This document discusses blood flow and its properties. It covers topics like cardiovascular physiology, the physical properties of blood including viscosity, steady and oscillatory blood flow models like Poiseuille flow and the Windkessel model. It discusses concepts like entrance length, application of Bernoulli's equation, vascular resistance and branching effects. Unsteady flow models like the Wommersley equations are also covered. The goal is to understand blood flow to improve medical devices and understand cardiovascular disease development.
This document discusses the components and function of the cardiovascular system. It describes the main parts of the circulatory system including arteries, arterioles, capillaries, venules and veins. It explains how blood flows through vessels, defining concepts like blood flow, velocity, resistance and hemodynamics. Key factors that affect blood flow dynamics are vessel size, blood viscosity, resistance and vessel elasticity. Equations are provided for calculating velocity and blood flow based on factors like pressure gradient and resistance.
Baroreceptors And Negative Feedback MechanismSulav Shrestha
Baroreceptors are mechanoreceptors located in the carotid arteries and aorta that detect changes in blood pressure. As part of a negative feedback system called the baroreflex, baroreceptors send signals to the brain to increase or decrease heart rate and vascular resistance to maintain normal blood pressure. When blood pressure rises, baroreceptors inhibit the vasomotor center of the brain to decrease sympathetic nervous system activity and lower blood pressure. Conversely, lower blood pressure activates the vasomotor center to increase sympathetic activity and raise blood pressure. In addition to short term regulation, baroreceptors can reset over days to the new blood pressure level in cases of chronic high blood pressure.
This document discusses the regulation of arterial blood pressure. It defines terms related to blood pressure and lists factors that can cause physiological variations. The determinants of arterial blood pressure are cardiac output and total peripheral resistance. Blood pressure is regulated through short, intermediate, and long-term control mechanisms involving the nervous system, kidneys, hormones, and local factors. The baroreceptor and renin-angiotensin systems help maintain normal blood pressure levels.
The document discusses key concepts in cardiovascular physiology including:
1. Hemodynamic parameters such as blood flow, pressure, pressure gradient, vessel diameter, blood velocity, and peripheral resistance and how they are interrelated.
2. Physical laws governing blood flow including Bernoulli's principle, Poiseuille's law, and Ohm's law and how they describe the relationship between flow, pressure, resistance, and vessel geometry.
3. Factors that determine blood flow and resistance including viscosity, vessel length, radius and the "fourth power law".
The cardiac cycle describes the sequence of events that occur with each heartbeat. It involves mechanical, electrical, and pressure changes in the heart. The cycle begins with ventricular relaxation and atrial filling in diastole. Upon electrical stimulation, the ventricles contract in systole to pump blood out of the heart. This is accompanied by characteristic pressure and volume changes in the chambers as well as events on an electrocardiogram like the P, QRS, and T waves. The cycle repeats with each heartbeat to sustain blood circulation.
This document discusses the regulation of blood pressure on short, intermediate, and long term timescales.
Short term regulation occurs over seconds to minutes and involves baroreceptors, chemoreceptors, and the central nervous system ischemic response. Intermediate regulation over minutes to hours is mediated by capillary fluid shifts and stress relaxation in blood vessels. Long term regulation over days to years involves the renal body fluid mechanism and renin-angiotensin system to control extracellular fluid levels and blood pressure.
Cardiac output is defined as the volume of blood pumped by the heart each minute and is regulated intrinsically by factors affecting preload and afterload as well as extrinsically by the autonomic nervous system and hormones. Venous return is a primary extrinsic regulator of cardiac output, increasing stretch of cardiac muscles and stimulating an increase in heart rate. A combination of preload, contractility, afterload and heart rate determine cardiac output under normal resting conditions and during physical activity.
This document discusses the components and function of the cardiovascular system. It describes the main parts of the circulatory system including arteries, arterioles, capillaries, venules and veins. It explains how blood flows through vessels, defining concepts like blood flow, velocity, resistance and hemodynamics. Key factors that affect blood flow dynamics are vessel size, blood viscosity, resistance and vessel elasticity. Equations are provided for calculating velocity and blood flow based on factors like pressure gradient and resistance.
Baroreceptors And Negative Feedback MechanismSulav Shrestha
Baroreceptors are mechanoreceptors located in the carotid arteries and aorta that detect changes in blood pressure. As part of a negative feedback system called the baroreflex, baroreceptors send signals to the brain to increase or decrease heart rate and vascular resistance to maintain normal blood pressure. When blood pressure rises, baroreceptors inhibit the vasomotor center of the brain to decrease sympathetic nervous system activity and lower blood pressure. Conversely, lower blood pressure activates the vasomotor center to increase sympathetic activity and raise blood pressure. In addition to short term regulation, baroreceptors can reset over days to the new blood pressure level in cases of chronic high blood pressure.
This document discusses the regulation of arterial blood pressure. It defines terms related to blood pressure and lists factors that can cause physiological variations. The determinants of arterial blood pressure are cardiac output and total peripheral resistance. Blood pressure is regulated through short, intermediate, and long-term control mechanisms involving the nervous system, kidneys, hormones, and local factors. The baroreceptor and renin-angiotensin systems help maintain normal blood pressure levels.
The document discusses key concepts in cardiovascular physiology including:
1. Hemodynamic parameters such as blood flow, pressure, pressure gradient, vessel diameter, blood velocity, and peripheral resistance and how they are interrelated.
2. Physical laws governing blood flow including Bernoulli's principle, Poiseuille's law, and Ohm's law and how they describe the relationship between flow, pressure, resistance, and vessel geometry.
3. Factors that determine blood flow and resistance including viscosity, vessel length, radius and the "fourth power law".
The cardiac cycle describes the sequence of events that occur with each heartbeat. It involves mechanical, electrical, and pressure changes in the heart. The cycle begins with ventricular relaxation and atrial filling in diastole. Upon electrical stimulation, the ventricles contract in systole to pump blood out of the heart. This is accompanied by characteristic pressure and volume changes in the chambers as well as events on an electrocardiogram like the P, QRS, and T waves. The cycle repeats with each heartbeat to sustain blood circulation.
This document discusses the regulation of blood pressure on short, intermediate, and long term timescales.
Short term regulation occurs over seconds to minutes and involves baroreceptors, chemoreceptors, and the central nervous system ischemic response. Intermediate regulation over minutes to hours is mediated by capillary fluid shifts and stress relaxation in blood vessels. Long term regulation over days to years involves the renal body fluid mechanism and renin-angiotensin system to control extracellular fluid levels and blood pressure.
Cardiac output is defined as the volume of blood pumped by the heart each minute and is regulated intrinsically by factors affecting preload and afterload as well as extrinsically by the autonomic nervous system and hormones. Venous return is a primary extrinsic regulator of cardiac output, increasing stretch of cardiac muscles and stimulating an increase in heart rate. A combination of preload, contractility, afterload and heart rate determine cardiac output under normal resting conditions and during physical activity.
1. The document discusses hemodynamic factors like pressure, blood flow, resistance, and compliance and their interrelationships.
2. It defines terms like blood pressure, blood flow, resistance, compliance, laminar and turbulent blood flow. It also discusses how changes in vessel diameter affect resistance and flow.
3. The document compares arterial and venous compliance, noting that veins are more compliant and act as reservoirs due to their thin walls, storing over 60% of the blood volume.
Cardiac action potentials arise from the coordinated movement of ions through membrane channels in cardiac cells. The cardiac action potential has 5 phases: rapid upstroke (phase 0) due to sodium influx, early rapid repolarization (phase 1) mediated by potassium currents, plateau phase (phase 2) maintained by calcium and potassium currents, final rapid repolarization (phase 3) due to potassium currents, and resting phase (phase 4) where the cell prepares for the next action potential. Precisely regulated ion channel function underlies the generation and propagation of action potentials and ensures normal cardiac rhythm.
The document discusses the structure and function of chemical synapses. It begins by defining a synapse as the junction between two nerve cells. It then describes the key anatomical components of a chemical synapse, including the presynaptic knob, synaptic cleft, and postsynaptic membrane. It explains the process of neurotransmission, including the release of neurotransmitters into the synaptic cleft, their binding to receptors on the postsynaptic membrane, and the resulting postsynaptic potentials. The document also discusses inhibition at synapses, the properties of synaptic transmission, and examples of neurotransmitters.
The cardiac cycle begins with the spontaneous generation of an action potential in the sinus node which triggers contractions that move through the heart. It consists of systole, where the heart contracts to pump blood, and diastole, where the heart relaxes and refills with blood. Each cycle takes approximately 0.8 seconds and involves coordinated opening and closing of valves between the atria and ventricles and between the ventricles and arteries. Pressure and volume curves change dynamically throughout the cycle as the heart contracts and relaxes, pumping blood through the body.
Cardiac muscle cells have characteristics that allow the heart to contract rhythmically and conduct electrical impulses throughout. Key properties include automaticity which allows the cells to spontaneously depolarize without external stimulation, rhythmicity which enables contraction at regular intervals, excitability to respond to electrical signals, and conductivity to propagate the signals. The refractory period after contraction is longer for cardiac muscle than skeletal muscle. Electrical conduction is faster through specialized fibers but slower in nodal pathways due to fewer connections between cells.
Tunica Interna – innermost endothelium of simple squamous epithelium + basement membrane
Arteries – have an “internal elastic lamina” of elastic CT to allow for expansion under pressure
Veins – may have “valves” (folds of endothelium + CT) to prevent backflow of blood due to low pressure Microscopic, very thin-walled vessels comprised of endothelium with basement membrane; allows for filtration and reabsorption Found in all tissues of the body except for those that are “avascular” Usually form branching networks (“capillary beds”) within tissues for increased surface area blood flow into capillaries may be regulated by “pre- capillary sphincters” may have a central or “thoroughfare” channel that provides direct connection between “metarteriole” (terminal end of arteriole) & venule
The document discusses countercurrent exchange systems in various organs and tissues of the body including the kidney. It describes how the countercurrent multiplier system in the loop of Henle establishes a gradient that is maintained by the countercurrent exchanger system of the vasa recta, allowing the kidney to produce concentrated urine through the medullary countercurrent system. It also discusses how diuretics work by targeting different sites along the nephron to increase urine output.
The conducting system of the heart consists of specialized cardiac muscle tissue that generates and transmits electrical impulses to initiate and coordinate heart muscle contraction. It includes the sinoatrial node, atrioventricular node, bundle of His, Purkinje fibers and their left and right branches. These structures work together to conduct electrical signals from the upper to lower chambers and allow synchronized, rhythmic pumping of blood throughout the body. Damage to parts of this system can lead to arrhythmias or require treatment like artificial pacemakers.
Normal arterial blood pressure ranges from 90-140/60-90 mmHg. Systolic pressure is the maximum pressure when blood is ejected from the heart, while diastolic is the minimum pressure when the heart is resting between beats. Mean arterial pressure, which averages 93 mmHg, is the main driving force for blood flow. Blood pressure is regulated through short term mechanisms like baroreceptor and chemoreceptor reflexes which control heart rate and vascular tone, and long term factors like blood volume and vessel elasticity. Strict control of blood pressure is important to ensure adequate blood flow to vital organs.
Cardiac cycle refers to a complete heartbeat from its generation to the beginning of the next beat.
Cardiac events that occur from –
beginning of one heart beat to the beginning of the next are called the cardiac cycle.
The document provides an overview of cardiovascular physiology, including:
- The cardiovascular system functions to circulate blood throughout the body, transporting oxygen, nutrients, hormones, and removing waste.
- The heart is the central organ that pumps blood through two main circulations - pulmonary circulation to the lungs and systemic circulation to the rest of the body.
- The functional anatomy of the heart includes four chambers, cardiac muscle tissue, valves that ensure one-way blood flow, and a conducting system that coordinates contractions.
The document discusses lung elastance, compliance, and work of breathing. It defines key terms like elastance, compliance, and surface tension. It describes the elastance of the thoracic cage and lungs, the role of pulmonary surfactant in reducing surface tension, and how compliance is measured. It also explains the different components of work of breathing, including overcoming elastic, viscous, and airway resistance, and how work of breathing is affected in restrictive and obstructive lung diseases.
The document discusses capillary function and structure. It notes that capillaries are the smallest blood vessels, connecting arterioles and venules. They allow for exchange of water, gases, nutrients, and waste through diffusion, filtration, and active transport. Capillaries come in three types - continuous, fenestrated, and sinusoidal - depending on the thickness of their endothelial lining and presence of gaps or pores to facilitate exchange. Tight junctions between endothelial cells help control permeability at different capillary beds.
ACTION POTENTIAL - IONIC BASIS AND RECORDINGAnu Priya
The document discusses the ionic basis and recording of action potentials. It begins with an introduction to excitable tissues and how they generate electrical signals. It then covers the history of discoveries in this area including Galvani's work in the 18th century and seminal contributions from Hodgkin, Huxley, Eccles and Neher and Sakmann who won the Nobel Prize. The document discusses the resting membrane potential and how it is maintained, as well as graded and action potentials. It details the ionic basis of the action potential involving sodium, potassium and other ion channels. Finally, it addresses recording techniques, types of action potentials, and some applied aspects and clinical correlates.
DETERMINANTS AND FACTORS AFFECTING CARDIAC OUTPUTakash chauhan
This document discusses the determinants and factors affecting cardiac output. It defines cardiac output as the volume of blood pumped by the heart each minute, which is determined by stroke volume and heart rate. Ejection fraction is explained as the fraction of blood ejected from the ventricles with each heartbeat. Cardiac output can vary due to physiological factors like age, sex, exercise, and pathological factors like fever or shock. Cardiac output is maintained by four main factors - venous return, force of contraction, heart rate, and peripheral resistance. Venous return depends on respiratory pumping, muscle pumping, gravity, and venous pressure.
This document discusses the physiology of the heart. It begins by describing the different types of cardiac muscle and how cardiac muscle cells are interconnected. It then covers the cardiac cycle, including diastole and systole. Action potentials in cardiac muscle are longer than in skeletal muscle due to slow calcium channels. Contraction is triggered by calcium release from the sarcoplasmic reticulum and extracellular fluids. The heart pumps in two stages - the atria prime the ventricles, then the ventricles eject blood. Various waves in pressures, ECG, and sounds are related to the different cardiac cycle events.
William Harvey was the first modern physiologist in the 16th century. He proved that blood circulates in a continuous loop from the heart to the arteries and back to the veins and heart, overturning the long-held Galenic view of two separate circulatory systems. The circulatory system consists of arteries, which carry blood away from the heart; capillaries, where gas and nutrient exchange occurs; and veins, which carry blood back to the heart. Arteries have thicker muscular walls than veins and carry oxygenated blood except in the pulmonary circulation.
The cardiac cycle consists of systole and diastole. During systole, the heart contracts and pumps blood, while during diastole the heart relaxes and fills with blood. The cycle takes approximately 0.8 seconds and is initiated by the sinoatrial node firing an electrical impulse. Key events in the cycle include atrial systole, isovolumic contraction, rapid ejection, slow ejection, isovolumic relaxation, and rapid and slow ventricular filling. Diseases associated with abnormalities in the cardiac cycle include angina, congestive heart failure, myocardial infarction, and valve disorders like mitral stenosis.
This document discusses the conduction system of the heart, including:
1. The key components of the conduction system are the sinoatrial node, atrioventricular node, bundle of His, and Purkinje fibers which coordinate the contraction of the atria and ventricles.
2. The sinoatrial node initiates the heartbeat and spreads impulse through the internodal pathways and Bachman's bundle to the atria.
3. The atrioventricular node receives impulses and spreads them through the bundle of His to the Purkinje fibers which rapidly conduct throughout the ventricles.
The document discusses capillary circulation and microcirculation. It covers the structure of capillaries including their thin endothelial cell walls allowing for exchange of nutrients, wastes, and fluid. It describes the Starling forces that govern fluid filtration and exchange between blood and tissues, including capillary pressure, plasma and interstitial fluid oncotic pressures, and other factors. It also discusses edema, the accumulation of excess fluid in tissues, which can occur intracellularly or extracellularly due to various causes that impact capillary permeability or lymph flow.
Goodbye Windows 11: Make Way for Nitrux Linux 3.5.0!SOFTTECHHUB
As the digital landscape continually evolves, operating systems play a critical role in shaping user experiences and productivity. The launch of Nitrux Linux 3.5.0 marks a significant milestone, offering a robust alternative to traditional systems such as Windows 11. This article delves into the essence of Nitrux Linux 3.5.0, exploring its unique features, advantages, and how it stands as a compelling choice for both casual users and tech enthusiasts.
Let's Integrate MuleSoft RPA, COMPOSER, APM with AWS IDP along with Slackshyamraj55
Discover the seamless integration of RPA (Robotic Process Automation), COMPOSER, and APM with AWS IDP enhanced with Slack notifications. Explore how these technologies converge to streamline workflows, optimize performance, and ensure secure access, all while leveraging the power of AWS IDP and real-time communication via Slack notifications.
1. The document discusses hemodynamic factors like pressure, blood flow, resistance, and compliance and their interrelationships.
2. It defines terms like blood pressure, blood flow, resistance, compliance, laminar and turbulent blood flow. It also discusses how changes in vessel diameter affect resistance and flow.
3. The document compares arterial and venous compliance, noting that veins are more compliant and act as reservoirs due to their thin walls, storing over 60% of the blood volume.
Cardiac action potentials arise from the coordinated movement of ions through membrane channels in cardiac cells. The cardiac action potential has 5 phases: rapid upstroke (phase 0) due to sodium influx, early rapid repolarization (phase 1) mediated by potassium currents, plateau phase (phase 2) maintained by calcium and potassium currents, final rapid repolarization (phase 3) due to potassium currents, and resting phase (phase 4) where the cell prepares for the next action potential. Precisely regulated ion channel function underlies the generation and propagation of action potentials and ensures normal cardiac rhythm.
The document discusses the structure and function of chemical synapses. It begins by defining a synapse as the junction between two nerve cells. It then describes the key anatomical components of a chemical synapse, including the presynaptic knob, synaptic cleft, and postsynaptic membrane. It explains the process of neurotransmission, including the release of neurotransmitters into the synaptic cleft, their binding to receptors on the postsynaptic membrane, and the resulting postsynaptic potentials. The document also discusses inhibition at synapses, the properties of synaptic transmission, and examples of neurotransmitters.
The cardiac cycle begins with the spontaneous generation of an action potential in the sinus node which triggers contractions that move through the heart. It consists of systole, where the heart contracts to pump blood, and diastole, where the heart relaxes and refills with blood. Each cycle takes approximately 0.8 seconds and involves coordinated opening and closing of valves between the atria and ventricles and between the ventricles and arteries. Pressure and volume curves change dynamically throughout the cycle as the heart contracts and relaxes, pumping blood through the body.
Cardiac muscle cells have characteristics that allow the heart to contract rhythmically and conduct electrical impulses throughout. Key properties include automaticity which allows the cells to spontaneously depolarize without external stimulation, rhythmicity which enables contraction at regular intervals, excitability to respond to electrical signals, and conductivity to propagate the signals. The refractory period after contraction is longer for cardiac muscle than skeletal muscle. Electrical conduction is faster through specialized fibers but slower in nodal pathways due to fewer connections between cells.
Tunica Interna – innermost endothelium of simple squamous epithelium + basement membrane
Arteries – have an “internal elastic lamina” of elastic CT to allow for expansion under pressure
Veins – may have “valves” (folds of endothelium + CT) to prevent backflow of blood due to low pressure Microscopic, very thin-walled vessels comprised of endothelium with basement membrane; allows for filtration and reabsorption Found in all tissues of the body except for those that are “avascular” Usually form branching networks (“capillary beds”) within tissues for increased surface area blood flow into capillaries may be regulated by “pre- capillary sphincters” may have a central or “thoroughfare” channel that provides direct connection between “metarteriole” (terminal end of arteriole) & venule
The document discusses countercurrent exchange systems in various organs and tissues of the body including the kidney. It describes how the countercurrent multiplier system in the loop of Henle establishes a gradient that is maintained by the countercurrent exchanger system of the vasa recta, allowing the kidney to produce concentrated urine through the medullary countercurrent system. It also discusses how diuretics work by targeting different sites along the nephron to increase urine output.
The conducting system of the heart consists of specialized cardiac muscle tissue that generates and transmits electrical impulses to initiate and coordinate heart muscle contraction. It includes the sinoatrial node, atrioventricular node, bundle of His, Purkinje fibers and their left and right branches. These structures work together to conduct electrical signals from the upper to lower chambers and allow synchronized, rhythmic pumping of blood throughout the body. Damage to parts of this system can lead to arrhythmias or require treatment like artificial pacemakers.
Normal arterial blood pressure ranges from 90-140/60-90 mmHg. Systolic pressure is the maximum pressure when blood is ejected from the heart, while diastolic is the minimum pressure when the heart is resting between beats. Mean arterial pressure, which averages 93 mmHg, is the main driving force for blood flow. Blood pressure is regulated through short term mechanisms like baroreceptor and chemoreceptor reflexes which control heart rate and vascular tone, and long term factors like blood volume and vessel elasticity. Strict control of blood pressure is important to ensure adequate blood flow to vital organs.
Cardiac cycle refers to a complete heartbeat from its generation to the beginning of the next beat.
Cardiac events that occur from –
beginning of one heart beat to the beginning of the next are called the cardiac cycle.
The document provides an overview of cardiovascular physiology, including:
- The cardiovascular system functions to circulate blood throughout the body, transporting oxygen, nutrients, hormones, and removing waste.
- The heart is the central organ that pumps blood through two main circulations - pulmonary circulation to the lungs and systemic circulation to the rest of the body.
- The functional anatomy of the heart includes four chambers, cardiac muscle tissue, valves that ensure one-way blood flow, and a conducting system that coordinates contractions.
The document discusses lung elastance, compliance, and work of breathing. It defines key terms like elastance, compliance, and surface tension. It describes the elastance of the thoracic cage and lungs, the role of pulmonary surfactant in reducing surface tension, and how compliance is measured. It also explains the different components of work of breathing, including overcoming elastic, viscous, and airway resistance, and how work of breathing is affected in restrictive and obstructive lung diseases.
The document discusses capillary function and structure. It notes that capillaries are the smallest blood vessels, connecting arterioles and venules. They allow for exchange of water, gases, nutrients, and waste through diffusion, filtration, and active transport. Capillaries come in three types - continuous, fenestrated, and sinusoidal - depending on the thickness of their endothelial lining and presence of gaps or pores to facilitate exchange. Tight junctions between endothelial cells help control permeability at different capillary beds.
ACTION POTENTIAL - IONIC BASIS AND RECORDINGAnu Priya
The document discusses the ionic basis and recording of action potentials. It begins with an introduction to excitable tissues and how they generate electrical signals. It then covers the history of discoveries in this area including Galvani's work in the 18th century and seminal contributions from Hodgkin, Huxley, Eccles and Neher and Sakmann who won the Nobel Prize. The document discusses the resting membrane potential and how it is maintained, as well as graded and action potentials. It details the ionic basis of the action potential involving sodium, potassium and other ion channels. Finally, it addresses recording techniques, types of action potentials, and some applied aspects and clinical correlates.
DETERMINANTS AND FACTORS AFFECTING CARDIAC OUTPUTakash chauhan
This document discusses the determinants and factors affecting cardiac output. It defines cardiac output as the volume of blood pumped by the heart each minute, which is determined by stroke volume and heart rate. Ejection fraction is explained as the fraction of blood ejected from the ventricles with each heartbeat. Cardiac output can vary due to physiological factors like age, sex, exercise, and pathological factors like fever or shock. Cardiac output is maintained by four main factors - venous return, force of contraction, heart rate, and peripheral resistance. Venous return depends on respiratory pumping, muscle pumping, gravity, and venous pressure.
This document discusses the physiology of the heart. It begins by describing the different types of cardiac muscle and how cardiac muscle cells are interconnected. It then covers the cardiac cycle, including diastole and systole. Action potentials in cardiac muscle are longer than in skeletal muscle due to slow calcium channels. Contraction is triggered by calcium release from the sarcoplasmic reticulum and extracellular fluids. The heart pumps in two stages - the atria prime the ventricles, then the ventricles eject blood. Various waves in pressures, ECG, and sounds are related to the different cardiac cycle events.
William Harvey was the first modern physiologist in the 16th century. He proved that blood circulates in a continuous loop from the heart to the arteries and back to the veins and heart, overturning the long-held Galenic view of two separate circulatory systems. The circulatory system consists of arteries, which carry blood away from the heart; capillaries, where gas and nutrient exchange occurs; and veins, which carry blood back to the heart. Arteries have thicker muscular walls than veins and carry oxygenated blood except in the pulmonary circulation.
The cardiac cycle consists of systole and diastole. During systole, the heart contracts and pumps blood, while during diastole the heart relaxes and fills with blood. The cycle takes approximately 0.8 seconds and is initiated by the sinoatrial node firing an electrical impulse. Key events in the cycle include atrial systole, isovolumic contraction, rapid ejection, slow ejection, isovolumic relaxation, and rapid and slow ventricular filling. Diseases associated with abnormalities in the cardiac cycle include angina, congestive heart failure, myocardial infarction, and valve disorders like mitral stenosis.
This document discusses the conduction system of the heart, including:
1. The key components of the conduction system are the sinoatrial node, atrioventricular node, bundle of His, and Purkinje fibers which coordinate the contraction of the atria and ventricles.
2. The sinoatrial node initiates the heartbeat and spreads impulse through the internodal pathways and Bachman's bundle to the atria.
3. The atrioventricular node receives impulses and spreads them through the bundle of His to the Purkinje fibers which rapidly conduct throughout the ventricles.
The document discusses capillary circulation and microcirculation. It covers the structure of capillaries including their thin endothelial cell walls allowing for exchange of nutrients, wastes, and fluid. It describes the Starling forces that govern fluid filtration and exchange between blood and tissues, including capillary pressure, plasma and interstitial fluid oncotic pressures, and other factors. It also discusses edema, the accumulation of excess fluid in tissues, which can occur intracellularly or extracellularly due to various causes that impact capillary permeability or lymph flow.
Goodbye Windows 11: Make Way for Nitrux Linux 3.5.0!SOFTTECHHUB
As the digital landscape continually evolves, operating systems play a critical role in shaping user experiences and productivity. The launch of Nitrux Linux 3.5.0 marks a significant milestone, offering a robust alternative to traditional systems such as Windows 11. This article delves into the essence of Nitrux Linux 3.5.0, exploring its unique features, advantages, and how it stands as a compelling choice for both casual users and tech enthusiasts.
Let's Integrate MuleSoft RPA, COMPOSER, APM with AWS IDP along with Slackshyamraj55
Discover the seamless integration of RPA (Robotic Process Automation), COMPOSER, and APM with AWS IDP enhanced with Slack notifications. Explore how these technologies converge to streamline workflows, optimize performance, and ensure secure access, all while leveraging the power of AWS IDP and real-time communication via Slack notifications.
Unlocking Productivity: Leveraging the Potential of Copilot in Microsoft 365, a presentation by Christoforos Vlachos, Senior Solutions Manager – Modern Workplace, Uni Systems
Best 20 SEO Techniques To Improve Website Visibility In SERPPixlogix Infotech
Boost your website's visibility with proven SEO techniques! Our latest blog dives into essential strategies to enhance your online presence, increase traffic, and rank higher on search engines. From keyword optimization to quality content creation, learn how to make your site stand out in the crowded digital landscape. Discover actionable tips and expert insights to elevate your SEO game.
HCL Notes and Domino License Cost Reduction in the World of DLAUpanagenda
Webinar Recording: https://www.panagenda.com/webinars/hcl-notes-and-domino-license-cost-reduction-in-the-world-of-dlau/
The introduction of DLAU and the CCB & CCX licensing model caused quite a stir in the HCL community. As a Notes and Domino customer, you may have faced challenges with unexpected user counts and license costs. You probably have questions on how this new licensing approach works and how to benefit from it. Most importantly, you likely have budget constraints and want to save money where possible. Don’t worry, we can help with all of this!
We’ll show you how to fix common misconfigurations that cause higher-than-expected user counts, and how to identify accounts which you can deactivate to save money. There are also frequent patterns that can cause unnecessary cost, like using a person document instead of a mail-in for shared mailboxes. We’ll provide examples and solutions for those as well. And naturally we’ll explain the new licensing model.
Join HCL Ambassador Marc Thomas in this webinar with a special guest appearance from Franz Walder. It will give you the tools and know-how to stay on top of what is going on with Domino licensing. You will be able lower your cost through an optimized configuration and keep it low going forward.
These topics will be covered
- Reducing license cost by finding and fixing misconfigurations and superfluous accounts
- How do CCB and CCX licenses really work?
- Understanding the DLAU tool and how to best utilize it
- Tips for common problem areas, like team mailboxes, functional/test users, etc
- Practical examples and best practices to implement right away
Building Production Ready Search Pipelines with Spark and MilvusZilliz
Spark is the widely used ETL tool for processing, indexing and ingesting data to serving stack for search. Milvus is the production-ready open-source vector database. In this talk we will show how to use Spark to process unstructured data to extract vector representations, and push the vectors to Milvus vector database for search serving.
Dr. Sean Tan, Head of Data Science, Changi Airport Group
Discover how Changi Airport Group (CAG) leverages graph technologies and generative AI to revolutionize their search capabilities. This session delves into the unique search needs of CAG’s diverse passengers and customers, showcasing how graph data structures enhance the accuracy and relevance of AI-generated search results, mitigating the risk of “hallucinations” and improving the overall customer journey.
Sudheer Mechineni, Head of Application Frameworks, Standard Chartered Bank
Discover how Standard Chartered Bank harnessed the power of Neo4j to transform complex data access challenges into a dynamic, scalable graph database solution. This keynote will cover their journey from initial adoption to deploying a fully automated, enterprise-grade causal cluster, highlighting key strategies for modelling organisational changes and ensuring robust disaster recovery. Learn how these innovations have not only enhanced Standard Chartered Bank’s data infrastructure but also positioned them as pioneers in the banking sector’s adoption of graph technology.
In the rapidly evolving landscape of technologies, XML continues to play a vital role in structuring, storing, and transporting data across diverse systems. The recent advancements in artificial intelligence (AI) present new methodologies for enhancing XML development workflows, introducing efficiency, automation, and intelligent capabilities. This presentation will outline the scope and perspective of utilizing AI in XML development. The potential benefits and the possible pitfalls will be highlighted, providing a balanced view of the subject.
We will explore the capabilities of AI in understanding XML markup languages and autonomously creating structured XML content. Additionally, we will examine the capacity of AI to enrich plain text with appropriate XML markup. Practical examples and methodological guidelines will be provided to elucidate how AI can be effectively prompted to interpret and generate accurate XML markup.
Further emphasis will be placed on the role of AI in developing XSLT, or schemas such as XSD and Schematron. We will address the techniques and strategies adopted to create prompts for generating code, explaining code, or refactoring the code, and the results achieved.
The discussion will extend to how AI can be used to transform XML content. In particular, the focus will be on the use of AI XPath extension functions in XSLT, Schematron, Schematron Quick Fixes, or for XML content refactoring.
The presentation aims to deliver a comprehensive overview of AI usage in XML development, providing attendees with the necessary knowledge to make informed decisions. Whether you’re at the early stages of adopting AI or considering integrating it in advanced XML development, this presentation will cover all levels of expertise.
By highlighting the potential advantages and challenges of integrating AI with XML development tools and languages, the presentation seeks to inspire thoughtful conversation around the future of XML development. We’ll not only delve into the technical aspects of AI-powered XML development but also discuss practical implications and possible future directions.
Communications Mining Series - Zero to Hero - Session 1DianaGray10
This session provides introduction to UiPath Communication Mining, importance and platform overview. You will acquire a good understand of the phases in Communication Mining as we go over the platform with you. Topics covered:
• Communication Mining Overview
• Why is it important?
• How can it help today’s business and the benefits
• Phases in Communication Mining
• Demo on Platform overview
• Q/A
Maruthi Prithivirajan, Head of ASEAN & IN Solution Architecture, Neo4j
Get an inside look at the latest Neo4j innovations that enable relationship-driven intelligence at scale. Learn more about the newest cloud integrations and product enhancements that make Neo4j an essential choice for developers building apps with interconnected data and generative AI.
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In his public lecture, Christian Timmerer provides insights into the fascinating history of video streaming, starting from its humble beginnings before YouTube to the groundbreaking technologies that now dominate platforms like Netflix and ORF ON. Timmerer also presents provocative contributions of his own that have significantly influenced the industry. He concludes by looking at future challenges and invites the audience to join in a discussion.
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2. Introduction
The study of blood flow CONTENTS
behavior: Cardiovascular physiology
Physical properties of
• Improving the design of implants
blood
(heart valves, artificial heart) and
extra-corporeal flow devices Viscosity
(blood oxygenators, dialysis Steady blood flow
machines) Poiseuille’s equation
• Understanding the connection Entrance effects
between flow characteristics and Bernoulli’s equation
the development of cardiovascular Oscillatory blood flow
diseases (atherosclerosis, Windkessel model
thrombosis)
January 2008 Blood Flow
Wommersley 2
3. Cardiovascular Physiology
• HEART: atrium, ventricles mean diameter number of
[mm] vessels
• BLOOD VESSELS: aorta, aorta 19 - 4.5 1
arteries, arterioles, arteries 4 – 0.15 110.000
capillaries, veinules, veins arterioles 0.05 2.7 ∙106
capillaries 0.008 2.8 ∙109
right ventricle
lungs left
atrium
MAIN FUNCTIONS:
• to deliver oxygen and
nutrients to the cells
• to remove cellular wastes
left ventricle and carbon dioxide
aorta organs • to maintain organs at a
and tissues right
atrium constant temperature and pH
January 2008 Blood Flow 3
4. Poiseuille flow
• Steady flow in a rigid cylindrical tube
– Pressure gradient Fp = 2π r ( p1 − p2 )δ r
– Viscous force Fv = −
∂
∂r
(2π rLµ
∂v
∂r
)δ r
The forces are equal and
opposite: p1 − p2
∂ 2 v 1 ∂v
+ + =0
∂r 2 r ∂r µL
p1 − p2
v (r ) = −r 2 + A ln r + B
v(r=R)=0 4µ L
v(r=0)≠∞ p1 − p2
v (r ) = (R 2 − r 2 )
4µ L
L
r R
p1 − p2
r Q = ∫ 2π v(r )rdr = π R 4 volume flow
8µ L
r2
0
v
v=
Q
= R2
p1 − p2 1
= v ( r = 0) =
vmax average
p1 p2 π R2 8µ L 2 2 velocity
January 2008 Blood Flow 4
5. Poiseuille flow - assumptions
• Newtonian fluid
– in large blood vessels (at high shear rates)
• Laminar flow
– Reynold’s numbers below the critical value of about
2000
• No slip at the vascular wall
– endothelial cells
x
• Steady flow
– pulsatile flow in arteries
x
• Cylindrical shape
– elliptical shape (veins, pulmonary arteries), taper
x
• Rigid wall
– visco-elastic arterial walls
x
• Fully developed flow
– entrance length; branching points, curved sections
January 2008 Blood Flow 5
6. Physical properties of blood
BLOOD =
plasma + blood cells
( 55%) (45%)
electrolyte Red blood cells (95%)
solution
White blood cells (0.13%)
containing
8% of Platelets (4.9%)
proteins
Reference values
RBC 1 μm PLASMA WHOLE
: BLOOD
density 1035 kg/m 3 1056 kg/m 3
8 μm
viscosit 1.3×10 -3 Pa 3.5 × 10 -3 Pa s
January 2008 Bloody s
Flow 6
7. Viscosity
• Viscosity varies with samples
– variations in species
– variations in proteins and RBC
• Temperature dependent
– decrease with increasing T
In small tubes the blood
• Blood viscosity has a very low value
because of a cell-free zone near
– a non-Newtonian fluid at low the wall.
shear rates (the agreggates of
RBC) Fahraeus-Lindqvist
effect
– a Newtonian fluid above shear
rates of0 50 s -1 dv / dr
τ = τ + Kc
– Casson’s equation
January 2008 Blood Flow 7
8. Fahraeus-Lindqvist Effect
Cell-free marginal layer The Sigma effect theory
model velocity profile is not
Core region μc , vc , 0rR- continuous
small tubes ( N red blood
region near the wall μ , v , R-r R
Cell-free plasma p p
cells move abreast)
μp , vp
r
μc , vc
R
∆p 1 d dv the volume flow is
− = µr ÷
L r dr dr π∆p R 3rewritten
2 µL ∫
Q= r dr
the volume flow 0
N concentric laminae,
π R ∆p 1
4
Q= ( 1 − (1 − δ / R)4 (1 − µ p / µc ) ) each of thickness ε
8L µp
π∆p N π∆pR 4 1 ε
Q= ∑(nε )ε = 8L µ 1 + R ÷
2 µL n =1
3
1/μ
1/μ
January 2008 Blood Flow 8
9. Entrance length
• The flow of fluid from a reservoir to a pipe
– flat velocity profile at the entrance point
– the fluid in contact with the wall has zero velocity (‘no slip’)
– retardation due to shearing adjacent to the wall
– boundary layer (where the viscous effects are present)
– acceleration in the core region to maintain the same volume of
flow
– parabolic velocity profile FULLY DEVELOPED FLOW
d dv
Fvisc = µ ÷ A(r2 − r1 ) viscous force
dr dr
- boundary layer
µU thickness at z
Fvisc = 2 A(r2 − r1 )
δ U - free stream
velocity
U2
Fi = ρ aV = ρ A(r2 − r1 ) inertial force
z
* a=U/t=U/(z/U)
January 2008 Blood Flow 9
10. Entrance length
U2 U
• equating the viscous and inertial force ρ
z
= kµ 2
σ
k – proportionality constant derived from experiments, approximately 0.06
• the boundary layer thickness
µz
δµ
ρU
• the entrance length (when =D/2 the flow Pulsatile flow –
the entrance
becomes fully established)
Uρ length fluctuates
z0 = kD 2
µ
The above derivation is valid only for
the flow originating from a very large
reservoir, where the velocity profile
at the entrance point is relatively flat.
In other cases, the entrance length
is shorter.
January 2008 Blood Flow 10
11. Application of Bernoulli Equation
Bernoulli
equation p + ρ gz + 1 ρ v 2 = const.
2
• Flow trough stenosis • Flow in aneurysms
p1 A1
A1 v1 p2, v2, A2 p1v p2, v2, A2
A1v1 = A2v2 1
– v2 > v1 – v2 < v1
– p 2 < p 1 : caving or closing – p 2 > p 1 : expansion and
of the vessel bursting of the vessel
– decrease in v 2
– reopening of the vessel – caused by the weakening
– fluttering of the arterial wall
January 2008 Blood Flow 11
12. Vacular resistance and branching
• Vascular resistance • Succesive branching:
∆p – Increase in the total cross-
Rv = section area
Q
8µ L
Rv =
– for Poiseuille flow π R4
– major drop in the mean
pressure in arterioles (60
mmHg)
autonomic nervous system
controls muscle tension
arterioles distend or contract
2
v1 nR2
= 2 =d
Mean pressure values [mmHg]: v2 R1
– d A 1= n A 2:
∆p1 nR2 d 2
4
- arteries 100 = 4 =
∆p2 R1 n
- capillaries 30-34 at arterial end,
12-15 at venous end velocity decreases,
n≥2
pressure gradient
average d=1.26 increases
January 2008 Blood Flow 12
13. Turbulent Flow
• Reynolds number
v ρD for flow in rigid straight
Re = critical value Re > 2000 cylindrical pipes
µ
• Flow in the circulatory system is
normally laminar
• Flow in the aorta can destabilize
during the deceleration phase of late
systole
– too short time period for the flow to
become fully turbulent
• Diseased conditions can result in
turbulent blood flow
– vessel narrowing at atherosclerosis,
defective heart valves
– weakening of the wall, progression of the
disease
January 2008 Blood Flow 13
14. Unsteady flow models
• The pressure pulse:
– generated by the contraction of the left ventricle
– travels with a finite speed through the arterial wall
– change in a shape due to interaction with reflected waves
• Windkessel model
– the arteries: a system of interconnected tubes with a
storage capacity
– distensibility Di = dV/dp
– Inflow – Outflow = Rate of Storage A typical pressure pulse curve.
p − pV dV dp
Q (t ) − = = Di b
RS dt dt
systole diastole
SYSTOLE DIASTOLE
Q=Q 0 , 0 t t s Q=0, t s t T
ts T
p(t) b-(b-p 0 )e -t/a p(t) e (T-t)/a p0
January 2008 Blood Flow 14
15. Wommersley equations
• The equation for the motion of a
viscous liquid in a cylindrical tube
(general form):
∂ 2 w 1 ∂w 1 ∂p ρ ∂w
+ + =
∂r 2 r ∂r µ ∂z µ ∂t
• Arterial pulse = periodic function iωt
∂p
the sum of harmonics ∂z ∑
= Ae
The flow velocity pulse and the arterial
pressure pulse (femoral artery of a dog). • The solution:
A * R2 J 0 (α yi 3/ 2 ) iωt
w= 1 − 3/ 2
e
i µα 2 J 0 (α i )
– Wommersley number
– J 0 (xi 3/2 ) is a Bessel function of the
α = R (ωρ / µ ) first kind of order zero and
complex argument
– y=r/R
January 2008 Blood Flow 15
16. The role of Wommersley number
- unsteady inertial forces vs. viscous forces
(viscous forces dominate when 1) 10-3 18
The velocity profiles for capillaries aorta
the first four harmonics : 3.34 4.72 5.78 6.67
resulting from the
pressure gradient cos ωt
Parabolic profile is
not formed
The laminae near
the wall move first
Solid mass in the
centre
Increase in :
flattening of the central
region, reduction of
amplitude and reversal
of flow at the wall
January 2008 Blood Flow 16
17. The sum of harmonics
y=r/R
Parabolic shape in
the fast systolic rush
Phase lag between
the pressure gradient
and the movement of
the liquid
The reversal begins
in the peripheral The time dependence of
laminae (the point of velocity at different distances y.
flow reversal: 25°
after the pressure gradient)
The first four harmonics summed The peak forward
together with a parabola (representing Back flow: and backward
the steady forward flow). harmonics are out of velocities: 165
phase and the profile cm/s at 75° 35
is flattened cm/s at 165°
January 2008 Blood Flow 17
18. Conclusion
• What have we learned? • Why am I interested in
blood flow?
future experiment:
dissolving blood clots
under physiological
conditions
PULSATILE FLOW
Artificial heart.
- basic equations of blood
flow
January 2008 Blood Flow 18
19. Non-Newtonian fluid behavior
Power law fluid Bingham plastic
Cassons fluid
Velocity profiles in a round rigid tube.
January 2008 Blood Flow