Beneficial Effects of Long-Term Use of the Antioxidant Probucol in Heart Failure in the Rat

Background—Congestive heart failure (CHF) is a disease that is characterized by progressive left ventricular (LV) dysfunction and dilatation. Oxidative stress is thought to contribute to the progression of CHF, and antioxidants have been shown to have beneficial effects when started early after myocardial infarction (MI). In this study, we tested whether the powerful antioxidant probucol would attenuate progression of CHF once it was established after MI in the rat. Methods and Results—Ligation of a coronary artery was used to create an MI in rats (n=266). Survivors were then randomized 20 days after MI to either probucol 61 mg · kg−1 · d−1 or vehicle and followed up for a total of 100 days after MI. Studies of cardiac hemodynamics, LV remodeling, cardiac apoptosis and morphology, systemic neurohumoral activation, oxidative stress, and renal function were then evaluated. Probucol improved LV function (LV maximum rate of pressure rise from 3103 to 4250 mm Hg/s, P <0.05, and LV end-diastolic pressure decrease from 28 to 24 mm Hg, P <0.05), reduced pulmonary weights, prevented right ventricular systolic hypertension, and preserved renal function compared with vehicle. Probucol also prevented LV dilatation, prevented wall thinning (1.70 versus 1.42 mm, P <0.05), reduced cardiac fibrosis and cardiac apoptosis, attenuated increased myocardial cell cross-sectional area, and increased scar thickness. Conclusions—In chronic CHF, probucol exerts multiple beneficial morphological effects that result in better LV remodeling and function, reduced neurohumoral activation, and preserved renal function.

[1]  J. Rouleau,et al.  Improved post-myocardial infarction survival with probucol in rats: effects on left ventricular function, morphology, cardiac oxidative stress and cytokine expression. , 2002, Journal of the American College of Cardiology.

[2]  P. Singal,et al.  Adriamycin-Induced Early Changes in Myocardial Antioxidant Enzymes and Their Modulation by Probucol , 2000, Circulation.

[3]  Hiroyuki Tsutsui,et al.  Treatment With Dimethylthiourea Prevents Left Ventricular Remodeling and Failure After Experimental Myocardial Infarction in Mice: Role of Oxidative Stress , 2000, Circulation research.

[4]  R. Weiss,et al.  Antioxidants attenuate myocyte apoptosis in the remote non-infarcted myocardium following large myocardial infarction. , 2000, Cardiovascular research.

[5]  V. Palace,et al.  Mobilization of antioxidant vitamin pools and hemodynamic function after myocardial infarction. , 1999, Circulation.

[6]  J. Rouleau,et al.  Endothelin A receptor blockade causes adverse left ventricular remodeling but improves pulmonary artery pressure after infarction in the rat. , 1998, Circulation.

[7]  A. Matsumori,et al.  Cytokine gene expression after myocardial infarction in rat hearts: possible implication in left ventricular remodeling. , 1998, Circulation.

[8]  W. MacLellan,et al.  Death by design. Programmed cell death in cardiovascular biology and disease. , 1997, Circulation research.

[9]  L. J. Eldik,et al.  S100 beta induces apoptotic cell death in cultured astrocytes via a nitric oxide-dependent pathway. , 1996, Biochimica et biophysica acta.

[10]  Y. Hayakawa,et al.  Expression of bcl-2 protein, an inhibitor of apoptosis, and Bax, an accelerator of apoptosis, in ventricular myocytes of human hearts with myocardial infarction. , 1996, Circulation.

[11]  P. Singal,et al.  Role of oxidative stress in transition of hypertrophy to heart failure. , 1996, Journal of the American College of Cardiology.

[12]  M. Yazdanpanah,et al.  Determination of aldehydes and other lipid peroxidation products in biological samples by gas chromatography-mass spectrometry. , 1995, Analytical biochemistry.

[13]  P. Singal,et al.  Probucol protects against adriamycin cardiomyopathy without interfering with its antitumor effect. , 1995, Circulation.

[14]  R. Lefkowitz,et al.  Myocardial expression of a constitutively active alpha 1B-adrenergic receptor in transgenic mice induces cardiac hypertrophy. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[15]  J. Rouleau,et al.  Markedly different effects on ventricular remodeling result in a decrease in inducibility of ventricular arrhythmias. , 1994, Journal of the American College of Cardiology.

[16]  M. Pfeffer,et al.  Ventricular Remodeling After Myocardial Infarction: Experimental Observations and Clinical Implications , 1990, Circulation.