Regulation of myocardial β-adrenergic receptor function in adult and neonatal rabbits

被引:9
作者
Sun, LS
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Anesthesiol, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Pediat, New York, NY 10032 USA
来源
BIOLOGY OF THE NEONATE | 1999年 / 76卷 / 03期
关键词
beta-adrenergic receptor; adenylyl cyclase; newborn rabbits; development; contractility; beta-adrenergic receptor desensitization;
D O I
10.1159/000014157
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
beta-Adrenergic receptor (beta AR) desensitization is the decrease in response following sustained agonist stimulation by catecholamines. While developmental changes in beta AR response have been well documented in the mammalian heart, much less is known regarding the regulation of beta AR function in immature hearts. The purpose of the present study was to determine whether there are developmental differences in myocardial beta AR desensitization. We used an isolated heart preparation to examine the beta AR-mediated inotropic response before and after sustained exposure to 1 mu M isoproterenol in adult and neonatal rabbits. We also assayed the adenylyl cyclase activity and performed radioligand-binding studies to determine beta AR characteristics in adult and neonatal ventricular tissues with and without exposure to isoproterenol. Both adult and neonatal rabbit hearts showed a concentration-dependent increase in systolic function, namely, isovolumic left ventricular developed pressure (LVDP) and maximal positive dP/dt of LVDP (dP/dt(max)) in response to isoproterenol. Adults, however, showed a significantly greater response than neonates. After sustained exposure to isoproterenol, the subsequent beta AR-mediated responses in LVDP and dP/dt(max) were significantly attenuated in adults, but much less so in neonates. The adenylyl cyclase activity in response to isoproterenol was significantly different between adult, but comparable in neonatal tissues both exposed or not to isoproterenol. The total beta AR density was higher in neonatal than in adult tissues without isoproterenol exposure, but there was no significant change in beta AR density in either group following isoproterenol exposure. In addition, isoproterenol exposure increased the amount of the inhibitory G protein in adult, but not neonatal tissues. Our results suggest that there were developmental differences in myocardial beta AR functional responses in beta AR desensitization.
引用
收藏
页码:181 / 192
页数:12
相关论文
共 26 条
[1]   DEVELOPMENTAL-CHANGES IN MODULATION OF CONTRACTILITY OF RABBIT HEARTS [J].
AKITA, T ;
KUMAR, R ;
JOYNER, RW .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1995, 25 (02) :240-251
[2]   Developmental changes in beta-adrenergic modulation of L-type Ca2+ channels in embryonic mouse heart [J].
An, RH ;
Davies, MP ;
Doevendans, PA ;
Kubalak, SW ;
Bangalore, R ;
Chien, KR ;
Kass, RS .
CIRCULATION RESEARCH, 1996, 78 (03) :371-378
[3]   INOTROPIC RESPONSES CHANGE DURING POSTNATAL MATURATION IN RABBIT [J].
ARTMAN, M ;
KITHAS, PA ;
WIKE, JS ;
STRADA, SJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (02) :H335-H342
[4]   CARDIAC BETA-ADRENOCEPTORS DURING NORMAL GROWTH OF MALE AND FEMALE RATS [J].
BAKER, SP ;
POTTER, LT .
BRITISH JOURNAL OF PHARMACOLOGY, 1980, 68 (01) :65-70
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   Seminars in medicine of the Beth Israel Hospital, Boston - Adrenergic receptors - Evolving concepts and clinical implications [J].
Flier, J ;
Insel, PA .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (09) :580-585
[7]   RAPID DESENSITIZATION OF NEONATAL RAT-LIVER BETA-ADRENERGIC RECEPTORS - A ROLE FOR BETA-ADRENERGIC-RECEPTOR KINASE [J].
GARCIAHIGUERA, I ;
MAYOR, F .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (03) :937-943
[8]   TURNING OFF THE SIGNAL - DESENSITIZATION OF BETA-ADRENERGIC-RECEPTOR FUNCTION [J].
HAUSDORFF, WP ;
CARON, MG ;
LEFKOWITZ, RJ .
FASEB JOURNAL, 1990, 4 (11) :2881-2889
[9]  
HOU QC, 1989, J DEV PHYSIOL, V11, P305
[10]   DEVELOPMENTAL-CHANGES IN BETA-ADRENOCEPTORS, MUSCARINIC CHOLINOCEPTORS AND CA-2+ CHANNELS IN RAT VENTRICULAR MUSCLES [J].
KOJIMA, M ;
ISHIMA, T ;
TANIGUCHI, N ;
KIMURA, K ;
SADA, H ;
SPERELAKIS, N .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 99 (02) :334-339