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(Hypertension. 2004;43:154.)
© 2004 American Heart Association, Inc.
Editorial Commentaries |
From the Clinica Medica, Dipartimento di Medicina Clinica, Prevenzione e Biotecnologie Sanitarie, Università Milano-Bicocca, Monza (Milano), Centro Interuniversitario di Fisiologia Clinica e Ipertensione and Centro Auxologico Italiano, Milano, Italy.
Correspondence to Professor Guido Grassi, Clinica Medica, Ospedale S. Gerardo dei Tintori, Via Donizetti 106, 20052 Monza (MI), Italia. E-mail guido.grassi@unimib.it
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
Since the demonstrationthat the sympathetic nervous system exerts a fundamental role in the homeostatic control of blood pressure, the hypothesis has been advanced that abnormalities in the adrenergic regulation of either cardiac output or peripheral vascular resistance might represent the pathophysiological hallmarks of the essential hypertensive state of "neurogenic" nature. To date, the evidence supporting this hypothesis can be summarized as follows. First, the early stages of hypertension frequently display hyperkinetic circulation characterized by an increase in cardiac output coupled with an elevated heart rate (ie, by hemodynamic abnormalities that have been shown to be triggered by a blunted parasympathetic and an enhanced sympathetic cardiovascular drive).1 Second, a meta-analysis of all published studies that have made use of plasma norepinephrine assay for evaluating adrenergic tone has provided evidence that, even accounting for some negative results, an indirect marker of the sympathetic function, such as plasma norepinephrine, is significantly elevated in essential hypertensive patients as compared with age-matched normotensive controls.2 Third, by using the technique based on the intravenous tracer infusion of small doses of radiolabeled norepinephrine, it has been possible to show3 that the rate of norepinephrine spillover from the sympathetic neuroeffector junctions is augmented in young subjects with borderline blood pressure elevation and that this enhanced release is particularly manifest in the kidney and in the heart (ie, in two organs of key importance in the homeostatic process of blood pressure control). Fourth, hypertensive patients display at the 123I-metaiodobenzylguanidine cardiac imaging technique a lower uptake and a greater washout
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