Related Experiment Video
Updated: Oct 14, 2025

Measuring the Carotid to Femoral Pulse Wave Velocity Cf-PWV to Evaluate Arterial Stiffness
Published on: May 3, 2018
High Pulsatile Load Decreases Arterial Stiffness: An ex vivo Study
Cédric H G Neutel1, Giulia Corradin2, Pauline Puylaert3
1Laboratory of Physiopharmacology, Faculty of Medicine and Health Sciences, University of Antwerp, Campus Drie Eiken, Antwerp, Belgium.
Insights
Pulse pressure significantly affects ex vivo arterial stiffness measurements by softening aortic tissue. This pulsatile load also impacts vascular smooth muscle cell function, with different aortic regions responding uniquely.
Area of Science:
- Biomedical Engineering
- Cardiovascular Physiology
- Biophysics
Background:
- Arterial stiffness is a key predictor of cardiovascular events and mortality.
- Current in vivo methods for measuring arterial stiffness offer limited information.
- Ex vivo experiments provide a more detailed analysis of arterial biomechanical properties.
Purpose of the Study:
- To investigate the impact of pulsatile load on ex vivo arterial stiffness measurements.
- To determine how pulse pressure influences the biomechanical properties of aortic tissue.
- To explore the effects of pulse pressure on vascular smooth muscle cell function.
Main Methods:
- Dynamic ex vivo testing of aortic tissue segments.
- Application of controlled pulsatile load mimicking physiological pressures.
- Assessment of arterial stiffness and vascular smooth muscle cell responses.
Main Results:
- Increasing pulsatile load softens aortic tissue in ex vivo settings.
- Vascular smooth muscle cell contraction and tonus depend on pulse pressure amplitude.
- Distinct regional differences in aortic response to pulse pressure were observed between the thoracic descending aorta and abdominal infrarenal aorta.
Conclusions:
- Pulse pressure is a critical variable that modulates ex vivo arterial stiffness measurements.
- Further research is needed to elucidate pulse pressure-sensitive biomechanical properties.
- Understanding these properties could advance blood vessel biomechanics and therapeutic strategies.
Abstract:
Measuring arterial stiffness has recently gained a lot of interest because it is a strong predictor for cardiovascular events and all-cause mortality. However, assessing blood vessel stiffness is not easy and the in vivo measurements currently used provide only limited information. Ex vivo experiments allow for a more thorough investigation of (altered) arterial biomechanical properties. Such experiments can be performed either statically or dynamically, where the latter better corresponds to physiological conditions. In a dynamic setup, arterial segments oscillate between two predefined forces, mimicking the diastolic and systolic pressures from an in vivo setting. Consequently, these oscillations result in a pulsatile load (i.e., the pulse pressure). The importance of pulse pressure on the ex vivo measurement of arterial stiffness is not completely understood. Here, we demonstrate that pulsatile load modulates the overall stiffness of the aortic tissue in an ex vivo setup. More specifically, increasing pulsatile load softens the aortic tissue. Moreover, vascular smooth muscle cell (VSMC) function was affected by pulse pressure. VSMC contraction and basal tonus showed a dependence on the amplitude of the applied pulse pressure. In addition, two distinct regions of the aorta, namely the thoracic descending aorta (TDA) and the abdominal infrarenal aorta (AIA), responded differently to changes in pulse pressure. Our data indicate that pulse pressure alters ex vivo measurements of arterial stiffness and should be considered as an important variable in future experiments. More research should be conducted in order to determine which biomechanical properties are affected due to changes in pulse pressure. The elucidation of the underlying pulse pressure-sensitive properties would improve our understanding of blood vessel biomechanics and could potentially yield new therapeutic insights.
Related Concept Videos
Autoregulation of Blood Flow
Chemical Signaling in Autoregulation
Chemical signaling operates at the precapillary sphincter level, inciting either contraction or relaxation....
Pulse
The pulse serves as a clinical...
Blood Pressure
Measurement of Blood Pressure

