Where are we with probucol: A new life for an old drug?

被引:160
作者
Yamashita, Shizuya [1 ]
Matsuzawa, Yuji [2 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Cardiovasc Med, Suita, Osaka 5650871, Japan
[2] Sumitomo Hosp, Osaka, Japan
关键词
Probucol; Anti-oxidant; Atherosclerosis; Familial hypercholesterolemia; Coronary artery disease; Risk factor; HDL-cholesterol; Cholesteryl ester transfer protein; FAMILIAL HYPERCHOLESTEROLEMIA; ATHEROSCLEROSIS; CHOLESTEROL; ANGIOPLASTY; ACCUMULATION; RESTENOSIS; CILOSTAZOL; EXPRESSION; PREVENTS; RABBIT;
D O I
10.1016/j.atherosclerosis.2009.04.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Probucol has a long history of clinical application with established efficacy and safety profiles. Probucol is a potent anti-oxidant drug that has been in clinical use during the past few decades for the treatment and prevention of cardiovascular diseases. Here we review the current status of knowledge on the pharmacology, clinical benefits, and the mechanism of actions of this unique drug. Probucol has diverse pharmacological properties with therapeutic effects on the cardiovascular systems. Its mechanism of pharmacologic actions at the molecular level has recently been elucidated with the new concept of HDL metabolism associated with cholesteryl ester transfer protein (CETP) or scavenger receptor class B type I (SR-BI). HDL-C reduction may not be a "side effect" but it most likely might reflect a mechanism of action of probucol. Probucol could be reconsidered as an option at least in case statins, which are known to be effective in lowering low-density lipoproteins (LDL) and coronary artery disease (CAD) risk, are not effective. In particular, a marked CAD risk reduction has been recently reported in long-term probucol treatment of patients with heterozygous familial hypercholesterolemia (FH) in Japan. Therefore, probucol could be a more common therapeutic drug for the treatment of patients with FH as well. There is more than enough reason to believe that this old drug has much more to offer than hitherto known. (C) 2009 Published by Elsevier Ireland Ltd.
引用
收藏
页码:16 / 23
页数:8
相关论文
共 57 条
[31]   INHIBITION OF HYPERCHOLESTEROLEMIA-INDUCED ATHEROSCLEROSIS IN THE NONHUMAN PRIMATE BY PROBUCOL .1. IS THE EXTENT OF ATHEROSCLEROSIS RELATED TO RESISTANCE OF LDL TO OXIDATION [J].
SASAHARA, M ;
RAINES, EW ;
CHAIT, A ;
CAREW, TE ;
STEINBERG, D ;
WAHL, PW ;
ROSS, R .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :155-164
[32]   Effects of Probucol and pravastatin on common carotid atherosclerosis in patients with asymptomatic hypercholesterolemia - Fukuoka Atherosclerosis Trial (FAST) [J].
Sawayama, Y ;
Shimizu, C ;
Maeda, N ;
Tatsukawa, M ;
Kinukawa, N ;
Koyanagi, S ;
Kashiwagi, S ;
Hayashi, J .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 39 (04) :610-616
[33]   Effects of probucol and cilostazol alone and in combination on frequency of poststenting restenosis [J].
Sekiya, M ;
Funada, J ;
Watanabe, K ;
Miyagawa, M ;
Akutsu, H .
AMERICAN JOURNAL OF CARDIOLOGY, 1998, 82 (02) :144-147
[34]   Viability of developing CETP inhibitors [J].
Sirtori, Cesare R. ;
Mombelli, Giuliana .
CARDIOVASCULAR THERAPEUTICS, 2008, 26 (02) :135-146
[35]  
STEINBERG D, 1989, NEW ENGL J MED, V320, P915
[36]   Role of oxidative modifications in atherosclerosis [J].
Stocker, R ;
Keaney, JF .
PHYSIOLOGICAL REVIEWS, 2004, 84 (04) :1381-1478
[37]   Lipid management to reduce cardiovascular risk - A new strategy is required [J].
Superko, H. Robert ;
King, Spencer, III .
CIRCULATION, 2008, 117 (04) :560-568
[38]   PROBUCOL-INDUCED QT PROLONGATION AND SYNCOPE [J].
TAMURA, M ;
UEKI, Y ;
OHTSUKA, E ;
ORIBE, M ;
SEITA, M ;
ORIBE, K ;
ITO, M .
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION, 1994, 58 (05) :374-377
[39]   Probucol inhibits neointimal formation in carotid arteries of normocholesterolemic rabbits and the proliferation of cultured rabbit vascular smooth muscle cells [J].
Tanaka, K ;
Hayashi, K ;
Shingu, T ;
Kuga, Y ;
Nomura, K ;
Kajiyama, G .
CARDIOVASCULAR DRUGS AND THERAPY, 1998, 12 (01) :19-28
[40]   Effects of AGI-1067 and probucol after percutaneous coronary interventions [J].
Tardif, JC ;
Grégoire, J ;
Schwartz, L ;
Title, L ;
Laramée, L ;
Reeves, F ;
Lespérance, J ;
Bourassa, MG ;
L'Allier, PL ;
Glass, M ;
Lambert, J ;
Guertin, MC .
CIRCULATION, 2003, 107 (04) :552-558