scholarly journals The Importance of Vascular Elasticity in the Circulatory System of the Cephalopod Octopus Vulgaris

1990 ◽  
Vol 152 (1) ◽  
pp. 471-484
Author(s):  
R. E. SHADWICK ◽  
E. K. NILSSON
Keyword(s):  
Pressure Wave ◽  
Vena Cava ◽  
Circulatory System ◽  
Octopus Vulgaris ◽  
Arterial Tree ◽  
Windkessel Model ◽  
Arterial Circulation ◽  
Vascular Impedance ◽  
Elastic Reservoir

The passive mechanical properties of the dorsal aorta and the vena cava of Octopus vulgaris were investigated in vitro. Both vessels are highly distensible structures that exhibit non-linear elasticity, but have substantially different material properties. The volume compliance of each vessel is maximal within the resting physiological pressure range (2–3 kPa in the aorta and 0–0.5 kPa in the vena cava) but is five times greater in the vena cava than in the aorta. The aorta is mechanically suited to function as an elastic storage reservoir in the arterial circulation, while the vena cava is appropriately designed to be a low-pressure capacitance element. Pressure wave velocity in the aorta was calculated from the elastic modulus to be 1.8 ms−1 under resting conditions. Therefore, pressure changes will occur almost simultaneously throughout the arterial tree and pressure wave transmission properties can be described by a two-element Windkessel model. Predictions of vascular impedance amplitude made from this model are presented. The effectiveness of the aorta as an elastic reservoir appears to be severely reduced during exercise in Octopus. Because blood pressure increases while heart rate does not, the efficiency of the Windkessel will be diminished as the time constant of the system decreases and the pulsatile work of the heart subsequently increases. Note: Address for reprint requests.

Tuning of pulmonary arterial circulation evidenced by MR phase mapping in healthy volunteers

2001 ◽  
Vol 90 (2) ◽  
pp. 469-474 ◽  
Author(s):  
Eric Laffon ◽  
Virginie Bernard ◽  
Michel Montaudon ◽  
Roger Marthan ◽  
Jean-Louis Barat ◽  
...  
Keyword(s):  
Healthy Volunteers ◽  
Pressure Wave ◽  
Main Pulmonary Artery ◽  
Cross Sectional ◽  
Arterial Circulation ◽  
Vascular Impedance ◽  
Pulmonary Arterial ◽  
Phase Mapping ◽  
The Right

Magnetic resonance (MR) phase mapping was used to noninvasively assess both blood flow and cross-sectional area (CSA) in the main pulmonary artery (MPA) of 12 healthy volunteers. Flow and CSA patterns exhibited two positive peaks: high systolic and small diastolic. This finding can be explained using a simple “distributed” theoretical model that takes into account the role of a reflected pressure wave from pulmonary vascular impedance in generating a diastolic flow. The mean reflection coefficient of pressure wave, MPA input impedance, and pulmonary vascular impedance were assessed. We verified, in this series, that pressure wave velocity appears to be age-dependent. MR phase mapping has been used to observe the tuning (resonance) of the right cardiovascular system at rest under physiological conditions. MR phase mapping could be used to assess pathological modifications of the tuning that occurs in cases of pulmonary arterial hypertension.

Assessment of Aortic Graft Impact on Hemodynamics

2011 ◽  
Author(s):  
Orestis Vardoulis ◽  
Eline Coppens ◽  
Bryn Martin ◽  
Philippe Reymond ◽  
Nikos Stergiopulos
Keyword(s):  
Reflection Coefficient ◽  
Pressure Wave ◽  
Wave Reflection ◽  
Characteristic Impedance ◽  
Physiological Mechanism ◽  
In Vivo Studies ◽  
In Vitro Tests ◽  
Aortic Graft ◽  
Arterial Tree

In vivo studies have revealed that aortic grafts augment heart load and alter blood pressure and flow waveforms [1]. A one-dimensional model of the arterial tree was developed in order to analyze the different mechanisms by which proximal and distal aortic grafts affect hemodynamics. Graft compliance and properties were based on in vitro tests. Predicted pressures at the aortic root were compared for the control, proximal and distal graft case. Pulse pressure increased by 21% and 10% in presence of a proximal and distal graft, respectively. The distal graft resulted in a wave reflection coefficient of 0.62 while for the proximal graft the wave reflection coefficient was 0.46. The physiological mechanism behind the rise of pressure is dual and it is critically affected by the graft’s compliance and position. In case of a proximal graft, the primary reason for aortic pressure increase is the augmentation of aortic characteristic impedance, which augments the forward running pressure wave, while for the distal graft the wave reflections are major contributors to the total pressure wave. Overall, the proximal graft altered hemodynamics to a greater extent than a distal aortic graft.

The effects of extracts from neurosecretory cells in the anterior vena cava and pharyngo-ophthalmic vein upon the hearts of intact free-moving octopuses

1980 ◽  
Vol 84 (1) ◽  
pp. 319-334
Author(s):  
M. J. Wells ◽  
K. Mangold
Keyword(s):  
Vena Cava ◽  
Neurosecretory Cells ◽  
Octopus Vulgaris ◽  
Release Point ◽  
Branchial Heart ◽  
Cardiac Regulation ◽  
Branchial Vessel ◽  
Normal Performance

Recordings of pressure and frequency were made from the hearts of free-moving Octopus vulgaris. The effects of extracts from neurosecretory endings in the anterior vena cava (AVC) and the pharyngo-ophthalmic vein (POV), injected through fine cannulae into a branchial heart, efferent branchial vessel or the dorsal aorta, were studied and compared with the effects of acetylcholine, 5-hydroxytryptamine, adrenaline, histamine and tyramine. AVC and POV extracts each produce a different spectrum of effects, unlike those of any of the drugs tested. AVC extract is effective at doses of less than 2% of the material extractable from a single vein per kg, increasing the force and amplitude of the heartbeats. With a natural release point just upstream of the branchial hearts the AVC material must be relevant to the normal performance of the hearts. POV extract is effective only at doses equivalent to several veins per kg, and is unlikely to have a role in cardiac regulation. Section of the visceral nerves did not affect the action of drugs or extracts, indicating that effects were not indirectly mediated via the CNA. Further experiments were made with hearts and the aorta in vitro with effects that did not always parallel those found in vivo. Reasons for these differences are discussed.

The Effect of Pentosan Polysulphate (SP54) on the Fibrinolytic Enzyme System - A Human Volunteer and Experimental Animal Study

1985 ◽  
Vol 54 (04) ◽  
pp. 833-837 ◽  
Author(s):  
N A Marsh ◽  
P M Peyser ◽  
L J Creighton ◽  
M Mahmoud ◽  
P J Gaffney
Keyword(s):  
Plasminogen Activator ◽  
Surface Effect ◽  
Ex Vivo ◽  
Vena Cava ◽  
Tissue Type ◽  
Similar Response ◽  
Small Contribution ◽  
Thrombosis Model ◽  
Pentosan Polysulphate

SummaryPentosan polysulphate causes an increase in plasminogen activator activity in plasma both after oral ingestion and after subcutaneous injection. The effect is greatest after 3 h and has disappeared by 6 h. Repeat doses by mouth over 5 days elicit a similar response. The recorded increase in activity is due largely to the release of tissue-type plasminogen activator (tPA) from the endothelium according to the antigen assay although there could be a small contribution from Factor XH-related “intrinsic” fibrinolysis induced in vitro. SP54 enhances activity ex vivo by a non-specific surface effect, and this phenomenon may contribute the increased levels of activity seen in vitro. Administration of SP54 to animals elicits a similar increase in activator activity, the intramuscular route being slightly more effective. Results with an inferior vena cava thrombosis model in the rat suggest that pentosan polysulphate may induce a thrombolytic effect.

scholarly journals A modular microfluidic system based on a multilayered configuration to generate large-scale perfusable microvascular networks

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Tao Yue ◽  
Da Zhao ◽  
Duc T. T. Phan ◽  
Xiaolin Wang ◽  
Joshua Jonghyun Park ◽  
...  
Keyword(s):  
Large Scale ◽  
Circulatory System ◽  
Vertical Direction ◽  
Microfluidic System ◽  
Vital Role ◽  
Microvascular Networks ◽  
Biological Studies ◽  
Wide Range ◽  
High Flexibility

AbstractThe vascular network of the circulatory system plays a vital role in maintaining homeostasis in the human body. In this paper, a novel modular microfluidic system with a vertical two-layered configuration is developed to generate large-scale perfused microvascular networks in vitro. The two-layer polydimethylsiloxane (PDMS) configuration allows the tissue chambers and medium channels not only to be designed and fabricated independently but also to be aligned and bonded accordingly. This method can produce a modular microfluidic system that has high flexibility and scalability to design an integrated platform with multiple perfused vascularized tissues with high densities. The medium channel was designed with a rhombic shape and fabricated to be semiclosed to form a capillary burst valve in the vertical direction, serving as the interface between the medium channels and tissue chambers. Angiogenesis and anastomosis at the vertical interface were successfully achieved by using different combinations of tissue chambers and medium channels. Various large-scale microvascular networks were generated and quantified in terms of vessel length and density. Minimal leakage of the perfused 70-kDa FITC-dextran confirmed the lumenization of the microvascular networks and the formation of tight vertical interconnections between the microvascular networks and medium channels in different structural layers. This platform enables the culturing of interconnected, large-scale perfused vascularized tissue networks with high density and scalability for a wide range of multiorgan-on-a-chip applications, including basic biological studies and drug screening.

scholarly journals Effect of cannulation site on emboli travel during cardiac surgery

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Mira Puthettu ◽  
Stijn Vandenberghe ◽  
Stefanos Demertzis
Keyword(s):  
Cardiac Surgery ◽  
In Vitro Study ◽  
Blood Stream ◽  
Air Bubbles ◽  
Arterial Tree ◽  
Air Bubble ◽  
Cannulation Site ◽  
The Brain

Abstract Background During cardiac surgery, micro-air emboli regularly enter the blood stream and can cause cognitive impairment or stroke. It is not clearly understood whether the most threatening air emboli are generated by the heart-lung machine (HLM) or by the blood-air contact when opening the heart. We performed an in vitro study to assess, for the two sources, air emboli distribution in the arterial tree, especially in the brain region, during cardiac surgery with different cannulation sites. Methods A model of the arterial tree was 3D printed and included in a hydraulic circuit, divided such that flow going to the brain was separated from the rest of the circuit. Air micro-emboli were injected either in the HLM (“ECC Bubbles”) or in the mock left ventricle (“Heart Bubbles”) to simulate the two sources. Emboli distribution was measured with an ultrasonic bubble counter. Five repetitions were performed for each combination of injection site and cannulation site, where air bubble counts and volumes were recorded. Air bubbles were separated in three categories based on size. Results For both injection sites, it was possible to identify statistically significant differences between cannulation sites. For ECC Bubbles, axillary cannulation led to a higher amount of air bubbles in the brain with medium-sized bubbles. For Heart Bubbles, aortic cannulation showed a significantly bigger embolic load in the brain with large bubbles. Conclusions These preliminary in vitro findings showed that air embolic load in the brain may be dependent on the cannulation site, which deserves further in vivo exploration.

In Vitro Evaluation of Capturing and Dissolving the Clot by Magnetic Nanoparticles Carrying a Thrombolytic Agents Instead of Temporary Inferior Vena Cava (IVC) Filter

2020 ◽  
Vol 16 (11) ◽  
pp. 1623-1632
Author(s):  
Abbas Moghanizadeh ◽  
Fakhreddin Ashrafizadeh ◽  
Jaleh Varshousaz ◽  
Mahshid Kharaziha
Keyword(s):  
Magnetic Field ◽  
Magnetic Nanoparticles ◽  
Vena Cava ◽  
Simple Method ◽  
Thrombolytic Agents ◽  
Blood Clots ◽  
Life Threatening ◽  
The Magnetic Field ◽  
Different Levels

This study aims to evaluate the efficiency of a novel in vitro technique in clot capturing and dissolving them by applying magnetic force on magnetic nanoparticles (MNP) carrying thrombolytic agents. It is a quick and simple method to protect patients from a life-threatening pulmonary embolism in an emergency to provide time for the medical team. To analyze the in vitro efficiency of nano-magnetic capturing and dissolving of clots (NCDC), different levels of process parameter including strength magnetic field (0.1, 0.2 and 0.3 T) and fluid flow rate (2.5, 5 and 7 l/min) are exposed to different blood clots sizes from 5 × 10 to 20 × 10 mm2 (length × diameter), in an in vitro flow model. The results show that by increasing the parameters to their maximum values, it is possible to immobilize 100% of the clots and dissolve around 61.4% of clots weight. In addition, the clot-dissolving is directly proportional to the magnetic field strength. NCDC is an efficient technique in immobilizing and dissolving the clots and its efficiency depends on process parameters especially the magnetic field.

Nervous control of the heartbeat in octopus

1980 ◽  
Vol 85 (1) ◽  
pp. 111-128 ◽  
Author(s):  
M. J. Wells
Keyword(s):  
Circulatory System ◽  
Aortic Pressure ◽  
Surgical Removal ◽  
Cardiac Ganglion ◽  
Nervous Control ◽  
Cardiac Ganglia ◽  
Before And After ◽  
Branchial Heart ◽  
Systemic Heart

The circulatory system of cephalopods is based on a trio of hearts, with two pairs of associated ganglia linked to the CNS by a pair of visceral nerves. The beat of the hearts was recorded from free-moving octopuses before and after surgical removal or disconnexion of elements of the nervous system. Severing the visceral nerves does not stop the hearts, which continue to beat in a powerful well co-ordinated manner in isolation from the CNS. The nerves seem to be concerned in raising the cardiac output in exercise, and with stopping the hearts when mantle movements cease, but they are not necessary for the initiation of maintenance of the normal rhythm. Removal of the fusiform ganglia severs all nervous connexions between the ywo gill hearts, and deprives the systemic heart of its nerve supply. The trio of hearts continues to beat as strongly as before. Removal or disconnexion of a cardiac ganglion disrupts the beat of the corresponding gill heart which now tends to contract in an ill-coordinated and rather feeble manner, though at much the same frequency as before; with both cardiacs gone the systemic heart, which contracts only when it is filled, tends to drop in frequency and the mean aortic pressure falls. The system remains rhythmic, however, and the beat may recover, to the point where aortic pressures and frequencies approach those found in intact animals at rest; even octopuses with both fusiform and both cardiac ganglia removed can survive for many hours. From the performance of the isolated branchial heart, the existence of a pulsating vesicle in each cardiac ganglion, the effects of cardiac ganglion removal and the remarkable steadiness of heartbeat frequency shown by intact animals under a variety of conditions, it is argued that the heartbeat rhythm is normally controlled by pacemakers in the branchial heart/ cardiac ganglion complexes, and perhaps, in intact animals, from within the cardiac ganglia themselves. The picture of the control of the heartbeat that emerges from the study of free moving essentially intact animals is quite different from that arising from in vitro and acute preparation studies. It suggests that the conventional wisdom about the control of the heartbeat in cephalopods (and perhaps by implication, in other molluscs) may need to be considerably revised.

Abstract 34: Endogenous Superoxide Dismutase Protects From Impaired Generation of Activated Protein C and Enhanced Susceptibility to Experimental Thrombosis in Mice

2014 ◽  
Vol 34 (suppl_1) ◽  
Author(s):  
Sanjana Dayal ◽  
Sean X Gu ◽  
Katinan M Wilson ◽  
Ryan Hutchins ◽  
Steven R Lentz
Keyword(s):  
Superoxide Dismutase ◽  
Protein C ◽  
Activated Protein C ◽  
Vena Cava ◽  
Oxidative Modification ◽  
Mrna Levels ◽  
Endothelial Protein C Receptor ◽  
Experimental Thrombosis

In vitro studies have suggested that reactive oxygen species such as superoxide can produce prothrombotic effects, including enhanced platelet activation, increased tissue factor (TF) expression, and an oxidative modification in thrombomodulin impairing its capacity to enhance the generation of activated protein C (APC) by thrombin. It is not known, however, if elevated levels of superoxide accelerate susceptibility to experimental thrombosis in vivo . We used mice genetically deficient in superoxide dismutase-1 (SOD1, an antioxidant enzyme that dismutates superoxide to hydrogen peroxide), to test the hypothesis that lack of SOD1 enhances susceptibility to thrombosis. Susceptibility to carotid artery thrombosis in a photochemical injury model demonstrated that Sod1-/- mice formed stable occlusions significantly faster than Sod1+/+ mice (P<0.05). In an inferior vena cava (IVC) stasis model Sod1- /- mice developed significantly larger thrombi 48 hours after IVC ligation (P<0.05 vs. Sod1+/+ mice). After activation with thrombin (0.5 U/ml) or convulxin (200 ng/ml), no differences in surface expression of P-selectin or binding of fibrinogen were observed between platelets from Sod1-/- and Sod1+/+ mice. The expression of TF mRNA in lung measured by real time qPCR showed similar levels in Sod1-/- and Sod1 +/+ mice. However, the activation of exogenous protein C by thrombin in lung homogenates was decreased in Sod1 -/- mice (P<0.05 vs. Sod1 +/+ mice). Further, in vivo generation of activated protein C in response to thrombin (40 U/Kg) infusion was significantly lower in Sod1-/- mice (P<0.05 vs. Sod1+/+ mice). No differences in mRNA levels for thrombomodulin or endothelial protein C receptor were detected in Sod1 -/- mice vs. Sod1 +/+ mice, suggesting that altered generation of activated protein C in Sod1-/- mice may be related to a direct oxidative effect on thrombomodulin. In accordance, thrombomodulin treated with xanthine/hypoxanthine showed 40% loss of ability to activate protein C that was overcome by addition of SOD and catalase (P<0.05). We conclude that endogenous SOD1 in mice protects from impaired generation of activated protein C and accelerated thrombosis.

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