Modulation of myocardial SOD and iNOS during ischemia-reperfusion by antisense directed at ACE mRNA

被引:8
作者
Mehta, JL
Chen, HJ
Li, DY
Phillips, MI
机构
[1] Univ Arkansas Med Sci, Div Cardiovasc Dis, Little Rock, AR 72205 USA
[2] Univ Florida, Coll Med, Dept Med, Gainesville, FL USA
[3] Univ Florida, Coll Med, Dept Physiol, Gainesville, FL USA
[4] VA Med Ctr, Gainesville, FL USA
关键词
cardioprotection; nitric oxide; superoxide dismutase;
D O I
10.1006/jmcc.2000.1254
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Renin-angiotensin system (RAS) is involved in the regulation of superoxide dismutase (SOD) and nitric oxide (NO) equilibrium and its modulation protects hearts from ischemic dysfunction. We examined the effect of a new antisense-oligodeoxynucleotides (AS-ODNs) directed at ACE mRNA on SOD and iNOS expression during myocardial ischemia, Sprague-Dawley rats were treated with saline. AS-ODNs, or inverted-ODNs (IN-ODNs), given with liposome DOTAP/DOPE. Hearts were excised and subjected to 25 min of ischemia followed by 30 min of reperfusion, Ischemia-reperfusion in saline-treated hearts resulted in a decrease in the expression of SOD and an increase in the expression of inducible NOS (iNOS) genes concurrently with myocardial dysfunction, AS-ODNs, but not IN-ODNs, protected hearts against functional deterioration, and upregulated SOD expression and inhibited the expression of iNOS, ACE protein expression was decreased in the rat hearts of the AS-ODNs-treated group, but not in the IN-ODNs group. Thus manipulation of RAS with AS-ODNs directed at ACE mRNA can ameliorate cardiac dysfunction and modulate expression of SOD and iNOS at genomic level, (C) 2000 Academic Press.
引用
收藏
页码:2259 / 2268
页数:10
相关论文
共 48 条
[31]  
NICKLAS JM, 1992, NEW ENGL J MED, V327, P685
[32]   Selective inhibition of inducible nitric oxide synthase prevents ischaemic brain injury [J].
Parmentier, S ;
Böhme, GA ;
Lerouet, D ;
Damour, D ;
Stutzmann, JM ;
Margaill, I ;
Plotkine, M .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 127 (02) :546-552
[33]   ACTIVATION OF ANGIOTENSIN-CONVERTING ENZYME EXPRESSION IN INFARCT ZONE FOLLOWING MYOCARDIAL-INFARCTION [J].
PASSIER, RCJJ ;
SMITS, JFM ;
VERLUYTEN, MJA ;
STUDER, R ;
DREXLER, H ;
DAEMEN, MJAP .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 269 (04) :H1268-H1276
[34]   FREE-RADICALS AND INFLAMMATION - SUPEROXIDE-DEPENDENT ACTIVATION OF A NEUTROPHIL CHEMOTACTIC FACTOR IN PLASMA [J].
PETRONE, WF ;
ENGLISH, DK ;
WONG, K ;
MCCORD, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (02) :1159-1163
[35]   EFFECT OF CAPTOPRIL ON MORTALITY AND MORBIDITY IN PATIENTS WITH LEFT-VENTRICULAR DYSFUNCTION AFTER MYOCARDIAL-INFARCTION - RESULTS OF THE SURVIVAL AND VENTRICULAR ENLARGEMENT TRIAL [J].
PFEFFER, MA ;
BRAUNWALD, E ;
MOYE, LA ;
BASTA, L ;
BROWN, EJ ;
CUDDY, TE ;
DAVIS, BR ;
GELTMAN, EM ;
GOLDMAN, S ;
FLAKER, GC ;
KLEIN, M ;
LAMAS, GA ;
PACKER, M ;
ROULEAU, J ;
ROULEAU, JL ;
RUTHERFORD, J ;
WERTHEIMER, JH ;
HAWKINS, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (10) :669-677
[36]   Antisense inhibition and adeno-associated viral vector delivery for reducing hypertension [J].
Phillips, MI .
HYPERTENSION, 1997, 29 (01) :177-187
[37]   Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NADH/NADPH oxidase activation - Contribution to alterations of vasomotor tone [J].
Rajagopalan, S ;
Kurz, S ;
Munzel, T ;
Tarpey, M ;
Freeman, BA ;
Griendling, KK ;
Harrison, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (08) :1916-1923
[38]  
SANDS H, 1994, MOL PHARMACOL, V45, P932
[39]   Characterization of cationic liposome-mediated gene transfer in vivo by intravenous administration [J].
Song, YK ;
Liu, F ;
Chu, SY ;
Liu, DX .
HUMAN GENE THERAPY, 1997, 8 (13) :1585-1594
[40]   Myocardial protection with endogenous overexpression of manganese superoxide dismutase [J].
Suzuki, K ;
Sawa, Y ;
Ichikawa, H ;
Kaneda, Y ;
Matsuda, H .
ANNALS OF THORACIC SURGERY, 1999, 68 (04) :1266-1271