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on June 24, 2002

Circulation. 2002
Published online before print June 24, 2002, doi: 10.1161/01.CIR.0000021430.04195.51
A more recent version of this article appeared on July 16, 2002
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Submitted on March 4, 2002
Revised on April 24, 2002
Accepted on April 24, 2002

Probucol Attenuates Left Ventricular Dysfunction and Remodeling in Tachycardia-Induced Heart Failure. Roles of Oxidative Stress and Inflammation

Ryo Nakamura MD, Kensuke Egashira MD*, Youji Machida MD, Shunji Hayashidani MD, Motohiro Takeya MD, Hideo Utsumi MD, Hiroyuki Tsutsui MD, and Akira Takeshita MD

From the Department of Cardiovascular Medicine, School of Medical Sciences (R.N., K.E., Y.M., S.H., M.T., H.T., A.T.), and Department of Biophysics, Faculty of Pharmaceutical Sciences (H.U.), Kyushu University, Fukuoka, Japan.

* To whom correspondence should be addressed. E-mail: egashira{at}cardiol.med.kyushu-u.ac.jp.

Background—Oxidative stress and inflammation are potentially involved in the pathogenesis of heart failure (HF). We examined whether antioxidant and antiinflammatory treatment with probucol decreases myocardial oxidative stress and inflammation and attenuates the progression of left ventricular (LV) dysfunction and remodeling (dilatation) in tachycardia-induced HF.

Methods and Results—We studied 3 groups of dogs: a sham-operated control group and 2 other groups that underwent ventricular pacing at 240 bpm with and without probucol treatment (100 mg/kg IP per week) for 4 weeks. Dogs that underwent ventricular pacing for 4 weeks developed signs of HF, such as a reduction in the LV ejection fraction and increases in the LV end-diastolic dimension and LV end-diastolic pressure. Myocardial oxidative stress, as measured by electron spin resonance spectroscopy with 4-hydroxy-2,2,6,6,-tetramethyl-piperidine-N-oxyl (hydroxy-TEMPO), was significantly increased. There was an increase in myocardial monocyte infiltration, monocyte chemoattractant protein-1 expression, and renin-angiotensin system and matrix metalloproteinase activity. Probucol treatment prevented increases in oxidative stress, inflammation, and matrix metalloproteinase activity and attenuated LV dysfunction and remodeling.

Conclusions—Probucol attenuated LV dysfunction and remodeling, possibly through its antioxidant and/or antiinflammatory effects in ventricular pacing--induced HF. These data suggest that inflammatory disorders, which cause an abnormal interaction between failing myocardium and activated monocytes, have an important role in the progression of HF.


Key words: heart failure • stress • remodeling • inflammation • leukocytes




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