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Implantation of Combined Telemetric ECG and Blood Pressure Transmitters to Determine Spontaneous Baroreflex Sensitivity in Conscious Mice
Published on: February 14, 2021
Brain systems for baroreflex suppression during stress in humans
Peter J Gianaros1, Ikechukwu C Onyewuenyi, Lei K Sheu
1Department of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania 15213, USA. gianarospj@upmc.edu
Human Brain Mapping
|May 14, 2011
Summary
Psychological stressors reduce the arterial baroreflex
Area of Science:
- Neuroscience
- Cardiovascular Physiology
- Psychophysiology
Background:
- The arterial baroreflex regulates blood pressure homeostasis.
- Psychological stressors impair baroreflex sensitivity (BRS) in humans and animals.
- Human brain mechanisms linking stress to BRS suppression remain unclear.
Purpose of the Study:
- To investigate the human brain systems involved in stress-induced suppression of baroreflex sensitivity.
- To correlate brain activity and functional connectivity with changes in BRS during a psychological stressor.
Main Methods:
- 97 adults underwent beat-to-beat blood pressure and heart rate monitoring during a cognitive stress task.
- Spontaneous baroreflex sensitivity (BRS) was quantified using a validated sequence method.
- Functional magnetic resonance imaging (fMRI) measured brain activity and functional connectivity during the task.
Main Results:
- Task performance increased blood pressure and heart rate, and reduced BRS.
- Reduced BRS correlated with increased activity in central autonomic and cardiovascular control regions (cingulate cortex, insula, amygdala, PAG).
- Task performance enhanced functional connectivity between the anterior insula and the cingulate cortex, amygdala, midbrain PAG, and pons.
Conclusions:
- This study provides human evidence for brain systems suppressing baroreflex function during psychological stress.
- Findings elucidate neurobiological mechanisms of stressor-related cardiovascular reactivity.
- These insights are relevant for understanding essential hypertension and atherosclerotic heart disease risk.
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