Week 3 (The Blood) Flashcards

1
Q

The Blood

A

Blood is a fluid connective tissue, composed of formed cellular elements suspended in a liquid medium called plasma.

 formed cellular elements:
*erythrocytes (red blood cells, RBCs)
*leukocytes (white blood cells, WBCs)
*thrombocytes (platelets)

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2
Q

Functions of the Blood

A

 Transportation
*deliver O2, nutrients eg. glucose, amino acids to cells
*transport waste products eg. CO2 from cells for
elimination
* transport hormones
*distribute heat throughout the body

 Regulation (helps maintain homeostasis)
*maintain pH (carries buffers)
*maintain fluid and electrolyte balance
*maintain body temperature

 Protection
*coagulation (clotting): prevent blood loss
*immunologic: prevent infection (WBCs, antibodies)

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3
Q

Physical Properties of Blood

A

Blood Volume:
5-6 L in males
4.5-5.5 L in females

pH: 7.35 – 7.45

Specific Gravity: 1.050

Viscosity: 4.5 – 5.5

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4
Q

Hematopoiesis (Blood Cell Formation)

A

(Blood Cell Formation)

*Occurs in red bone marrow.

*Sites of hematopoiesis in adults:
Skull, sternum, ribs, upper ends of long limb bones (humerus, femur), vertebrae, and pelvis.

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5
Q

BLOOD CELL COUNTS AND HEMATOCRIT

A

Blood Cell Counts
Red Blood Cells
Male: 4.7 to 6.1 million/μL
Female: 4.2 to 5.4 million/μL

White Blood Cells
4000 to 11 000 /μL

Platelets
150 000 to 450 000 /μL

Hematocrit
packed cell volume (PCV)
volume % of erythrocytes in blood
Male: 42 to 52 %
Female: 37 to 47 %

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6
Q

Blood Components

A

*Plasma (55%) – Contains water, ions, plasma proteins, respiratory gases, nutrients, waste products, and hormones.

*Cells (45%) – RBCs, WBCs, and platelets develop from stem cells in red bone marrow.

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7
Q

Plasma Components

A

*Water (90%)

*Plasma Proteins (8%)
Albumin: Acts as a buffer and helps maintain osmotic pressure.
Gamma Globulins: Antibodies.
Fibrinogen and Other Clotting Factors.
Complement Proteins and Transport Proteins.
Electrolytes, Nutrients, and Waste

*Products. (~1%)

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8
Q

Erythrocytes (Red Blood Cells)

A

*Manufactured by erythropoiesis.

*Shape: Circular, biconcave, and disc-shaped.

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9
Q

Advantages of Biconcave Shape

A

*Increased surface area for gas exchange.

*Flexibility to pass through capillaries.

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10
Q

Factors Affecting Erythropoiesis

A

 Tissue Oxygenation
Hypoxia (triggers erythropoietin (EPO) release)

 Erythropoietin (EPO)
Hormone produced by the kidneys to stimulate RBC production.

 State of Bone Marrow

 State of Liver

 Nutritional Factors
Vitamins:
Vitamin B12
Folic Acid
Vitamin B6, B2, C, A, E
Nicotinic Acid (Niacin)

 Protein: Amino acids

 Minerals:
Iron
Copper
Cobalt

 Other Hormones
Androgens
Estrogens
Growth Hormone
Thyroxine
Cortisol

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11
Q

Characteristics of Mature RBCs

A

 Anucleate (no nucleus).

 Lack mitochondria and organelles to maximize space for hemoglobin.

  • do not divide / reproduce
  • ↑ efficiency- more space to carry haemoglobin

*↓ weight- travel faster

*more O2 delivered to the tissues as organelles not present to consume it

*Life span: 100–120 days.

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12
Q

Functions of RBCs

A

 Transport O₂ and CO₂.
 Buffer blood pH.
 Contribute to blood viscosity.

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13
Q

Hemoglobin (Hb)

A

– Primary Content of RBCs

 Gives RBCs their characteristic red color.

 Iron-containing protein with a quaternary structure.

 Composed of two parts: Haem and Globin.

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14
Q

Functions of Hemoglobin

A

 Transports O₂ and CO₂.
 Maintains blood pH.
 Controls vascular tone, mediated by nitric oxide (NO).

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15
Q

Normal Mean Concentration of Hb in Blood

A

 adult males:
15.5 g/dL (range 14 – 18 g/dL)

 adult females:
14 g/dL (range 12 – 16 g/dL)

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16
Q

Hemoglobin Structure

A
  1. Globin (97% of Hb Molecule)
    Protein component of Hb.
    Tetramer structure: consists of two α subunits and two β subunits.
    Each subunit binds to a haem group.
  2. Haem Group (3% of Hb Molecule)
    Iron-containing porphyrin ring, composed of 4 pyrrole rings.
    Each haem group contains one iron atom, which binds reversibly with one molecule of O₂.

(1 Hb molecule carries 4 molecules of O₂.)

17
Q

Types of Hemoglobin

A
  1. Oxyhemoglobin
    Hb bound to O₂ (bright red).
    O₂ loading occurs in the lungs.
  2. Deoxyhemoglobin
    Hb after O₂ is released (dark red).
    Occurs in the tissues.
  3. Carbaminohemoglobin
    Hb bound to CO₂.
    20% of CO₂ in the blood binds to the globin component of Hb.
    CO₂ loading occurs in the tissues.
18
Q

Red Blood Cells – Life Cycle

A

Lifespan: 100–120 days

 Destruction: Occurs in macrophages of the spleen, liver, and bone marrow

 Hemoglobin (Hb) Breakdown:
*Hb is split into haem and globin components
*Globin chains are broken down into amino acids for reuse
*Iron from the haem group is released and transported to:
+Various tissues for storage
+Red bone marrow for the synthesis of new hemoglobin

 Haem Group Conversion:
*The remaining haem is converted into biliverdin, then into bilirubin
*Bilirubin metabolism occurs in the liver, with its derivatives:
+Secreted in bile and excreted in feces (gives feces its characteristic color)
+Excreted in urine, contributing to its color

19
Q

Leukocytes (White Blood Cells)

A

WBCs are the only blood components that are complete cells with a nucleus and organelles.

20
Q

Functions of White Blood Cells

A

 Defend against diseases and infections.

 Remove toxins and tumor cells.

 Can leave capillaries by diapedesis (migration).

21
Q

Categories of WBCs

A

 Granulocytes:
Contain membrane-bound granules.
*Neutrophils (60-70%)
*Eosinophils (1-4%)
*Basophils (0.25-0.5%)

 Agranulocytes
Lack granules.
*Lymphocytes (25-33%)
*Monocytes (2-6%)

22
Q

Neutrophils

A

Nucleus: Multilobed (3–6 lobes)
Function: Phagocytize bacteria

23
Q

Eosinophils

A

Nucleus: Bilobed

Granules: Coarse, stain deep red to crimson

Functions:
*Defense against parasites (release digestive enzymes; worms too large to be ingested)
*Lessen the severity of allergies
*Phagocytize antigen-antibody complexes
*Release histaminase (reduces inflammation)

24
Q

Basophils

A

Nucleus: Lobed, U- or S-shaped with 2 or 3 conspicuous constrictions

Granules: Coarse, dark purple or black

Functions:
*Release histamine (inflammatory chemical) and other mediators of inflammation
*Attract other WBCs to the area
*Contain heparin (anticoagulant)

25
Lymphocytes
Nucleus: Large, dark-purple, circular; can be spherical or indented Location: Found mostly in lymphoid tissue Types: T Cells – Direct cell attack B Cells – Produce antibodies (give rise to plasma cells) Function: Mount an immune response
26
Monocytes
Nucleus: Large, purple-staining, U- or kidney-shaped Size: Largest leukocytes Function: *Phagocytosis *Differentiate into macrophages when entering tissues *Activate lymphocytes to mount an immune response
27
Thrombocytes (Platelets)
Structure: Not true cells; cytoplasmic fragments of large megakaryocytes found in bone marrow Functions: *Secrete vasoconstrictors to induce vascular spasms after blood vessel injury *Form temporary platelet plugs to stop bleeding *Secrete chemicals to attract neutrophils and monocytes to sites of inflammation *Secrete growth factors that stimulate fibroblasts and smooth muscle growth, aiding in blood vessel maintenance *Dissolve blood clots that have outlasted their usefulness
28
Hemostasis
(Stopping of Bleeding) + A vital process to prevent excessive blood loss. + Blood clot typically forms within 3 to 6 minutes. + Positive Feedback Mechanism: Coagulation amplifies clotting until bleeding stops.
29
Three Phases of Hemostasis
1) Vascular Spasms: Immediate vasoconstriction to reduce blood flow. 2) Platelet Plug Formation: Platelets stick to damaged site and release chemicals to attract more platelets. 3) Coagulation (Clotting): Fibrin threads form a mesh that traps RBCs and platelets.