Immediate-early gene responses to different cardiac loads in the ejecting rabbit left ventricle

被引:13
作者
Slinker, BK [1 ]
Stephens, RL [1 ]
Fisher, SA [1 ]
Yang, QL [1 ]
机构
[1] CASE WESTERN RESERVE UNIV, DIV CARDIOL, CLEVELAND, OH 44106 USA
关键词
cellular oncogenes; proto-oncogenes; c-fos; c-jun; egr-1; cardiac hypertrophy; isolated heart preparation;
D O I
10.1006/jmcc.1996.0147
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Clinical and experimental observations in humans and animals have shown that different cardiac adaptations occur in response to different types of hemodynamic overload. However, very little is known about how different hemodynamic loads lead to these different cardiac adaptations. Accordingly, we studied the acute response of ejecting isolated rabbit hearts to independently varied systolic and diastolic mechanical loads at constant coronary perfusion pressure. We studied the combined effects of low end-diastolic volume (EDV) and low systolic ejection pressure (P-ej), compared to low EDV and high P-ej, high EDV and low P-ej, and high EDV and high P-ej, on the expression of c-fos, c-jun, and egr-1. Further, although we did not seek to clarify the role of these immediate-early genes in cardiac hypertrophy, we hypothesized that they should not all respond in the same manner to these different mechanical loads. In these ejecting hearts we found that the expression of these immediate-early genes did not all respond alike to the different mechanical loads: both c-fos and egr-1 were strongly induced at both 30 and 60 min. However, at 30 min only c-fos depended on the level of EDV (P = 0.01). Neither c-fos nor egr-1 was influenced by EDV at 60 min. The expression of c-inn was largely insensitive to all loading conditions. We conclude that EDV, independent of P-ej, influences the pattern and time course of expression of some immediately-early genes and that these different immediate-early genes do not respond in parallel to changes in cardiac loading. (C) 1996 Academic Press Limited.
引用
收藏
页码:1565 / 1574
页数:10
相关论文
共 40 条
[1]
BISHOPRIC NH, 1992, J BIOL CHEM, V267, P25535
[2]
EXPRESSION OF NUCLEAR PROTOONCOGENES IN ISOPROTERENOL-INDUCED CARDIAC-HYPERTROPHY [J].
BRAND, T ;
SHARMA, HS ;
SCHAPER, W .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1993, 25 (11) :1325-1337
[3]
PROTOONCOGENE EXPRESSION IN PORCINE MYOCARDIUM SUBJECTED TO ISCHEMIA AND REPERFUSION [J].
BRAND, T ;
SHARMA, HS ;
FLEISCHMANN, KE ;
DUNCKER, DJ ;
MCFALLS, EO ;
VERDOUW, PD ;
SCHAPER, W .
CIRCULATION RESEARCH, 1992, 71 (06) :1351-1360
[4]
SINGLE PERTURBED BEAT VS STEADY-STATE BEATS FOR ASSESSING SYSTOLIC FUNCTION IN THE ISOLATED HEART [J].
CAMPBELL, KB ;
TAHERI, H ;
KIRKPATRICK, RD ;
SLINKER, BK .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (06) :H1631-H1639
[5]
SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[6]
DODGE H T, 1973, Progress in Cardiovascular Diseases, V16, P1, DOI 10.1016/0033-0620(73)90002-9
[8]
GUPTA MP, 1991, J BIOL CHEM, V266, P12813
[9]
IN-VITRO WORK LOAD AND RAT-HEART METABOLISM .1. EFFECT ON PROTEIN-SYNTHESIS [J].
HJALMARSON, A ;
ISAKSSON, O .
ACTA PHYSIOLOGICA SCANDINAVICA, 1972, 86 (01) :126-+
[10]
QUANTITATIVE ANGIOCARDIOGRAPHY .3. RELATIONSHIPS OF LEFT VENTRICULAR PRESSURE VOLUME AND MASS IN AORTIC VALVE DISEASE [J].
KENNEDY, JW ;
TWISS, RD ;
BLACKMON, JR ;
DODGE, HT .
CIRCULATION, 1968, 38 (05) :838-&