Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Imaging Studies VII: Vascular Imaging01:19

Imaging Studies VII: Vascular Imaging

158
DefinitionRenal angiography, also known as renal arteriography, is an imaging technique used to obtain a comprehensive view of blood flow and the vascular structure of blood vessels in the kidneys and surrounding areas.PurposeRenal angiography detects blood vessel abnormalities in the kidneys, such as aneurysms, stenosis, thrombosis, vascular tumors, and renal artery stenosis. It evaluates kidney function and guides interventional treatments like angioplasty or stent placement.Pre-Procedure...
158
Physiological Pharmacokinetic Models: Blood Flow-Limited Versus Diffusion-Limited Models00:57

Physiological Pharmacokinetic Models: Blood Flow-Limited Versus Diffusion-Limited Models

235
Physiological pharmacokinetic models, often called flow-limited or perfusion models, typically assume a swift drug distribution between tissue and venous blood, creating a rapid drug equilibrium. This premise is based on the idea that drug diffusion is extremely fast, and the cell membrane presents no barrier to drug permeation. In this scenario, where no drug binding occurs, the drug concentration in the tissue equals that of the venous blood leaving the tissue. This greatly simplifies the...
235
Model Approaches for Pharmacokinetic Data: Physiological Models01:15

Model Approaches for Pharmacokinetic Data: Physiological Models

187
Physiological models in pharmacokinetics are instrumental in understanding the distribution and elimination of drugs within the body. These models describe the drug concentration within target organs, influenced by factors such as drug uptake, tissue volume, and blood flow. Drug uptake is governed by the partition coefficient, which signifies the drug concentration ratio in tissue to that in the blood. The blood flow rate to a specific tissue is expressed as Qt, and the rate of change in tissue...
187
Autoregulation of Blood Flow01:17

Autoregulation of Blood Flow

7.2K
Autoregulation mechanisms are characterized by their inherent capacity for self-regulation without necessitating specific nervous stimulation or endocrine control. These mechanisms facilitate the adjustment of blood flow and, therefore, perfusion specific to each tissue region. This self-regulation encompasses chemical signals and myogenic controls.
Chemical Signaling in Autoregulation
Chemical signaling operates at the precapillary sphincter level, inciting either contraction or relaxation....
7.2K
Imaging Studies for Cardiovascular System V: CT01:28

Imaging Studies for Cardiovascular System V: CT

161
Cardiac computed tomography (CT) scanning is an advanced cardiac imaging technique that utilizes CT technology, with or without intravenous (IV) contrast, to produce accurate cross-sectional virtual slices of specific areas of the heart, coronary circulation, and major blood vessels such as the aorta, pulmonary veins, and arteries. The computer processes these slices to generate three-dimensional images. Multidetector CT (MDCT) is a rapid form of CT scanning that captures multiple slices...
161
Imaging Studies for Cardiovascular System IV: CMRI01:21

Imaging Studies for Cardiovascular System IV: CMRI

227
Cardiovascular magnetic resonance imaging, or CMRI, is a non-invasive diagnostic test that employs a magnetic field and radiofrequency waves to create precise images of the heart and arteries. It provides comprehensive information about cardiac anatomy, function, perfusion, and tissue characterization without ionizing radiation.IndicationsCMRI diagnoses various heart conditions, including tissue damage from heart attacks, ischemic heart disease, myocarditis, aortic issues (tears, aneurysms,...
227

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Biaxial biomechanics of aged human carotid arteries.

Journal of the mechanical behavior of biomedical materials·2026
Same author

Two Years of Menaquinone-7 Supplementation and Coronary Artery Calcification: A Randomized Clinical Trial.

JAMA cardiology·2026
Same author

Delta (Δ) 12-lead electrocardiography and vectorcardiography to identify the origin of focally induced atrial and ventricular premature depolarizations in horses.

Journal of veterinary internal medicine·2026
Same author

Subclavian or axillary artery cannulation for extracorporeal membrane oxygenation: A systematic review.

JTCVS open·2026
Same author

In silico modelling of changes in spinal cord blood flow after endovascular aortic aneurysm repair.

Computer methods and programs in biomedicine·2026
Same author

Editorial for "Detection of Coronary Microvascular Dysfunction in Diabetic Mice Using Arterial Spin Labeling Cardiac MRI: A Multimodality Imaging Comparison".

Journal of magnetic resonance imaging : JMRI·2026

Related Experiment Video

Updated: Dec 3, 2025

Dual-mode Imaging of Cutaneous Tissue Oxygenation and Vascular Function
11:35

Dual-mode Imaging of Cutaneous Tissue Oxygenation and Vascular Function

Published on: December 8, 2010

16.8K

Complementing sparse vascular imaging data by physiological adaptation rules.

Maarten H G Heusinkveld1, Robert J Holtackers2, Bouke P Adriaans3

  • 1Department of Biomedical Engineering, Maastricht University, Maastricht, The Netherlands.

Journal of Applied Physiology (Bethesda, Md. : 1985)
|October 29, 2020
PubMed
Summary
This summary is machine-generated.

This study introduces a new method for personalized pulse wave propagation (PWP) modeling that uses physiological adaptation rules to estimate missing vascular geometry data, improving clinical decision-making.

Keywords:
computational modelhemodynamicsimagingsparse datavascular adaptation

More Related Videos

Quantification of Vascular Parameters in Whole Mount Retinas of Mice with Non-Proliferative and Proliferative Retinopathies
12:28

Quantification of Vascular Parameters in Whole Mount Retinas of Mice with Non-Proliferative and Proliferative Retinopathies

Published on: March 12, 2022

4.0K
Author Spotlight: Creating Human Vascularized Micro-Tumors as Models for Translational Cancer Research
07:26

Author Spotlight: Creating Human Vascularized Micro-Tumors as Models for Translational Cancer Research

Published on: September 15, 2023

2.2K

Related Experiment Videos

Last Updated: Dec 3, 2025

Dual-mode Imaging of Cutaneous Tissue Oxygenation and Vascular Function
11:35

Dual-mode Imaging of Cutaneous Tissue Oxygenation and Vascular Function

Published on: December 8, 2010

16.8K
Quantification of Vascular Parameters in Whole Mount Retinas of Mice with Non-Proliferative and Proliferative Retinopathies
12:28

Quantification of Vascular Parameters in Whole Mount Retinas of Mice with Non-Proliferative and Proliferative Retinopathies

Published on: March 12, 2022

4.0K
Author Spotlight: Creating Human Vascularized Micro-Tumors as Models for Translational Cancer Research
07:26

Author Spotlight: Creating Human Vascularized Micro-Tumors as Models for Translational Cancer Research

Published on: September 15, 2023

2.2K

Area of Science:

  • Biomedical Engineering
  • Computational Biology
  • Cardiovascular Physiology

Background:

  • Personalized pulse wave propagation (PWP) models require complete vascular geometry data, which is often unavailable in clinical practice.
  • Existing PWP models struggle with incomplete patient-specific datasets, limiting their clinical utility.
  • Vascular adaptation to mechanical load is a physiological process that can potentially fill data gaps.

Purpose of the Study:

  • To develop and validate an adaptive PWP model that estimates missing vascular geometries using physiological adaptation rules.
  • To assess the accuracy of the adaptive model in predicting arterial dimensions and waveform characteristics compared to a complete model.
  • To enable personalized PWP modeling even with incomplete patient data.

Main Methods:

  • Implemented homeostatic feedback loops in a validated PWP model to simulate vessel geometry adaptation.
  • Used vascular MRI and ultrasound data from 10 healthy subjects.
  • Compared adapted models (using limited data) with reference models (using complete data) for geometry and waveform accuracy.

Main Results:

  • The adaptive PWP model accurately predicted arterial radius and wall thickness, with limits of agreement of 0.2 ± 2.6 mm and -140 ± 557 µm, respectively.
  • Pressure and flow waveforms from the adapted models more closely resembled those from the reference models.
  • The adaptation-based model demonstrated improved accuracy over non-adapted models with incomplete data.

Conclusions:

  • The developed adaptation-based PWP model successfully personalizes vascular geometries using physiological adaptation rules, even with incomplete datasets.
  • This approach offers a valuable tool for facilitating personalized cardiovascular modeling in clinical settings where data is often missing.
  • The method enhances the feasibility of using PWP models for clinical decision-making by overcoming data limitations.