Key result
Sustained cardiac sympathetic stimulation progressively reduces norepinephrine overflow by ~79% over 10 minutes.
Why the study?
Does sustained cardiac sympathetic nerve stimulation with or without norepinephrine reuptake blockade affect norepinephrine overflow rates in anaesthetized dogs?
Does sustained cardiac sympathetic nerve stimulation with or without norepinephrine reuptake blockade affect norepinephrine overflow rates in anaesthetized dogs?
Sustained cardiac sympathetic nerve stimulation leads to a progressive decline in norepinephrine overflow due to curtailed neuronal release rather than accelerated reuptake.
Answers are grounded in this paper and cite their sources.
Does not support reuptake blockade to sustain norepinephrine overflow; leaves open translation to human sympathetic regulation models.
The left ansa subclavia was stimulated at supramaximal intensity at a frequency of Hz in open-chest, anaesthetized dogs for periods of about 10 min. Arterial blood pressure, myocardial contractile force, and coronary sinus blood flow reached peak values after 1 or 2 min of stimulation, and then declined gradually throughout the remainder of stimulation. In hearts that averaged 159 +/- 10 (SEM) g, the norepinephrine (NE) overflow rose to a peak value of 470 +/- 128 ng/min at the end of 1 min of sympathetic stimulation in the control animals. By the 10th min of stimulation, the NE overflow had diminished to 97 +/- 24 ng/min. In animals pretreated with cocaine (5 mg/kg) or with phenoxybenzamine (5 mg/kg), the peak NE overflow rates were 288 +/- 62 and 980 +/- 148 mg/min, respectively, and the rate of NE overflow declined to levels of 104 +/- 39 and 128 +/- 30 ng/min, respectively by the 10th min of stimulation. Since there was a profound, progressive diminution in the rate of NE overflow during sustained cardiac sympathetic stimulation regardless of whether or not NE reuptake was suppressed, it is concluded that the reduction in NE overflow reflects a curtailment of neuronal release of NE rather than an acceleration of reuptake.
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Levy et al. (1976) studied Cardiac sympathetic nerve stimulation in anaesthetized dogs. Left ansa subclavia stimulation (with or without cocaine or phenoxybenzamine pretreatment) vs. Control animals without cocaine or phenoxybenzamine pretreatment was evaluated on Norepinephrine (NE) overflow rate. Sustained cardiac sympathetic stimulation progressively reduced norepinephrine overflow from 470 to 97 ng/min over 10 minutes in control dogs, regardless of reuptake suppression.
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