Simulation of Empirical Correlations Between Temperatures and Blood Perfusion During Heating Using a Temperature-Dependent Blood Perfusion Model

2004 ◽  
Author(s):  
Cuiye Chen ◽  
Robert B. Roemer
Keyword(s):  
Blood Flow ◽  
Blood Perfusion ◽  
Step Function ◽  
Human Muscle ◽  
Tissue Temperature ◽  
Thigh Muscle ◽  
Temperature Dependent ◽  
In Vivo Experiments ◽  
Perfusion Model

This study applies a recently developed temperature-dependent blood perfusion model (TDBPM) coupled with a modified, one-dimensional Pennes bioheat transfer equation to predict the blood perfusion and temperature responses to step function microwave heating applied in the in vivo experiments performed by Sekins’ et al. [1] on human thigh muscle. The TDBPM model links the perfusion increase to the tissue temperature elevation based on physiological mechanisms underlying this temperature-blood-perfusion change phenomenon, i.e., a pharmacokinetic compartmental model. This physiology-based model avoids using ad hoc time delays between blood perfusion increases and tissue temperature elevations as done in previous efforts. It also includes a mechanism that produces the threshold temperature for blood flow increases that has been observed in vivo. In our recent study [2], the TDBPM model was used to simulate both the constant temperature water bath heating used in the in vivo experiments on rat leg muscle performed by Song et al. [3], and the step function microwave heating applied in the in vivo experiments on canine thigh muscle performed by Roemer et al. [4]. The blood perfusion rates predicted by the model are compared with those in vivo experimental data obtained in rat muscle and human muscle and good agreement was obtained. The TDBPM provides a possible explanation to the biochemical and biophysical origins of the relationships between temperature and blood flow that observed in rat muscle and human muscle. The physiology-based TDBPM is a simple, generic model of muscle blood flow responses of different animals to different heating conditions, which provides the type of fundamental information needed for the design of methods to thermally control blood flow in medical applications.

Lumped Parameter Thermal Model for the Study of Vascular Reactivity in the Fingertip

2008 ◽  
Vol 130 (3) ◽  
Author(s):  
O. Ley ◽  
C. Deshpande ◽  
B. Prapamcham ◽  
M. Naghavi
Keyword(s):  
Heat Flux ◽  
Blood Flow ◽  
Thermal Model ◽  
Vascular Reactivity ◽  
Arterial Occlusion ◽  
Blood Perfusion ◽  
Cost Effective ◽  
Venous Occlusion ◽  
Cardiovascular Complications ◽  
Tissue Temperature

Vascular reactivity (VR) denotes changes in volumetric blood flow in response to arterial occlusion. Current techniques to study VR rely on monitoring blood flow parameters and serve to predict the risk of future cardiovascular complications. Because tissue temperature is directly impacted by blood flow, a simplified thermal model was developed to study the alterations in fingertip temperature during arterial occlusion and subsequent reperfusion (hyperemia). This work shows that fingertip temperature variation during VR test can be used as a cost-effective alternative to blood perfusion monitoring. The model developed introduces a function to approximate the temporal alterations in blood volume during VR tests. Parametric studies are performed to analyze the effects of blood perfusion alterations, as well as any environmental contribution to fingertip temperature. Experiments were performed on eight healthy volunteers to study the thermal effect of 3min of arterial occlusion and subsequent reperfusion (hyperemia). Fingertip temperature and heat flux were measured at the occluded and control fingers, and the finger blood perfusion was determined using venous occlusion plethysmography (VOP). The model was able to phenomenologically reproduce the experimental measurements. Significant variability was observed in the starting fingertip temperature and heat flux measurements among subjects. Difficulty in achieving thermal equilibration was observed, which indicates the important effect of initial temperature and thermal trend (i.e., vasoconstriction, vasodilatation, and oscillations).

Endothelin-1 and pancreatic islet vasculature: studies in vivo and on isolated, vascularly perfused pancreatic islets

2007 ◽  
Vol 292 (6) ◽  
pp. E1616-E1623 ◽  
Author(s):  
En Yin Lai ◽  
A. Erik G. Persson ◽  
Birgitta Bodin ◽  
Örjan Källskog ◽  
Arne Andersson ◽  
...  
Keyword(s):  
Blood Flow ◽  
Pancreatic Islet ◽  
Vascular Reactivity ◽  
Blood Perfusion ◽  
Receptor Subtype ◽  
Endothelin 1 ◽  
Islet Blood Flow ◽  
Endothelin B

Endothelin-1 (ET-1) is a potent endothelium-derived vasoconstrictor, which also stimulates insulin release. The aim of the present study was to evaluate whether exogenously administered ET-1 affected pancreatic islet blood flow in vivo in rats and the islet arteriolar reactivity in vitro in mice. Furthermore, we aimed to determine the ET-receptor subtype that was involved in such responses. When applying a microsphere technique for measurements of islet blood perfusion in vivo, we found that ET-1 (5 nmol/kg) consistently and markedly decreased total pancreatic and especially islet blood flow, despite having only minor effects on blood pressure. Neither endothelin A (ETA) receptor (BQ-123) nor endothelin-B (ETB) receptor (BQ-788) antagonists, alone or in combination, could prevent this reduction in blood flow. To avoid confounding interactions in vivo, we also examined the arteriolar vascular reactivity in isolated, perfused mouse islets. In the latter preparation, we demonstrated a dose-dependent constriction in response to ET-1. Administration of BQ-123 prevented this, whereas BQ-788 induced a right shift in the response. In conclusion, the pancreatic islet vasculature is highly sensitive to exogenous ET-1, which mediates its effect mainly through ETA receptors.

Temperature Distributions During Thermoradiotherapy: A Sensitivity Study With a Transient Numerical Model of the Rabbit Eye

1997 ◽  
Vol 119 (2) ◽  
pp. 153-158 ◽  
Author(s):  
D. T. Tompkins ◽  
S. A. Klein ◽  
R. A. Steeves
Keyword(s):  
Numerical Model ◽  
Thermal Model ◽  
Choroidal Melanoma ◽  
Blood Perfusion ◽  
Sensitivity Study ◽  
Temperature Dependent ◽  
Rabbit Eye ◽  
Temperature Distributions ◽  
Perfusion Model ◽  
Choroidal Melanomas

An approach to the treatment of medium-sized choroidal melanomas combines radiation with ferromagnetic hyperthermia. The study herein discusses results with a numerical thermal model of a choroidal melanoma in the rabbit eye as treated with episcleral, thermoradiotherapy plaques. The sensitivity of a temperature–dependent blood perfusion model is investigated.

scholarly journals Revealing intraosseous blood flow in the human tibia with ultrasound

2021 ◽  
Author(s):  
Sebastien Salles ◽  
Jami Shepherd ◽  
Hendrik J. Vos ◽  
Guillaume Renaud
Keyword(s):  
Blood Flow ◽  
Cortical Bone ◽  
Femoral Artery ◽  
Bone Growth ◽  
Critical Role ◽  
Blood Perfusion ◽  
Blood Velocity ◽  
Bone Disorders ◽  
Peak Blood

Intraosseous blood circulation is thought to have a critical role in bone growth and remodeling, fracture healing, and bone disorders. However, it is rarely considered in clinical practice due to the absence of a suitable non-invasive in vivo measurement technique. In this work, we assessed blood perfusion in tibial cortical bone simultaneously with blood flow in the superficial femoral artery with ultrasound imaging in 5 healthy volunteers. After suppression of stationary signal with Singular-Value-Decomposition, pulsatile blood flow in cortical bone tissue is revealed, following the heart rate measured in the femoral artery. Using a method combining transverse oscillations and phase-based motion estimation, two-dimensional vector flow was obtained in the cortex of the tibia. After spatial averaging over the cortex, the peak blood velocity along the long axis of the tibia was measured four times larger than the peak blood velocity across the bone cortex. This suggests that blood flow in central (Haversian) canals is larger than in perforating (Volkmann's) canals, as expected from the intracortical vascular organization in humans. The peak blood velocity indicates a flow from the endosteum to the periosteum and from the heart to the foot for all subjects. Because aging and the development of bone disorders are thought to modify the direction and velocity of intra-cortical blood flow, their quantification is crucial. This work reports for the first time an in vivo quantification of the direction and velocity of blood flow in human cortical bone.

Sensitivity Analysis of One-Dimensional Heat Transfer in Tissue With Temperature-Dependent Perfusion

1997 ◽  
Vol 119 (1) ◽  
pp. 77-80 ◽  
Author(s):  
C. R. Davies ◽  
G. M. Saidel ◽  
H. Harasaki
Keyword(s):  
Heat Transfer ◽  
Sensitivity Analysis ◽  
Heated Surface ◽  
Experimental Studies ◽  
Total Artificial Heart ◽  
Tissue Temperature ◽  
Model Parameters ◽  
Temperature Dependent ◽  
One Dimensional

Design criteria for implantable, heat-generating devices such as the total artificial heart require the determination of safe thresholds for chronic heating. This involves in-vivo experiments in which tissue temperature distributions are obtained in response to known heat sources. Prior to experimental studies, simulation using a mathematical model can help optimize the design of experiments. In this paper, a theoretical analysis of heat transfer is presented that describes the dynamic, one-dimensional distribution of temperature from a heated surface. Loss of heat by perfusion is represented by temperature-independent and temperature-dependent terms that can reflect changes in local control of blood flow. Model simulations using physiologically appropriate parameter values indicate that the temperature elevation profile caused by a heated surface adjacent to tissue may extend several centimeters into the tissue. Furthermore, sensitivity analysis indicates the conditions under which temperature profiles are sensitive to changes in thermal diffusivity and perfusion parameters. This information provides the basis for estimation of model parameters in different tissues and for prediction of the thermal responses of these tissues.

scholarly journals Organic nanoparticle-doped microdroplets as dual-modality contrast agents for ultrasound microvascular flow and photoacoustic imaging

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Yu Xu ◽  
Guoyun Sun ◽  
Eshu Middha ◽  
Yu-Hang Liu ◽  
Kim Chuan Chan ◽  
...  
Keyword(s):  
Blood Flow ◽  
Nude Mice ◽  
Photoacoustic Imaging ◽  
Imaging Techniques ◽  
Contrast Effects ◽  
In Vivo Evaluation ◽  
Dual Modality ◽  
In Vivo Experiments

Abstract Tumor blood vessels are chaotic and abundantly distributed, owing to their heterogeneity. Therefore, imaging techniques which reveal abnormalities of tumor vasculature play significant roles in both mechanistic and clinical diagnostic tumor studies. Photoacoustic (PA) imaging uses the intrinsic characteristics of hemoglobin, to acquire tumor hemodynamic information, while ultrasound (US) imaging provides information about tumoral vessel structures and blood flow. To improve the imaging contrast performance, hydrogel-based microdroplets were designed for both US blood flow and PA imaging in this study. The microdroplets served as carriers for PA contrast agent solution in the innermost part while oil and hydrogel formed the inner and outer layers of the droplets. In vitro experiments firstly demonstrated the dual modality contrast effects of the microdroplets on US flow determination and PA imaging. In vivo experiments were then carried out in both healthy nude mice and nude mice with subcutaneous tumor to validate the contrast effects and to monitor the duration of contrast effects in animals. Using the dual-modality microdroplets, we were able to obtain distinct edges of tumor and blood flow mapping of the tumor microvascular with improved sensitivity up to 11.09 dB for PA and 6.69 dB for US flow. Besides, the in vivo evaluation with microdroplets showed US flow enhancement for more than 60 min. Therefore, the microdroplets are able to provide the contrast effects for both US flow and PA in a relative long duration and have potential to be applied in the tumor related diagnoses and studies.

Positioning of bone marrow hematopoietic and stromal cells relative to blood flow in vivo: serially reconstituting hematopoietic stem cells reside in distinct nonperfused niches

Blood ◽  
2010 ◽  
Vol 116 (3) ◽  
pp. 375-385 ◽  
Author(s):  
Ingrid G. Winkler ◽  
Valérie Barbier ◽  
Robert Wadley ◽  
Andrew C. W. Zannettino ◽  
Sharon Williams ◽  
...  
Keyword(s):  
Bone Marrow ◽  
Blood Flow ◽  
Stromal Cells ◽  
Blood Perfusion ◽  
Low Oxygen ◽  
Hematopoietic Stem ◽  
Single Host ◽  
Differentiation Stage

Abstract Hematopoietic stem cell (HSC) niches have been reported at the endosteum or adjacent to bone marrow (BM) vasculature. To investigate functional attributes of these niches, mice were perfused with Hoechst 33342 (Ho) in vivo before BM cell collection in presence of pump inhibitors and antibody stained. We report that the position of phenotypic HSCs, multipotent and myeloid progenitors relative to blood flow, follows a hierarchy reflecting differentiation stage, whereas mesenchymal stromal cells are perivascular. Furthermore, during granulocyte colony-stimulating factor–induced mobilization, HSCs migrated closer to blood flow, whereas stromal cells did not. Interestingly, phenotypic Lin−Sca1+KIT+CD41−CD48−CD150+ HSCs segregated into 2 groups (Honeg or Homed), based on degree of blood/Ho perfusion of their niche. HSCs capable of serial transplantation and long-term bromodeoxyuridine label retention were enriched in Honeg HSCs, whereas Homed HSCs cycled more frequently and only reconstituted a single host. This suggests that the most potent HSC niches are enriched in locally secreted factors and low oxygen tension due to negligible blood flow. Importantly, blood perfusion of niches correlates better with HSC function than absolute distance from vasculature. This technique enables prospective isolation of serially reconstituting HSCs distinct from other less potent HSCs of the same phenotype, based on the in vivo niche in which they reside.

NEW INSIGHTS INTO THE CONTROL OF HUMAN MUSCLE BLOOD FLOW AND METABOLISM STUDIED IN VIVO

1995 ◽  
Vol 27 (Supplement) ◽  
pp. S63
Author(s):  
R. S. Richardson ◽  
B. Saltin ◽  
J. Bangsbo ◽  
T. Graham ◽  
L. B. Rowell
Keyword(s):  
Blood Flow ◽  
Muscle Blood Flow ◽  
Human Muscle

scholarly journals Absence of Flow-Mediated Vasodilation in the Rabbit Femoral Artery

2010 ◽  
pp. 331-338
Author(s):  
P S Clifford ◽  
J A Madden ◽  
J J Hamann ◽  
J B Buckwalter ◽  
Z Valic
Keyword(s):  
Blood Flow ◽  
Femoral Artery ◽  
Outer Diameter ◽  
Solution Ph ◽  
Physiological Range ◽  
In Vivo Experiments ◽  
Exercise Hyperemia ◽  
Femoral Artery Blood Flow ◽  
Flow Mediated Vasodilation

The purpose of this study was to determine if there is flowmediated vasodilation of the femoral artery in response to progressive increases in flow within a physiological range observed in the in vivo experiments. Femoral artery blood flow was determined in conscious rabbits (n=5) using chronically implanted flowprobes. Resting blood flow was 8.3±0.6 ml/min and increased to 39.9±5.4 ml/min during high intensity exercise. Femoral arteries (n=12, 1705±43 µm outer diameter) harvested from a separate group of rabbits were mounted on cannulas and diameter was continuously monitored by video system. Functional integrity of the endothelium was tested with acetylcholine. The arteries were set at a transmural pressure of 100 mm Hg and preconstricted with phenylephrine to 73±3 % of initial diameter. Using a roller pump with pressure held constant, the arteries were perfused intraluminally with warmed, oxygenated Krebs' solution (pH=7.4) over a physiological range of flows up to 35 ml/min. As flow increased from 5 ml/min to 35 ml/min, diameter decreased significantly (p<0.05) from 1285±58 µm to 1100±49 µm. Thus, in vessels with a functional endothelium, increasing intraluminal flow over a physiological range of flows produced constriction, not dilation. Based on these results, it seems unlikely that flow-mediated vasodilation in the rabbit femoral artery contributes to exercise hyperemia.

scholarly journals Comparison of In Vivo Tissue Temperature Profile and Lesion Geometry for Radiofrequency Ablation with High Power-Short Duration and Moderate Power-Moderate Duration: Effects of Thermal Latency and Contact Force on Lesion Formation

2021 ◽  
Author(s):  
Hiroshi Nakagawa ◽  
Atsushi Ikeda ◽  
Tushar Sharma ◽  
Assaf Govari ◽  
John Ashton ◽  
...  
Keyword(s):  
Temperature Profile ◽  
High Power ◽  
Lesion Size ◽  
Tissue Temperature ◽  
Thigh Muscle ◽  
Muscle Preparation ◽  
Tissue Heating ◽  
Moderate Power ◽  
Rf Applications

Background - With short radiofrequency (RF) applications, tissue temperature continues to rise after RF-termination ("thermal latency"), which may result in lesion growth after RF-termination. The purpose was to compare in-vivo tissue temperature profile (thermal latency), lesion size and the incidence of steam pop and thrombus between RF-ablation with very-high-power-very-short-RF(90W/4s), high-power-short-RF(50W/10s) and moderate-power-moderate-RF(30W/30s) in a canine thigh muscle preparation and beating heart. Methods - In the thigh muscle preparation (5dogs), a 3.5mm ablation-electrode with 66 or 56 small irrigation holes (QDOT-Micro or ThermoCoolSmartTouch-SF, respectively) was held perpendicular or parallel to the muscle at 10 or 30g contact force (CF). Total of 120RFs were delivered at 90W/4s(QDOT-catheter), 50W/10s or 30W/30s(SF-catheter). Electrode temperature, electrode-tissue-interface temperature and tissue temperatures at 3mm and 7mm-depths were measured. In 6 closed-chest dogs, total of 72RFs were delivered in the ventricle at 90W/4s, 50W/10s or 30W/30s. Results - In the thigh muscle preparation, tissue temperatures and lesion size (depth, diameter and volume) were lowest/smallest for RFs at 90W/4s, followed by 50W/10s and greatest for 30W/30s. Thermal latency (Δtemperature and duration) was greatest for RFs at 90W/4s, followed by 50W/10s and smallest for 30W/30s ( p <0.01). Effective tissue heating (area under curve≥50°C at 3mm-depth) was observed after RF-termination in 88.0±7.6% with 90W/4s, 57.7±14.6% with 50W/10s, and only 31.9±8.5% with 30W/30s ( p <0.01). In beating hearts, lesion size was also smallest with 90W/4s and greatest with 30W/30s RFs. Increasing CF significantly increased lesion depth in all three groups. There was no significant difference in the incidence of steam pop or thrombus between three groups. Conclusions - Tissue temperatures and lesion size (depth, diameter and volume) were lowest/smallest for RF-applications at 90W/4s, followed by 50W/10s and greatest for 30W/30s. The greater thermal latency for 90W/4s RF-applications suggests that a significant portion of lesion is created after RF-termination due to conductive tissue heating.

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