BLOOD FUNCTIONS
Transport
Immunity (later in semester )
Hemostasis
Homeostasis
BLOOD:
Volume (in L) = approx. 6 - 8 % OF BODY
WEIGHT (in Kg)
4.5 - 6.0 L
BLOOD COMPONENTS
Plasma (Vs. Serum)
Proteins
Lipids
Carbohydrates
Ions
Water
Cellular
Leukocytes
Polymorphonuclear or granulocytes
Neutrophil
Basophil
Eosinophil
Monomorphonuclear or agranulocytes
Monocytes (m??
Lymphocytes
ERYTHROCYTES
MEN: 4.5 - 6.5 x 106 cells/µl
WOMEN: 3.8 - 5.8 x 106
cells/µl
HEMATOCRIT
Blood Properties
Hematocrit (42±5% & 47±5%)
Density or specific gravity 1.050 g/ml
Viscosity (3.5 - 5.5 x H2O)
Erythrocyte sedimentation rate (2-8 mm/hr)
HEMOGLOBIN
2 - 3 X108 molecules/RBC
12 - 16 gms/100 mls of BLOOD
Fig. 13.2
WHY PUT HEMOGLOBIN IN A CELL?
[O2] + [Hb] --> [Hb(O2)4]
98% of O2 in blood is bound
to Hb
1.34 mls O2/gm of Hb
20.1 mls of O2 carried/100 mls
blood
ADULT HEMOGLOBIN (HbA) Fig 13.2
MW = 64,458
4 polypeptide chains - 2 pairs
2 - 141 amino acids
2 - 146 amino acids
4 heme groups
Porphyrin
Iron
OTHER TYPES OF Hb
HbF - Fetal Hemoglobin
2 & either
(2OR 2CHAINS)
-- High affinity for oxygen
HbS
Replace #6 amino acid glutamic acid with valine in
chain
See Figures 16.8 16.10 !!!!
P50
P50 = [O2] in mm Hg that yields 50% saturation of Hb with O2
INCREASE P50 OR DECREASE
Hb AFFINITY FOR O2
DECREASE pH
INCREASE TEMPERTATURE
(Hb UNLOADS MORE O2
@ GIVEN PO2)
BLOOD TYPES
See page 730 in the text !!!!
Web sites to visit:
http://opbs.okstate.edu/~melcher/MG/MGW1/MG11121.html
http://ftp.bbc.co.uk/tw/9798/9801blood.shtml
ABO Blood types
Blood Type | Antigen | Antibodies |
O | NONE | ANTI A
ANTI B |
A | A | ANTI B |
B | B | ANTI A |
AB | A & B | NONE |
Rh FACTOR
1. MAKE ANTI-RHESIS MONKEY RED
CELL ANTIBODIES IN RABBIT
2. IF ANTI-Rh REACTS WITH HUMAN RBC
--> Rh+
3. IF ANTI-Rh DOES NOT REACT WITH HUMAN
RBC ---> Rh -
Rh FACTOR PROBLEMS
Rh - MOTHER CONCEIVES Rh + FETUS
FETAL RBCs LEAK INTO MATERNAL CIRCULATION
MOTHER PRODUCES ANTI Rh ANTIBODIES
(IgG)
SECOND Rh + CHILD: FETAL RBCs
ATTACKED BY MATERNAL IgG
SECOND Rh + CHILD: FETAL RBCs ATTACKED BY MATERNAL IgG
ERYTHROBLASTOSIS FETALIS
Rh TREATMENTS
RHOGAM: ANTI - Rh TO MOTHER AFTER BIRTH
OF FIRST CHILD.
TRANSFUSION OF SECOND CHILD
QUESTION:
WHY DOES Rh FACTOR POSE A PROBLEM WHILE ABO
BLOOD TYPES DO NOT???
Erythropoietin:
Stimulus?
Tissue Hypoxia
STEM CELL + ERYTHROPOETIN
---->
ERYTHROBLAST
---->
NORMOBLAST
---->
RETICULOCYTE ---->
MATURE RBC
(MAKE ABOUT 2.3 X 108/DAY)
ANEMIA
Hemorrhagic - blood loss
Aplastic - marrow damage
certain organics, x-rays, etc.
Hemolytic
Sickle Cell & Snake Venoms
Pernicious ( vitamin B12 deficit)
Intrinsic & Extrinsic Factors
Fe3+ deficiency
Destruction of hemoglobin
Polypeptide chains ------> amino acids
Iron (Fe3+)
released from m
transferrin in plasma
ferritin in cells, esp. liver
Heme group ----> BILIRUBIN
Jaundice
Elevated Free ---> Liver Problems
Elevated Conjugated ---> Kidney Malfunction
Problem For Some New Borns (Use UV Light)
HEMOSTASIS: CLOTTING
VASCULAR SPASM PAIN --->SYMPATHETIC
RESPONSE
PLATELET PLUG
CLOT FORMATION
PLATELET PLUG
Fig 13.4
PLATELETS (2 - 4 µM DIAMETER)
ADHERE TO - CHARGED SURFACE, e.g., COLLAGEN
IN CUT BVs
DEGRANULATION (SEROTONIN, ADP, PROSTAGLANDINS,
etc.)
PLATELETS
140,000 - 300,000 / mm3
TOO FEW ---> THROMBOCYTOPENIA PURPURA
NOTE: ASPIRIN, etc. AS BLOOD THINNERS
Platelet Plug
von Willebrand Factor (vWf)
From megakaryocytes, platelets & endothelial
cells of blood vessels
Serotonin & epinephrine
Local vasoconstriction
ADP - causes adhesiveness and aggregation
Thromboxane A2 (TXA2)
From arachidonic acid
Aggregation, ADP release & vasoconstriction
Prevention of Platelet Plug
Prostacyclin (PGI2)
Nitric Oxide
Both released by healthy, intact endothelial
cells
CLOT FORMATION
FIBRINOGEN (340,000) ---> FIBRIN (LOOSE
CLOT)
FSF COVALENTLY LINKS FIBRIN THREADS (TIGHT
CLOT)
See Figs 13.5 - 7
FIBRININOGEN ---> FIBRIN
PROTHROMBIN ---> THROMBIN (ACTIVE ENZYME)
FACTOR Xinactive --->
FACTOR X active
ACTIVATE FACTOR X
Extrinsic mechanism: tissue thromboplastin
+ lipids
Intrinsic mechanism: IX via XI via
XII activated by collagen or negatively charged surface
ANTI-COAGULANTS
Ca++ Chelators + siliconized
glass
Heparin from mast cells and basophils
Coumarin derivatives (vitamin k analogs;
Dicoumarol; Warfarin)
Coumarin
Analog of Vitamin K
Vitamin K is required for addition of carboxyl
group to glutamic acid residues of clotting factors
This addition bestows Ca++ binding
site and function to clotting factor
Vit K inhibits this addition, rendering
clotting factors inactive
CLOT RETRACTION
Profibrinolysin --->Fibrinolysin
or
Plasminogen ---> Plasmin
Activated By Thrombin, Factor XII, Tissue
Enzymes
Blood vessels: Structures and Functions
Figs 13.8 & 12 and pages 411 - 417
Artery --> arteriole --> capillary
-->
venule --> veins
Starlings Capillary Hypothesis
Hydrostatic Pressure
Plasma Osmotic or Oncotic Pressure
(pi)
= RT C
= osmotic
pressure
R = Gas constant
T = temperature, oK
C
= difference in concentration of impermeant solute molecules
Across capillaries, the solutes are plasma proteins
Capillary barrier is selectively permeable to solutes > 69,000 mw
Lymphatic system drains the interstitial space of proteins and water
FILTRATION = REABSORPTION
Edema:
Filtration > Reabsorption
Tissue Dehydration:
Filtration < Reabsorption
Factors influencing movement of water across
capillaries
BP
Dehydration
Hydration
Add Osmotic Solute
Capillary Damage
Lymphatic Blockage