Alterations in cardiac adrenergic terminal function and b-adrenoceptor density in pacing-induced heart failure

Kawai, Hiroya, Amy Mohan, Jason Hagen, Erdan Dong, Jacqueline Armstrong, Suzanne Y. Stevens, and Chang-seng Liang. Alterations in cardiac adrenergic terminal function and b-adrenoceptor density in pacing-induced heart failure. Am J Physiol Heart Circ Physiol 278: H1708– H1716, 2000.—Congestive heart failure is associated with cardiac adrenergic nerve terminal changes and b-adrenoceptor density downregulation. To study the temporal sequence of these changes, we performed studies in rabbits at 2, 4, and 8 wk of cardiac pacing (360 beats/min) and at 1, 2, and 4 wk after cessation of pacing. Rapid pacing produced left ventricular (LV) dysfunction and an increase in plasma norepinephrine (NE) in 1–2 wk. At week 2, NE uptake activity, NE uptake-1 density, and adenylyl cyclase responses to isoproterenol, 58-guanylyl imidodiphosphate [Gpp(NH)p], and forskolin reduced. However, immunostained tyrosine hydroxylase profile, b-adrenoceptor density, and NE histofluorescence did not reduce until 4–8 wk of pacing. After cessation of cardiac pacing, LV function normalized quickly, followed by return of tyrosine hydroxylase and NE profiles in 1 wk and adenylyl cyclase responses to agonists and NE uptake activity in 2 wk. Myocardial b-adrenoceptor density returned to normal by 4 wk after cessation of pacing. Our results suggest that there is no permanent structural neuronal damage in the myocardium within the first 8 wk of rapid cardiac pacing. Abnormal myocardial NE reuptake mechanism may play an important pathophysiological role in heart failure.