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Chapter 19 blood

blood

liqud connective tissue consisting of cells surrounded by liquid matrix (plasma)

Blood

metallic taste, scarlet to dark red, 38 C, approx 8%, 5-6L males, 4-5L females

Buffy Coat

WBC, about 1 percent of blood, contains the components of immune infection

Blood plasma

91.5% of water and 8.5% solutes which most are proteins

Albumin proteins (plasma)

largest amount of protein in plasma

helps maintain osmotic pressure; important factor in exchange of fluids across blood capillary walls

Albumin protein

Globulin protein (plasma)

produce immunoglobulins

immunoglobulin help attack viruses and bacteria

Globulin protein

transports iron, lipids and fat-soluble vitamins

alpha and beta globulins

fibrinogen protein (plasma)

plays essential role in blood clottng

RBCs

erythrocytes

transport O2 from lungs to body tissues and CO2 from body tissue to lungs

RBCs

WBC (formed elements)

leukocytes

protects the body from pathogens and foreign substances

WBC (formed element)

platelets (formed element)

cell fragments that release chemicals to promote blood clotting

Serum

yellowish liquid

blood plasma minus the clotting factors

Serum

hematocrit

percentage of RBCs out of total blood volume

hemopoiesis (hematopoisiesis)

process by which the formed elements of blood is developed

Hemocytoblasts

pluripotent stem cells found in red blood marrow that forms blood cells

RBC (erythrocytes)

contain the oyxgen-protein hemoglobin which gives the blood the red color

Biconcave discs

shape of RBCs (no nuclues) which allows them to carry O2 more efficiently

Reticulocytes

immature RBCs-mature in 1 to 2 days

heme (structure of hemoglobin)

nonprotein pigment that is attached to each polypeptide chain and an iron ion in the center of each heme

Globin (hemoglobin structure)

has 4 polypeptide chains (2 alpha, 2 beta)

Iron ions (hemoglobin structure)

in the center of a heme

binds reversibly to an O2 molecule which allows each hemoglobin molecule to bind 4 O2 molecules

Iron ions (hemoglobin structure)

Hemoglobin

major function to carry O2 to cells and CO2 to lungs

consist of a protein globin

hemoglobin

involved in regulating blood flow and BP via the release of nitric oxide which causes vasodilation

Hemoglobin

Erythopoietin

hormone released by the kidneys in response to hypoxia, stimulates differentiation of hematopoietic stem cells into erythocytes

only survives only to 5 to 9 days

platelets

Megakaryocytes

located in red bone marrow that splinters into 2000-3000 fragments to create platelets that contain many vesicles but no nucleus

Cord-blood transplant

stem celss are collected and frozen from an umbilical cord after birth and used later if needed

Hemorrhage

large loss of blood from blood vessels

Hemostasis

stops bleeding

1. vasscular spasm 2. platelet plug formation 3. blood clotting (coagulation)

hemostasis

Tissue Factor (thromboplastin)

a tissue protein leaks into the blood from cells outside the blood vessel and begins the formation of prothrobinase

Intrinsic Pathway

activators are present inside the blood and outside tissue damage is not needed-platelet phospholipids, Ca2+, and clotting factors lead to prothrombinase formation

formation of prothrombinase in both extrinsic pathway and intrinsic pathway

common pathway

Vitamin K

needed for normal clot formation bc it is used in synthesis of 4 clotting factors

fat-sluble vitamin produce in large intestine by bacteria

Vitamin K

Anemia

blood has abnormally low-oxygen carrying capacity, s/s fatigue, paleness, SOB, chills

Unvierasl recipient

AB group-can receive all blood types w/o negative reaction

Universal Donor

O group

Neurophils (WBC)

"bacteria slayer"

first WBC to respond during an inflammatory process chemical use to destroy pathgen

Neutrophils (WBC)

releases lysozyme, defensin, strong oxidants to destroy pathogen

Neutrophils (WBC)

Eosinophils (WBC)

attacks parasitic worms

enter tissue and release enzymes such as histamine; high account in allergic conditions and parasistic infections

Eosinophils

Basophils (WBC)

involved in hypersensitivity and allergic reacions

enters site of inflammation and release granules that contain histamine, heparin, and serotonin which intesifies the inflammatory reaction

Basophils (WBC)

Lymphpcytes (WBC)

major pathogen fighters in lympathetic system

B cells (lymphocytes)

effective in bateria destruction and inactivating their toxins

T cells (lymphocytes)

attack infected body and tumor cells

Natural killer cells (lymphocytes)

attack infected body cells and tumor cells

high count indicates viral infection

Lymphocytes (WBC)

Monocytes (WBC)

arrrives later than neutrophils in infection, but destroys more microbes

wandering macrophages that cleans up debris and microbes by phagocytes

Monocytes (WBC)

high count indicates viral or fungal infections such as TB

Monocytes (WBC)

Fibrin

major protein of blood clot

Thrombus

the clot in an unbroken blood vessel

Embolus

when a thrombus becomes dislodged and swept away by bloodstream

Pulmonary emboli

can impair the ability of the body to obtain O2

Cerebral emboli

can cause strokes

anticoagulants

substances in blood that delay, suppress, or prevent blood clot such as heparin

Antigens

glycoprotein and glycolipid found on the surface of RBC

how blood is characterized depending on its absence or presence

antigens

Labeled A, B, AB, O

antigens

Antibodies

reacts with A or B antigens called anti-A antibodies and anti B antibodies

ABO group A

classificatio is based on antigens labeled A, B, or AB with O being absence of the A and B antigens

Rh group

antigen present in 85% of humans; individual presentsthe Rh antigen is said to be Rh+

hemmorrhagic anemia

result of acute or chronic loss of blood

hemolytic anemia

prematurely ruptured RBCs

Aplastic anemia

destruction or inhibition of red bone marrow

Iron-deficiency anemia

secondary result of hemorrhagic anemia; inadequate intake of iron; impaire iron absorption

Pernicious anemia

deficiency of Vit B12; lacks intrinsic factor that absorbs Vit B12

Sickle-Cell disease

gentic anemia; indvidual w/ this disease contain Hemoglobin-S (HB-S)

Hemolytic disease in Newborns

transferred anti-Rh antibodies from mother to fetus will attack some of fetus' RBCs causing agglutination and hemolysis

RhoGram (drug)

given to Rh- patients before and after delivery; destroys any Rh+ cells from the baby before the mother's immune sytem can become sensitive to it

1. Globin & heme separate 2. Globin turns into amino acids 3. Iron is removed from heme portion and attaches to TRANSFERRIN. 4. In muscle fibers, liver and spleen, the iron detaches from TRANSFERRIN and attaches to protein FERRITIN. 5. Iron transferred to red bone marrow to produce new RBCs 6. Heme downgraded to yellow pigment called BILIRUBIN. 7. BILIRUBIN goes to liver, then intestine, secreted as BILE. 8. Intenstines metabolize BILE to UROBILINOGEN. 9. UROBILINOGEN leaves body in urine called UROBLIN and in feces called STERCOBLIN.

Erythocytes (destruction and recycling)

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