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AJP - Heart and Circulatory Physiology, Vol 270, Issue 2 575-H582, Copyright © 1996 by American Physiological Society
ARTICLES |
C. C. Yang, T. B. Kuo and S. H. Chan
Center for Neuroscience, National Yang-Ming University, Taipei, Taiwan, Republic of China.
We applied auto- and cross-spectral analysis of systemic arterial pressure (SAP) and heart rate (HR) signals to quantify the effects of pentobarbital sodium on short-term cardiovascular fluctuations in adult, male Sprague-Dawley rats. Intravenous administration of pentobarbital, delivered as a bolus injection (5, 10, or 20 mg/kg) or continuous infusion (10, 20, or 40 mg.kg-1.h-1), elicited only mild hypotension and tachycardia. This was accompanied by a dose-related depression of the very low (0-0.25 Hz) and low (0.25-0.8 Hz)-frequency components of both SAP and HR signals and high (0.8-2.4 Hz)-frequency component of HR signals. Cross-spectral analysis of SAP and HR signals during intravenous infusion of pentobarbital revealed a maintained coherence in the high-frequency range, together with a gradual and dose-related decrease in magnitude of transfer function and baro-receptor reflex sensitivity. Stable plasma concentration and all hemodynamic parameters were observed during 120 min of infusion at 20 mg.kg-1.h-1. Under this dosing condition, autonomic blockade by phentolamine, propranolol, or atropine still evoked discernible but differential reductions in the SAP and HR spectral components. Our data suggest that continuous intravenous administration of pentobarbital at 20 mg.kg-1.h-1 offers maintained anesthesia while preserving the capacity of cardiovascular regulation.
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