Development of the cardiovascular system

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Development of the cardiovascular system

ETP CVS

ETP CVS

Introduction to the cardiovascular system
Anatomy of the heart
Anatomy of the coronary circulation
Anatomy clinical correlates: Heart
Anatomy of the superior mediastinum
Anatomy of the inferior mediastinum
Anatomy clinical correlates: Mediastinum
Development of the cardiovascular system
Fetal circulation
Cardiac muscle histology
Artery and vein histology
Arteriole, venule and capillary histology
Cardiovascular system anatomy and physiology
Lymphatic system anatomy and physiology
Coronary circulation
Blood pressure, blood flow, and resistance
Pressures in the cardiovascular system
Laminar flow and Reynolds number
Resistance to blood flow
Compliance of blood vessels
Control of blood flow circulation
Microcirculation and Starling forces
Measuring cardiac output (Fick principle)
Stroke volume, ejection fraction, and cardiac output
Cardiac contractility
Frank-Starling relationship
Cardiac preload
Cardiac afterload
Law of Laplace
Cardiac and vascular function curves
Altering cardiac and vascular function curves
Cardiac cycle
Cardiac work
Pressure-volume loops
Changes in pressure-volume loops
Physiological changes during exercise
Cardiovascular changes during hemorrhage
Cardiovascular changes during postural change
Normal heart sounds
Abnormal heart sounds
Action potentials in myocytes
Action potentials in pacemaker cells
Excitability and refractory periods
Cardiac excitation-contraction coupling
Cardiac conduction system
Cardiac conduction velocity
ECG basics
ECG rate and rhythm
ECG intervals
ECG QRS transition
ECG axis
ECG normal sinus rhythm
ECG cardiac infarction and ischemia
ECG cardiac hypertrophy and enlargement
Baroreceptors
Chemoreceptors
Renin-angiotensin-aldosterone system
Arterial disease
Angina pectoris
Stable angina
Unstable angina
Myocardial infarction
Prinzmetal angina
Coronary steal syndrome
Peripheral artery disease
Subclavian steal syndrome
Aneurysms
Aortic dissection
Vasculitis
Hypertension
Hypertensive emergency
Conn syndrome
Hypotension
Orthostatic hypotension
Abetalipoproteinemia
Familial hypercholesterolemia
Hypertriglyceridemia
Hyperlipidemia
Chronic venous insufficiency
Thrombophlebitis
Deep vein thrombosis
Lymphedema
Lymphangioma
Shock
Vascular tumors
Human herpesvirus 8 (Kaposi sarcoma)
Angiosarcomas
Persistent truncus arteriosus
Transposition of the great vessels
Total anomalous pulmonary venous return
Hypoplastic left heart syndrome
Atrial septal defect
Coarctation of the aorta
Patent ductus arteriosus
Tetralogy of Fallot
Ventricular septal defect
Atrial flutter
Atrial fibrillation
Premature atrial contraction
Atrioventricular nodal reentrant tachycardia (AVNRT)
Wolff-Parkinson-White syndrome
Ventricular tachycardia
Brugada syndrome
Premature ventricular contraction
Long QT syndrome and Torsade de pointes
Ventricular fibrillation
Atrioventricular block
Bundle branch block
Pulseless electrical activity
Tricuspid valve disease
Pulmonary valve disease
Mitral valve disease
Aortic valve disease
Dilated cardiomyopathy
Restrictive cardiomyopathy
Hypertrophic cardiomyopathy
Heart failure
Cor pulmonale
Endocarditis
Myocarditis
Rheumatic heart disease
Pericarditis and pericardial effusion
Cardiac tamponade
Dressler syndrome
Cardiac tumors
Acyanotic congenital heart defects: Pathology review
Cyanotic congenital heart defects: Pathology review
Atherosclerosis and arteriosclerosis: Pathology review
Coronary artery disease: Pathology review
Peripheral artery disease: Pathology review
Valvular heart disease: Pathology review
Cardiomyopathies: Pathology review
Heart failure: Pathology review
Supraventricular arrhythmias: Pathology review
Ventricular arrhythmias: Pathology review
Heart blocks: Pathology review
Aortic dissections and aneurysms: Pathology review
Pericardial disease: Pathology review
Endocarditis: Pathology review
Hypertension: Pathology review
Shock: Pathology review
Vasculitis: Pathology review
Cardiac and vascular tumors: Pathology review
Dyslipidemias: Pathology review
Sympatholytics: Alpha-2 agonists
Adrenergic antagonists: Presynaptic
Adrenergic antagonists: Alpha blockers
Adrenergic antagonists: Beta blockers
ACE inhibitors, ARBs and direct renin inhibitors
Thiazide and thiazide-like diuretics
Calcium channel blockers
cGMP mediated smooth muscle vasodilators
Class I antiarrhythmics: Sodium channel blockers
Class II antiarrhythmics: Beta blockers
Class III antiarrhythmics: Potassium channel blockers
Class IV antiarrhythmics: Calcium channel blockers and others
Lipid-lowering medications: Statins
Lipid-lowering medications: Fibrates
Miscellaneous lipid-lowering medications
Positive inotropic medications
Cardiomyopathies: Clinical
Congenital heart defects: Clinical
Valvular heart disease: Clinical
Infective endocarditis: Clinical
Pericardial disease: Clinical
Chest trauma: Clinical
Hypertension: Clinical
Pulmonary hypertension
Aortic aneurysms and dissections: Clinical
Raynaud phenomenon
Peripheral vascular disease: Clinical
Heart failure: Clinical
Coronary artery disease: Clinical
Deep vein thrombosis and pulmonary embolism: Pathology review
Fascia, vessels and nerves of the upper limb
Vessels and nerves of the forearm
Vessels and nerves of the hand
Anatomy of the abdominal viscera: Blood supply of the foregut, midgut and hindgut
Fascia, vessels and nerves of the lower limb
Vessels and nerves of the gluteal region and posterior thigh
Anatomy of the popliteal fossa
Ventilation
Ventilation-perfusion ratios and V/Q mismatch
Gas exchange in the lungs, blood and tissues
Oxygen binding capacity and oxygen content
Oxygen-hemoglobin dissociation curve
Carbon dioxide transport in blood
Trypanosoma cruzi (Chagas disease)
Yellow fever virus
Rickettsia rickettsii (Rocky Mountain spotted fever) and other Rickettsia species
Arteriovenous malformation
Cerebral circulation

Flashcards

Development of the cardiovascular system

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The cardiovascular system starts developing at the beginning of week 3 of intrauterine life.

At that point, the embryo is a flat little pancake made up of two layers: the epiblast on the dorsal, or back, side, and the hypoblast on the ventral, or front, side.

A line called the primitive streak appears on the epiblast back of this two-layered creature.

Cells migrate along the primitive streak during gastrulation, resulting in a three-layered embryo pancake, with each layer containing germ cells that form organs and tissues of the body.

The ventral, or bottom, germ layer is called endoderm, the dorsal, or top, germ layer is called ectoderm, and the layer in between these two is called mesoderm.

The heart derives from a part of the mesoderm called the visceral mesoderm.

Let’s look at this three-week-old creature from above. Mesoderm cells go through the primitive streak and make their way up to the embryo’s head, forming an area that’s called the primary heart field, a horseshoe-shaped area that has two limbs, with one on either side of the future brain.

This region lies on a blanket of endoderm cells that secrete vascular endothelial growth factor, which is called VEGF for short.

VEGF signals the cells in the limbs of the horseshoe to self-organize into two heart tubes.

A primitive pericardial cavity also appears lateral to each endocardial tube.

At its inferior end, each endocardial tube connects to a vitelline vein, which comes from an extraembryonic tissue called the yolk sac and through which blood enters the endocardial tube.

Blood exits each endocardial tube at its superior end through a dorsal aorta, which then continues down the embryo’s back.

During lateral folding, the flat embryo goes from a trilaminar disc to a more cylindrical shape.

The lateral borders of the embryo reach out towards each other and meet anteriorly at the midline, forming a cylindrical shape.

This process makes the two endocardial tubes fuse into one, forming the primitive heart tube.

The left and right vitelline veins also fuse to form the sinus venosus, which is the inflow tract of the heart tube.

Similarly, the aortae fuse to form the aortic sac, which is the outflow tract of the heart tube.

The two pericardial cavities also unite around the heart tube and form the singular pericardial cavity.

The heart tube remains attached to the back wall of the pericardial cavity by a sheet of mesoderm called the dorsal mesocardium.

The heart tube itself has two layers: an endothelial lining on the inside, which turns into the endocardium, and cardiac myoblasts on the outside, which become the myocardium.

Some of the myocardial cells in the sinus venosus begin to produce a rhythmic electrical discharge at this early stage.

However, the conduction system and working myocardium are still underdeveloped, and they can’t contract in perfect sync, so we don’t hear the familiar “lub-dub” of the heart at this point.

During craniocaudal folding, the now-cylindrical embryo curves down its length, forming more of a shrimp-like creature, and this process pushes the heart tube down towards the chest.

By the beginning of week 4, the heart tube reaches the thorax, and blood can be seen going through the heart tube.

The heart tube develops sections. First there’s the sinus venosus, which has a left and a right sinus horn that bring blood in.

Above it, there’s the primitive atrium and then the primitive ventricle, which are separated from one another by the atrioventricular sulcus.

The primitive atrium gives rise to the left and right atria, and the primitive ventricle forms the left ventricle.

The primitive ventricle is separated from the next region, called the bulbus cordis, by the bulboventricular sulcus.

The first part of the bulbus cordis forms the right ventricle, as well as the outflow tracts for both ventricles.

Finally, at the top of the heart tube, there’s the truncus arteriosus, which pumps blood through the aortic sac into an early version of the circulatory system that’s made up of aortic arches.

This organization of structures doesn’t mirror the adult heart, so during week 4 the heart tube undergoes looping, which is a fancy way of saying the tube elongates, its walls become thicker, and sections of the heart move around so that they end up in their right place.

The heart tube is held in place inside the pericardial cavity by blood vessels at both ends, and looping starts with the heart tube folding into a “C” shape.

The truncus arteriosus and bulbus cordis move down and to the right to form the top portion of the “C”, while the primitive ventricle bends to the right of the midline and a little to the front, forming the middle of the “C”.

Finally, the primitive atrium and sinus venosus form the bottom of the “C” and snuggle deeper inside the pericardial cavity.

As development continues, the growing ventricle moves to the left, so it crosses over the midline again, covering the primitive atrium.

By the end of week 4, the cardiac loop starts to take on the general appearance of the adult heart.

Also, by this point, visceral pericardium has attached to the outside of the heart, forming the epicardium.

Key Takeaways

The cardiovascular system develops at the beginning of week three during prenatal life. The development of the primitive heart starts with a horseshoe-shaped structure called the primary heart field, which has a pair of tubes that fold so that the heart structures will be in the proper position. Next, septa appear, which help to partition the heart into two atria and two ventricles.

The electrical conduction system of the primitive heart initially lies in the sinus venosus. As the sinus venous becomes absorbed by the right atria, the pacemaker cells appear in the sinoatrial node in the right atrium wall. The development of blood vessels involves the endothelium, which undergoes a process called angiogenesis, which is the formation of new blood vessels from pre-existing ones. This process is driven by growth factors such as VEGF (vascular endothelial growth factor).