Week 10 Flashcards

(47 cards)

1
Q

What are the two main components of blood and their proportions?

A

Blood is composed of Plasma (~55%) and Formed Elements (~45%), which include red blood cells, white blood cells, and platelets.

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2
Q

What are the structure and main functions of red blood cells (erythrocytes)?

A
  • Structure: Biconcave, flexible, anucleate, 33% hemoglobin.
  • Function: Transport oxygen and carbon dioxide via hemoglobin.
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3
Q

What is the life cycle of a red blood cell?

A

Produced in bone marrow → lives ~120 days → removed by spleen and liver when old or damaged.

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4
Q

What are the two types of white blood cells and examples of each?

A

Granulocytes: Neutrophils, Eosinophils, Basophils.
Agranulocytes: Lymphocytes, Monocytes.

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5
Q

What are the functions of the five types of white blood cells?

A
  • Neutrophils: Phagocytose bacteria.
  • Eosinophils: Attack parasites, allergic response.
  • Basophils: Release histamine/heparin, allergy/inflammation.
  • Lymphocytes: Immune memory, viral defense.
  • Monocytes: Become macrophages, phagocytosis.
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6
Q

What are the structure and roles of platelets (thrombocytes)?

A
  • Structure: Cell fragments from megakaryocytes, no nucleus.
  • Functions: Clotting, vessel repair, immune response, release of clotting factors and growth factors.
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7
Q

What is plasma made of and what are its functions?

A
  • Composition: ~92% water, proteins (albumin, globulins, fibrinogen), nutrients, gases, electrolytes, wastes.
  • Functions: Transport, osmotic balance, immune defense, clotting.
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8
Q

What are haematocrit and haemoglobin, and how are they measured or characterized?

A
  • Haematocrit: % of blood made up of RBCs (≈42% in females, 47% in males).
  • Haemoglobin: Oxygen-carrying protein in RBCs with 4 O₂ binding sites and iron that gives blood its red color.
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9
Q

Why is it important to keep red blood cell (RBC) numbers within a homeostatic range?

A
  • Too few RBCs: Reduced oxygen-carrying capacity → risk of hypoxia.
  • Too many RBCs: Increased blood viscosity, resistance, and risk of clotting.
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10
Q

What hormone regulates red blood cell production and how?

A
  • Erythropoietin (EPO), produced mainly by the kidneys, stimulates erythropoiesis.
    -Circulates at low levels to maintain RBCs at a basal rate; increases in response to low oxygen levels.
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11
Q

How does the body maintain a constant RBC count?

A

Through a negative feedback loop balancing RBC production (stimulated by EPO) and destruction, ensuring stable oxygen delivery.

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12
Q

What is haemostasis and why is it essential?

A

Haemostasis is the process that stops bleeding when a blood vessel is injured. It prevents blood loss even from small cuts by initiating rapid defensive reactions like clot formation.

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13
Q

What prevents platelet activation in healthy blood vessels?

A

The endothelium of intact vessels secretes Nitric Oxide (NO) and Prostacyclin (PGI₂), which inhibit platelet adhesion and activation, keeping the vessel surface smooth.

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14
Q

What is the first step in haemostasis and its function?

A

Step 1: Vascular spasm – Injured vessels contract (vasoconstriction) to reduce blood flow and limit blood loss. Triggered by injury, pain, and inflammation.

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15
Q

What happens during platelet plug formation (Step 2 of haemostasis)?

A

Platelets aggregate, swell, become sticky, and release ADP, thromboxane A₂, and serotonin to recruit more platelets and form a temporary plug at the injury site.

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16
Q

How does coagulation (Step 3) stabilize the platelet plug?

A

Fibrinogen is converted to fibrin, forming a solid mesh that reinforces the plug and traps red blood cells, creating a stable clot to seal the vessel.

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17
Q

What is coagulation and what does it involve?

A

Coagulation is the process of blood clot formation. It involves:
- Activation, adhesion, and aggregation of platelets
- Deposition and maturation of fibrin to form a stable clot

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18
Q

What is the coagulation cascade?

A

The coagulation cascade is a series of enzyme-driven reactions involving clotting factors that activate each other.

Initiated by intrinsic or extrinsic pathways
Both pathways converge at Factor X, leading to the formation of fibrin, which forms a mesh that traps blood cells to stabilize the clot

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19
Q

What are natural anticoagulants that regulate coagulation?

A

Protein C: Degrades Factors Va and VIIIa
Antithrombin: Inhibits thrombin, Factors IXa, Xa, XIa, XIIa
Plasmin: Breaks down fibrin
Prostacyclin: Inhibits platelet activation

20
Q

What are coagulation disorders and their effects?

A

Coagulation disorders are imbalances in clotting ability.

  • Haemorrhage: Too little clotting → excessive bleeding
  • Thrombosis: Too much clotting → blood flow obstruction
21
Q

What are two serious conditions caused by excessive clotting?

A

Deep Vein Thrombosis (DVT): Clot in a deep leg vein
Pulmonary Embolism: Clot travels to the lungs, potentially life-threatening

22
Q

What is the purpose of clot retraction and how does it help wound healing?

A

Clot retraction stabilizes the clot and helps close the wound by using actin and myosin to contract fibrin strands, squeezing out serum and drawing wound edges together. PDGF stimulates tissue regrowth.

23
Q

What is fibrinolysis and why is it important?

A

Fibrinolysis is the process of breaking down clots after healing. It prevents vessel blockage by removing unneeded clots, which form naturally and continuously throughout the body.

24
Q

What enzyme is responsible for breaking down fibrin and how is it activated?

A

Plasmin digests fibrin. It is formed from plasminogen, which is activated by tissue plasminogen activator (tPA), thrombin, and Factor XII after a clot forms.

25
What is PDGF and what role does it play in healing?
Platelet-Derived Growth Factor (PDGF) is released by platelets and stimulates smooth muscle cells and fibroblasts to divide and repair the vessel wall.
26
How does Warfarin prevent blood clotting?
Warfarin inhibits Vitamin K epoxide reductase, reducing active Vitamin K hydroquinone, which is needed to synthesize clotting factors II, VII, IX, and X → decreases coagulation.
27
What is the mechanism and effect of Aspirin on haemostasis?
Aspirin inhibits COX-1, blocking thromboxane A₂ production → reduces platelet activation and aggregation, disrupting early platelet plug formation.
28
Why are antithrombotic drugs important and what conditions do they help prevent?
They prevent excessive clotting (thrombosis), helping avoid dangerous conditions like embolisms by reducing or inhibiting clot formation in arteries or veins.
29
What are the two main branches of the immune system and their purposes?
Innate immune defense: Immediate, non-specific response to pathogens. Adaptive immune defense: Specific, targeted response with memory. Purpose: Protects the body from harmful pathogens and toxins.
30
What are key features of the innate immune response?
- Acts quickly (minutes to hours) - Non-specific and always active - Includes physical barriers, chemical defenses, phagocytes, inflammation, and fever
31
What are key features of the adaptive immune response?
- Specific and slower (days after exposure) - Provides immunological memory - Involves B cells (antibodies) and T cells (targeted cell destruction and immune regulation)
32
What are macrophages and their role in immunity?
Macrophages perform phagocytosis and present antigens to adaptive immune cells, acting as a bridge between innate and adaptive responses.
33
What is the function of neutrophils in the immune system?
Neutrophils are the most abundant WBCs, arrive first at infection sites, perform phagocytosis, and release antimicrobial substances.
34
What are the functions of B-lymphocytes (B-cells)?
B-cells recognize specific antigens and produce antibodies. They differentiate into: Plasma cells → secrete antibodies Memory B-cells → fast response upon re-exposure
35
What are the types and roles of T-lymphocytes (T-cells)?
- Helper T-cells (CD4⁺): Activate B-cells, cytotoxic T-cells, and macrophages - Cytotoxic T-cells (CD8⁺): Kill infected or abnormal cells - Regulatory T-cells: Suppress overactive immune responses
36
What roles do eosinophils, basophils, and mast cells play in the immune system?
- Eosinophils: Attack parasites, involved in allergies - Basophils: Release histamine during allergic reactions - Mast cells: Tissue-based cells releasing histamine and other mediators in inflammation
37
What is the main trigger of the adaptive immune response?
The recognition of antigens, which are specific molecules (usually proteins or polysaccharides) found on pathogens or foreign substances.
38
What are the two main types of lymphocytes in adaptive immunity and their roles?
- B cells → Humoral immunity; produce antibodies - T cells → Cell-mediated immunity; kill infected cells or help activate other immune cells
39
What are the main functions of antibodies produced by B cells?
Neutralization of pathogens Opsonization (tagging pathogens for destruction) Activation of the complement system
40
How do cytotoxic and helper T cells function in the immune response?
- Cytotoxic T cells: Kill infected or cancerous cells - Helper T cells: Activate B cells, cytotoxic T cells, and macrophages
41
What are antigens and what can act as one?
Antigens are foreign substances that trigger immune responses. Examples: bacteria, fungi, parasites, plant pollen, insect venom, and transplanted tissues.
42
What is the difference between complete and incomplete antigens (haptens)?
- Complete antigens: Have immunogenicity and reactivity (e.g., proteins, lipids) - Haptens: Small molecules that become immunogenic only when attached to body proteins (e.g., penicillin allergy)
43
What are antigenic determinants (epitopes)?
Specific parts of an antigen that bind to antibodies or lymphocyte receptors. Most antigens have multiple antigenic determinants.
44
What is the basic structure of an antibody?
- Heavy and light chains - Disulfide bonds - Variable region: binds antigens - Constant region: determines the antibody class (IgG, IgA, IgM, IgE, IgD)
45
What is antibody neutralization?
Antibodies bind to pathogens or toxins, blocking their ability to infect cells and marking them for destruction.
46
What are agglutination and the complement system in antibody function?
- Agglutination: Antibodies bind multiple antigens, forming clumps that enhance phagocytosis. - Complement activation: Antibodies initiate the complement system, promoting cell lysis and inflammation.
47