Karl Landsteiner discovered the ABO blood group system in 1900. He found that mixing blood samples together could cause agglutination, or clumping. Based on this, he identified the main blood groups: A, B, AB, and O. The presence of antigens A or B on red blood cells determines blood group. Rh factor is another important blood group - a person can be either RhD positive or negative. Blood typing involves testing blood against different antibodies to identify a person's blood group. Matching donor and recipient blood by ABO and RhD type is crucial for safe blood transfusions.
A blood type (also called a blood group) is a classification of blood based on the presence or absence of inherited antigenic substances on the surface of red blood cells (RBCs). These antigens may be proteins, carbohydrates, glycoproteins, or glycolipids, depending on the blood group system.
Although individual humans (and all diploid organisms) can only have two alleles for a given gene, multiple alleles may exist at the population level.
“Three or more kinds of gene which occupy the same locus are referred to as multiple alleles.”
Abo blood group system by Pandian M, Tutor, Dept of Physiology, DYPMCKOP.Pandian M
SLO’s
INTRODUCTION
HISTORICAL REVIEW
EVOLUTION
CLASSIFICATION
ABOUT CLASSICAL ABO BLOOD GROUPING SYSTEM
AGGLUTINOGENS
AGGLUTININS
TYPES OF ABO BLOOD GROUPS
POPULATION DISTRIBUTION
INHERITANCE
DETERMINATION
CLINICAL IMPRTANCE
A blood type (also called a blood group) is a classification of blood based on the presence or absence of inherited antigenic substances on the surface of red blood cells (RBCs). These antigens may be proteins, carbohydrates, glycoproteins, or glycolipids, depending on the blood group system.
Although individual humans (and all diploid organisms) can only have two alleles for a given gene, multiple alleles may exist at the population level.
“Three or more kinds of gene which occupy the same locus are referred to as multiple alleles.”
Abo blood group system by Pandian M, Tutor, Dept of Physiology, DYPMCKOP.Pandian M
SLO’s
INTRODUCTION
HISTORICAL REVIEW
EVOLUTION
CLASSIFICATION
ABOUT CLASSICAL ABO BLOOD GROUPING SYSTEM
AGGLUTINOGENS
AGGLUTININS
TYPES OF ABO BLOOD GROUPS
POPULATION DISTRIBUTION
INHERITANCE
DETERMINATION
CLINICAL IMPRTANCE
1
BIOL 102: Lab 9
Simulated ABO and Rh Blood Typing
Objectives:
After completing this laboratory assignment, students will be able to:
• explain the biology of blood typing systems ABO and Rh
• explain the genetics of blood types
• determine the blood types of several patients
Introduction:
Before Karl Landsteiner discovered the ABO human blood groups in 1901, it was thought that all blood was the
same. This misunderstanding led to fatal blood transfusions. Later, in 1940, Landsteiner was part of a team
who discovered another blood group, the Rh blood group system. There are many blood group systems known
today, but the ABO and the Rh blood groups are the most important ones used for blood transfusions. The
designation Rh is derived from the Rhesus monkey in which the existence of the Rh blood group was
discovered.
Although all blood is made of the same basic elements, not all blood is alike. In fact, there are eight different
common blood types, which are determined by the presence or absence of certain antigens – substances that
can trigger an immune response if they are foreign to the body – on the surface of the red blood cells (RBCs
also known as erythrocytes).
ABO System:
The antigens on RBCs are agglutinating antigens or agglutinogens. They have been designated as A and B.
Antibodies against antigens A and B begin to build up in the blood plasma shortly after birth. A person
normally produces antibodies (agglutinins) against those antigens that are not present on his/her erythrocytes
but does not produce antibodies against those antigens that are present on his/her erythrocytes.
• A person who is blood type A will have A antigens on the surface of her/his RBCs and will have
antibodies against B antigens (anti-B antibodies). See picture below.
• A person with blood type B will have B antigens on the surface of her/his RBCs and will have antibodies
against antigen A (anti-A antibodies).
• A person with blood type O will have neither A nor B antigens on the surface of her/his RBCs and has
BOTH anti-A and anti-B antibodies.
• A person with blood type AB will have both A and B antigens on the surface of her/his RBCs and has
neither anti-A nor anti-B antibodies.
The individual’s blood type is based on the antigens (not the antibodies) he/she has. The four blood groups
are known as types A, B, AB, and O. Blood type O, characterized by an absence of A and B agglutinogens, is
the most common in the United States (45% of the population). Type A is the next in frequency, found in 39%
of the population. The incidences of types B and AB are 12% and 4%, respectively.
2
Table 1: The ABO System
Blood
Type
Antigens on
RBCs
Antibodies
in the Blood
Can GIVE Blood
to Groups:
Can RECEIVE
Blood from Groups:
A A Anti-B A, AB O, A
B B Anti-A B, AB O, B
AB A and B
Neither anti-A
nor anti-B
AB O, A, B, AB
O
Neither A nor
B
Both anti-A.
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.
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
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
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
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
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.
2. How blood group is determined !
As per Mendel, every character is controlled by one pair of alleles. There are only two
optional forms, one of which is Dominant and the other one is Recessive. Cases are
observed where there are more than two optional forms of a gene for one character.
Thus when three or more alleles are responsible for a single characteristic, they are
known as multiple alleles. All these alleles occupy the same specific locus on the
chromosomes. In a diploid cell, only two alleles can be present at a time on the
homologous chromosomes. A well known example is the ABO blood type in humans.
There are 4 main blood groups (types of blood) :–
A, B, AB and O. Your blood group is determined by the genes you inherit from your
parents.
Each group can be either RhD positive or RhD negative, which means in total there are 8
blood groups.
Rh was First discovered in Rhesus Monkey , That’s why called Rhesus Factor
3. Blood genotypes
Here the inheritance is based on three
alleles i.e. IA , IB , i . IA and IB are
dominant and i is recessive. The gene
for producing antigen I and it’s allele for
non producing antigen is i . IA is
responsible for producing Antigen-A.
Gene 1B is responsible for producing
Antigen-B.
These two alleles are co-dominant
which means that both can express
themselves in presence of each other.
Thus three alternatives are possible.
Various persons in different blood
groups can have following probable
genotype.
4. To work out your blood group, your red cells are
mixed with different antibody solutions. If, for
example, the solution contains anti-B antibodies and
you have B antigens on your cells (you're blood
group B), it will clump together.
If the blood does not react to any of the anti-A or
anti-B antibodies, it's blood group O. A series of
tests with different types of antibody can be used to
identify your blood group.
If you have a blood transfusion – where blood is
taken from one person and given to another – your
blood will be tested against a sample of donor cells
that contain ABO and RhD antigens. If there's no
reaction, donor blood with the same ABO and RhD
type can be used.
Blood group Serum test
5. In practice of blood transfusion. Karl Landsteiner discovered the ABO blood group in 1900 when he separated
cellular and liquid components from both his and his colleagues’ blood mixed in combination. As indicated by the
negative symbol (-) in the table , no agglutination of red blood cells was observed when both components from the
same individuals were mixed. However, RBC agglutination was observed in some combinations, as indicated with
the positive symbol (+). From the results gleaned from his studies, Landsteiner realized that people could be
grouped depending on the agglutination pattern of their RBCs. For example, Dr. St. and Mr. Land. belong to one
group. Similarly, Dr. Plee. and Mr. Zar. belong to a disparate second group, and Dr. Sturl. and Dr. Erdh belong to a
third group. In the next year, a fourth group was discovered by Sturle and von Decastello, Landsteiner's colleagues,
and these four groups became what is now known as the ABO group system (A, B, AB, and O groups). However, the
most important finding obtained from these experiments is that only ABO-matched blood that does not cause RBC
agglutination should be used for transfusion.
Experiment
6. In order to explain the RBC agglutination phenomenon, Landsteiner postulated that 2 different
antigens (A and B) are found on the surface of RBCs, and the "naturally occurring" antibodies
against these antigens are found in the plasma of individuals who do not express them (The
Landsteiner’s Law). For example, blood group A individuals express the A antigen on their RBCs
and possess anti-B antibodies in their plasma. Similarly, blood group B individuals express the B
antigen on their RBCs and possess anti-A antibodies in their plasma. Blood group AB individuals
express both A and B antigens on their RBCs and possess neither anti-A nor anti-B antibodies,
whereas blood group O individuals express neither A nor B antigens on their RBCs but possess
both anti-A and anti-B antibodies.
ABO blood groups are hereditary, and their mode of inheritance was explained by Bernstein’s one
gene-three allelic model. In this model, Bernstein postulated that there are three alleles, A, B, and
O, at a single ABO genetic locus, and that A and B alleles are co-dominant against the recessive O
allele. This produces 6 genotypes (AA, AO, BB, BO, AB, and OO) resulting in 4 phenotypes.
Landsteiner’s discovery
7. Pregnant women are always given a blood group test. This is because if the
mother is RhD negative but the child has inherited RhD-positive blood from
the father, it could cause complications if left untreated.
RhD-negative women of child-bearing age should always only receive RhD-
negative blood.
Rhesus disease is uncommon these days because it can usually be prevented
using injections of a medication called anti-D immunoglobulin.
Pregnancy
8. Giving blood
Most people are able to give blood, but only 1 in 25 people actually do. You can donate
blood if you:
are fit and healthy
weigh at least 50kg (7st 12lb)
are 17-66 years old (or 70 if you've given blood before)
are over 70 and have given blood in the last 2 years