Location via proxy:   [ UP ]  
[Report a bug]   [Manage cookies]                

Blood 200L

Download as pptx, pdf, or txt
Download as pptx, pdf, or txt
You are on page 1of 38

Blood

By

Dr. Alfred Ehiaghe


Components of Whole Blood

Plasma
(55% of whole
blood)

Buffy coat:
leukocyctes
and platelets
(<1% of whole blood)
Formed
elements
Erythrocytes
1 Withdraw blood 2 Centrifuge (45% of whole blood)
and place in tube

• Hematocrit
• Males: 47% ± 5%
• Females: 42% ± 5%
Components of plasma
(90% water rest
solids) Solids

Plasma Proteins Regulatory &


protective Organic and inorganic substances
6‐8 gm/dL proteins

Albumin Waste material


Hormones
3‐4
Antibodies Nutritive material
gm/dL
Globulin
2.5‐4 gm/ Enzymes Ions

dL
Fibrinogen
0.3 gm/ dl
Functions of blood
Distributive
• Carries O2 (from lungs) and nutrients (from
GIT and body stores) to all cells
• Carries wastes from all cells to elimination
sites (lungs for CO2, liver for bilirubin and
kidneys for nitrogenous wastes)
• Carries hormones (chemical signals) from
endocrine organs to target tissues.
Functions of blood…
Regulatory functions
• Body T° by absorbing and distributing heat
• pH by virtue of its many buffers
•Maintains adequate fluid volume in the body
Protective functions
• Prevents blood loss by initiating clotting
mechanisms in response to blood vessel damage
• Prevents infection via WBCs and plasma immune
proteins
Formation of cellular elements of
blood
In fetus: Extramedullary hematopoiesis(3 stages)
• Mesoblastic: (16‐19 days): Clusters of
mesenchymal cells in yolk sac ends by 12
weeks
• Hepatic (Second trimester) Liver, spleen
and lymph node
• Myeloid(Last month of gestation+ after birth):
Bone marrow
Bone marrow is the site of synthesis of
all formed elements of blood after
birth
Red bone marrow
Formation of cellular elements of
blood
Upto 5 yrs: all bone marrow
Upto 20 yrs: bone marrow of membranous +
ends of long bones
After 20 yrs: bone marrow of membranous
bone
Erythropoiesis: Formation of RBCs

This development takes about 7 days


and involves three to four mitotic cell
divisions, so that each stem cell
gives rise to 8 or 16 cells.
Erythropoiesis

Basophilic Polychromatophil Orthochromatic


erythroblast erythroblast erythroblast

Early Intermediate Late


Megaloblast normoblast normoblast normoblast

7‐10 µ m
15‐20µ m Nucleus: size 10‐14 µ m Nucleus: cart
Nucleus: Big Nucleoli: absent Nucleus: Size wheal‐ pyknotic
Hb: absent Hb: absent Hb: Starts Hb: increases
appearing
Reticulocytes VS mature RBC
• Size: 8 μm • Size: 7 μm
• Shape:Polylobulated • Shape: Biconcave disc
• Adhesiveness more • Adhesiveness less
• RNA and ribosomes • RNA and ribosomes
present absent
• Transferrin receptors • Transferrin receptors
present absent
• Hemoglobin • No more hemoglobin
synthesis synthesis
Erythrocytes (RBCs)

Figure 17.3
PBS under low power
PBS under high power
RBC indices
• MCV gives you the average volume of
erythrocytes.
• MCH gives you the average weight of
hemoglobin per eyrthrocyte.
• MCHC gives you the average hemoglobin
concentration per erythrocyte.
RBC indices
MCV: Average volume of the RBC
MCV= PCV in % X 10 cubic microns
RBC count in
millions/mm3
MCH: Average Hb
concentration of a RBC
MCH= Hb(gm/dl) X10 picogram
RBC count in million/mm3
MCHC: Ave. Hb concentration per RBC
MCHC= Hb(gm/dl) X100
PCV(%)
Biconcave disc shape of RBC
• Increased ratio of surface area : volume(40%
more membrane)
Facilitates gas transport
• More deformable
Maintenance of biconcave shape
• Elastic forces within the membrane
• Surface tension
• Electrical forces on the membrane surface due
to albumin adsorption
• Osmotic /hydrostatic forces
Spherocyt
e

Observed in immune induced hemolysis,


post blood transfusions, and congenital
anemia
Target cell

Observed in hemoglobinopathy, hepatic


diseases, iron deficiency anemia, hemolytic
anemia, and splenectomy.
Schistiocytes

Uremia, microangiopathic hemolytic anemias,


hemolytic anemias cause by physical agents,
and disseminated intravascular coagulation
(DIC)
Ovalocytes

Hereditary defect present in the RBC


cytoskeletal proteins (the spectrin chain),
iron deficiency anemia, leukemia
associated anemias, thalassemia, and
dyserythropoiesis
Poikilocytosis

Indicator of abnormal erythropoiesis due to


bone marrow effects and/or abnormal RBC
destruction
Howell‐Jolly bodies

Observed in hemolytic anemias, pernicious


anemia, post‐operative conditions,
splenectomy, or splenic atrophy
Echinocyte

Observed in uremia, acute blood loss,


stomach cancer, and pyruvate kinase
deficiency
Burr cell

Observed in uremia, acute blood loss,


stomach cancer, and pyruvate kinase
deficiency
Basophilic stippling

Observed in lead poisoning, alcoholism


megaloblastic anemias
Hematocrit/ Packed cell volume
Percentage of the total volume of blood that is
occupied by packed red blood cell
Normal values are as follows:
• Adult male = 42% to 53%
• Adult female = 36% to 46%
• Newborn = 50% to 62%
• One year = 31% to 39%
Hematocrit
• Increased
Polycythemia
Shock associated with surgery, burns, or traumas
Dehydration
• Decreased
Anemias
Pregnancy
receiving IV fluids
Cardiac decompensation (a failure to maintain a good blood
circulation)
Erythropoietin
Site of synthesis

90% kidney

10% liver & hepatocytes


Sites of erythropoiesis
Mechanism of red cell destruction
Averege life span 120 days
4 major mechanisms of destruction
1. Osmotic lysis
2. Erythrophagocytosis
3. Complement induced cytolysis
4. Fragmentation
Heme oxygenase system responsible for
hemoglobin degradation is located in the
phagocytic cells of Liver, Spleen& Bone marrow
Sites of erythrocyte destruction
• Extravascular hemolysis(80‐90 %)
Spleen, Liver, Macrophages, Lymph node and
Bone marrow
• Intravascular hemolysis
Hemoglobin is discharged directly into the
circulation & is removed by several
mechanisms
THANKS

You might also like