Weeks 1, 2 and 3 Flashcards

1
Q

Does the lymphatic system return leaked fluid to the blood, also helps in transporting absorbed lipids from the gut?

A

Yes

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2
Q

What are lacteals?

A

Specialised lymph capillaries present in intestinal mucosa.

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3
Q

Do lymphatic trunks, which are formed by union of largest collecting vessels, drain large areas of the body?

A

Yes

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4
Q

Are lymphatic vessels named for regions of the body they drain?

A

Yes.

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5
Q

Are some of the names for lymphatic vessels the following:

  • Paired lumbar
  • Paired bronchomediastinal
  • Paired subclavian
  • Paired jugular trunks
  • Single intestinal trunks
A

Yes.

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6
Q

What is lymphangitis?

A

A condition in which lymphatic vessels appear as painful red lines under the skin.

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7
Q

Is lymphangitis caused by inflammation of larger lymphatic vessels that contain vaso
vasora?

A

Yes.

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8
Q

In lymphangitis, do the vaso vasora become congested with blood?

A

Yes.

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9
Q

Do larger lymphatics, like blood vessels, receive their nutrients from branching vasa vasorum?

A

Yes.

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10
Q

Is the lymph system a low-pressure system like venous system?

A

Yes.

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11
Q

Is lymph propelled by:
– Milking action of skeletal muscle
Pressure changes in thorax during breathing
– Valves to prevent backflow
– Pulsations of nearby arteries
– Contractions of smooth muscle in walls of lymphatics

A

Yes.

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12
Q

Physical activity increases flow of lymph;
Immobilization of area keeps needed inflammatory material in area
for faster healing

A

Yes.

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13
Q

Lymphedema: severe localized oedema

A

Yes.

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14
Q

Caused by anything that prevents normal return of lymph to blood
– Examples: tumours blocking lymphatics or removal of lymphatics during cancer
surgery
– Lymphedema may improve if some lymphatic pathways remain and enlarge

A

Yes.

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15
Q

• Immune system cells
– T cells: attack and destroy infected cells
– B cells: produce plasma cells, which secrete antibodies

A

Yes.

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16
Q

Other lymphoid immune cells
– Macrophages
– Dendritic cells

A

Yes.

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17
Q

Supporting lymphoid cell

– Reticular cells produce reticular fibers called stroma in lymphoid organs

A

Yes.

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18
Q

Lymphoid Tissue
Houses and provides proliferation sites for lymphocytes
– Offer surveillance

A

Yes.

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19
Q

Lymphoid Tissue
Largely composed of reticular connective tissue, a type of loose
connective tissue

A

Yes.

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20
Q

Are there two main types of lymphoid tissues?

A

Yes.

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21
Q

Diffuse lymphoid tissue: loose arrangement of lymphoid cells and
some reticular fibers
– Found in virtually every body organ
– Larger collections in lamina propria of mucous membranes

A

Yes.

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22
Q

Lymphoid follicles (nodules): solid, spherical bodies consisting of tightly
packed lymphoid cells and reticular fibers
– Contain germinal centers of proliferating B cells
– May form part of larger lymphoid organs (nodes)
– Isolated aggregations in Peyer’s patches and in appendix

A

Yes.

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23
Q

Are lymph nodes the principal secondary lymphoid organs of body?

A

Yes.

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24
Q

Are the two main functions of lymph nodes:
1. Cleansing the lymph: act as lymph “filters”
2. Immune system activation: offer a place for lymphocytes to become
activated and mount an attack against antigens

A

Yes.

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25
Q

Do lymph nodes vary in shape and size, but most are bean shaped?

A

Yes.

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26
Q

Are lymph nodes small, less than 2.5 cm (~1 inch)?

A

Yes.

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27
Q

Are lymph nodes surrounded by external fibrous capsule?

A

Yes.

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28
Q

Lymph nodes: Do capsule fibers extend inward as trabeculae that divide node into
compartments

A

Yes.

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29
Q

Two histologically distinct regions of lymph node:
– Cortex
– Medulla

A

Yes.

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30
Q

Spleen functions
– Site of lymphocyte proliferation
– Cleanses blood of aged cells removes debris
– Stores breakdown products of RBCs (e.g., iron) for later reuse
– Stores blood platelets and monocytes for release into blood when needed
– May be site of foetal erythrocyte production

A

Yes.

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31
Q

• Spleen is encased by fibrous capsule and also has trabeculae

A

Yes.

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32
Q

• Histologically, consists of two components
– White pulp
– Red pulp

A

Yes.

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33
Q

Clinical homeostatic imbalance:
The spleen has a thin capsule, so direct blow or severe infection may
cause it to rupture, spilling blood into peritoneal cavity

A

Yes.

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34
Q

Splenectomy: surgical removal of ruptured spleen

A

Yes.

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35
Q

If spleen must be removed, liver and bone marrow take over most of its
functions

A

Yes.

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36
Q

Splenectomy: in children younger than 12, spleen will regenerate if a small part is left

A

Yes

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37
Q

Mucosa-associated lymphoid tissue (MALT)

– Lymphoid tissues in mucous membranes throughout body

A

Yes.

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38
Q

MALT: Protects from pathogens trying to enter body

A

Yes.

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39
Q

Malt: found in mucosa of respiratory tract, genitourinary organs, and
digestive tract; largest collections of MALT found in
– Tonsils
– Peyer’s patches
– Appendix

A

Yes.

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40
Q

Tonsils: Simplest lymphoid organs

A

Yes.

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41
Q

Tonsils: Form ring of lymphatic tissue around pharynx; appear as swellings of
mucosa

A

Yes.

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42
Q

Tonsils:Named according to location

– Palatine tonsils, Lingual tonsil, Pharyngeal tonsil, Tubal tonsils

A

Yes.

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43
Q

• Tonsil function - gather and remove pathogens

A

Yes.

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44
Q

Appendix: An offshoot of first part of large intestine

A

Yes.

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45
Q

Appendix: Contains a large number of lymphoid follicles

A

Yes.

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46
Q

Appendix: Location aids in functions (like Peyer’s patches)

A

Yes.

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47
Q

Appendix:

  1. Destroy bacteria, preventing them from breaching intestinal wall
  2. Generate “memory” lymphocytes
A

Yes.

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48
Q

Thymus: A bilobed lymphoid organ found in inferior neck

A

Yes.

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49
Q

Thymus: Functions as lymphoid organ where T cells mature

A

Yes.

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50
Q

Thymus is broken into lobules that contain outer Cortex and inner
Medulla

A

Yes

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51
Q

Thymus differs from other lymphoid organs
– Has no follicles
– Does not directly fight antigens
– Stroma is made up of epithelial cells, not reticular fibers

A

Yes.

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52
Q

The lymphatic vessels form a one-way system in which lymph flows only
toward the heart
– Returning leaked fluid back to the circulation
– Transporting absorbed nutrients (lipids) from the gut

A

Yes.

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53
Q

• The lymphoid organs and tissues provide the structural basis of the
immune system
– Lymph nodes, spleen, thymus, MALT and tonsils
– Lymphoid cells are housed and mature here
– Some lymphoid organs perform additional functions

A

Yes.

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54
Q
Immune system:
Innate (nonspecific)
defense system
• Always prepared
• Responding within minutes
• Two lines of defenses
• Inflammation
A

Yes.

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55
Q
Immune system:
Adaptive (specific)
defense system
• Takes longer to react than
innate
• Third line of defense
A

Yes

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56
Q
Innate
defenses
Surface barriers
• Skin
• Mucous membranes
A

Yes.

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57
Q
Innate
defenses
Internal defenses
• Phagocytes
• Natural killer cells
• Inflammation
• Antimicrobial proteins
• Fever
A

Yes.

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58
Q

Adaptive
defenses
Humoral immunity
• B cells

A

Yes.

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59
Q

Adaptive
defenses
Cellular immunity
• T cells

A

Yes.

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60
Q

First Line of Defense
Physical barriers
– Keratinized epithelial membrane and intact mucosae
– Hairs inside the nose
– Cilia in the upper respiratory tract
– Sticky mucus in digestive and respiratory tract

A

Yes.

61
Q

First Line of Defense
Chemicals & enyzmes
– Acid mentle inhibits bacterial growth (skin, vagina,stomach)
– Lysozyme of saliva, respiratory mucus, and lacrimal fluid, Enzymes in stomach
– Defensins control bacterial and fungal colonization
– Sebum and dermicidin in sweat are toxic to some bacteria

A

Yes.

62
Q

Second Line of Defense: Cells and Chemicals
Phagocytes
• Natural killer (NK) cells
• Antimicrobial proteins (interferons and complement)
• Inflammatory response (macrophages, WBCs, mast celles, and
inflammatory chemicals)
• Fever

A

Yes.

63
Q

Phagocytosis
Opsonization: immune system uses antibodies or complement proteins
as opsonins that coat pathogens
• Cytoplasmic extensions (pseudopods) bind to and engulf particle in
vesicle called phagosome
• Phagosome fuses with lysosome, forming phagolysosome
• Phagolysosome is acidified, and lysosomal enzymes digest particles
• Indigestible and residual waste is exocytosed from phagocyte

A

Yes.

64
Q
Inflammation: Tissue Response to Injury
Inflammation is triggered whenever body tissues are injured
• Trauma, heat, irritating chemicals, or infections by microorganisms
• Benefits of inflammation:
• Localize the damage and set a reparation of affected tissue
• Alert the adaptive immune system
• Cardinal signs of acute inflammation:
• Redness
• Heat
• Swelling
• Pain
• Impairment of function
A

Yes.

65
Q
Inflammation’s benefits
It prevents the spread of damaging agents to nearby tissue
It desposes of cell debris and pathogens
It alerts the adaptive immune system
It sets the stage for repair
A

Yes.

66
Q

Inflammation: Tissue Response to Injury
Stages of inflammation
– Chemical ALARM
• Histamine released by mast cells
• Macrophages and epithelial cells of respiratory tissues, intestine have Toll-like
receptors (TLRs)  CYTOKINES
• Kinins, prostaglandins (PGs), and complement
– Vasodilation and increased vascular permeability
• Role of OEDEMA  Translocation of foreign material into lymphatics
• Role of FIBRIN MASH  Isolate injured area
– Phagocyte mobilization
• Neutrophils flood area first; macrophages follow

A

Yes.

67
Q

Antimicrobial Proteins
Antimicrobial proteins enhance innate defense
– Attacking microorganisms directly
– Hindering microorganisms’ ability to reproduce
• Most important antimicrobial proteins
– Interferons
– Complement proteins
• Complement system can be activated by three different pathways:
– Classical pathway
– Lectin pathway
– Alternative pathway

A

Yes.

68
Q

Complement
• Inactive plasma proteins
• Major mechanism for destroying foreign substances
• Amplify inflammatory process
• Promote phagocytosis
• Lyses and kill certain bacteria (Membrane attack complex)

A

Yes.

69
Q

Fever
• Abnormally high body temperature that systemic response to invading
microorganisms
• Leukocytes and macrophages exposed to foreign substances secrete
pyrogens
• Pyrogens act on body’s thermostat in hypothalamus, raising body
temperature
• Benefits of moderate fever
– Causes liver and spleen to sequester iron and zinc (needed by microorganisms)
– Increases metabolic rate, which increases rate
of repair

A

Yes.

70
Q

Non-self substances, INTRUDERS, that can mobilize Antigens
adaptive defenses
and provoke an immune response
• Targets of all adaptive immune responses
• Most are large, complex molecules not normally found in body
• PROTEINS, POLYSACCHARIDES, LIPIDS, NUCLEIC ACIDS

A

Yes.

71
Q

Do both B and T lymphocyte precursors originate in

red bone marrow?

A

Yes.

72
Q
Role of Antigen-Presenting Cells (APCs)
• Engulf and present fragments of Ag to T cells for recognition
• Major types
– Dendritic cells
– Macrophages
• Role of MHC proteins
A

Yes.

73
Q

Activation and Differentiation of B Cells
• B cells are activated when antigens bind to surface receptors, crosslinking adjacent receptor
• Clonal selection, follows proliferation and differentiation of B cell into
effector cells
• Most clone cells become plasma cells, antibody-secreting effector cells
• Clone cells that do not become plasma cells become memory cells
– Provide immunological memory
– Mount an immediate response to future exposures to same antigen

A

Yes.

74
Q

Immunological Memory
• Primary immune response: cell proliferation and differentiation upon
exposure to antigen for the first time (3-6 days after Ag encounter)
• Secondary immune response
- Re-exposure to same antigen gives faster, more prolonged, more
effective response
– Sensitized memory cells provide immunological memory

A

Yes.

75
Q

Immunization by Injection of Antigens
• Immunization has been used for many years to produce acquired
immunity against specific diseases
• A person can be immunized by
– Injecting dead organisms that are no longer capable of causing disease but that still have
some antigens
– Toxins that have been treated with chemicals to destroy their toxic nature even though
their antigens for causing immunity are still intact
– And, finally, a person can be immunized by being infected with live organisms that have
been “attenuated”

A

Yes.

76
Q

Antibodies
• Antibodies, called Immunoglobulins (Igs)—are proteins secreted by
plasma cells
- Gamma globulin portion of blood proteins
• Bind specifically with Ag detected by B cells
• Five Immunoglobulin (Ig) classes

A

Yes

77
Q

In Summary…
• B Cells are activated (similar to T Cells) by Antigen Presenting Cells
• B Cells, upon activation, become Plasma Cells which are giant factories
of Antibody production
• Memory cells are also formed
• Secondary response is quicker and longer lasting than the primary
response
• Antibodies are of various types, each having its specific function

A

Yes.

78
Q

Cellular Immune Response
• T cells provide defense against intracellular antigens
• T cell are best suited for cell to cell interaction
- For example: cells infected with viruses or bacteria, cancerous or abnormal cells,
foreign (transplanted) cells
• Some T cells directly kill cells; others release chemicals that regulate
immune response

A

Yes.

79
Q

MHC Proteins and Antigen Presentation
• T cells respond only to processed fragments of antigens displayed on
surfaces of cells by major histocompatibility complex (MHC) proteins
• Antigen presentation is vital for activation of naive T cells and normal
functioning of effector T cells
• Two classes of MHC proteins:
• Class I MHC proteins: displayed by all cells except RBCs
• Class II MHC proteins: displayed by APCs (dendritic cells, macrophages, and B
cells)

A

Yes.

80
Q

MHC Proteins and Antigen Presentation
• Class I MHC proteins
- Located on the surface of virtually all body cells
- Class I MHC crucial for CD8 cell activation
– Act as antigen holders; form “self” part that T cells recognize
– Inform cytotoxic T cells of microorganisms hiding in cells (cytotoxic T cells ignore
displayed self-antigens)

A

Yes.

81
Q

MHC Proteins and Antigen Presentation
• Class II MHC proteins
- Less widespread than class I
- Bind with longer fragments (14–17 amino acids) of exogenous (extracellular)
antigens that have been engulfed and broken down in a phagolysosome by
antigen-presenting cell
- Class II MHC proteins recognized by naive CD4 and helper T cells
– Signal CD4 cells that help is required

A

Yes.

82
Q

Activation and Differentiation of T cells
• Cytokines
- IL-2 is a key growth factor, acting on same cells that release it and other T cells
• Encourages activated T cells to divide rapidly
- Other cytokines amplify and regulate innate and adaptive responses
• Example: gamma interferon enhances killing power of macrophages

A

Yes.

83
Q

Cellular Immune Response
• Helper T (TH
) cells
- Play central role in adaptive immune response
- Activate both humoral and cellular arms
- Once primed by APC presentation of antigen, helper T cells:
• Help activate B cells and other T cells
• Induce T and B cell proliferation
• Secrete cytokines that recruit other immune cells
• Without TH
, there is no immune response

A

Yes.

84
Q

Cellular Immune Response
- Activation of CD8 cells
– CD8 cells require TH
cell to become activated into destructive cytotoxic T cells
– Cause dendritic cells to express co-stimulatory molecules required for CD8 cell
activation
– Cytotoxic T cells attack infected and cancerous cells

A

Yes.

85
Q

Regulatory T (TReg) cells
- Diminish immune response by direct contact or by secreting inhibitory cytokines
such as IL-10 and transforming growth factor beta (TGF- )
- Important in preventing autoimmune reactions
– Suppress self-reactive lymphocytes in periphery (outside lymphoid organs)
– Research into using them to induce tolerance to transplanted tissue and alleviate
the severity of autoimmune diseases

A

Yes.

86
Q

In Summary…
• T cells are responsible for “cell-mediated immunity”
• They are activated when APCs present antigen in association with MHC
proteins
• T-cells sensitive to the antigen are activated upon contact (clonal
expansion)
• T cells attack the antigen (cytotoxic T cells) and stimulate B cells (helper
T cells)
• Memory cells are also formed

A

Yes.

87
Q

Immune disorders
• Autoimmune disorders
– Immune response mistakenly targets normal cells
• Immunodeficiency diseases
– Immune system does not develop properly or is blocked

A

Yes.

88
Q

Autoimmune disorders
• Immune response mistakenly targets normal cells
• Failure of the Tolerance Mechanism Causes Autoimmune Disease
– Diseases like rheumatic fever, myasthenia gravis, lupus erythematosus
• Treatment of autoimmune diseases may include immunomodulatory
drugs. These drugs suppress immune system and make host susceptible
to develop infections!

A

Yes.

89
Q

Immunodeficiency diseases
• An immunocompromised host is a patient with defects in host defenses
that predispose to infection.
• Risk factors include neutropenia, immune system defects (from disease
or immunosuppressive drug therapy), compromise of natural host
defenses, environmental contamination, and changes in normal flora of
the host.
• Immunocompromised patients are at high risk for a variety of bacterial,
fungal, viral, and protozoal infections.

A

Yes.

90
Q
Hypersensitivity (Allergy)
• Inappropriate or excessive immune response to allergens…
– Immediate hypersensitivity (type I)
– Cytotoxic reactions (type II)
– Immune complex disorders (type III)
– Delayed hypersensitivity (type IV)
• Anaphylaxis
– Circulating allergen affects mast cells throughout body
A

Yes.

91
Q
Skin: Consists of two distinct regions
1. Epidermis—superficial region
• Epithelial tissue
2. Dermis—underlies epidermis
• Mostly fibrous connective tissue
A

Yes.

92
Q

Hypodermis (superficial fascia)

  1. Subcutaneous layer deep to skin
  2. Not part of skin but shares some functions
  3. Mostly adipose tissue that absorbs shock & insulates
  4. Anchors skin to underlying structures – mostly muscles
A

Yes

93
Q
EPIDERMIS
Keratinized stratified squamous epithelium
Four (or five) distinct layers
1. Stratum basale
2. Stratum spinosum
3. Stratum granulosum
4. Stratum lucidum (only in thick skin)
5. Stratum corneum
A

Yes

94
Q

Four cell types

  1. Keratinocytes
  2. Melanocytes
  3. Dendritic (Langerhans) cells
  4. Tactile (Merkel) cells
A

Yes

95
Q
EPIDERMIS 4 CELL TYPES
Keratinocytes
– Produce fibrous protein keratin
– Most cells of epidermis
– Tightly connected by desmosomes
A

Yes

96
Q

EPIDERMIS 4 CELL TYPES
Melanocytes
– 10–25% of cells in deepest epidermis
– Produce pigment melanin – packaged into melanosomes
• Protect apical surface of keratinocyte nucleus from UVdamage
• Absorbs UV rays and dissipates the energy as heat

A

Yes.

97
Q

EPIDERMIS 4 CELL TYPES
Dendritic (Langerhans) cells
– Macrophages – key activators of immune system (APC)

A

Yes

98
Q

EPIDERMIS 4 CELL TYPES
4. Tactile (Merkel) cells
– Sensory touch receptors

A

Yes.

99
Q

CELL DIFFERENTIATION IN EPIDERMIS
• Cells change from stratum basale to stratum corneum
Accomplished by specialized form ofapoptosis
– Controlled cellular suicide
• Cells slough off as dandruff and dander
• Shed ~ 50,000 cells every minute
• ~18Kgs/lifetime
– Support microscopic organism:
– House dust mite (type of dermatophagoids)
– House dust allergy: allergy to inhaled feaces of mites

A

Yes

100
Q
DERMIS
Strong, flexible connective tissue
• Cells
– Fibroblasts, macrophages, and
occasionally mast cells and
white blood cells
• Fibers in matrix bind body together
• Contains nerve fibers; blood and lymphatic vessels
• Contains epidermal hair follicles; oil and sweat glands
• Twolayers
1. Papillary
2. Reticular
A

Yes.

101
Q

DERMIS: PAPILLARY LAYER
Areolar connective tissue with collagenand elastic fibres and bloodvessels
• Loosetissue
– Phagocytes can patrol for microorganisms
• Dermal papillae
– Superficial peg like projections
• Most contain capillary loops
• Some contain Meissner’s corpuscles (touch receptors)
• Some contain free nerve endings (pain receptors)
• Thick skin that lies atop dermal ridges, causes epidermal ridges
• Collectively ridges called friction ridges
• Enhance grippingability
• Contribute to sense of touch
• Pattern isfingerprints

A

Yes.

102
Q
DERMIS: RETICULAR LAYER
• ~80% of dermal thickness
• Dense fibrous connective tissue
1. Elastic fibers
– Provide stretch-recoil properties
2. Collagen fibers
– Provide strength and resiliency
– Bind water
• Cleavage lines: most collagen fibers parallel to skin surface
• Externally invisible
• Important tosurgeons
• Incisions parallel to cleavage lines gap less and heal more readily
A

Yes.

103
Q

THE EVOLUTION OF SKINCOLOUR
UV light: 2 adverseeffects
– Causes skin cancer
– Breaks down folic acid (a vitamin B) needed:
• Cell division, fertility, fetal development
_ UV Bone deformities
• UV light desirable effect
– Stimulates keratynocytes to synthesize vitamin D
• Needed for absorption of
dietary Calcium, bone growth

A

Yes.

104
Q
SKIN COLOUR
Three pigments contribute to skincolour
1. Melanin (tyrosine polymer)
• Only pigment made in skin
2. Carotene
• Accumulates in stratum corneum and in fatty
tissues of hypodermis
3. Haemoglobin
• Oxygenated pigment in red blood cells
Distribution is notrandom
– Near equator AND
Higher altitude:
greater protection required
from sun
A

Yes.

105
Q

HOMEOSTATIC IMBALANCES
Excessive sun exposure
elastic fibers clump&raquo_space;leathery skin depressed immune system
altered DNA of skin cells&raquo_space; skin cancer
2. UV radiation destroys body’s folic acid stores (DNA synth.)
pregnancy: impair embryo CNS development
3. Chemical induced photosensitivity- skin rash antibiotics,
antihistamines, perfumes, detergents
4. Sunspots (tinea versicolour) are fungal infection;
not related to melanin

A

Yes.

106
Q

SKIN COLOUR IN DIAGNOSIS
• Cyanosis
– Blue skin color - low oxygenation of hemoglobin
– Heart failure, severe respiratory disorders
– Dark skinned: masking of melatonin
• Where red cast can be observed, so can blue
• Nail beds
• Erythema (or redness)
– Fever, hypertension, inflammation, allergy
– Blushing
• Pallor (or blanching): pale
– Emotional stress (fear, anger)
– Anemia, low blood pressure

A

Yes.

107
Q

SKIN COLOUR IN DIAGNOSIS
• Jaundice (yellow cast)
– Liver disorder
– Yellow bile pigments (bilirubin) accumulate in the blood
• Bronzing
– Inadequate steroid hormones in Addison’sdisease
– Pituitary gland tumor: inappropriate secretion of
melanocyte-stimulating hormone
• Bruises
– Clotted blood beneath skin

A

Yes.

108
Q
APPENDAGES OF THE SKIN
• Derivatives of theepidermis
– Hairs and hair follicles
• Dead keratinized cells of hard keratin
– More durable than soft keratin of skin
• Hair bulb
– Hair follicle receptor (root hair plexus)
– Sensory nerve endings - touch receptors
– Hair matrix
• Actively dividingarea
– Nails
– Sweat glands
– Sebaceous (oil) glands
A

Yes

109
Q

THE HAIR CYCLE
Average 2.25 mm growth per week
• Lose 90 scalp hairs daily

A

Yes.

110
Q

FUNCTIONS OF THE HAIR
Trunk, limbs
• Warn of insects on skin, parasites crawling (lice, fleas)
Scalp:
• Physical trauma
• Minimize heat loss
– Brain: rich warm blood supply, scalp lacks insulatingfat
– Heat is easily conducted through the bones of theskull
– Wind
• Sunlight
–These may be the reasons why we still have hair
Eyebrow
• Non-verbal communication, enhance expressiveness
• Apes uses them: greetings, dominance

A

Yes.

111
Q
NAILS
Scalelike modifications of epidermis
• Protective cover for distal, dorsal surfaceof fingers and toes
– Useful tool: scratch an itch
• Contain hard keratin (<>skin: softkeratin)
• Nail matrix
– Nail growth
– Cells produced are keratinized
– Slides distally
A

Yes.

112
Q
SWEAT GLANDS
 Also called sudoriferous glands
• All skin surfaces except nipples and parts of external genitalia
• ~3 million per person
• Two main types
1. Eccrine (merocrine) sweat glands
2. Apocrine sweat glands
• Contain myoepithelial cells
– Contract upon autonomic nervous system
stimulation to force sweat into ducts
A

Yes.

113
Q
SWEAT GLANDS
Eccrine Sweat Glands
• Most numerous
• Abundant on palms, soles, andforehead
• Ducts connect topores
• Function in thermoregulation
– Regulated by sympathetic nervous system
• Their secretion issweat
• Confined to axillary and anogenital areas
• Sweat + fatty substances +proteins
– Viscous; milky or yellowish
– Odourless until bacterial interaction  body odour
A

Yes.

114
Q
SEBACEOUS (OIL) GLANDS
• Widely distributed
– Not in thick skin of palms and soles
• Most develop from hair follicles and secrete into hair follicles
• Relatively inactive until puberty
– Stimulated by hormones, especially androgens
• Secrete sebum
– Oily holocrine secretion
– Bactericidal
– Softens hair and skin
A

Yes.

115
Q

Digestive Process in the stomach
Mainly catabolic action – little absorption
• Proteins denatured (unravelled) by HCl
• Pepsin carries out enzymatic digestion of proteins.
Milk protein (casein) is denatured and partially
broken down by by rennin in infants
• Very little absorption: lipid-soluble alcohol
and aspirin are absorbed into blood
• Only stomach function essential to life is secretion
of intrinsic factor for vitamin B12 absorption

A

Yes.

116
Q

Neural & hormonal control of gastric secretion
Gastric mucosa  up to 3 L gastricjuice/day
• Neural mechanisms (short and long reflexes)
– Local enteric stimulation secretion 
– Vagus nerve stimulation  secretion 
– Sympathetic stimulation  secretion 
• Hormonal control mainly gastrin from stomach mucosa
– Enzyme and HCl secretion
– Other local gastric “hormones” involved (eg histamine for  HCl
synthesis)
– Some Gastrin released by small intestine (short term)
– Small intestine secretes Gastrin antagonists (Secretin, CCK)
“Enterogastrones”

A

Yes.

117
Q
HCl Formation
Carbonic acid (H2CO3
) breaks
down in Parietal cells
• Produces H+ and HCO3
-
− H+ pumped into stomach
lumen
− K+ moves into parietal cells
from stomach lumen to
balancecharge
• HCO3
-
from carbonic acid breakdown actively exchanged for plasma Cl–
• HCO3
-
flows into blood (via Cl– and HCO3
– antiporter)
• Blood leaving stomach more alkaline  Alkaline tide
• Cl– then moves across Parietal cell into lumen
• Combination of H+ and Cl–→ HCl in the lumen
A

Yes.

118
Q

Intestinal phase
Begins with a brief stimulatory component followed
by inhibition
– Stimulatory component-partially digested food
– Inhibitory effects of 2 factors

A

Yes.

119
Q

Response of the Stomach toFilling
Stomach stretches to accommodate incoming
food
– Pressure constant until 1.5 L food ingested
1. Receptive relaxation (Reflex-mediated)
• Anticipation and response to food send signal
• Coordinated by swallowing center of brain stem
2. Gastric accommodation
• Plasticity (stress-relaxation response) of smooth muscle

A

Yes.

120
Q
Gastric Contractile Activity
Peristaltic waves
– begins at gastroesophageal
sphincter
• Gentle (thin stomach wall)
– move toward pylorus at rate of 3/minute
• More powerful (stronger wall)
• Control- Enteric pacemaker cells
A

Yes.

121
Q
Small Intestine: Gross Anatomy
Major organ of digestion and absorption
• 6-7 m long
• From pyloric sphincter to ileocecal valve
− Sphincters control entry and exit
• Subdivisions
– Duodenum
– Jejunum
– Ileum
A

Yes.

122
Q
Duodenum
Curves around head of pancreas
• Shortest part of small intestine ≈ 25 cm long
• Receives secretions from liver/gall bladder and pancreas
– Separate ducts join at
hepatopancreatic
ampulla
– Enter duodenum at
major duodenal papilla
– Entry controlled by
hepatopancreatic
sphincter
• Most digestion takes
place in duodenum
A

Yes.

123
Q
Jejunum and Ileum
Jejunum
– Extends from duodenum to ileum
– About 2.5 m long
– most absorption of breakdown
products occurs here
• Ileum
– Joins large intestine
at ileocecal valve
– About 3.6 m long
A

Yes.

124
Q

Blood and Nerve supply to Small Intestine
Innervation: (from the “involuntary” nervous sytem)
• Parasympathetic: Excitatory
• Sympathetic: Inhibitory
Blood circulation: extensive arterial and venous supply
• Superior mesenteric artery brings blood supply to the
Small Intestine – picks up nutrients
• Veins (carrying nutrient-rich blood) drain into superior
mesenteric veins  hepatic portal vein liver

A

Yes.

125
Q

Structural Modifications of Small Intestine
Increase surface area of proximal part for
nutrient absorption
1. Circular folds (mucosa and sub-mucosa)
2. Villi (mucosa)
3. Microvilli (mucosa)
4. Intestinal Crypts (mucosa)

A

Yes.

126
Q

Structural Modifications
Circular folds
– Permanent folds of mucosa and submucosa (~1 cm
deep) that force chyme to slowly spiral through lumen
 more nutrient absorption

A

Yes.

127
Q

Structural Modifications
Villi
– Fingerlike extensions (~1 mm high) of mucosa with
capillary bed and lymphatic lacteal for absorption
– Epithelial cells of the villi are called absorptive
cells (enterocytes)

A

Yes.

128
Q

Structural Modifications
• Microvilli (brush border of villi themselves)
– Contain enzymes for carbohydrate, protein and some lipid
breakdown to complete digestion in small intestine

A

Yes.

129
Q
Intestinal Crypts
Contain a range of cells
1. Enterocytes -intestinal juices
2. Goblet cells - mucus
3. Enteroendocrine cells –
Enterogastrones – CCK &amp;
Secretin, etc
4. Paneth Cells – defensins &amp;
lysozyme
5. Stem cells divide to produce crypt cells
A

Yes.

130
Q

Microvilli

Contain many digestive enzymes on their brush border

A

Yes.

131
Q

Other specialised intestinal cells
• Mucosa associated lymphoid tissue (MALT)
− Protect against bacteria etc
− Peyer’s patches – macrophages & lymphocytes
• Duodenal (Brunner’s) glands
− secrete alkaline mucus to neutralize acidic chyme

A

Yes.

132
Q

Intestinal Juice (mainly in duodenum)
− 1-2 L secreted daily from a variety of glands
− Slightly alkaline; isotonic with blood plasma
− Largely water; contains mucus, enzyme-poor
(enzymes of small intestine only in brush border);

A

Yes.

133
Q
Accessory organs of Duodenum
Liver, Gallbladder &amp; Pancreas
1. Liver - Many vital
functions
• Digestion: produces bile to aid in fat
absorption from small intestine
• “Non–digestive”: metabolism,
detoxification, storage, phagocytic
protection, synthesis (globin,
angiotensin), breakdown (bilirubin,
some hormones)
2. Gallbladder- bile storage
3. Pancreas – Pancreatic
Juice - enzyme rich
A

Yes.

134
Q
Liver
 Largest internal gland
– Four lobes—right, left,
caudate, and quadrate
– Well supplied with blood
vessels
– Basis cell type is the
hepatocyte
– Many functions
including producing bile
– Important in health and
disease
A

Yes.

135
Q

Bile
Produced by the liver
• 900 ml/day, some stored in gall bladder
• Contains Bile Salts – cholesterol derivatives
− Act like detergent to aid digestion of lipids (micelles)
− Reabsorbed in ileum → liver
• Also contain Bilirubin – from the breakdown of
heme
− Provides much of the green/yellow colour of bile
− Further breakdown provides pigments which give
urine and feces their colour

A

Yes.

136
Q

The Gallbladder
Thin-walled muscular sac on ventral surface of
liver
1. Stores and concentrates bile from liver
(produced/recirculated)
2. Muscular contractions release bile via cystic
duct, which flows into bile duct
Homeostatic imbalance
Gallstones

A

Yes.

137
Q
Pancreatic Juice – Exocrine (vs Endocrine)
1200 – 1500 ml/day
• Watery alkaline solution (pH 8)
neutralizeschyme
• Electrolytes (primarily HCO3
–)
• Enzyme rich
• Amylase, lipases, nucleases
o active form secreted
o require ions or bile for
optimal activity
• Proteases
o inactive form secreted
o Activated by membrane
bound peptidase
A

Yes.

138
Q
Digestion in the Small Intestine
Chyme (acidic) from stomach contains
– Partially digested carbohydrates and proteins
– Undigested fats
• 3–6 hours in small intestine
– Most water absorbed
– ~ All nutrients absorbed
• Intestinal digestion relies on:
− Secretion of Intestinal Juice, Bile &amp; Pancreatic Juice
− Motility of the small intestine
− Opening/closing of pyloric sphincter for entry
and also ileocecal valve for exit
A

Yes.

139
Q
Large Intestine
Main Regions
• Cecum
• Appendix
• Colon
• Rectum
• Anal canal
A

Yes.

140
Q

Large Intestine: Microscopic Anatomy
• Thicker mucosa of simple columnar epithelium
except in anal canal
– stratified squamous to withstand abrasion in anus
• No circular folds, villi or digestive secretions
• Abundant deep crypts with goblet cells
– Secreting mucus to help movement
• Mucosal MALT cells help provide protection
against microorganisms

A

Yes.

141
Q

Digestive Processes in the Large Intestine
• Residue remains in large intestine 12–24 hours
• No food breakdown except by enteric bacteria
• Vitamins (B & K made by bacterial flora), water,
and electrolytes (especially Na+ Cl–) reclaimed
• Major functions:
– propulsion of feces to anus
– defecation
• Colon is not essential for life
– Ileostomy (ileum to abdominal wall)
– Ileoanal juncture (ileum-anal canal)

A

Yes.

142
Q

Bacterial Flora
• Enter from small intestine or anus
1. Colonize colon
2. Synthesize some B complex vitamins and
vitamin K
3. Metabolize some host-derived molecules
(mucin, heparin, hyaluronic acid)
4. Ferment indigestible carbohydrates
5. Release irritating acids and gases (~500 ml/day)

A

Yes.

143
Q

Intestinal Flora
• Viruses and protozoans
• Bacteria prevented from breaching mucosal
barrier
– Epithelial cells recruit dendritic cells to mucosa
 sample microbial antigens  present to T
cells of MALT  IgA antibody-mediated
response  restricts microbes

A

Yes.

144
Q
Always wanted to know…but never asked
• Flatulence or intestinal gas
• Large intestine contains: 7-10Lgas
• Average expelled amount: 500ml/day
– Swallowed air + bacterial flora production
– Mainly from intestines (70%)
• Main gases
− N2
, CO2
, H2
, CH4
,
– H2S, amines: indole, skatole
– H2
\: flammable
• Explosion in surgery
(500-600 in US/year)
A

Yes.

145
Q

Defecation
• Mass movements force feces toward rectum
• Distension initiates spinal defecation reflex
• Parasympathetic signals
– Stimulate contraction of sigmoid colon and rectum
– Relax internal anal sphincter
• Conscious control allows relaxation of external
anal sphincter

A

Yes.

146
Q

Defecation
• Mass movements force feces toward rectum
• Distension initiates spinal defecation reflex
• Parasympathetic signals
– Stimulate contraction of sigmoid colon and rectum
– Relax internal anal sphincter
• Conscious control allows relaxation of external
anal sphincter

A

Yes.

147
Q

Digestion and Absorption
• Digestion
– Catabolic process for the break down of
macromolecules  smaller molecules for
absorption
− Most breakdown of food is by hydrolysis
o Water reacts with food to break bonds
− Enzymes required
o Intrinsic and accessory gland enzymes speed up
the breakdown of food (“catalysts”)

A

Yes.

148
Q

Absorption: Vitamins, minerals water
Vitamins: essential, not produced by the body, small amounts
• Fat Soluble Vitamins – A,D, E, K
• Absorbed along with fats in small intestine
• Water soluble Vitamins – C and B Vitamins
− Mainly absorbed with water in the small intestine
− B12 is a large molecule and requires Intrinsic Factor (from stomach)
− B12 absorbed in the ileum through exocytosis
Minerals/electrolytes
• Most minerals actively absorbed along length of small intestine
• Fe++ and Ca++ in duodenum
− Fe++ bound to ferritin in mucosa/released as needed (heme)
− Ca++ absorption linked to parathyroid activity/Vitamin D
Water
• ≈ 9L enters GI daily
• 95% reabsorbed in small intestine; rest in large intestine
• Most movement is osmosis

A

Yes.

149
Q
Jejunum and Ileum (slide 17- typo)
• Jejunum
– Extends from duodenum to ileum
– About 2.5 m long
– most absorption of breakdown
products occurs here
• Ileum
– Joins large intestine
at ileocecal valve
– About 3.6 m long
A

Yes.