Adriamycin-induced early changes in myocardial antioxidant enzymes and their modulation by probucol

被引:151
作者
Li, TM
Singal, PK
机构
[1] St Boniface Gen Hosp, Res Ctr, Inst Cardiovasc Sci, Winnipeg, MB R2H 2A6, Canada
[2] Univ Manitoba, Fac Med, Dept Physiol, Winnipeg, MB, Canada
关键词
glutathione peroxidase; lipids; cardiomyopathy; heart failure;
D O I
10.1161/01.CIR.102.17.2105
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-The clinical usefulness of adriamycin is restricted by the development of congestive heart failure. It has been suggested that probucol, a strong antioxidant, completely prevents adriamycin-induced cardiomyopathy without interfering with its antitumor properties. The present study investigated the effects of adriamycin and probucol on myocardial antioxidant enzyme activities and immunoreactive protein levels in rats. Methods and Results-Activities and protein levels of glutathione peroxidase (GSHPx) were significantly decreased from 2 to 24 hours, and those of manganese superoxide dismutase were decreased at 1 and 2 hours after adriamycin treatment. These changes were prevented by probucol. Catalase activity was increased from 2 to 24 hours after adriamycin treatment, but its protein levels were not significantly changed. Copper zinc superoxide dismutase activity and protein level were not changed at any time. Myocardial lipid peroxidation was found to be significantly higher at all time points, and this change was also prevented by probucol. Treatment with probucol alone increased GSHPx activity at 2 weeks, and in these hearts, lipid peroxidation was lower than the control value. Within 24 hours, there was no mortality in any of the groups. Conclusions-It is suggested that an early and persistent decrease in GSHPx activity and protein may play an important role in the pathogenesis of adriamycin-induced cardiomyopathy, worsening heart failure and mortality.
引用
收藏
页码:2105 / 2110
页数:6
相关论文
共 29 条
[1]   Doxorubicin selectively inhibits brain versus atrial natriuretic peptide gene expression in cultured neonatal rat myocytes [J].
Chen, SC ;
Garami, M ;
Gardner, DG .
HYPERTENSION, 1999, 34 (06) :1223-1231
[2]  
CHOI KS, 1969, BIOCHEMISTRY-US, V8, P2827
[3]  
Claiborne A., 1985, Handbook of Methods of Oxygen Radicals Research, DOI DOI 10.1016/0531-5565(85)90021-X
[4]  
DOROSHOW JH, 1983, CANCER RES, V43, P460
[5]   ENZYMATIC DEFENSES OF THE MOUSE HEART AGAINST REACTIVE OXYGEN METABOLITES - ALTERATIONS PRODUCED BY DOXORUBICIN [J].
DOROSHOW, JH ;
LOCKER, GY ;
MYERS, CE .
JOURNAL OF CLINICAL INVESTIGATION, 1980, 65 (01) :128-135
[6]   A METHOD FOR DISTINGUISHING CU,ZN-CONTAINING AND MN-CONTAINING SUPEROXIDE DISMUTASES [J].
GELLER, BL ;
WINGE, DR .
ANALYTICAL BIOCHEMISTRY, 1983, 128 (01) :86-92
[7]   Mechanisms of beneficial effects of probucol in adriamycin cardiomyopathy [J].
Iliskovic, N ;
Hasinoff, BB ;
Malisza, KL ;
Li, T ;
Danelisen, I ;
Singal, PK .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1999, 196 (1-2) :43-49
[8]   SPIN-TRAPPING AND DIRECT ELECTRON-SPIN RESONANCE INVESTIGATIONS OF THE REDOX METABOLISM OF QUINONE ANTI-CANCER DRUGS [J].
KALYANARAMAN, B ;
PEREZREYES, E ;
MASON, RP .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 630 (01) :119-130
[9]   FREE-RADICALS AND THE HEART [J].
KAUL, N ;
SIVESKIILISKOVIC, N ;
HILL, M ;
SLEZAK, J ;
SINGAL, PK .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 1993, 30 (02) :55-67
[10]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+