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Am J Physiol Regul Integr Comp Physiol (October 12, 2006). doi:10.1152/ajpregu.00488.2006
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Submitted on July 12, 2006
Accepted on October 2, 2006

Optimal frequency ranges for extracting information on cardiovascular autonomic control from the blood pressure and pulse interval spectrograms in mice

Veronique Baudrie1, Dominique Laude1, and Jean-Luc Luc Elghozi2*

1 INSERM U652, Faculte de Medecine, Paris, France
2 INSERM U652, Faculte de Medecine, 15 rue de l'Ecole de Medecine, Paris, France

* To whom correspondence should be addressed. E-mail: elghozi{at}necker.fr.

The analysis of blood pressure (BP) and heart rate (HR) variability by spectral methods has proven a useful tool in many animal species for the assessment of the vagal and sympathetic contributions to oscillations of BP and HR. Continuous BP measures obtained in mice by telemetry were used to characterize the spectral bandwidths of autonomic relevance using an approach with no {alpha} priori. The paradigm was based on the autonomic blockades obtained with conventional drugs (atropine, prazosin, atenolol). The spectral changes were estimated in all the combinations of spectral bandwidths. The effect of hydralazine was also tested using the same systematic analysis, to detect the zones of sympathetic activation resulting reflexly from the vasodilatory action of the drug. Two zones of interest in the study of the autonomic control of BP and HR were observed. The first zone covered the 0.15-0.60 Hz range of the systolic BP spectrum and corresponds to the low frequency zone (or Mayer waves). This zone reflects sympathetic control since the power spectral density of this zone was significantly reduced with alpha1-adrenoceptor blockade (prazosin) while it was significantly amplified as a result of a reflex sympathetic activation (hydralazine). The second zone covered the 2.5-5.0 Hz range of the pulse interval spectrum and corresponded to the high frequency zone (respiratory sinus arrhythmia) under vagal control (blocked by atropine). These zones are recommended for testing the autonomic control of circulation in mice.




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