The fetal circulation differs from adult circulation in three key ways: 1) the placenta oxygenates blood rather than the lungs, 2) the lungs have high resistance so little blood flows through them, and 3) the hepatic portal system is less significant. In fetal circulation, oxygenated blood from the umbilical vein passes through the ductus venosus and foramen ovale to supply the heart and brain before returning to the placenta through the umbilical arteries. After birth, the ductus venosus, ductus arteriosus, foramen ovale, and umbilical vessels close or become ligaments, and the lungs begin oxygenating blood through pulmonary circulation. Patent ductus arteriosus
Describe the normal fetal circulation and mention the changes that occur in it is placental stage and after birth. Fetal circulation is composed of placenta, umbilical cord, heart and systemic blood vessels.
A major difference between the fetal circulation and postnatal circulation is that the lungs are not used during the fetal stage resulting in the presence of shunts to move oxygenated blood and nutrients from the placenta to the fetal tissue.
At birth, the start of breathing and the severance of the umbilical cord prompt various changes that quickly transform fetal circulation into postnatal circulation.
When the embryo develops into the fetus, it creates a functional cardiovascular system that cooperates with the mother's system.
During birth, there are functional physiological changes that transform the shared system into an individual one for the fetus.
In the fetus main filtration site for plasma nutrients and wastes in the placenta, which is outside of the body cavity.
In adults, the circulation occurs entirely inside the body.
The blood that flow to through the fetus is actually more complicated than after the baby is born (normal heart).
This is because the mother (the placenta) is doing the work that the baby's lungs will do after birth.
The placenta accepts the blood without oxygen from the fetus through blood vessels that leave the fetus through the umbilical cord (Umbilical arteries , there are two of them).
When blood goes through the placenta it pick up oxygwn.
The oxygen rich blood then returns to the fetus via the third vessels in the umbilical cord (Umbilical vein).
The oxygen rich blood that enters the fetus passes through the fetal liver and enters the right side of the heart.
The oxygen rich blood goes through one of the two extra connections in the fetal heart that will close after the baby is born.
The hole between the top two heart chmbers (right and left atrium) is called "Patent Foramen Ovale (PFO).
This hole allows the oxygen rich blood to go form the right atrium to left atrium and then to the left ventricle and out the aorta.
As a result the blood with the most oxygen gets to the brain.
Blood coming back from the fetus's body also enters the right atrium, but the fetus is able to send this oxygen poor blood from the right atrium to the right ventricle (the chamber that normally pumps blood to the lungs).
most of the blood that leaves the right ventricle in the fetus bypass the lungs through the second of the extra fetal connections known as the ductus arteriosus.
The ductus arteriosus sends the oxygen poor blood to the organs in the lower half of the fetal body. This also allows for the oxygen poor blood to leave the fetus through the umbilical arteries and get back to the placenta to pick up oxygen.
Since the patent foramen ovale and ductus arteriosus are normal findings in the fetus, it is impossible to predict whether or not these connections will close normally after birth in a normal fetal heart.
Describe the normal fetal circulation and mention the changes that occur in it is placental stage and after birth. Fetal circulation is composed of placenta, umbilical cord, heart and systemic blood vessels.
A major difference between the fetal circulation and postnatal circulation is that the lungs are not used during the fetal stage resulting in the presence of shunts to move oxygenated blood and nutrients from the placenta to the fetal tissue.
At birth, the start of breathing and the severance of the umbilical cord prompt various changes that quickly transform fetal circulation into postnatal circulation.
When the embryo develops into the fetus, it creates a functional cardiovascular system that cooperates with the mother's system.
During birth, there are functional physiological changes that transform the shared system into an individual one for the fetus.
In the fetus main filtration site for plasma nutrients and wastes in the placenta, which is outside of the body cavity.
In adults, the circulation occurs entirely inside the body.
The blood that flow to through the fetus is actually more complicated than after the baby is born (normal heart).
This is because the mother (the placenta) is doing the work that the baby's lungs will do after birth.
The placenta accepts the blood without oxygen from the fetus through blood vessels that leave the fetus through the umbilical cord (Umbilical arteries , there are two of them).
When blood goes through the placenta it pick up oxygwn.
The oxygen rich blood then returns to the fetus via the third vessels in the umbilical cord (Umbilical vein).
The oxygen rich blood that enters the fetus passes through the fetal liver and enters the right side of the heart.
The oxygen rich blood goes through one of the two extra connections in the fetal heart that will close after the baby is born.
The hole between the top two heart chmbers (right and left atrium) is called "Patent Foramen Ovale (PFO).
This hole allows the oxygen rich blood to go form the right atrium to left atrium and then to the left ventricle and out the aorta.
As a result the blood with the most oxygen gets to the brain.
Blood coming back from the fetus's body also enters the right atrium, but the fetus is able to send this oxygen poor blood from the right atrium to the right ventricle (the chamber that normally pumps blood to the lungs).
most of the blood that leaves the right ventricle in the fetus bypass the lungs through the second of the extra fetal connections known as the ductus arteriosus.
The ductus arteriosus sends the oxygen poor blood to the organs in the lower half of the fetal body. This also allows for the oxygen poor blood to leave the fetus through the umbilical arteries and get back to the placenta to pick up oxygen.
Since the patent foramen ovale and ductus arteriosus are normal findings in the fetus, it is impossible to predict whether or not these connections will close normally after birth in a normal fetal heart.
This is a presentation I had made for giving a seminar on Fetal Circulation in the first year of my MBBS course in Maharashtra.
Please share it with your juniors and colleagues.Thank You
Presentation By Tashif Jilani
the 1st aortic arch – disappears (a small portion persists and forms a piece of the maxillary artery)
the 2nd aortic arch – disappears (small portions of this arch contributes to the hyoid and stapedial arteries)
the 3rd aortic arch - has the same development on the right and left side
it gives rise to the initial portion of
the internal carotid artery,
the remainder of its trunk is
formed by the cranial portion of
the dorsal aorta + primitive internal
carotid
the external carotid is deriving from
the cranial portion of the ventral aorta
the common carotid corresponds to a
portion of the ventral aorta between
exits of the third and fourth arches
Fetal Circulation by Barkha Devi,Lecturer,Sikkim Manipal College of NursingBarkha Devi
This PowerPoint will provide you a short a sweet lecture about fetal circulation. Please give me your feed back .
-Discuss anatomy and physiology of fetal circulation
-Compare and contrast fetal circulation to infant circulation
-Define specialized structures of fetal circulation
Embryology of heart, Anatomy of heart, Physiology of heart, Fetal circulation, Neonatal circulation, Congenital cyanotic and acyanotic heart diseases of children.
Embark on a captivating exploration of #FetalCirculation in this presentation. Delve into the intricacies of the developing cardiovascular system, understanding how the fetus receives oxygen and nutrients for optimal growth within the womb. Uncover the role of critical structures such as the ductus venosus and foramen ovale in facilitating unique circulatory patterns. Gain insights into the transition from fetal to neonatal circulation and its crucial significance for newborns. This presentation provides a comprehensive overview of the physiological marvel that sustains life before the first breath.
This is a presentation I had made for giving a seminar on Fetal Circulation in the first year of my MBBS course in Maharashtra.
Please share it with your juniors and colleagues.Thank You
Presentation By Tashif Jilani
the 1st aortic arch – disappears (a small portion persists and forms a piece of the maxillary artery)
the 2nd aortic arch – disappears (small portions of this arch contributes to the hyoid and stapedial arteries)
the 3rd aortic arch - has the same development on the right and left side
it gives rise to the initial portion of
the internal carotid artery,
the remainder of its trunk is
formed by the cranial portion of
the dorsal aorta + primitive internal
carotid
the external carotid is deriving from
the cranial portion of the ventral aorta
the common carotid corresponds to a
portion of the ventral aorta between
exits of the third and fourth arches
Fetal Circulation by Barkha Devi,Lecturer,Sikkim Manipal College of NursingBarkha Devi
This PowerPoint will provide you a short a sweet lecture about fetal circulation. Please give me your feed back .
-Discuss anatomy and physiology of fetal circulation
-Compare and contrast fetal circulation to infant circulation
-Define specialized structures of fetal circulation
Embryology of heart, Anatomy of heart, Physiology of heart, Fetal circulation, Neonatal circulation, Congenital cyanotic and acyanotic heart diseases of children.
Embark on a captivating exploration of #FetalCirculation in this presentation. Delve into the intricacies of the developing cardiovascular system, understanding how the fetus receives oxygen and nutrients for optimal growth within the womb. Uncover the role of critical structures such as the ductus venosus and foramen ovale in facilitating unique circulatory patterns. Gain insights into the transition from fetal to neonatal circulation and its crucial significance for newborns. This presentation provides a comprehensive overview of the physiological marvel that sustains life before the first breath.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
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Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
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Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
2. Objectives
• Describe the fate of the foetal structures once postnatal circulation
begins.
• Describe the importance of the hepatic portal system
3.
4. •Fetal Circulation
• fetal circulation is different from that of adult circulation
• three basic reasons for this difference:
• 1. Blood in the fetus is oxygenated by placenta and not by lungs
• 2. During fetal life, the lungs are collapsed, hence the resistance to blood flow
through the lung is much higher
• result, only minimal amount of blood passes through the lungs to supply
oxygen and nutrients to the lungs.
• 3. Portal circulation is of little significance
5.
6. • Before birth, the oxygenated blood from the placenta returns to the fetus by
the left umbilical vein
• umbilical vein traverses through the umbilical cord
• enters the abdomen through umbilicus, and passes to the liver through
falciform ligament
• In the liver, the left umbilical vein joins the left branch of portal vein
• most of blood from left umbilical vein bypasses the sinusoids of the liver by
passing through ductus venosus—a channel that connects left branch of portal
vein to the inferior vena cava
• small amount of blood of left umbilical vein enters the liver sinusoids and mixes
with the blood from the portal circulation
7. • the inferior vena cava opens into the right atrium
• the inferior vena cava, richly oxygenated blood mixes with the deoxygenated
blood returning from the lower limbs
• this blood enters in the right atrium, it is guided by the valve of inferior vena
cava towards foramen ovale
• most of blood from the inferior vena cava passes through foramen ovale into
the left atrium
• small amount of blood is prevented from entering left atrium by the lower
edge of septum secundum—the crista dividens
8.
9. • Some blood remains in the right atrium
• it mixes with the deoxygenated blood from the superior vena cava and passes
to the right ventricle
• Blood from the right ventricle passes through pulmonary trunk, and right and
left pulmonary arteries
• due to high resistance in pulmonary tissue during fetal life only a small amount
of blood enters the pulmonary circulation
• most of it passes into the aorta through the ductus arteriosus (DA)—a channel
that connects the left pulmonary artery to arch of aorta
10. • left atrium receives mainly rich oxygenated blood from the right atrium
through the foramen ovale
• a small amount of deoxygenated blood enters the left atrium from the lungs
through the pulmonary veins
• Blood from the left atrium passes to the left ventricle
• Blood from the left ventricle enters into the ascending aorta
• through its three large branches (brachiocephalic artery, left common carotid
artery, and left subclavian artery) supply oxygenated blood to head, neck,
brain, and superior extremity
11.
12. • the coronary and carotid arteries are the first branches of the aorta
• the heart musculature and brain are supplied by well oxygenated blood
• the arch of aorta receives poorly oxygenated blood from the pulmonary trunk
through the ductus arteriosus
• blood is distributed by the aorta and common iliac arteries to the lower part of
the body
• lower part of the body is supplied with relatively less oxygenated blood as
compared with the upper part of the body
13. • two umbilical arteries arising from internal iliac branches of common iliac
arteries pass through umbilicus
• enter the placenta through the umbilical cord, where it is oxygenated
14. • Changes in Fetal Circulation Just after Birth
• After birth, the placenta—fetal organ of respiration—is separated from
newborn and lung starts oxygenating the blood
• 1. Umbilical vein, as it no longer carries any blood from the placenta,
obliterates and forms a fibrous ligament called ligamentum teres hepatis
• 2. Ductus venosus obliterates to form a fibrous ligament called ligamentum
venosum
• 3. As the lungs are inflated and the pulmonary circulation is established,
pulmonary veins bring more blood to the left atrium
15. • pressure of blood in the left atrium is more than that in the right atrium the
septum primum is pushed to the right and the foramen ovale is closed
• first the closure of foramen ovale is physiological
• later septum primum fuses with the septum secundum and there is an
anatomical closure of foramen ovale
• The closed foramen ovale forms fossa ovalis
• 4. Ductus Arteriosus obliterates to form a fibrous ligament called the
ligamentum arteriosum
16. • 5. Umbilical arteries (right and left) obliterate
• their proximal parts remain open
• proximal parts of umbilical arteries form superior vesicle arteries
• distal parts form fibrous ligaments called medial umbilical ligaments
17.
18. • Clinical Correlation
• 1. Patent ductus arteriosus (PDA) :
• occurs when ductus arteriosus, a connecting channel between left pulmonary
artery and the arch of aorta, fails to close
• The PDA causes shunting of blood from aorta back into the pulmonary
circulation
• The PDA is one of the most common congenital anomalies of the great vessels
• occurring in 8/10,000 births, especially in premature female babies born to
mothers who had suffered from rubella infection in the early part of pregnancy
19.
20. • Functional closure of the ductus arteriosus (DA) occurs at birth by contraction
of smooth muscles of the DA.
• Anatomical closure occurs by proliferation of tunica intima of DA 1–3 months
after birth
• It is mediated by bradykinin—a substance released from lungs, during their
initial inflation
21. • 2. Coarctation of aorta :
• The coarctation means narrowing of the aorta
• It occurs due to extension of the process of obliteration of DA into the aorta
• The coarctation of aorta is of two types: preductal and postductal
• (a) Preductal type of coarctation of aorta:
• In this type, a narrow segment of arch of aorta is proximal to entrance of the
DA
• The DA persists in this type.
• (b) Postductal type of coarctation of aorta:
• In this type, a narrow segment of arch of aorta is distal to the entrance of the
DA
• The DA usually obliterates in this type
22.
23. • Hepatic portal circulation
• carries venous blood from the gastrointestinal organs and spleen to the liver
• vein that carries blood from one capillary network to another is called a portal
vein
• hepatic portal vein receives blood from capillaries of gastrointestinal organs
and spleen , delivers it to the sinusoids of the liver
• superior mesenteric and splenic veins unite to form the hepatic portal vein