Title: The Cardiovascular System: The Blood
1Chapter 19
- The Cardiovascular System The Blood
2What is blood?
- Blood is a connective tissue composed of a liquid
extracellular matrix called plasma. It has cells
and cell fragments dissolved in it. - The cardiovascular system is made up of blood,
the heart, and blood vessels.
3Functions of Blood
- Transportation
- O2, CO2, metabolic wastes, nutrients, heat
hormones - Regulation
- helps regulate pH through buffers
- helps regulate body temperature
- helps regulate water content of cells
- Protection from disease loss of blood
- Hematology is study of blood and blood disorders
4Physical Characteristics of Blood
- Thicker than water and therefore flows more
slowly than water - Feels sticky
- Temperature of 100.4 degrees F
- pH 7.4 (7.35-7.45)
- 8 of total body weight
- Blood volume
- 5 to 6 liters in average male
- 4 to 5 liters in average female
5Techniques of Blood Sampling
- Venipuncture
- Most common method
- sample taken from vein with hypodermic needle
syringe - Finger or heel stick
- Used by diabetics to monitor blood sugar
- Used to test blood of infants
- Arterial stick used to determine oxygen levels
6COMPONENTS OF BLOOD
- Blood consists of 55 plasma and 45 of cells.
- Blood plasma consists of 91.5 water and 8.5
solutes. - Principal solutes include nutrients, enzymes,
hormones, respiratory gases, electrolytes, and
waste products.
7Blood Cells
- Red blood cells, 40 ( erythrocytes )
- White blood cells, 20 ( leukocytes )
- neutrophils, eosinophils, basophils
- lymphocytes T cells, B cells, and natural
killer cells - monocytes
- Platelets, 30 (special cell fragments)
8Hematocrit
- Hematocrit is the percentage of total blood
volume occupied by RBCs. - Anemia
- not enough RBCs or not enough hemoglobin
- Can be due to leukemia, iron deficiency, or B12
deficiency - Vitamins or injections of iron can treat anemia
- Polycythemia
- too many RBCs (over 65)
- dehydration, blood loss (including menstruation),
blood doping in athletes (common in professional
cycling to increase O2 supplies to the blood,
muscles, and lungs)
9Formation of Blood Cells
- Most blood cells types need to be continually
replaced - die within hours, days or weeks
- process of blood cells formation is hematopoiesis
or hemopoiesis - In the embryo
- occurs in yolk sac, liver, spleen, thymus, lymph
nodes red bone marrow - In adults
- occurs only in red marrow of flat bones like
sternum, ribs, skull pelvis and ends of long
bones
10Red Blood Cells or Erythrocytes
- Contain oxygen-carrying protein hemoglobin that
gives blood its red color - 1/3 of cells weight is hemoglobin
- Biconcave disk 8 microns in diameter
- increased surface area/volume ratio
- flexible shape for narrow passages
- no nucleus or other organelles
11RBC Life Cycle
- RBCs live only 120 days
- wear out from bending to fit through capillaries
- no repair possible due to lack of organelles
- Worn out cells removed by macrophages in spleen
liver
12Erythropoiesis Production of RBCs
- Erythrocyte formation, called erythropoiesis,
occurs in adult red bone marrow of certain bones. - It takes 1-2 days for a mature red blood cell to
be formed and released into the blood stream.
13Hemoglobin
- Each RBC has 280 million hemoglobin molecules
- Each one can bind 4 molecules of oxygen (to the
iron at the center of the molecule). - Hemoglobin removes CO2 from the blood
- Hemoglobin also regulates blood pressure by
regulating nitric oxide in the blood
14WHITE BLOOD CELLS
- Leukocytes (WBCs) have a nucleus but do not have
hemoglobin. - Granular leukocytes include eosinophils,
basophils, and neutrophils based on the straining
of the granules. - Agranular leukocytes do not have cytoplasmic
granules and include the lymphocytes and
monocytes.
15WBC Physiology
- Less numerous than RBCs
- 5000 to 10,000 cells per drop of blood
- 1 WBC for every 700 RBC
- Leukocytosis is a high white blood cell count
- microbes, disease, strenuous exercise,
anesthesia, cancer or surgery - Leukopenia is low white blood cell count
- radiation, shock or chemotherapy
- Only 2 of total WBC population is in circulating
blood at any given time - rest is in lymphatic fluid, skin, lungs, lymph
nodes spleen
16Neutrophils (Granulocyte)
- The most abundant WBC
- 60 to 70 of circulating WBCs
- First cells to migrate to the site of bacterial
infection or cancer formation. - Also involved in healing injuries
- release lysozymes which destroy/digest bacteria
- release defensin proteins that act like
antibiotics poke holes in bacterial cell walls
destroying them - release strong oxidants (bleach-like, strong
chemicals) that destroy bacteria
17Eosinophils (Granulocyte)
- 2 to 4 of circulating WBCs
- Combat parasites and infections
- Fight allergies and asthma
18Basophils (Granulocyte)
- Less than 1 of circulating WBCs
- Store histamine and can contribute to allergic
reactions - Also contain heparin, which prevents blood from
clotting too quickly
19Lymphocyte (Agranulocyte)
- 20 to 25 of circulating WBCs
- The main soldiers in the immune system battles
- B cells
- destroy bacteria and their toxins
- turn into plasma cells that produces antibodies
- T cells
- attack viruses, fungi, transplanted organs,
cancer cells some bacteria - Natural killer cells (NKC)
- attack many different microbes some tumor cells
- destroy foreign invaders by direct attack
20Monocyte (Agranulocyte)
- 3 to 8 of circulating WBCs
- Stored in the spleen
- Produce macrophages which attack bacteria
- Destroy microbes and clean up dead tissue
following an infection
21PLATELETS
- Platelets help stop blood loss from damaged
vessels by forming a platelet plug. -
- Their granules also contain chemicals that
promote blood clotting.
22Platelet (Thrombocyte) Anatomy
- Disc-shaped cell fragment with no nucleus
- They are produced in the bone marrow and live 5
to 9 days in the blood stream before being
recycled by the spleen and liver.
23Bone Marrow Transplant
- Bone marrow transplant replaces diseased marrow
with healthy marrow. - Patients diseased marrow is destroyed by cancer
or disease. - Healthy marrow is supplied by a donor or the
patient. It is removed (painfully) by sticking a
needle into the hipbone. - Risks to recipient include
- Infection due to decreased WBC
- T cells might attack new bone marrow
- Must take immunosuppressant drugs for life
24Cord-Blood Transplant
- Stem cells are taken from the umbilical cord and
frozen - This method offers several advantages over marrow
transplant. - Easy to obtain
- More abundant
- Are not rejected by patient
- Dont transmit infections
- Can be stored, frozen, forever
25Hemostasis
- Stoppage of bleeding in a quick localized
fashion when blood vessels are damaged - Prevents hemorrhage (loss of a large amount of
blood) - Methods utilized
- vascular spasm
- platelet plug formation
- blood clotting
26Vascular Spasm
- Damage to blood vessel produces stimulates pain
receptors - Small blood vessels are contracted which reduces
blood flow to the injury site
27Platelet Plug Formation
- Steps in the process
- (1) platelet adhesion (2) platelet release
reaction (3) platelet aggregation
28Platelet Adhesion
- Platelets stick to exposed collagen underlying
damaged cells in vessel wall
29Platelet Release Reaction
- Platelets activated by adhesion
- Extend projections to make contact with each
other - This decreases blood flow to injury site
30Platelet Aggregation
- Activated platelets stick together and activate
new platelets to form a mass called a platelet
plug - Plug reinforced by fibrin threads formed during
clotting process
31Clot Retraction Blood Vessel Repair
- The plug stops the bleeding, then
- Edges of damaged vessel are pulled together
- Fibroblasts endothelial cells repair the blood
vessel
32Blood Clotting
- Blood drawn from the body thickens into a gel
- gel separates into liquid (serum) and a clot of
insoluble fibers (fibrin) in which the cells are
trapped - If clotting occurs inside the body, it is called
a thrombosis - Having vitamin K in your diet can help prevent
blood clotting
33Blood Groups and Blood Types
- RBC surfaces are marked by antigens, which
determine blood type
34ABO Blood Groups
- Blood types in humans are
- display only antigen A -- blood type A
- display only antigen B -- blood type B
- display both antigens A B -- blood type AB
- display neither antigen -- blood type O
- Type O is the universal donor
- Type AB is the universal receiver
35RH blood groups
- Antigen was discovered in blood of Rhesus monkey
- People with Rh agglutinogens on RBC surface are
Rh. - Most people are Rh
- If an Rh - woman is pregnant and the baby is Rh,
the mothers body may reject the pregnancy she
must take anti-rejection drugs and be closely
monitored.
36DISORDERS HOMEOSTATIC IMBALANCES
- Anemia
- Sickle-cell
- Hemophilia
- Disseminated intravascular clotting
- Acute leukemia
- chronic leukemia
37Anemia Not Enough RBCs
- Symptoms
- oxygen-carrying capacity of blood is reduced
- fatigue, cold intolerance paleness
- Types of anemia
- iron-deficiency lack of absorption or loss of
iron - pernicious lack of intrinsic factor for B12
absorption - hemorrhagic loss of RBCs due to bleeding
(ulcer) - hemolytic defects in cell membranes cause
rupture - thalassemia hereditary deficiency of hemoglobin
- aplastic destruction of bone marrow
(radiation/toxins)
38Sickle-cell Anemia
- Genetic defect in hemoglobin molecule
- RBC is deformed
- sickle-shaped cells rupture easily causing
anemia clots - Found among populations in malaria belt
- Mediterranean Europe, sub-Saharan Africa Asia
39Hemophilia
- Inherited deficiency of clotting factors
- bleeding spontaneously or after minor trauma
- subcutaneous intramuscular hemorrhaging
- nosebleeds, blood in urine, articular bleeding
pain - Treatment is transfusions of fresh plasma or
concentrates of the missing clotting factor
40Disseminated Intravascular Clotting
- Life threatening paradoxical presence of blood
clotting and bleeding at the same time throughout
the whole body - Associated with infections, hypoxia, low blood
flow rates, trauma, hypotension hemolysis - Clots cause necrosis leading to multisystem organ
failure
41Leukemia
- Acute leukemia
- uncontrolled production of immature leukocytes
- crowding out of normal red bone marrow cells by
production of immature WBC - prevents production of RBC platelets
- Chronic leukemia
- accumulation of mature WBC in bloodstream because
they do not die