-
Blood plasma
- Straw colored liquid portion of unclotted blood
- 55-60% of blood volume
- 92% water
- 8% solutes
- -7% plasma proteins: Albumins, Globulins, Fibrinogen
- -1% other solutes: electrolytes, nutrients, gases, hormones, wastes
-
Albumin
- A low-molecular-weight plasma protein synthesized in the liver
- contributes to blood viscosity and maintains blood pressure
- - does not diffuse freely across the vascular endothelium
- Acts on an osmotically-active carrier molecule- carries billiruben
-
clotting factors
- Soluble factors (protiens) that are activated to produce a insoluble clot
- Fibrinogen (factor 1) is the most plentiful
- They promote clotting in a cascading fashion
-
Red blood Cells (RBC)/ Erythrocytes
- lifespan 80-120 days
- Functions in gas transport
- high surface-to-volume ratio
- reversible deformity
-
Why would a biconcave disc be a better shape for a RBC than a sphere?
it has a high surfac-to-volume ratio
-
Hematocrit (Hct)
- % of whole blood volume occupied by red blood cells
- Females: 38-46%
- Males: 40-54%
-
Hemoglobin (Hgb)
- Oxygen carrying molecule
- Heme (4) +4 globin proteins
- 14-16 g/dl
-
RBC count
4.00-6.00 x 106/mm3
-
Lymphatic system
- A system consisting of organs and lymph vessels through which lymphatic fluid passes.
- It functions to:
- -drain interstitial fluid
- -Transport dietary lipids absorbed by the GI tract to the blood
- -Facilitate an immune response
-
Lymphatic Organs
- Primary: Thymus, bone marrow
- Secondary: spleen, lymph nodes, tonsils, and Pever Patches of the small intestine
- Lymph organs ling the hematologic and immune system.
-
structures in the lymphatic system
- Lymph Vessels- pass through lymph nodes
- Lymph Nodes- full of WBCs waiting for invaders
- Right and left lymphatic duct
- Tonsils
- spleen
- Thymus
- Bone marrow
-
Spleen
- Filters and cleanses the blood from foreign invaders
- Contains masses of lymphoid tissue (whit pulp)
- Remove old or damaged cells from the blood
- Storage area for extra blood that can be released by sympathetic stimulation
- Storage of platelets, up to 1/3 of blood supply
-
Lymph Nodes
- Serve as filters for lymph fluid
- Foreign objects are trapped and destroyed
- Important groups of lymph nodes: submandibular, cervical, axillary, inguinal
- Lymph node enlargement may often indicate a pathological condition
-
Hematopoiesis
- Formed element production
- Cells are formed in red bone marrow from pluripotent stem cells and mature in bone marrow or lymphoid tissue (spleen, thymus, tonsils, lymph nodes)
-
Totipotent
- a cell that can produce any kind of cell
- Ex: Fertilized egg
-
Pluripotent stem cells
can become many different things (cells) but not everything
-
Unipotent
gives rise to only one thing
-
Impotent/ terminally differentiated cells
cant produce cells anymore.
-
Hematopoiesis and cytokines
Hematopoietic cells will develop, proliferate, and differentiate if they are provided with specific growth factors (Colony stimulating factors)
-
Colony stimulating factors (CSF)
- These cytokines act as hormones to stimulate the proliferation of progenitor (early) cells
- Specific CSFs are necessary for growth of myeloid, erythroid, lymphoid and megakaryocitic cells
-
Hematopoiesis and cytokines
See table in study guide. p.113
-
Alpha and Beta globulins
Act individually as carrier molecules. Collectively, they control blood osmotic pressure
-
Gamma globulins
Immunoglobulins or antibodies. Made by plasma cells (activated B lymphocytes)
-
Granulocytes
Neutrophils, Eosinophils, Basophilsmost die doing their jobslife span .5-9 days
-
Agranulocytes
Monocytes/Macrophages, Lymphocyteslymphocytes live from days to decadesmonocytes live for several monthsphagocytes or immunocytes
-
Leukocytosis
- Increase in WBC count >10 thousand (10 x 10^3/mm^3)
- *Normal physiological response to disease, up to a certain point
- Occurs in both viral and bacterial infections
-
Leukopenia
- Decrease in WBC count < 5 thousand (5 x 10^3/mm^3)
- *Never a normal response
-
G-CSF (Granulocyte colony stimulating factor)
- Cell Origin: Macrophage, fibroblastCell
- Stimulated: Granulocytes
-
GM-CSF (Granulocyte, Monocyte colony stimulating factor)
- Cell Origin: T cellCell
- Stimulated: Neutrophil, Macrophage
-
Intrinsic pathway
Activated by contact with the injured vessel (collagen and endothelium)
-
Common pathway
Extrinsic and Intrinsic converge here with Factor X
-
Thrombocytes (Platelets)
- Cell fragmants
- -150-400x10/mm3originate from megakaryocytes
- Aids in clotting by clumping (agglutination) and the release of biochemical mediators
- Thrombocytopenia: Low platelet count
- Thrombocytosis: Increased platelet count
-
the clotting cascade
- positive feedback system
- Begins with the activation of several soluble, inactive clotting factors stimulated in cascading fashion
- Two main pathways:
- -Extrinsic Pathway- activated by things out side of us
- -Intrinsic Pathway- activated by things inside of us
- Both systems or pathways merge at a common point, forming the common pathway
- coagulation is usually fast and localized
-
Stages of coagulation
- Extrinsic and intrinsic activation
- the common pathway begins with the formation of prothrombinase (prothrombin activator)
- The prothrombin activator activates prothrombin to thrombin
- Thrombin induces the formation of fibrin from fibrinogen
-
Clot Retraction
- After 30-6- min, the platelets contract
- -platelets contain actin and myosin proteins
- -this squeezes out the serum
- The clot becomes impacted and the edges of the blood vessel are brought closer together
- Healing is also begining
- -Smooth muscle cells & fibroblasts are stimulated to divide
- Endothelial cells begin to restore endothelial lining of the vessel
- Now the clot has to remove
- -Fibrinolysis- breaking apart the clot
-
Fibrinolysis
- Removing a clot
- Large amounts of plasminogen (a plasma protein) are incorporated into clots
- when endothelial cells produce tissue plasminogen activator (TPA), it causes the plasminogen to become plasmin
- Factors within the coagulation cascade (factor XII and thrombin) also change plasminogen into its active form, plasmin
- Either way when plasmin is formed it digests clots
- -TPA ("clot buster") is widely used in stroke/MI patients.
-
Bone Marrow biopsy
- Small amounts of bone marrow tissue are removed from the bone and observed microscopically
- Usually collected from the posterior iliac crest
- Assists in the diagnosis of: anemias, leukemias, platelet, disorders, immunoglobulin disorders, etc
-
Complete Blood Count
- White blood cell (WBC) count
- Whit blood cell differential
- Red blood cell (RBC) count
- Hemoglobin
- Hematocrit
- Platelet count
- MCV
- MCH
- MCHC
- Red cell distribution width (RDW)
-
Whit blood cell differential
- Physicians use the percentage of the individual white blood cells in the blood to aid in the diagnosis of specific diseases
- -
-
Coagulation tests
- Prothrombin Time/ International Normalized ratiio (PT/NR)
- -Measures the extrinsic pathway
- -Usually to check status after anticoagulent administration
- Activated Patial Thromboplastin Time (APTT)
- -Measures the intrinsic pathaway
- Bleeding Time
- Measures platelet function, not platelet number
- -New instrumentation is replacing this test
-
Reticulocyte count
- Low retic count (<0.5%) indicates low rate of erythropoiesis
- High retic count (>1.5%) indicates high rate of erythroopoiesis
|
|