NEUROLOGY, 2005, 252 : 97 - 97
  • [23] Upregulation of cyclo-oxygenase-2 in an animal model of familial amyotrophic lateral sclerosis
    Almer, G
    Vukosavic, S
    Romero, N
    Przedborski, S
    NEUROLOGY, 2000, 54 (07) : A304 - A304
  • [24] Effects of specific inhibition of cyclo-oxygenase-1 and cyclo-oxygenase-2 in the rat stomach with normal mucosa and after acid challenge
    Gretzer, B
    Maricic, N
    Respondek, M
    Schuligoi, R
    Peskar, BM
    BRITISH JOURNAL OF PHARMACOLOGY, 2001, 132 (07) : 1565 - 1573
  • [25] Induction of cyclo-oxygenase-2 by acute liver allograft rejection and cytomegalovirus infection in the rat
    Martelius, TJ
    Wolff, H
    Bruggeman, CA
    Höckerstedt, KA
    Lautenschlager, IT
    TRANSPLANT INTERNATIONAL, 2002, 15 (12) : 610 - 614
  • [26] Heme oxygenase-1 induction by nitric oxide in RAW 264.7 macrophages is upregulated by a cyclo-oxygenase-2 inhibitor
    Alcaraz, MJ
    Habib, A
    Créminon, C
    Vincente, AM
    Lebret, M
    Lévy-Toledano, S
    Maclouf, J
    BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2001, 1526 (01): : 13 - 16
  • [27] Use of the cyclo-oxygenase-2 (COX-2) inhibitor DFU in experimental glaucoma surgery.
    Lesk, MR
    Ponomarenko, S
    Beaudoln, N
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S81 - S81
  • [28] Function of cyclo-oxygenase-1 and cyclo-oxygenase-2 in the ductus arteriosus from foetal lamb: differential development and change by oxygen and endotoxin
    Coceani, F
    Ackerley, C
    Seidlitz, E
    Kelsey, L
    BRITISH JOURNAL OF PHARMACOLOGY, 2001, 132 (01) : 241 - 251
  • [29] Selective cyclo-oxygenase-2 inhibitors and their influence on the protective effect of a mild irritant in the rat stomach
    Gretzer, B
    Ehrlich, K
    Maricic, N
    Lambrecht, N
    Respondek, M
    Peskar, BM
    BRITISH JOURNAL OF PHARMACOLOGY, 1998, 123 (05) : 927 - 935
  • [30] Selective cyclo-oxygenase-2 inhibitors aggravate ischaemia-reperfusion injury in the rat stomach
    Maricic, N
    Ehrlich, K
    Gretzer, B
    Schuligoi, R
    Respondek, M
    Peskar, BM
    BRITISH JOURNAL OF PHARMACOLOGY, 1999, 128 (08) : 1659 - 1666