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Clonidine reduces blood pressure and heart rate oscillations in hypertensive patients
J L Elghozi1, D Laude, F Janvier
1Laboratory of Pharmacology, CNRS I61670, Faculty of Medicine Necker-E.M., Paris, France.
Insights
Clonidine significantly reduced blood pressure (BP) and heart rate (HR) variability in hypertensive men. This suggests clonidine improves BP and HR control by enhancing baroreflex sensitivity.
Area of Science:
- Cardiology
- Pharmacology
- Physiology
Background:
- Essential hypertension is characterized by short-term fluctuations in blood pressure (BP) and heart rate (HR).
- Understanding the autonomic nervous system's role in BP and HR variability is crucial for managing hypertension.
Purpose of the Study:
- To investigate the effects of clonidine on BP and HR variability in men with essential hypertension.
- To explore the underlying mechanisms of clonidine's hypotensive effects, particularly baroreflex sensitivity.
Main Methods:
- A double-blind, crossover, placebo-controlled study involving eight men with essential hypertension.
- Continuous BP and HR monitoring using a Finapres device with spectral analysis via fast Fourier transform.
- Assessment of BP (SAP, DAP, MAP) and HR variability before and after a 150-microgram oral dose of clonidine.
Main Results:
- Clonidine (150 micrograms) significantly reduced BP and HR variability by 21-36.7% after 90 minutes.
- Average BP decreased by 10.6-19.7 mm Hg and HR by 1.0 beat/min.
- Spectral analysis revealed clonidine reduced BP and HR oscillations in the mid-frequency range (66-129 mHz), linked to autonomic activity.
Conclusions:
- Clonidine effectively reduces BP and HR variability in hypertensive individuals.
- The findings suggest clonidine enhances baroreflex sensitivity, leading to improved BP and HR regulation.
- Clonidine's impact on autonomic nervous system activity is a key factor in its therapeutic effects.
Abstract:
Short-term fluctuations in blood pressure (BP) and heart rate (HR) were analyzed in a group of eight men with essential hypertension. Indirect finger BP was measured by a Finapres device. Analog-to-digital conversion of the BP was used to determine systolic (SAP), diastolic (DAP), and mean arterial pressure (MAP) and HR every second. The equidistant sampling allowed a direct spectral analysis using a fast Fourier transform algorithm. The effects of an oral dose of clonidine (150 micrograms) were studied in a double-blind, crossover, placebo-controlled study. Clonidine markedly reduced the variability of BP and HR after 90 min as indicated by a reduction in the standard deviations of BP by 36.7% for SAP, 21.0% for DAP, 22.1% for MAP, and 26.0% for HR. At this time clonidine reduced the average BP by 19.7 mm Hg for SAP, 10.6 mm Hg for DAP, 16.0 mm Hg for MAP, and 1.0 beat/min for HR. Spectral profiles of BP and HR illustrated the alterations in the spontaneous oscillations underlying the standard deviation changes. Clonidine dramatically reduced the amplitude of BP and HR oscillations in the mid-frequency region 66-129 mHz, which depends on the activity of the autonomic nervous system. We suggest that an increased sensitivity of the baroreflex is responsible for the apparent better control of BP and HR with clonidine.
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