introduction to the cardiovascular system
DESCRIPTION
Introduction to the Cardiovascular System. A circulating transport system A pump (the heart) A conducting system (blood vessels) A fluid medium ( blood ) Is specialized fluid of connective tissue Contains cells suspended in a fluid matrix. Functions of Blood. - PowerPoint PPT PresentationTRANSCRIPT
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Introduction to the Cardiovascular System
A circulating transport system
A pump (the heart)
A conducting system (blood vessels)
A fluid medium (blood)
Is specialized fluid of connective tissue
Contains cells suspended in a fluid matrix
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Functions of Blood
Transport of blood cells and dissolved substances
such as oxygen and carbon dioxide
Regulation of pH and ions
Restriction of fluid losses at injury sites
Defense against toxins and pathogens
Stabilization of body temperature
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Physical Characteristics of Blood
Whole Blood Composition
Plasma
Fluid consisting of: ______________________________________________
______________________________________________
______________________________________________
Formed elements:
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Physical Characteristics of Blood
Three Types of Formed Elements
Red blood cells (RBCs) or erythrocytes
Transport oxygen and carbon dioxide
White blood cells (WBCs) or leukocytes
Protection from toxins and infection
Platelets
Cell fragments involved in clotting
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Physical Characteristics of Blood
Figure 19–1c The Composition of Formed Elements of Blood
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Physical Characteristics of Blood
Hemopoiesis
Process of producing formed elements
By myeloid and lymphoid stem cells
Occurs in red bone marrow and lymphatic
tissues
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Physical Characteristics of Blood
Three General Characteristics of Blood
38°C (100.4°F) is normal temperature
High viscosity:
Slightly alkaline pH:
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Physical Characteristics of Blood
Blood volume (liters) = 7% of body weight
(kilograms)
Adult Volume:
Normovolemic:
Hypovolemic
Hypervolemic:
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Plasma
Makes up 50–60% of blood volume
More than 90% of plasma is water
Extracellular fluids
Interstitial fluid (IF) and plasma
Materials plasma and IF exchange across capillary walls
Water
Ions
Small solutes
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Plasma
Plasma Proteins Albumins (60%)
Transport some lipid soluble substances Largely responsible for ability of blood to retain fluid
Globulins (35%) Antibodies, also called immunoglobulins Transport globulins bind to and carry some circulating
molecules
Fibrinogen (4%) Molecules that form clots and produce long, insoluble
strands of fibrin
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Plasma
Other Plasma Proteins
1% of plasma
Changing quantities of specialized plasma proteins
Enzymes and hormones
Most are made in liver
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Summary of Plasma Composition
Figure 19–1b The Composition of a Typical Sample of Plasma
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Red Blood Cells
Red blood cells (RBCs) make up 99.9% of blood’s formed
elements
Transports _______________________
Average about 8 micrometers in diameter
Oxygen and Carbon dioxide
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RBC Values
Red blood cell count: the number of RBCs in 1 microliter of
whole blood
Male: 4.5–6.3 million
Female: 4.2–5.5 million
Hematocrit (packed cell volume, PCV): percentage of RBCs in
centrifuged whole blood
Male: 40–54
Female: 37–47
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RBC Composition
No nucleus (enucleate) No membranous organelles Hemoglobin
Red, ___ containing molecules Transport oxygen and carbon dioxide
Bind oxygen in the lungs and release it in tissues Bind some carbon dioxide in the tissues and release it in
lungs 280 millions molecules per RBC
iron
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Hemoglobin Composition
Protein (globin) part Made of four polypeptides – blue part
Oxygen Binding parts – red parts four iron containing heme groups – iron binds
oxygen
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Hemoglobin Values
Normal hemoglobin (adult male)
14–18 g/dL whole blood
Normal hemoglobin (adult female)
12–16 g/dL, whole blood
If values are too low you are ___________.
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RBC Formation and Turnover
1% of circulating RBCs wear out per day
About 3 million RBCs per second
Macrophages of liver, spleen, and bone marrow
Monitor RBCs
Engulf RBCs before membranes rupture (hemolyze)
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Red Blood Cells
Hemoglobin Conversion and RecyclingPhagocytes break hemoglobin into
components Globin (protein part) to amino acids
Heme to Biliverdin
Iron
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Red Blood Cells
Iron Recycling
Iron removed from heme leaving biliverdin
To transport proteins (transferrin)
To storage proteins (ferritin and hemosiderin)
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Red Blood Cells
Breakdown of Biliverdin
Biliverdin (green) is converted to bilirubin
(yellow)
Bilirubin is:
Excreted by liver (bile)
Jaundice is caused by bilirubin buildup
Converted by intestinal bacteria to urobilins and
stercobilins
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Hemoglobin Recycling
Heme
Globin Amino Acids recycled
Biliverdin
Iron
BilirubinExcreted in urine and Feces
Stored in liver and spleen as ferritin and hemosiderin for later use
Hemoglobin
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Red Blood Cell Recycling
Figure 19–5 Recycling of Red Blood Cell Components
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Red Blood Cells
RBC Production
Erythropoiesis
Occurs only in myeloid tissue (red bone marrow) in adults
Stem cells mature to become RBCs
Hemocytoblasts
Stem cells in myeloid tissue divide to produce
Myeloid stem cells: become RBCs, and most WBCs
Lymphoid stem cells: become lymphocytes
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Red Blood Cell Maturation
Proerythroblasts form from myeloid stem cells become
Erythroblasts __________________________________
Normoblasts lose their nucleus and become reticulocytes
Reticulocytes enter blood to become _______________________________________
Erythrocytes are not able tomake _________________.Why?
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Regulation of RBC Formation (erythropoiesis)
Building red blood cells requires
Amino acids for:
Iron for:
Vitamins B12, B6, and folic acid:
pernicious anemia Low RBC production
Due to unavailability of vitamin B12
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Hormonal Control of Erythropoiesis
Erythropoietin (EPO) from Kidneys and liver
Also called erythropoiesis-stimulating hormone
Secreted when oxygen in peripheral tissues is low
(hypoxia)
Due to disease or high altitude
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Blood Types
ABO and Rh are most important types
Karl Landsteiner developed classifications for ABO blood types in 1901 Awarded Nobel Prize in medicine in 1930
Landsteiner and Alexander Wiener dicovered Rh type in 1937
Antigens (glycoproteins and glycolipids) called _____________ on surface of RBC’S determine blood types.
These antigens are inherited, thus blood types are inherited
Antibodies (agglutinins) against the antigens may be in the plasma
The following slides will illustrate
agglutinogens
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ABO Blood Types
Four ABO Blood Types
A (surface antigen A)
B (surface antigen B)
AB (antigens A and B)
O (neither A nor B)
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Blood Type Antibodies
Type A Type B antibodies
Type B Type A antibodies
Type O Both A and B antibodies
Type AB Neither A nor B antibodies
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ABO Blood Types Illustrated
ABO Type
Antigen on
RBC’s
Antibodies in Plasma
A A Anti-B
B B Anti-A
AB A&B Neither
O Neither Both
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Rh Blood Type
Rh blood type is determined by presence of absence of Rh (D) _____
(_________) on the surface of RBCsIf Rh agglutinogen present, the type is
Rh . If no agglutinogens are present, the type is Rh .
agglutinogen
antigen
+
-
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People with Rh- type lack anti-Rh antibodies (agglutinins), but if they receive Rh+ blood, their immune systems will be stimulated to produce them, and they are then _________. Future exposure to Rh+ blood will cause a dangerous blood reaction.
sensitized
Rh Blood Type
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Hemolytic Disease of the Newborn (HDN)
Results from Rh incompatibility between ___ mother and her ____child
If Rh+ RBC’s of first born child enter mother’s circulation, mother will be ________, and her plasma will carry anti-Rh agglutinins (antibodies)
Rh- Rh+
sensitized
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The first child is not harmed, but the mother’s _________, acquired by exposure to the first child’s blood, easily pass across the placenta where they _________ and destroy the second child’s RBC’s.
How is it prevented?
antibodies
agglutinate
Hemolytic Disease of the Newborn (HDN)
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HDN Illustrated
Figure 19–9 Rh Factors and Pregnancy
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Hemolytic Disease of Newborn
Figure 19–9 Rh Factors and Pregnancy
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The greatest concern with blood types involves _________
Person giving blood is the ______, person getting blood is the ________
If RBCs of a donor are incompatible with the blood of a recipient, antibodies in the plasma of the recipient will bind to the antigens of the donated RBCs.
This reaction will ______ (__________) and destroy (cause hemolysis of) the donated RBCs, resulting in a serious and possibly fatal reaction.
clump agglutinate
Transfusions and Blood Typing
transfusions
donorrecipient
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ABO and Rh Donors and Recipients
ABO and Rh Types
Can be donated to types
Can receive from types
A+ A+ and AB+ A+, A-, O+, O-
A- A+, AB+, AB- A-, O-
B+ B+, AB+ B+, B-, O+, O-
B- B+, B-, AB+, AB- B-, O-
AB+ AB+ All ABO and Rh types
AB- AB+, AB- All ABO Rh+ types
O+ All ABO Rh+ types O+, O-
O- All ABO and Rh Types
O-
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ABO and Rh Donors and Recipients
Use previous table to answer the following questionsDo you understand why some blood types
are compatible and some are not? What ABO Rh type is the universal donor?
What makes it the universal donor?Why is universal donor important
What is the universal recipient?What makes it the universal recipient?
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Blood Typing
To assure blood type compatibilities Blood type must be typed or Blood must be cross-matched (check page 664)
Supplies for blood typing: Sample of blood to be typed Three separate bottles of sera containing Anti-A,
Anti-B and Anti-Rh (D) antibodies Slide with three spaces marked A, B and Rh Three toothpicks to stir the the samples
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Blood Typing
Procedure for blood typing Put drops of blood (all the same) in the A, B and Rh
spaces Put drops of each serum in respective bloods
Anti-A serum in A space Anti-B serum in B space Anti-Rh (D) serum in Rh space
Mix each sample, being careful not to contaminate, and observe sample for any changes in appearance
What does it mean if sample clumps? What does it mean if sample does not clump?
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Determining ABO and Rh Types
Figure 19–8 Blood Type Testing
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Blood Type Cross Reactions
Figure 19–7b Blood Types and Cross-Reactions
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Percentage of Blood Types
Notice how percentages vary in different populations Notice that Native South Americans are all type O+
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White Blood Cells
Also called leukocytes
Have nuclei and other organelles
WBC functions
Defend against pathogens
Remove toxins and wastes
Attack abnormal cells
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White Blood Cells
WBC Circulation and Movement
Most WBCs in
Connective tissue proper
Lymphoid system organs
Small numbers in blood
5000 to 10,000 per microliter
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White Blood Cells
WBC Circulation and Movement
Characteristics of circulating WBCs
Can migrate out of bloodstream
Have amoeboid movement
Attracted to chemical stimuli (positive chemotaxis)
Some are phagocytic:
What does phagocytic mean?
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Types of WBCs
Granulocytes Granules in cytoplasm
Neutrophils
Eosinophils
Basophils
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Types of WBCs
Agranulocytes No granules in cytoplasm
Monocytes
Lymphocyte
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Facts About White Blood Cells
Neutrophils
Also called polymorphonuclear leukocytes
50–70% of circulating WBCs
Pale cytoplasm granules with
Lysosomal enzymes
Bactericides (hydrogen peroxide and superoxide)
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Facts About White Blood Cells
Neutrophil Actions Very active, first to attack bacteria
Phagocytes - engulf pathogens and digest
pathogens
Defensins (peptides from lysosomes) attack
pathogen membranes and destroy them
Form pus
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Facts About White Blood Cells
Eosinophils 2–4% of circulating WBCsCounteract inflammationAttack large parasitesAre sensitive to allergens
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Facts About White Blood Cells
Basophils
Are less than 1% of circulating WBCs
Are small
Help cause inflammation by accumulating in
damaged tissue and releasing histamine
Release heparin to prevent blood clotting
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Facts About White Blood Cells
Monocytes
2–8% of circulating WBCs
Are large and spherical
Enter peripheral tissues and become
macrophages
Engulf large particles and pathogens
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Facts About White Blood Cells
Lymphocytes
20–30% of circulating WBCs
Are larger than RBCs
Migrate in and out of blood
Mostly in connective tissues and lymphoid organs
Are part of the body’s specific defense (immune)
system
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White Blood Cells
The Differential Count and Changes in WBC Profiles
Percentage range for different WBCs
Detects changes in WBC populations during:
Infections, inflammation, and allergic reactions
Will learn differential for WBCs in lab
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WBC Disorders
Leukopenia
Abnormally low WBC count
Leukocytosis
Abnormally high WBC count
Leukemia
Cancer of WBC forming tissues
Results in extremely high WBC count and other symptoms
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WBC Production - Leukopoiesis
All blood cells originate from hemocytoblasts
They produce myeloid stem cells and lymphoid stem cells
Myeloid Stem Cells
Differentiate into progenitor cells, which produce all WBCs
except lymphocytes
Lymphoid Stem Cells
Produce lymphocytes
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Leukopoiesis -WBC Formation
Granulocytes and Monocytes develop in red bone marrow from myeloid stem cells Myeloid stem cells become myeloblasts and
monoblasts Myeloblasts become granular WBC’s Monoblasts become monocytes
Lymphocytes develop from lymphoid stem cells of the bone marrow and lymph tissues Lymphoid stem cells become lymphoblast Lymphoblasts become lymphocytes
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Leukopoiesis Diagram
Myeloblasts
Neutrophils, eosinophils and basophils
Monocytes
Lymphoblasts
Lymphocytes
Myeloid Stem Cells Lymphoid Stem Cells
Monoblasts
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Platelets
Cell fragments involved in human clotting system
Nonmammalian vertebrates have thrombocytes (nucleated
cells)
Circulate for 9–12 days
Are removed by spleen
2/3 are reserved for emergencies
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Platelets
Platelet Counts
150,000 to 500,000 per microliter
Thrombocytopenia
Abnormally low platelet count
Thrombocytosis
Abnormally high platelet count
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Platelets
Three Functions of Platelets:
1. Release important clotting chemicals
2. Temporarily patch damaged vessel walls
3. Actively contract tissue after clot formation
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Platelets
Platelet Production
Also called thrombocytopoiesis
Occurs in bone marrow
Megakaryocytes
Giant cells in bone marrow
Manufacture platelets from cytoplasm
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Platelet Formation (thrombocytopoiesis)
Myeloid Stem Cells
Megakaryoblasts
Megakaryocytes
Platelets (thrombocytes)
fragmentation
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Hemostasis
Hemostasis is the cessation of bleeding
Consists of three phases
Vascular phase
Platelet phase
Coagulation phase
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Hemostasis Stages
Vascular Phase Muscles in cut
vessels constricts Blood loss is
immediately reduced
Clotting factors concentrate faster
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Hemostasis Stages
Platelet Phase Platelet adhesion
Platelet release reaction
Platelet aggregation
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Coagulation Phase - Clot Formation
Clot consists of a gel of _____ and trapped formed elements
Clot closes cut vessel
Clotting process called __________
fibrin
coagulation
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Coagulation Phase - Clot Formation
Three Coagulation Pathways
Extrinsic pathway
Begins in the vessel wall
Outside bloodstream
Intrinsic pathway
Begins with circulating proenzymes
Within bloodstream
Common pathway
Where intrinsic and extrinsic pathways converge
Ends with formation of clot
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Basic Steps in Clotting
Clotting is a cascade of chemical reactions as follows: When vessels are cut or damaged, several
clotting factors from the extrinsic and intrinsic pathways interact to form the enzyme _____________
In common pathway prothrombinase catalyzes the conversion of the plasma protein ___________ to _________
In turn, above chemical acts as an enzyme to convert __________ to ____
prothrombinase
prothrombin thrombin
Fibrinogen fibrin
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Basic Coagulation Diagram
Several clotting factors released from damaged tissues, vessel wall and platelets
Prothrombinase
Ca2+
Prothrombin Thrombin
Fibrinogen Fibrin (clot)Thrombin
Ca2+ CommonPathway
Extrinsic andIntrinsic Pathways
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*More Complete Coagulation Diagram
Figure 19–13a The Coagulation Phase of Hemostasis
Check Table 19-4, page 676 for list of Clotting Factors
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Electron Micrograph of Coagulation
Figure 19–13b The Coagulation Phase of Hemostasis
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Calcium (Ca2+) and Vitamin __ needed to form four of the clotting factors
Within 30 minutes platelets begin to _____ the clot by pulling edges of cut vessel together
Clots may form within closed vessels
K
retract
More Fact About Clotting
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Intravascular Clot
Intravascular clot – clot within closed vessel Damaged vessel lining or slowing of blood flow Platelets aggregate and release clotting factors Resulting clot called a ________ Moving piece of the clot is an _______ Clot moves downstream and blocks smaller vessel
________ May cut off blood supply to organ
thrombus
embolus
embolism
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Clot Dissolution (Dissolving)
As repair of a cut or damaged vessel proceeds, a series of enzyme catalyzed reactions called _________ slowly dissolves the clot
An enzyme called ____________________ catalyzes the conversion of inactive enzyme ___________ to active enzyme plasmin
Plasmin catalyzes the dissolving of clot
fibrinolysis
tissue plasminogen activator
plasminogen
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Clot Dissolving Diagram
Plasminogen PlasminTissue plasminogen activator
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*Anticoagulants
Chemicals that decrease or prevent blood clotting are called ___________
Heparin is administered medically and it occurs naturally in our bodies. It works by decreasing thrombin production
Coumadin (warfarin) is effective as a long-term anticoagulant. It is an antagonist of vitamin K.
EDTA and CPD are used in blood banks to keep the donated blood from clotting. They both work by tying-up and removing calcium.
anticoagulants
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Clinical Terms
Polycythemia High RBC count
Anemia Low RBC count (hematocrit) or low hemoglobin
Hemophilia Bleeder’s disease, inherited from mom to son
Leukophilia (leukocytosis) High WBC count
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Clinical Terms
Leukopenia Low WBC count
Thrombocytopenia Low platelet count
Sickle cell disease Inheritance of faulty hemoglobin causing
RBC’s to sickle. Mostly in people of African and Mediterranean ancestry
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Clinical Terms
Hemoglobinuria Hemoglobin breakdown products in urine due
to excess hemolysis in bloodstream
Hematuria Whole red blood cells in urine due to kidney or
tissue damage
Jaundice Yellowing of eyes and skin due to buildup
of excess bilirubin