ALTERED RESPONSIVENESS OF HYPERTROPHIED RAT HEARTS TO ALPHA-ADRENERGIC AND BETA-ADRENERGIC STIMULATION

被引:27
|
作者
FOSTER, KA
HOCK, CE
REIBEL, DK
机构
[1] THOMAS JEFFERSON UNIV, JEFFERSON MED COLL, DEPT PHYSIOL, 1020 LOCUST ST, PHILADELPHIA, PA 19107 USA
[2] UNIV MED & DENT NEW JERSEY, SCH OSTEOPATH MED, DEPT MED, DIV RES, CAMDEN, NJ 08103 USA
关键词
ALPHA-ADRENOCEPTORS; BETA-ADRENOCEPTORS; CAMP; CARDIAC HYPERTROPHY; FORSKOLIN; ISOPROTERENOL; PHENYLEPHRINE;
D O I
10.1016/0022-2828(91)90042-K
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inotropic responsiveness to α- and β-adrenergic agents was examined in pressure-overload hypertrophied rat hearts. Pressure overload was induced in rats by abdominal aortic constriction. Three weeks post-constriction, hearts were isolated and perfused with buffer containing various concentrations of (1) calcium (2) isoproterenol (3) forskolin, or (4) phenylephrine. The change in rate of left ventricular pressure development (Δ + dP dt) with increasing perfusate calcium concentrations was comparable in hypertrophied hearts of aortic-constricted rats (AC) and hearts of sham-operated rats (SO). However, with isoproterenol or forskolin stimulation, inotropic responsiveness (Δ + dP dt) was 50% lower in hypertrophied hearts of AC. This was associated with significantly lower tissue cAMP levels. Beta-adrenoceptor number and affinity were unchanged in the hypertrophied myocardium. Maximum inotropic responsiveness to phenylephrine was also lower in hypertrophied hearts and was associated with reduced α-adrenoceptor numbers. The data suggest that altered inotropic responsiveness to α-adrenergic stimulation may, in part, be due to reduced cardiac α-adrenoceptor density. However, post-receptor mechanisms including alterations in cAMP metabolism may contribute to the reduced responsiveness to β-adrenergic stimulation in hypertrophied hearts of AC. © 1991.
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页码:91 / 101
页数:11
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