Chapter 19 Flashcards

1
Q

what are the functions of cardiovascular system

A
  1. transport gas, nutrients, hormones & metabolic wastes
  2. regulation of pH and ion composition of interstitial fluid (neutralizes lactic acid, controls Ca++ and K+ concentration) - buffers in the blood
  3. restriction of fluid loss at injury sites
  4. defence against toxins & pathogens
  5. stabilization of body temp (thermoregulation)
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2
Q

what are the components of Cardiovascular system:

A

1) blood - transport medium =4-6L, 38*C, pH (7.35-7.45)
2) heart - muscular pump that moves blood around the body
3) system of tubes/ vessels - arteries, veins, capillaries

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3
Q

What is body fluid compartments

A

total fluid 60% of body weight

intracellular fluid 40% of body weight
extracellular fluid 20% of body weight
* itnerstitial fluid 80% ECF
* plasma 20% ECF

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4
Q

What are the intracellular fluid & extracellular fluid

A
  • 60% of our body weight is made up of water (40L in a 70kg male), water occupies two main compartments within the body:

1) intracellular fluid: fluid found within the cells of the body
2) extracellulra fluid (ECF) fluid outside of cells
- interstitial flud: the water surrounding cells within tissues
- plasma: thw ater found within the blood stream
- others: CSF, lymph, eye, synovial fluid, etc
*note that the electrolyte concentrations of all ECF is roughly the same

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5
Q

what is the plasma composition

A

= plasma proteins (7%), other solutes (1%), water (92%) - transports organics and inorganic molecules, formed elements and heat
1) plasma proteins
* albumins (60%) - major cobtriutors to somotic pressur eof plasm; transport lipids, steroid hormones
* globulins (35%) - transport ions, hormones, lipids; immune function
* fibrinogen (4%) - essential component of clotting system; can be converted to insoluble fibrin
* regulatory proteins (<1%) - enzymes, proenzymes, hormones

2) other solutes:
* electrolytes: normal extracellular fluid ion composition essential for vital cellular activities
-Ions contribute to osmotic pressure of body fluids (major plasma electrolytes are Na+, K+, Ca2+, Mg2+)
* other nutrients: used for ATP production, growth and maintenance of cells; include (fatty acids, cholesterol, glycerides), carnohydrates (primarily glucose) and amino acids
* organic wastes: carried to sites of breakdown or excretion; include urea, uric acid, creatinine, bllirubin, ammonlum ions

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6
Q

what is the plasma

A

Blood is a connective tissue = plasma + formed elements
* 55% of blood is plasma: composition similar to interstitial fluid with addition of dissolved proteins; plasma is the liquid matrix that supports and surrounds the blood cells
* although it does not contain collagen and elastin like other connective tissue matrices,
the blood plasma contains a number of dissolved proteins involved in…
1) transport and clooting
2) dissolved gases, electrolytes, and organic nutrients, platelets = cell fragments involved in clotting
* leukocytes = white blood cells (WBCs) involved in immune response

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7
Q

the kinds of dissolved plasma proteins

A
  1. albumin: 60% of plasma protein
    - the most abundant proeint int he plasma is involved in transporting lipid soluble susbtances (i.e. fattu acods ad steroid hrmones) in the blood, and is produced in the liver. Responsible for the majority of the blood colloid osmotic force
  2. globulins: 35% of plasma protein: includes Antibodies (immunoglobulins) and transport globulins produced in the liver (transport vitamins, lipids, metal ions and hormones) e.g. lipoprotein (travelling around)
  3. antibodies: specialize proteins involved in immunity produced in lymph tissue
  4. fibrinogen and prothrombin: 4% of plasma protein - produced in the liver and are invovld in blood clotting. require vitamin K during ynthesis
  5. lipoproteins: produced in the liver and involved in transporting triglycerides and cholesterol in the blood (e.g. HDS & LDS)
  6. hormones and enzymes: specialized funcitons
  • sources of most plasma proteins: liver
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8
Q

what are included in Gases (blood plsama)

A

: small amounts of oxygen and carbon dioxide are dissolved in the blood; however, Red blood cells (RBC) and bicarbonate play a more important role in gas transport

organic nutrients and metabolic wastes
- nutrients: monosaccharides, amino acids, and water soluble vitamins
- waste products such as lactate (glucose), urea (protein), uric acid (DNA/RNA), creatinine (creatine phosphate), and bilirubin (hemoglobin)
- electrolytes: ions such as Na+, K+, Ca++, H+, HCO3- and Cl-

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9
Q

what is hematocrit

A

% by volume of blood that is formed elements
male = 46 (higher average since they do have more skeletal muscles)
female = 42

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10
Q

what is erythyrocytes
(structure, what are required for the erythrocyte production, function and significance of shape)

A

structure: biconcave, no nucleus or membrane bound organelles, full of hemoglobin

erythrocyte production requires: Folic acid & vitamin B12

funcitons: transport O2 and CO2

significance of shape:
1) large surface area: volume ratio = increase - rapid RBC movement
2) form stacks 9ronleaux) that smoothly flow through narrow vessels
3) bend & flex through capillaries as narrow as 4 mM

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11
Q

the types of leukocytes

A
  1. neutrophlis: the most abundant phagocyte in the blood; contain extensive lysosomes
  2. eosinophils: destroy parastic worms & immune complexes
  3. basophils & mast cells: release histamine and heparin
  4. lymphocytes: involved in antibody production and the targeted specific immune response; only small amounts in blood the rest are in lymphatic tissues (nodes tonsils, and spleen)
  5. monocytes: can leave the blood steram and differentiate into powerful phagocytes called macrophages (fixed or free)

erythrocytes (RBC): transport oxygen and carbon dioxide
palatelets: anuclear cell-fragments formed from larger Megakaryocytes that are invovled in blood clotting

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12
Q

where are the blood cells produced from

A

all blood cells are formed in the bone marrow from a common blood stem cell, hemocytoblast
- once differentiated, mature cells enter the circulation
- some lymphocytes undergo additional maturation in the thymus gland (lymphoid tissue)

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13
Q

blood production 족보**

A

all from hemocytoblast
1. proerythroblast - polythromatic erythroblast - erythrocytes
2. myeloblast - progrnulocytes - basophil & eosinophil & neutrophil (granulocytes)
3. lymphoblast - lymphocyte (agranulocyte)
4. monoblast - monocyte (agranulocyte)
5. megakaryoblas - megakaryocyte - thromocytes (platelets)

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14
Q

what is hematopoiesis

A

= the process by which the formed elements of blood devleop is called hemopoesis (hematopoiesis). in adults, blood cells are formed in red bone marrow from pluripotent (multipotent) stem cells.
- they mature in bone marrow or lymphoid tissue
- born marrow harvesting for use in a bone marrow transplant
- multipotent stem cells = pluripotent stem cells: one stem cell becomes relevant cells in body (hemocytoblasts)

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15
Q

what is erythropoiesis

A

= the part of hematopoiesis that deals with the production of RBCs.
it increases when states of hypoxia (O2 deficiency) stimulate the kidneys to release the hormone erythropoietin (EPO)
- EPO circulates to the red marrow and speeds up the maturation and release of immature red cells
- EPO prod. can also be stim. by: throxine, grwoth hormone, testosterone (but not estrogen)

throxine = both work towards “growing tissues & maintaining tissues of your body

This triggers the level of RBC

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16
Q

what’s occuring during the evens in the red born marrow

A

developing RBCs absorb amino acids and Fe2+ from the bloodstream and synthesize new Hb molecules
1) cells destines to become RBCs fist differnetiate into prorythroblasts

2) proerythroblasts then differntiate into various stages of cells called erythroblasts, which actively synthesie hemoglobin.
- Erythroblasts are named according to total size, amount of hemoglobin present,a nd size and appearance of the nucleus

3) after roughly four days of differnetitation, the erythroblast, now called a normoblast, sheds its nucleus and becomes a reticulocyte, which contains 80% of the Hb of mature RBC

4) after two days in the bone marrow, reticulocytes enter the bloodsteram. After 24 hours in circulation, the reticulocytes complete their maturation and become indistinguishable from other mature RBCs

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17
Q

explain what reticulocytes are

A

the rate of erythropoiesis is measured by the number of immature RBCs (called reticulocytes or “retics”) in the peripheral circulation
- a low retic count (<0.5) indicates a low rate of reythropoiesis while an elevated rate (>2%) indicates a high rate of erythropoiesis
- the normal range is 1-2% of the RBCs being “retics”
- RBC production requires: amino acids, iron, B vitamins, and folic acid
- LOW RBC (or hemoglobin) production leads to fatigue, weakness and confusion due to lower O2 delivery (lack of oxygen)

brain is higly depends on oxygen

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18
Q

the protein chain of hemoglobin

A

4 poly peptide chains, each with a heme = pigment
the iron of each heme can bind to 1 oxygen molecule, O2
Hb + O2 <-> HbO2
deoxyhemoglobin <-> oxyhemoglobin

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19
Q

what is erythrocytes (RBCSs)

A
  • 45% of the blood is RBCs. the percentage is called the hematocrit value is % of formed elements
  • during differentiation RBCs synthesize larfe amounts of the protein hemoglobin. once hemoglobin production is complete, normoblasts eject their nucleus and organelles, and take ont he shape of a Biconcave Disk
  • once differntiated, the RBC cannot replicate, synthesize proetin, or produce ATP from aerobic pathways, and only live for 120 days (mitochondria x blood)
  • hemaglobin is a complex protein with four iron-containing heme groups. each heme group can reversibly bind to one oxygen molecule; therefore, each molecule of hemoglobin is called hemoglobin concentration
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20
Q

abnormalities of erythropoiesis

A

anemia: a condition of insufficient RBC or hemoglobin (quality or quantity)
- it is most often the result of low iron intake, hemolysis, autoimmune disease, blood loss, or lack of production in the bone marrow

polythemia: a condition of excess number of RBCs
- it occurs in response to hypoxia (natural “blood doping” is training at high alaltitude), shots of EPO (illegal “doping”), smoking (COPD, Chronic, obstructive pulmonary disease), or dehydration

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21
Q

plasma, buffy coat, hematocrit

A
  1. plasma: water, proteins, nutrient, hormones, etc.
  2. buffy coat: white blood cells, platelets
  3. hematocrit: red blood cells
22
Q

What are the kinds of anemias

A

Iron deficiency anemia is the most common aneia in the US, and affects primarily menstruating women
- in the US, 20% of all women of childbeaering age have iron deficiency anemia, compared with only 2% of adult men (women have lower iron reserve than a man and sometimes poor diet, preganancy or being vegetarian contribute to loewr iron levels as well)

**hemorrhagic anemia **= the result of precipitous blood loss, and results in an equal decrease in Hct, Hgb content and RBC count

pernicious anemia - due to low vitamin B12 in diet (or low intrinsic factor, which is required for vit. B12 absorption)

sickle-cell disease (SCD) also called sickle-cell anemia, is an autosomal recessive disorder. A genetic defect in the primary DNA sequence leads to production of a faulty Hb beta chain, and RBCs that take on a rigid, sickle-shape
* sickling decreases the cell’s flexibility and results in a variety of complications; life expectancy is shortened
* treatments include: medications, blood transfusions & bone marrow stem cell replacement

pernicious anemia: Vit B12 is required for cells to uptake folic acid (req for DNA synthesis)

23
Q

explain the erythrocyte life cycle

A
  1. low O2 levles in blood stimulate kidneys to produce erythropoletin
  2. erythropoletin levels rise in blood
  3. erythropoietin and necessary raw materials in blood promote erythropoiesis in red bone marrow
  4. new erythrocyles enter bloodstream; function about 120 days
  5. aged and damaged and blood cells are engulfed by macrophage of liver, spleen, and bone marrow; the hemoglobin is broken down
  6. raw materials are made avaible in blood for erythrocyte synthesis
    - iron is bound to transterin and released to blood from liver as needed for erythropoiesis

from hemoglobin
- heme - iron stored as ferrittin, hemosiderin and bailrubin goes to liver
- the bailrubin is picked up from blood by liver, secreted into intestine in bile, metabolized to sterocoblin by bacteria and excreted in feces
- (small intestine) food nutrients, including amino acids, Fe, B12 and folic acid, are absorbed from intetine and enter blood `

Fe (iron) rritin = protein that stores most of Fe
Hemosiderin = complex of rest of iron

24
Q

what does control the RBC production?

A

RBC production is controlled by the O2 saturation in the blood/ when this falls, the kidney released the hormone erythropoietin, which stimulates RBC synthesis in the bone marrow.
- RBC requires Fe, amino acids, vitamins B12 and folic acid

25
what happens if blood delivered to kidneys contain low O2?
1) some stimulus disrupts homeostasis by (decreasing) 2) oxygen delivery to kidneys (and other tissues) 3) receptors: kidney cells detect low oxygen level * input to the next (incnreased erythropoietin secreted into blood) 4) center center: proerythroblasts in red bone marrow mature more quickly into reticulocytes * output to the next (increased erythropoietin) 5) effecters: larger number of RBCs in circulation 6) increased oxygen delivery to tissues - return to homeostasis when oxygen delivery to kidneys increases to normal
26
Life span of a red blood cell & what are **erythropoiesis** and **multipotent** stem cells?
= **120** days - eventually they rupture, or are destroyed by immune system cells (WBCs) by phagocytosis - constantly replacing - rate of 1%/ day - most often by targeted phagocytosis of old RBCs by macrophages Formation of all blood cells (WBCs, RBCs & platelets) = hemopoiesis occurs in red bone marrow in adults: RBC formation = **erythropoiesis** all types of blood cells develop from hemocytoblasts = **multipotent stem cells**
27
how are the blood cells' types determined?
the number of each type of blood cell that is produced is determined by: - signals that stem cells receive in the form of hormones erythropoiesis = production of RBCs - controlled by hormone Erythropoetin (EPO) - produced by cells of the **kidney** (stimulation) **regulation**: tonic baseline production of erythropoietin - tonic production of RBCs - production increased in response to low tissue O2 levels (hypoxia)
28
WHat are the leukocytes (WBC)
* do have nuclei, organelles * function: non-specific and specific defence **most** white blood cells located: in connective tissue proper or organs of the lymphoid system (thymus, spleen, lymph nodes) **small** proportion: circulate in the bloodstream two groups depending on whether they contain conspicuous chemical-filled cytoplasmic granules (when stained) * granulocytes includ ethe neutrophils, eosinophils and basophils * agranulocytes are the monocytes and lymphocytes
29
special properties of circulating WBCs
1. **diapedesis** = process of squeezing out of capillaries and entering tissue 2. **amoeboid** movement = uses for the mocement 3. positive **chemotaxis** 4. **phagocytosis** (neutrophils, eosinophils, monocytes)
30
what is Neutrophil
* 50-70% of circulating WBCs * nucleus has 5 lobes, known as polymorphonuclear leukocytes (PMNs) * cytoplasm contains granuels (= secretory vesicles) * granules contain lysosomal enzymes & bactericidal compounds * specialize in fighting bacteria that have been identified and flagged by components of immune system (e.g., antibodies) * engulf and destorys bacterial cells (phagocytosis)
31
what is chemotaxis
chemicals relased by microbes and inflamed tissues attract phagocytes, a phenomenon called **chemotaxis** * this graphic shows a neutrophil phagocytizing a microbe for internal digestion and destruction
32
What is an eosinophil
* granules stain with red dye eosin and nucelus has 2 lobes * main role: release substances that fight multicellular pathoges (e.g. parastic worms) * have been associated with allergies (which are an abnormal over-active immune response to a non-harmful substance, e.g. pollen)
33
what granules contain:
digestive enzymes toxins chemicals that modulate the immune response
34
what are monocytes
* agranuclocytes * larget WBCs * nucleus - kidney bean shaped * remain in blood -24 hrs 1. enter tissue and transform 2. becomes macrophages (free or fixed) - larger phagocytic cells that patrol tissues, engulf foreign materials and release substances that attract neutrophils, monocytes, and fibroblasts 3. **chemotaxis**
35
what are basophils
- granules contain histamine & stain dark blue with basic stains - are very similar to Mat cells in function (some research suggests they are the same cells) - migrate to site of injury - release histamine (diluating) which dilate blood vessles; causing inflammation - release heparin, which prevents blood clotting - both basophils (circulating blood cells) and mast cells play a role in allergies and the inflammatory response
36
what are lymphocytes
large dark nucleus, little cytoplasm = 20-30% of circulating WBCs most located in **connective tiessue & lymphoid tissues** three types: 1. T cells: attack foreign cells 2. B cells: produce antibodies = those two are specific immue response (target & attack specific antigens) 3. natural killer (NK) cells: destructin of abnoraml tissue celll (e.g. cancer cell) - nonspecific immune response
37
what are platelets produced by
anuclear cell fragments produced by large cells = **megakaryocytes** - their granules contain chemicals that once released - play crucial role in clotting - usually 2/3 of platelets circulating and 1/3 of platelts are stored in spleen - anuclear = without nucleus; short life-span (5-9 days)
38
what is hemostasis
* hemostasis or blood clotting occurs whenver there is injury to a blood vessel * there are three stages to hemostatsis 1) **vascular spasms** 2) **platelet plug formation** 3) **congulation**
39
what are 3 stages of hemostasis
**1) vascular spasms** - smooth muscle contraction caused by reflex pain response & chemicals released from endothelial cells; blood vessles constrict preventing blood loss **2) platelet plug formation** - platelets 'stick' to the exposed collagen from the damaged endothelium of vessle. once stuck they release serotonin and thromboxane A, which leads to further constriction and platelet aggregation, leading to a temporary plug **3) coagulation** - soluble fibrinogen is converted to insoluble fibrin fibers, which stablizie the blood clot. this series of events is caused by the activation of prothrombin activator (F actor X) and can be acheived by instrinsic or extrinsic mechanism
40
what is vascular pahse
characterized by smooth muscle contraction - vesel contraction & constriction = vascular spasms result - minimize blood loss while next steps take place *endothelins = potent vasoconstrictors **triggered by**: direct damage to the wall of vessel, then endothelial cells: 1) contract, exposing underlying collagen fibers 2) release a variety of chemical messengers (ADP, tissue factor, prostacyclin and endothelins) 3) endothelial cell membranes become sticky
41
what is platelet phase:
platelet stick to endothelial cells and exposed collagen fibers - become platelet plug and release many chemical messengers including... **ADP** - attracts and activates platelet aggregation & secreation **thromboxane A2** - stimulate vascular spasms **proteins** - participate in clotting **Ca++** - required for Tissue factor and factor X platelet-derived growth factor - promotes vessel repair the platelet phase pgenerates a positive feedback loop that results in the formation of platelet plug & clotting at the site of the damage. to avoid an explosive positive feedback, undamaged endothelial cells produce **anticogulanuts** (e.g. prostacyclin) - inhibits platelet aggregation except at site of injury
42
what is coagulation
= blood clotting Involves complex chain reaction ending with conversion of the plasma protein - fibrinogen (soluble) to fibrin (insoluble) - fibrin forms meshwork over platelet plug **clotting factors** = molcules or ions required for clotting to proceed - include clotting factors, calcium & vitamin K
43
What activates coagulation stage
coagulation is caused by the activation of **Prothrombin Activator (Factor X)**. - this can occur through Instrinsic (from within the blood) or through extrinsic (by damaged tissue) mechanisms - **instrinsic factors** relesae from platelets can activate Prothrombin activator (factor X); however, this process is considered **slow** - **extrinsict factors**, such as tissue factor are released from damaged tissue & activate prothrombin activator (factor X) very **rapidly** - **calcium ions** are required for both instrinsic & extrinsic mechanisms
44
4 fibrinolysis and regeneration
platelets release **Platelets derived growth factor** (PDGF) - stimulates regeneration regenerated tissue releases **tissue plasminogen activator** (tPA) (a powerful digestive enzyme) that dissolves the clot - Plasminogen (dissolves clot) - plasmin **recovery** 1) **clot retraction** - platelets retract, pulling vessles closer 2) **fibrinolysis** - plasmin digests fibrin, the clot dissolves
45
what are the clot retraction & fibrinolysis
1) **clot retraction**: - occurs once l=platelets and RBCs entangled in fibrin mesh - platelets contract by pulling torn edges of vessel closer together, reducing the size of damaged area 2) **fibrinolysis**: - as repairs take place, **clot** dissolves - as enzyme plasmin digests fibrin **inactive plasmin** present in blood in form of plasminogen converted to plasmin as a result of **TPA (tissue plasminogen activator) activity** - plasminogen is incorporated into clot as it forms *serum = plasma with clotting proteins removed
46
WHat is antigen
the plasma membrane of our RBCs can contain a number of different protens, sometimes referred to as **antigens** - a person's antigens are genetically determined
47
what are the two antigens in body
two antigens (A and B) determine our blod type * **type A**: if our RBCs contain antigen A, we will produce an antibody to antigen B (anti-B antibody) * **type B**: if our RBCs contain antigen B, we will produce an antibody to antigen A (anti-A antibody) * **type AB**: if both antigens are present, neither antibody is present * **type O**: if neiteher antigen is present * if the matching antigens and antibodies are allowed to mix, the blood will **agglutinate** or clump
48
What's difference between Blood typing and Cross-match testing
1. blood typing (determine ABO) and 2. Cross-match testing (mix donor & recipient blood in well)
49
What is Rh factor
an additional fator called **Rh** can also be present (+) or absent (-) on the RBC - antibodies to Rh are only produced after exposeure e.g. second pregnancy (when a Rh- mother has carried a Rh+ baby)
50
Punnett squares in blood type
both parents contribute in determining their child's blood type there are 2 alleles (antigen A and antigen B) that determine ABO blood type) there are 2 alleles (on a separate gene loci) that determine whether the Rh antigen is produced
51
how does Rh (Phesus) work in fetal Rh disease resulting from Rh-mothers carrying Rh+ babies
the most common (86%) sensitizing event is childbrirth,but fetal blood may pass into the maternal circulation earlier during pregnancy it is part of modern antenatal care to give all Rh (-) pregnant women an anti-RhD IgG immunoglobulin injection at 28 weeks gestation, with a booster at 34 weeks. also a booster will be given within 72 hrs after any potentiallly sensitizing events that occur early in pregnancy cancadian medical hall of fame: Dr. B. Chown & JM. Bowman, U of Man, for development of the Canegene vaccine