The circulatory system consists of the heart, blood vessels, and blood. The heart pumps blood through arteries, capillaries, and veins to deliver oxygen and nutrients to tissues throughout the body. It has three layers - the inner endocardium, middle muscular myocardium, and outer epicardium. The heart's conducting system coordinates heartbeats and includes the sinoatrial and atrioventricular nodes and bundle of His. Blood vessels have three layers - the inner endothelium-lined tunica intima, middle smooth muscle-containing tunica media, and outer connective tissue tunica externa. Capillaries are the sites of nutrient exchange and have only an endothelium.
11.03.08(c): Histology of the Cardiovascular SystemOpen.Michigan
Slideshow is from the University of Michigan Medical School's M1 Cardiovascular / Respiratory sequence
View additional course materials on Open.Michigan:
openmi.ch/med-M1Cardio
Connective tissue is the tissue that connects or separates, and supports all the other types of tissues in the body. Like all tissue types, it consists of cells surrounded by a compartment of fluid called the extracellular matrix (ECM). However connective tissue differs from other types in that its cells are loosely, rather than tightly, packed within the ECM.
11.03.08(c): Histology of the Cardiovascular SystemOpen.Michigan
Slideshow is from the University of Michigan Medical School's M1 Cardiovascular / Respiratory sequence
View additional course materials on Open.Michigan:
openmi.ch/med-M1Cardio
Connective tissue is the tissue that connects or separates, and supports all the other types of tissues in the body. Like all tissue types, it consists of cells surrounded by a compartment of fluid called the extracellular matrix (ECM). However connective tissue differs from other types in that its cells are loosely, rather than tightly, packed within the ECM.
A PowerPoint review of photomicrographs depicting the various histological features of muscle tissues : skeletal, cardiac, and smooth. By Timothy Ballard, UNC Wilmington. Licensed under a Creative Commons License: Attribution Non-Commercial-NoDerivs. From http://www.lifescitrc.org/resource.cfm?submissionID=8992
A complete lecture of the Histology of Muscle Tissues, taught at First Moscow State Medical University, Moscow, in the Histology department, for the first year English medium foreign medical students.
Epithelium cellstissues histology
1. Chapter 4 Tissues and Histology • Tissues - collections of similar cells and the substances surrounding them • Tissue classification based on structure of cells, composition of noncellular extracellular matrix, and cell function • Major types of adult tissues – Epithelial – Connective – Muscle – Nervous • Histology: Microscopic Study of Tissues – Biopsy: removal of tissues for diagnostic purposes – Autopsy: examination of organs of a dead body to determine cause of death
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A PowerPoint review of photomicrographs depicting the various histological features of muscle tissues : skeletal, cardiac, and smooth. By Timothy Ballard, UNC Wilmington. Licensed under a Creative Commons License: Attribution Non-Commercial-NoDerivs. From http://www.lifescitrc.org/resource.cfm?submissionID=8992
A complete lecture of the Histology of Muscle Tissues, taught at First Moscow State Medical University, Moscow, in the Histology department, for the first year English medium foreign medical students.
Epithelium cellstissues histology
1. Chapter 4 Tissues and Histology • Tissues - collections of similar cells and the substances surrounding them • Tissue classification based on structure of cells, composition of noncellular extracellular matrix, and cell function • Major types of adult tissues – Epithelial – Connective – Muscle – Nervous • Histology: Microscopic Study of Tissues – Biopsy: removal of tissues for diagnostic purposes – Autopsy: examination of organs of a dead body to determine cause of death
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Histological review of the cardiac muscle-maha hammady.pptxMaha Hammady
Histological review of the cardiac muscle-maha hammady.pptx
for references and more details, check my article :
https://www.researchgate.net/publication/378439219_Enhancing_Our_Understanding_A_Comprehensive_Exploration_of_Heart_Histology_and_Cardiomyocyte_Molecular_Structure
Learning Objectives:
Compare and contrast the structure and function
of
Arteries
Veins
Capillaries
ulatory
system
Arteries
Arterioles
Capillaries
Venules
Veins
3 tunics
Lume
The Vessels
Functions:
Distribution of blood
Exchange of materials with tissues
Return of blood to the heart
Structure:
Most have the same basic structure:
– 3 layers surrounding a hollow lumen
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!
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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.
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
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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
2. The Circulatory System
-pumps and directs blood cells and substances carried in blood to all
tissues of the body.
- It includes both the blood and lymphatic vascular system.
3. Lecture outline:
• Heart
• 3 major layers
• Innate cardiac conducting system
• Purkinje fibers
• Cardiac skeleton
6. The CVS is composed of:
Heart- an organ whose function is to pump the blood.
Arteries- a series of efferent vessels that become smaller as they branch into
the various organs.
- carry the blood to the tissues.
Capillaries-the smallest blood vessels
- site of oxygen and carbon dioxide, nutrient and waste product
exchange between blood and tissues.
Veins- which result from the convergence of capillaries into a system of
larger channels that continue enlarging as they approach the heart,
toward which they convey the blood to be pumped again.
7. Endothelium
-is a single layer of a squamous epithelium that lined the internal
surface of all components of the blood.
Function:
1. Acts as a selectively permeable,antithrombogenic (inhibitory to clot
formation) barrier
2. Determines when and where white blood cells leave the circulation
for the interstitial space of tissues
3. Secretes a variety of paracrine factors for vessel dilation,
constriction and growth of adjacent cells.
8. Heart
• The heart is a muscular organ
that contracts rhythmically,
pumping the blood through the
circulatory system
• The right and left ventricles
pump blood to the lungs and the
rest of the body respectively
• The right and left atria receive
blood from the body and the
pulmonary veins respectively.
9. The Heart’s 3 major layers:
1. The inner endocardium of the endothelium and subendothelial
connective tissue.
2. The myocardium of cardiac muscle.
3. The epicardium, connective tissue with many adipocytes and
covered mesothelium.
10. The endocardium consists of:
Endothelium (En) -a thin layer of
connective tissue with smooth
muscle cells.
Subendothelial layer (Sen)- a layer of
variable thickness lacking smooth
muscle
11. Subendocardial layer
consists of:
• Small nerves
• Conducting (Purkinje) fibers (P) -
These fibers are cardiac muscle
cells joined by intercalated disks
but specialized for impulse
conduction rather than
contraction.
• Purkinje fibers are usually larger
than contractile cardiac muscle
fibers with large amounts of lightly
stained glycogen filling most of the
cytoplasm and displacing sparse
myofibrils to the periphery.
12. The cardiac conducting system
• This system consists of two nodes located in the right
atrium—the sinoatrial (SA) node (pacemaker) and the
atrioventricular (AV) node—and the atrioventricular
bundle (of His).
• The SA node is a small mass of modified cardiac muscle
cells that are fusiform, smaller and with fewer myofibrils
than neighboring muscle cells.
• The cells of the AV node are similar to those of the SA
node but their cytoplasmic projections branch in various
directions, forming a network.
• Distally fibers of the AV bundle become larger than
ordinary cardiac muscle fibers and acquire a distinctive
appearance. These conducting myofibers or Purkinje
fibers have one or two central nuclei and their cytoplasm
is rich in mitochondria and glycogen. Myofibrils are
sparse and restricted to the periphery of the cytoplasm
13. The Myocardium
• The thickest layer
• Consist mainly of cardiac muscle
with its fibers arranged spirally
around each heart chamber
14. The Epicardium
• Simple squamous mesothelium supported by a
layer of connective tissue containing blood vessels
and nerves.
• The epicardium, is the site of the coronary vessels
and contains considerable adipose tissue. This
section of atrium shows part of themyocardium
(M) and epicardium (Ep). The epicardium consists
of loose connective tissue (CT) containing both
autonomic nerves (N) and fat (F).
• The epicardium is the visceral layer of the
pericardium and is covered by the simple
squamous-to-cuboidal epithelium (arrows) that
also lines the pericardial space. These mesothelial
cells secrete a lubricate fluid that prevents friction
as the beating heart contacts the parietal
pericardium on the other side of the pericardial
cavity.
15. Cardiac skeleton
• Masses of dense irregular
connective tissue.
• Surrounds the bases of all heart
valves, separates the atria from
the ventricles, and provides
insertions for cardiac muscles.
• These fibrous tissue includes the
chordae tendinae, cords that
extend from the cusps and the
chordae tendinae to which they
attached.
16. Cardiac skeleton
Function:
• Anchors and supports the heart
valves
• Provides firm points of insertion
for cardiac muscle
• Helps coordinate the heartbeat
by acting a s electrical insulation
between atria and ventricles
18. Tissues of the vascular wall
• Walls of all blood vessels except capillaries contain smooth muscle
and connective tissue in addition to the endothelial lining.
• The endothelium is a specialized epithelium that acts as a
semipermeable barrier between two internal compartments: the
blood plasma and the interstitial tissue fluid.
19. Functions of Endothelial cells
1. Nonthrombogenic surface
2. Regulate local vascular tone and blood flow
3. Inflammation and local immune responses
4. Secrete growth factors
20. Walls of arteries, veins, capillaries
• tunica intima, tunica media, and
tunica externa (or adventitia)
• An artery has a thicker tunica media
and relatively narrow lumen.
• A vein has a larger lumen and its
tunica externa is the thickest layer.
The tunica intima of veins is often
folded to form valves.
• Capillaries have only an endothelium,
with no subendothelial layer or other
tunics.
21. • Simple squamous endothelial cells (arrows)
line the tunica intima (I) which has
subendothelial loose connective tissue and is
separated from the tunica media by the
internal elastic lamina (IEL), a prominent sheet
of elastin.
• The media (M) contains elastic lamellae and
fibers (EF) and multiple layers of smooth
muscle not seen well here. The tunica media is
much thicker in large arteries than veins, with
relatively more elastin.
• Elastic fibers are also present in the outer
tunica adventitia (A), which is relatively thicker
in large veins.
• Vasa vasorum (V) are seen in the adventitia of
the aorta. The connective tissue of the
adventitia always merges with the less dense
connective tissue around it.
Aorta Vena Cava
22.
23. Microvasculature
Arterioles (A), capillaries (C), and venules
(V) comprise the microvasculature where,
in almost every organ, molecular exchange
takes place between blood and the
interstitial fluid of the surrounding tissues.
Lacking media and adventitia tunics and
with diameters of only 4-10 μm, capillaries
(C) in paraffin sections can be recognized by
nuclei adjacent to small lumens or by highly
eosinophilic red blood cells in the lumen.
24. Microvascular bed
structure and perfusion
• In metarterioles, the smooth muscle cells are
dispersed as bands that act as precapillary
sphincters.
• The thoroughfare channel, lacks smooth
muscle cells and merges with the
postcapillary venule.
• The precapillary sphincters regulate blood
flow into the true capillaries.
• At any given moment, most sphincters are at
least partially closed and blood enters the
capillary bed in a pulsatile manner for
maximally efficient exchange of nutrients,
wastes, O2, and CO2 across the endothelium
25. Capillaries
Capillaries consist only of an
endothelium rolled as a tube, across
which molecular exchange occurs
between blood and tissue fluid. (a)
Capillaries are normally associated with
perivascular contractile cells called
pericytes (P) that have a variety of
functions. The more flattened nuclei
belong to endothelial cells.
26. Types of capillaries
(a) Continuous capillaries- have tight,
occluding junctions sealing the intercellular
clefts between all the endothelial cells to
produce minimal fluid leakage.
(b) Fenestrated capillaries- also have tight
junctions, but perforations (fenestrations)
through the endothelial cells allow greater
exchange across the endothelium.
c) Sinusoids, or discontinuous capillaries,
usually have a wider diameter than the other
types and have discontinuities between the
endothelial cells, large fenestrations through
the cells, and a partial, discontinuous
basement membrane.
27. Venules
• the last segment of the microvasculature where capillary beds
generally drain.
• Postcapillary venules- are the sites at which white blood cells enter
damaged or infected tissue
28. Venules
(a)Compared to arterioles (A), postcapillary venules (V) have
large lumens and an intima of simple endothelial cells, with
occasional pericytes (P).
(b)Larger collecting venules (V) have much greater diameters
than arterioles (A), but the wall is still very thin, consisting of an
endothelium with more numerous pericytes or smooth muscle
cells.
(c) The muscular venule cut lengthwise here has a better
defined tunica media, with as many as three layers of smooth
muscle (M) in some areas, a very thin intima (I) of endothelial
cells (E), and a more distinct adventitia (Ad). Part of an arteriole
(A) shows a thicker wall than the venule.
Postcapillary venules are important as the site in the vasculature
where these cells leave the circulation to become functional in
the interstitial space of surrounding tissues when such tissues
are inflamed or infected.
(d) Postcapillary venule (V) from an infected small intestine
shows several leukocytes adhering to and migrating across the
intima.
29. Arteriovenous shunts
In skin blood flow can be varied according to external
conditions by arteriovenous (AV) shunts, or anastomoses,
commonly coiled, which directly connect the arterial
and venous systems and temporarily bypass capillaries.
In venous portal systems one capillary bed drains into
a vein that then branches again into another capillary bed.
This arrangement allows molecules entering the blood in
the first set of capillaries to be delivered quickly and at high
concentrations to surrounding tissues at the second capillary
bed, which is important in the anterior pituitary gland
and liver.
30. Veins
(a) Small vein (V) shows a relatively large lumen
compared to the small muscular artery (A) with
its thick media (M) and adventitia (Ad). The wall
of a small vein is very thin, containing only two
or three layers of smooth muscle.
(b) Convergence between two small veins shows
valves (arrow). Valves are thin folds of intima
projecting well into the lumen, which act to
prevent backflow of blood.
(c) Medium vein (MV) shows a thicker wall but
still less prominent than that of the
accompanying muscular artery (MA). Both the
media and adventitia are better developed, but
the wall is often folded around the relatively
large lumen.
(d) Medium vein contains blood and shows
valve folds (arrows).
31. Wall of Large vein with valve
Large veins have a muscular
media layer (M) that is very thin
compared to the surrounding
adventitia (A) of dense irregular
connective tissue.
The wall is often folded with the
intima (I) projecting into the
lumen as a valve (V) composed of
the subendothelial connective
tissue with endothelium on both
sides.