Chapter 10 Blood
Chapter 10 Blood
Components of blood
Living cells
Formed elements – RBC & WBC
Non-living matrix
Plasma
When Blood is centrifuged
Colors:
Oxygen rich blood – scarlet red (bright)
Oxygen poor blood – dull red
Distribution:
Oxygen to lungs
Nutrients to digestive system
Transporting metabolic wastes from elimination sites
(lungs, kidneys, liver)
Hormones from glands to target organs
Functions of Blood
Regulation:
Maintain appropriate body temperature by absorbing and
distributing heat through body, encouraging skin for heat
loss
Maintain normal pH, blood holds an “alkaline” reserve to
raise pH when necessary
Maintain adequate fluid volume in circulation
Salts & blood protein – prevent excess fluid loss
Protection
Prevents blood loss
Prevents infection
Blood Plasma
Proteins include:
Albumin: regulates osmotic pressure
The pressure that keeps water in the blood
Essentially carries all proteins around the blood
High albumin almost always caused by dehydration
Low albumin can come from liver disease, kidney disease, & malnutrition
Globulins:
Alpha, beta: transport proteins that bind to lipids, metal ions, fat-soluble vitamins
Gamma: antibodies released during an immune response
Clotting proteins: help to stop blood loss when a blood vessel is injured
Antibodies: help protect the body from pathogens (disease)
Blood Plasma
Erythrocytes
Red blood cells (RBCs)
Leukocytes
Lymphocytes
Both are white
blood cells (WBCs)
Platelets
Cell fragments
Formed Elements
Erythrocytes
AKA Red blood cells (RBCs)
4-6 million (per mm3)
Developed in the bone marrow
Salmon – colored biconcave discs
Anucleate – CAN’T reproduce–produced in the bone marrow
Literally, sacs of hemoglobin
most organelles have been rejected
Structural protein called spectrin: spectrin net is deformable – allows
erthyrocytes to change shape as necessary to move through blood vessels
Each erythrocyte has 250 million hemoglobin sacs
Normal blood contains 12-18g per 100ml of blood
Functions:
Transport oxygen to lung capillary beds
Also transports small amounts of CO (about 20%)
Formed Elements
Erythrocytes
Women have lower RBC count (4.32 -5, versus 5.1 – 5.8
mm3)
As RBCs increase, blood viscosity increases, blood flow slows
Function:
Respiratory gas transport
Hemoglobin in RBC binds to oxygen
14-20 (g/100ml) – infants
13-18 – adult males
12 – 16 – adult females
Hemoglobin is inside RBCs to prevents the protein molecule
from breaking apart and leaking through the bloodstream
Formed Elements
Diseases of RBCs
Anemia
Decrease in oxygen carrying ability
Polycythemia
excessive or abnormal increase in
the number of RBCs
Formed Elements
Formed Elements: Leukocytes
Essential for body’s defense against pathogens
Agranulocytes
Lack of visible granules Basophils
Erythrocytes
Nuclei are spherical, oval or kidney – shaped
Include: lymphocytes & monocytes
Platelets
List of the WBCs from most to least abundant
Eosinophils
Neutrophils Never
Lymphocytes Let
Monocytes Monkeys
Eosinophils Eat
Basophils Bananas
Lymphocytes Monocytes Neutrophils
Formed Elements: Types of Leukocytes
Neutrophils
Multilobed nuclei with small granules
Acts as phagocyte at active site of
infection
“first responder” to inflammatory site
(trauma) – tell tale sign of acute
inflammation
Eosinophils
Large brick red granules
Shown in response to allergies, asthmatic
reactions or parasitic worms
May play a role in defense against viruses
Formed Elements: Types of Leukocytes
Basophils
Least common granulocytes
Contain histamine granules
Initiate inflammation
Contain heparin
Prevent blood from clotting too quickly
May regulate the behavior of T cells
Formed Elements: Types of Agranulocytes
Lymphocytes
Nucleus fills most of the cell
Plays an important role in the immune
system
Types of Lymphocytes:
Killer Cells (Killer T Cells)
Defend against tumors and virally infected
cells
T Cells (Thymus Cells)
Many subsets of t cells
All cell mediated immunity – pathogen
detection
B Cells (Bone cells)
Secretion of antibodies
Neutralize foreign objects like bacteria &
viruses
Formed Elements: Types of Agranulocytes
Monocytes
Largest WBC in size
~50% found in the spleen
Function as macrophages
Specific & non-specific defense
Act in response to inflammatory situations
to get rid of pathogen/allergic causing
antigen
Important in fighting chronic infection
WBC Abnormalities
Leukocytosis
WBC count above 11,000 leukocytes/mm3
Generally indicates an infection
But not indicative of any specific infection
It’s diagnostically similar to a fever
Leukopenia
Abnormally low leukocyte level
Commonly caused by certain drugs such as corticosteroids and anticancer agents
An important indicator of infection risk
Leukemia
Bone marrow becomes cancerous, turns out excess WBC
4 types: ALL (acute lymphoblastic), CLL, AML (acute myelogenous), & CML
Can be acute or chronic
Acute is more common in children, chronic in the elderly
Can be lymphoid or myeloid
Lymphoid is more common in children, myeloid is rare in children
http://www.youtube.com/watch?v=tDTLC2swhlQ
Formed Elements: Platelets
Aka thrombocytes
Small regular shaped cell fragments, derived from megakaryocytes (bone marrow
cell)
Average lifespan of a platelet is 5 to 9 days
If platelets are too low, excessive bleeding can occur; if too high, wanted/unwanted
clotting can occur.
Hematopoiesis
Blood cell formation in red bone marrow
Rate
Moreof RBC production is controlled by the hormone erthyropoietin
RBCs
levels
Formation of WBCs and platelets
Controlled by hormones
Colony stimulating factors (CSFs) and interleukins prompt bone
marrow to generate leukocytes
Thrombopoietin stimulates production of platelets
Hemostasis
break
PF from
Platelets
3
platelets become sticky & cling to the collagen fibers
Calcium
and other
Those platelets
+ clotting
release chemicals (PF3) to attract more platelets
factors
The in blood
platelets pile up to form a platelet plug
Tissue factor
plasma
in damaged
tissue
Coagulation (blood clotting)
Injured tissues
Phases of
coagulation Formationrelease
of TF (tissue factor)
(clotting prothrombin
PF interacts with TF, clotting factors & calcium ions to initiate the
cascade) 3 activator
clotting cascade
Prothrombin Thrombin
Prothrombin gets converted to thrombin by prothrombin activator.
Thrombin
Fibrinogen joins fibrinogen proteins into hair-like molecules of insoluble
Fibrin
(soluble) (insoluble)
fibrin
Fibrin forms a meshwork (the basis for a clot)
Hemostasis
Embolus
A thrombus that breaks away and floats freely in the bloodstream
In general, an embolus is ANY detached, itinerant intravascular mass –
they can be solid, liquid or gas
Can later clog vessels in critical areas such as the brain
Bleeding Disorders
Thrombocytopenia
Platelet deficiency = below 50,000 per
microliter
Normal platelet counts are between
150,000 – 450,000 per microliter of
blood (that’s a lot)
Even normal movements can cause
bleeding from small blood vessels
that require platelets for clotting
Symptoms include frequent bruising,
purpura, & petechiae
Bleeding Disorders
Haemophilia
Hereditary bleeding disorder
Normal clotting factors are missing
When bleeding occurs, a scab does
form, but it is temporary
The clotting factor prevents the fibrin
from reattaching and healing the blood
vessel
Blood Typing & Transfusions
Large losses of blood have serious consequences
Loss of 15–30% causes weakness
Loss of over 30% causes shock, which can be fatal
Blood is tested for a large number of diseases before giving to the patient who needs blood
Tested for:
All forms of HIV, All forms of hepatitis, syphillis, CMV, and West Nile virus – just to name a few
Complications:
Hemolytic reactions: you have antibodies again the donor’s RBCs –
symptoms include fever, chills, increased heart rate, shortness of breath, rapid drop in blood pressure.
Transfusion must be stopped immediately before kidney damage occurs
Allergic reactions: while blood banks look at the complete chemical make up of donor blood, if a
patient is unaware of allergies and these chemicals are in blood – an allergic reaction can occur
If severe, Usually easily fixed by dosing epinephrine to stop anaphylaxis
Human Blood Groups