Exam 2: Blood, Respiratory, Lymph Flashcards

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1
Q

What is the connective tissue that is involved in transportation within the body?

A

Vascular connective tissues

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2
Q

What is the function of blood?

A

Transportation of O2, CO2, nutrients, wastes, hormones

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3
Q

Can blood thermoregulate?

A

Yes, as blood takes heat to the skin

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4
Q

Can blood regulate pH?

A

Yes

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5
Q

What enables blood to regulate fluid volume?

A

Its osmotic properties

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6
Q

How can blood “protect”?

A

Through its immune system (leukocytes)

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7
Q

Can leukocytes cause inflammation?

A

Yes

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8
Q

Can leukocytes kill microbes and cancer?

A

Yes

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9
Q

Can leukocytes make antibodies?

A

Yes

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10
Q

What are antibodies also known as?

A

Immunoglobulins (Ig’s) or gamma globulins

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11
Q

How do Ig’s and gamma globulins get rid of pathogens?

A

They mark pathogens for destruction by the immune system

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12
Q

Does blood contain clotting factors?

A

Yes

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13
Q

Does blood contain proteins that destroy pathogens?

A

Yes

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14
Q

What is the extracellular fluid component of blood before clotting?

A

Plasma

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15
Q

What is the extracellular fluid component of blood after clotting?

A

Serum

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16
Q

What are cells and platelets a part of?

A

The formed elements

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17
Q

What blood cell transports oxygen?

A

Erythrocytes

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18
Q

What blood cell is a major component of the immune system?

A

Leukocytes

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19
Q

What cell fragments initiate blood clotting?

A

Platelets

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20
Q

What is the pH of blood?

A

7.35-7.45

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21
Q

How sensitive is the body to changes in blood pH?

A

Very. A slight change in pH indicates a dramatic change in hydrogen ion concentration

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22
Q

Could a blood pH of 6.8 or 8.0 kill?

A

Yes, this slight variance in pH may be lethal

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23
Q

What percent of your body’s weight is blood?

A

8%

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24
Q

What does CO2 and H20 form?

A

Carbonic acid

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25
Q

What is the formula for carbonic acid?

A

H2CO3

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26
Q

What enzyme breaks carbonic acid into CO2 and H20?

A

Carbonic anhydrase

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27
Q

What is the formula for bicarbonate?

A

HCO3-

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28
Q

Where are HCO3- and H+ produced?

A

In the body’s tissues

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29
Q

In most situations, do you want the formula to read right to left, or left to right?
CO2 + H2O <-> H2CO3 <-> HCO3 + H+

A

From right to left. You want to get rid of H+ by combining it into carbonic acid, then split the carbonic acid into H20 and CO2

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30
Q

Where is carbonic anhydrase found?

A

In the erythrocytes and kidney tubules

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31
Q

What is the law of mass action?

A

If you increase a component (reactant) on one side of an equation, it forces the equation to proceed in the other direction

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32
Q

What takes care of CO2?

A

It is dumped by the lungs

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33
Q

What is too much CO2 called?

A

Hypercapnia

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34
Q

What is too low CO2 called?

A

Hypocapnia

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35
Q

What happens to the H+ ions when you have a respiratory/pulmonary disease such as emphysema?

A

There’s a high concentration of H+ ions in the blood leading to respiratory acidosis (the equation is reversed to read left to right)

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36
Q

What is acidosis?

A

Elevated H+, loss of bicarbonate

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37
Q

What respiratory disease usually causes respiratory acidosis?

A

Hypercapnia (too high CO2)

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38
Q

What is the most common form of acidosis?

A

Respiratory acidosis

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39
Q

What causes metabolic acidosis?

A

Too much H+, lactic acid, ketoacidosis, bicarbonate loss

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40
Q

Where is ketoacidosis seen?

A

In diabetes

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41
Q

Does kidney failure elevate or lower retained H+?

A

Kidney failure prevents the body from excreting H+, thus raising it in the body

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42
Q

What might lower bicarbonate ions in the body?

A

Diarrhea

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43
Q

Is this a symptom of acidosis?
Compensatory hyperventilation

A

Yes

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44
Q

Is this a symptom of acidosis?
CNS elevation

A

No. The CNS would depress with acidosis

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45
Q

Is this a symptom of acidosis?
pH < 7.0

A

Yes

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46
Q

Can a pH < 7.0 induce a coma?

A

Yes

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47
Q

Is this a symptom of acidosis?
Confusion, lethargy, headaches

A

Yes

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48
Q

Is this a symptom of acidosis?
Hyperactive reflexes

A

No. Hypoactive reflexes are a symptom

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49
Q

What is alkalosis?

A

When there is not enough H+ in the body

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50
Q

What can anxiety, hyperventilation, liver failure, vomiting, and hypocapnia cause?

A

Alkalosis

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51
Q

Is this symptom acidosis or alkalosis?
Over excited CNS

A

Alkalosis

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52
Q

Is this symptom acidosis or alkalosis?
Under excited CNS

A

Acidosis

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53
Q

Is this symptom acidosis or alkalosis?
Hypoventilation

A

Alkalosis

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54
Q

Is this symptom acidosis or alkalosis?
Hyperventilation

A

Acidosis

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55
Q

Is this symptom acidosis or alkalosis?
Confusion, lethargy

A

Acidosis

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56
Q

Is this symptom acidosis or alkalosis?
Irritability, agitated state, hyperactive reflexes

A

Alkalosis

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57
Q

Is this symptom acidosis or alkalosis?
Muscle contraction/tetany/twitching/convulsions

A

Alkalosis

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58
Q

Low pH means high or low acidity?

A

Low pH = high acidity

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59
Q

Low pH means lots of H+ ions or few H+ ions?

A

Low pH = high H+ ions

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60
Q

High pH means high or low acidity?

A

High pH = low acidity

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61
Q

High pH means lots of H+ ions or few H+ ions?

A

High pH = low H+ ions

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62
Q

Is trauma a leading cause of death for those aged 1-44?

A

Yes

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63
Q

What is the number 1 cause of death in the United States (according to him)

A

Trauma

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64
Q

What percentage of death by trauma is caused by hemorrhaging?

A

40%

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65
Q

What term means to “bleed out”?

A

Exsanguination

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66
Q

What are the three components of the triad of death?

A

Hypothermia
Acidosis
Coagulopathy

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67
Q

What does hypothermia mean?

A

Body temperature gets below 35 degrees Celsius

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68
Q

What is coagulopathy?

A

Reduced ability to form a clot

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69
Q

What demonstrates a potentially catastrophic disruption of homeostatic balance?

A

The triad of death

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70
Q

What is normal body temperature?

A

36-37 degrees Celsius

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71
Q

What can cause hypothermia?

A

Massive blood loss

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72
Q

How does hypothermia affect the circulatory system?

A

It reduces heart function and O2 delivery to tissues

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73
Q

How does hypothermia affect clotting?

A

Reduces ability to clot

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74
Q

What is hypothermia’s effect on infection/immunity?

A

Decreases immunity, increases risk of wound infection, pneumonia, and sepsis

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75
Q

How does acidosis affect the circulatory system?

A

Reduces heart function and increases risk of ventricular fibrillation

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76
Q

How does acidosis affect muscles?

A

Reduces muscle strength and increases fatigue of respiratory muscles

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77
Q

How does acidosis affect mental state?

A

Decreases mental status and incudes coma

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78
Q

How does acidosis affect clotting?

A

Reduces ability to clot

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79
Q

What is fibrinolysis?

A

Dissolving clots faster than they form (causes bleeding out)

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80
Q

What causes fibrinolysis?

A

Massive traumatic injury and blood loss

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81
Q

How does coagulopathy affect breathing?

A

Increased anaerobic respiration (without O2)

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82
Q

How does anerobic respiration affect the levels of lactic acid and pH?

A

Increases lactic acid and reduces the pH (acidosis)

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83
Q

How does coagulopathy affect body temperature?

A

Lowers body temperature

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84
Q

What is the fluid component of blood prior to clotting?

A

Plasma

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85
Q

What is the fluid component of blood after clotting?

A

Serum

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86
Q

Is it better to use plasma or serum for lab testing?

A

Serum, as there are no clotting proteins present that may interfere with tests

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87
Q

Where are most of the proteins in the blood made?

A

The liver

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88
Q

What proteins are the exception/not made by the liver?

A

Antibodies

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89
Q

How many proteins are made by the liver?

A

Over 2,000

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90
Q

What % of plasma proteins are albumins?

A

60%

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91
Q

What do albumins regulate?

A

Osmotic pressure

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92
Q

What percentage of plasma proteins are globulins?

A

36%

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93
Q

Which globulins transport lipids, metal ions, and fat-soluble vitamins?

A

Alpha and Beta globulins

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94
Q

What globulins are the antibodies/immunoglobulins?

A

Gamma globulins

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95
Q

What do gamma globulins do?

A

Mark pathogens for destruction in the immune system

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96
Q

What makes gamma globulins?

A

Leukocytes called plasma cells

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97
Q

What percentage of the plasma proteins are fibrinogens?

A

4%

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98
Q

What are fibrinogens important for?

A

Blood clotting

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99
Q

Are enzymes proteins in blood?

A

Yes

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100
Q

How are enzymes relevant in diagnostics?

A

These spill out of dead cells and are measured to diagnose disease

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101
Q

Where do nitrogenous wastes come from in blood?

A

From breakdown of proteins (DNA & RNA)

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102
Q

What is the MAIN nitrogenous waste?

A

Urea

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103
Q

What are other nitrogenous wastes?

A

Uric acid, creatinine, ammonia salts

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104
Q

Where do nitrogenous wastes get eliminated?

A

The kidneys

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105
Q

What are considered nutrients in the blood?

A

Glucose, amino acids, fatty acids, triglycerides, cholesterol, vitamins

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106
Q

What are examples of electrolytes in blood?

A

Na+, K+, Mg++, Cl-, PO4-, SO3-2, HCO3- (Bicarbonate)

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107
Q

Are there respiratory gasses in blood?

A

Yes, O2 and CO2

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108
Q

What hormones are in blood?

A

Yes, steroid hormones and protein hormones

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109
Q

What is osmolarity?

A

How much solute is dissolved

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110
Q

What do “hypertonic”, “hypotonic”, and “isotonic” refer to?

A

Osmolarity. Comparing solutions based on how much solute is in them

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111
Q

What can effect osmolarity?

A

Electrolytes, proteins, lipids, carbohydrates

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112
Q

What is osmolarity measured in?

A

mOsm (milliosmoles)

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113
Q

Where does water always move towards? (High or low concentration)

A

Water moves to the high solute (What is hypertonic)

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114
Q

What is the diffusion of water?

A

Osmosis

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115
Q

Osmosis moves water from…

A

Low solute to high solute
(High water to low water)

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116
Q

What is osmotic pressure?

A

The amount of pressure required to stop osmosis of water

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117
Q

What does osmotic pressure rely on?

A

Osmolarity

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118
Q

What solution has a higher solute content in comparison?

A

Hypertonic

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119
Q

What solution has a lower solute content in comparison?

A

Hypotonic

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120
Q

What is it called when solutions have equal amounts of solute?

A

Isotonic

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121
Q

What is the isotonicity for all solutes? (Range and the “rough” #)

A

280-296, or 300 mOsm

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122
Q

What % of NaCl is isotonic in plasma?

A

0.9%

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123
Q

What % of glucose is isotonic in plasma?

A

5.0%

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124
Q

If your liver fails, how will this effect your blood?

A

There will be a drop in protein production, making the blood hypotonic

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125
Q

What is ascites?

A

Severe abdominal edema

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126
Q

What is the disease known for giving starving people “pot bellies”?

A

Kwashiorkor

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127
Q

Total volume of blood in a female vs a male?

A

Female: 5L
Male: 6L

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128
Q

What is the measure of the contribution over 2,000 plasma proteins make to the total osmolarity of the blood?

A

Osmotic pressure, or Colloid osmotic pressure (COP)

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129
Q

What are the plasma cell leukocytes that make antibodies?

A

B Lymphocytes

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130
Q

What are the two main types of lipids in the blood?

A

Triglycerides and phospholipids

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131
Q

What do triglycerides want the plasma levels to be?

A

<150 mg/dL

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132
Q

What do phospholipids want the plasma levels to be?

A

160-300 mg/dL

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133
Q

Where are phospholipids found?

A

Cell membrane

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134
Q

What do phospholipids tend to form?

A

Bilayers, due to having both hydrophobic and hydrophilic properties

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135
Q

What term means phospholipids have both hydrophilic and hydrophobic properties?

A

Amphiphilic/amphipathic

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136
Q

What part of the phospholipid is water soluble?

A

Fatty acid heads

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137
Q

What part of the phospholipid is fat soluble?

A

Fatty acid tails

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138
Q

What part of the phospholipid is polar?

A

Fatty acid heads

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139
Q

What part of the phospholipid is nonpolar?

A

Fatty acid tails

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140
Q

What part of the phospholipid is hydrophobic?

A

Fatty acid tails

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141
Q

What part of the phospholipid is hydrophilic?

A

Fatty acid heads

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142
Q

What part of the phospholipid is lipophobic?

A

Fatty acid heads

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143
Q

What part of the phospholipid is lipophilic?

A

Fatty acid tails

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144
Q

Which part of the phospholipid crosses membranes readily?

A

Fatty acid tails

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145
Q

Which part of the phospholipid does NOT cross membranes readily?

A

Fatty acid heads

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146
Q

Which part of the phospholipid breaks off to form prostaglandins?

A

Fatty acid tails

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147
Q

What does cholesterol want the plasma level to be?

A

<180 mg/dL or <200 mg/dL

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148
Q

What % cholesterol is made by the liver? What % is diet?

A

85% genetic
15% diet

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149
Q

Where are lipoproteins produced?

A

Liver

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150
Q

What do lipoproteins do?

A

Transport lipids in the blood

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151
Q

Which one is “bad” cholesterol?

A

Low density-lipoproteins (LDLs)

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152
Q

How much LDLs should a normal patient have?

A

<100 mg/dL

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153
Q

How much LDLs should high risk patients have?

A

<70 mg/dL

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154
Q

What diseases are correlated with high LDLs?

A

Coronary artery disease and atherosclerosis

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155
Q

What process do LDLs use to transport lipids into the cells?

A

Receptor mediated endocytosis

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156
Q

What is the process o receptor mediated endocytosis?

A

When an LDL binds to an LDL receptor on a cell wall, it opens allowing cholesterol to enter the cell

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157
Q

What happens when there’s too much LDL?

A

It gets under the endothelium, causes inflammation, and plaque builds up

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158
Q

What protein is part of the LDL that attaches to receptors found on most cells?

A

Apoprotein B100

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159
Q

What does apoprotein B100 do once inside the cell?

A

Metabolizes cholesterol

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160
Q

What can destroy LDLs?

A

Scavenger macrophages

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161
Q

What is arteriosclerosis?

A

Loss of elasticity of arterial wall (“hardening of the arteries”)

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162
Q

What is atherosclerosis?

A

A type of arteriosclerosis, where there’s clogging of the arteries (with plaque)

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163
Q

What is the plaque in atherosclerosis made of?

A

Lipids (such as cholesterol), WBC (such as macrophages), aberrant smooth muscle cells, and calcium

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164
Q

What can excess plaque in arteries cause?

A

The artery may rupture, causing hemorrhage

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165
Q

What part of atherosclerosis may cause a stroke?

A

Clots that form after an arterial rupture block O2 from going to the brain

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166
Q

What is familial hypercholesterolemia?

A

A genetic mutation in LDL receptors that prevent cholesterol from entering cells (so it stays in the plasma)

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167
Q

Are there high levels of cholesterol in familial hypercholesterolemia?

A

There are high levels of cholesterol in the blood, causing catastrophic arterial clogging

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168
Q

Does familial hypercholesterolemia only effect old people who eat like shit?

A

No, it’s genetic and young people suffer from it

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169
Q

What is “good” cholesterol?

A

High density lipoproteins (HDLs)

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170
Q

What do you want your HDLs to be at?

A

> 30 mm/dL

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171
Q

What is a normal range of HDLs?

A

30-80 mm/dL

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172
Q

What can an HDL of >60 mm/dL do?

A

Protect against heart disease

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173
Q

What do HDLs do?

A

Take cholesterol from the cells to the liver, where it will be a component of bile and excreted in feces

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174
Q

What is the movement of HDLs?

A

Receptor mediated endocytosis

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175
Q

What are normal blood glucose values?

A

70-110 mg/dL

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176
Q

Where is glucose stored in the body?

A

In the muscles and liver as glycogen

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177
Q

What makes glycogen go into the blood?

A

Glucagon

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178
Q

How many erythrocytes in a female vs male?

A

Female: 4.5 million/μL
Male: 5.5 million/μL

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179
Q

What is the diameter of erythrocytes?

A

7.5 μm

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180
Q

How long do erythrocytes last?

A

120 days

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181
Q

What removes erythrocytes at the end of their lifespan?

A

The spleen

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182
Q

What protein in blood carries O2?

A

Hemoglobin

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183
Q

How many hemoglobin molecules per erythrocyte cell?

A

280 million molecules

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184
Q

How much total hemoglobin in females vs males?

A

Females: 12-16 g/dL
Males: 13-18 g/dL

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185
Q

How many polypeptide chains does hemoglobin have?

A

4

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186
Q

What are the polypeptide chains hemoglobin has?

A

2 Alpha chains
2 Beta chains

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187
Q

How many hemes do each chain in hemoglobin have?

A

1 heme for each chain

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188
Q

How many hemes in 1 hemoglobin moloecule?

A

4

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189
Q

How many iron molecules does each heme have?

A

1 iron for each heme

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190
Q

How many irons in 1 hemoglobin molecule?

A

4

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191
Q

How many oxygens do each iron carry?

A

1

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192
Q

How many oxygens in each hemoglobin molecule?

A

4

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193
Q

What is the green pigment when hemoglobin breaks down?

A

Biliverdin

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194
Q

What is the yellow pigment made and released when hemoglobin is degraded by macrophages?

A

Bilirubin

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195
Q

What does the liver convert bilirubin into?

A

Bile components

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196
Q

Where do bile components go?

A

Secreted into the intestines

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197
Q

What is urobilinogen?

A

A by-product from bile degredation

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198
Q

What is the pigment from urobilinogen that gives feces a brown color?

A

Stercobilin

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199
Q

What is a yellow covering of skin/eyes due to excess bilirubin?

A

Jaundice

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200
Q

What causes jaundice?

A

Liver disease

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201
Q

What is the difference between oxyhemoglobin and deoxyhemoglobin?

A

Oxy: hemoglobin bound to O2
Deoxy: hemoglobin WITHOUT O2

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202
Q

What is carbaminohemoglobin?

A

Hemoglobin bound to CO2

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203
Q

What is hemoglobin bound to carbon monoxide?

A

Carboxyhemoglobin

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204
Q

What does hematocrit mean?

A

The % of centrifuged RBCs in blood

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205
Q

What’s a normal hematocrit in a female vs a male?

A

Female: 42%
Male: 47%

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206
Q

What does a high hematocrit % mean?

A

Infection

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207
Q

What does a low hematocrit % mean?

A

Heart and/or blood disorders

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208
Q

How do you calculate sedimentation (Sed) rate?

A

Measure the time required for RBCs to settle to the bottom of a tube containing a specific fluid

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209
Q

What does Sed rate tell you?

A

RBC density

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210
Q

What increases Sed rate/RBC density?

A

Pregnancy, disease (anemia, inflammation)

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211
Q

After 120, what happens to RBCs?

A

They become brittle and squeeze through holes in the spleen, causing them to rupture. They are then removed by macrophages

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212
Q

What is an RBC rupture called?

A

Hemolysis

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213
Q

Where does hemoglobin go when RBCs rupture?

A

It spills into the blood

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214
Q

What is hemopoiesis/hematopoiesis?

A

Blood formation within red bone marrow

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215
Q

What first makes the blood cells in humans?

A

The yolk sac in the embryo

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216
Q

When does the yolk sac make blood cells?

A

3-7 weeks of gestation

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217
Q

What are the precursor blood cells?

A

Hemopoietic stem cells

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218
Q

Where do hemopoietic stem cells migrate to and from?

A

Hemopoietic stem cells travel from the yolk sac to the embryo

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219
Q

What makes blood after the yolk sac?

A

Liver, spleen, and lymphatic tissues

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220
Q

When do the liver, spleen, and lymphatic tissues make blood?

A

At the end of the 2nd trimester or beginning o the 3rd

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221
Q

When does the liver stop making blood cells?

A

Birth

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222
Q

What type of blood cells do the spleen and lymphoid tissues continue to make?

A

Lymphocytes (a type of leukocyte)

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223
Q

What is it called when blood is made outside the medullary cavity?

A

Extramedullary hemopoiesis

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224
Q

Is extramedullary hemopoiesis normal?

A

No, in birthed humans this indicates loss of bone marrow function, possibly due to cancer, toxins, and radiation

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225
Q

Where does medullary hemopoiesis take place, and what is it called?

A

Red bone marrow occurs in the bone marrow cavity

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226
Q

When is red bone marrow in all bones?

A

From late fetal life until about 5 years old

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227
Q

What bones have red bone marrow after childhood? At what age?

A

Membranous bones by the age of 20

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228
Q

What are examples of membranous bones?

A

Sternum, ilium, vertebrae, ribs

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229
Q

What hormone from the liver and kidneys regulates erythropoiesis?

A

Erythropoietin (EPO)

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230
Q

What is erythropoiesis?

A

Production of erythrocytes

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231
Q

Why would you need more O2? (And subsequently, more erythrocytes)

A

Hemorrhaging, long term anemia, pulmonary/respiratory disease, living in high altitudes

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232
Q

What is natural “blood doping”?

A

Training in high altitudes where you get more EPO, which increases RBCs, which increases endurance

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233
Q

What element is used to make hemoglobin?

A

Iron

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234
Q

What is most of the body’s iron used for?

A

In hemoglobin

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235
Q

Is iron safe by itself?

A

No, it’s toxic, so it has to be bound to proteins

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236
Q

What is the primary extracellular protein that transports iron within the blood and makes iron available to cells (with the help of 2 other proteins)?

A

Transferrin

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237
Q

What are the 2 proteins that help transferrin make iron available to cells?

A

Ferritin and hemosiderin

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238
Q

Are ferritin and hemosiderin extracellular or intracellular proteins?

A

Intracellular proteins

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239
Q

What are the dietary iron ions?

A

Fe+2 and Fe+3

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240
Q

What form of iron can the intestines absorb?

A

Fe+2

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241
Q

What converts iron ions from Fe+3 to Fe+2 so it can be absorbed by the intestines?

A

The stomach

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242
Q

Where is vitamin B12 found?

A

Meat, brewers yeast

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243
Q

Why is vitamin B12 necessary?

A

DNA production and cell division

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244
Q

What is “intrinsic factor”?

A

A protein produced in the stomach that allows intestines to absorb B12

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245
Q

What pathology can be caused by failure to absorb B12?

A

Pernicious anemia

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246
Q

What are other names for folic acid?

A

Folate or folacin

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247
Q

Where can you get folate?

A

Dark leafy greens and beans

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248
Q

What is the purpose of folate?

A

DNA production and cell division

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249
Q

What pathology are folate deficiencies linked to?

A

Neural tube defects

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250
Q

What protein is used to diagnose NTD?

A

Elevated alpha fetal proteins

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251
Q

Where can you test the fetus for NTDs?

A

The maternal plasma

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252
Q

Does folate build up fast?

A

No, mothers should take folate prenatal vitamins months prior to being pregnant

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253
Q

What happens normally to the neural groove?

A

It closes to become the neural tube, or the beginning of the nervous system

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254
Q

When does the neural tube form/the neural groove close?

A

Days 9-22 of gestation

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255
Q

What NTD is the worst?

A

Anencephaly, a total lack of forebrain

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256
Q

Is anencephaly an anterior or posterior NTD?

A

Anterior

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257
Q

What are the posterior NTD from best to worst prognosis?

A

Spina bifida occulta
Meningocele
Myelomeningocele

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258
Q

What is the process leukocytes use to leave the blood vessels into the interstitum?

A

Diapedesis

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259
Q

What is the method of locomotion used by leukocytes to move within the interstitium?

A

Amoeboid movement

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260
Q

What is the process which leukocytes are attracted to locations by following the “scent” of chemicals?

A

Chemotaxis

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261
Q

What are organelles found in neutrophils which function as the body’s detoxifiers? (Found in the liver)

A

Peroxisomes

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262
Q

What are organelles found in various cells such as neutrophils that are the cells digestive system?

A

Lysosomes

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263
Q

What is the nonfunctional “drumsticks” seen on XX chromosomes?

A

Barr body

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264
Q

What does it mean if you find WBCs on a crime scene with drumsticks?

A

The blood is from a female

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265
Q

What WBC have barr bodies/drumsticks?

A

Neutrophils

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266
Q

What is the range of leukocytes in blood?

A

4,800-10,800 /µL

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267
Q

What type of leukocytes have granules and lobed nuclei?

A

Granulocytes or polymorphonuclear leukocytes

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268
Q

What are the most abundant WBC and what is their range?

A

Neutrophils: 2,500-8,000 /µL

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269
Q

What are neutrophil’s roles?

A

Primary phagocyte and inflammatory cell, dies to make pus

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270
Q

What % of WBC are neutrophils?

A

50-70%

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271
Q

What color are neutrophil’s cytoplasm and how many lobes does it have?

A

Clear, 3-6 lobes

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272
Q

What are antimicrobial compounds which digest holes in microbes?

A

Denfensins

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273
Q

What % of WBC are eosinophils?

A

2-4%

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274
Q

What color are eosinophil’s cytoplasm? How many lobes?

A

Red-pink, 2 lobes

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275
Q

What is the normal range of eosinophils?

A

<500/µL

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276
Q

When are eosinophil levels elevated?

A

During allergic reactions and parasitic worm infections

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277
Q

What % of WBC are basophils?

A

<1%

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278
Q

What is the normal range for basophils?

A

50-100/µL

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279
Q

What color are basophils?

A

Dark purple/blue

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280
Q

What are basophils role?

A

Produce histamine and heparin for anticlotting and inflammation during allergic reactions

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281
Q

What leukocytes are granulocytes or polymorphonuclear leukocytes?

A

Neutrophils
Eosinophils
Basophils

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282
Q

What type of leukocytes don’t have granules?

A

Agranulocytes or mononuclear leukocytes

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283
Q

What % of WBCs are lymphocytes?

A

25%

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284
Q

What is the normal range of lymphocytes?

A

1,000-4,500/µL

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285
Q

What do lymphocytes look like?

A

Small, dark purple, and round. Small crescent of cytoplasm

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286
Q

How big are lymphocytes?

A

As big as RBCs (7µm)

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287
Q

What % of WBCs are monocytes?

A

3-8%

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288
Q

What is the normal range of monocytes?

A

100-700 /µL

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289
Q

What do monocytes look like?

A

Large cells with abundant cytoplasm. Horseshoe shaped nuclei that is larger than other WBCs

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290
Q

What leukocytes become macrophages after diapedesis?

A

Monocytes

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291
Q

What leukocytes are agranulocytes or mononuclear leukocytes?

A

Lymphocytes
Monocytes

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292
Q

How many platelets are in the blood?

A

150,000-400,000 / µL

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293
Q

What are platelets?

A

Cell fragments that initate blood clotting

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294
Q

What do platelets come from?

A

Megakaryocytes

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295
Q

What hormone regulates the formation of platelets?

A

Thrombopoietin

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296
Q

What produces thrombopoietin?

A

Liver and kidneys

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297
Q

What is the body’s process for stopping bleeding called?

A

Hemostasis

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298
Q

What is the first step in hemostasis?

A

Vascular spasms

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299
Q

What are vascular spasms?

A

Vasoconstriction of blood vessels following damage

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300
Q

What is the second step of hemostasis, following vascular spasms?

A

Platelet plug formation

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301
Q

What is blood exposed to when there is damage to a blood vessel?

A

Collagen

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302
Q

What helps platelets aggregate on the collagen?

A

Von Willebrand factor (VWF)

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303
Q

What do platelets release on the collagen when you’re cut?

A

Serotonin, ADP, and thromboxane A2

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304
Q

What does thromboxane A2 do?

A

Keeps more platelets coming to the damaged site

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305
Q

What keeps platelets from adhering to undamaged endothelium?

A

Prostacyclin

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306
Q

What is the third step of hemostasis, which occurs after platelet plug formation?

A

Coagulation or blood clotting

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307
Q

How many clotting factors are involved in blood clotting?

A

13

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308
Q

What vitamin is necessary for clotting factors 2, 7, 9, 10?

A

Vitamin K

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309
Q

What is an anticoagulant that blocks the effect of vitamin K?

A

Coumadin (Warfarin)

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310
Q

What is the coumadin (warfarin) a main ingredient in?

A

May rat poisons

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311
Q

What is an anticoagulant that inhibits thrombin and clotting factor X (10)?

A

Heparin

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312
Q

What blocks the production of thromboxane A2 and prostaglandins?

A

Aspirin

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313
Q

What is the fourth step in hemostasis, after coagulation?

A

Prothrombin activator activates prothrombin

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314
Q

What does prothrombin change into?

A

The enzyme thrombin

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315
Q

What causes fibrinogen to form long strands of fibrin?

A

Thrombin

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316
Q

What does fibrin do?

A

Glue the platelets together to form the basis of the blood clot

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317
Q

What are blood types based off of?

A

The type of carbohydrate-protein (glycoprotein) on the outside of the erythrocyte’s membrane

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318
Q

What are the glycoproteins that determine your blood type called?

A

Antigens

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319
Q

What are the antibodies you are born with that attack the blood types you don’t have?

A

Agglutinins

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320
Q

If you have type A antigens, you have___ antibodies?

A

Anti-B

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321
Q

If you have type B antigens, you have___ antibodies?

A

Anti-A

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322
Q

If you have type A and B antigens, you have___ antibodies?

A

No antibodies against A or B

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323
Q

What is the universal recipient?

A

Type AB+

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324
Q

If you have type O, you have 0 antigens and anti-___?

A

No antigens and anti-A and anti-B antibodies

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325
Q

Why is O+ the universal donor?

A

It has no antigens so everyone can have it without attacking it

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326
Q

What is the Rh or Rhesus group?

A

The + or - that comes from having an Rh glycoprotein on your cell membrane

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327
Q

What did Type O and the Rh group used to be known as?

A

Types C and D

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328
Q

For the general US population, what % are: O

A

48%

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329
Q

For the general US population, what % are: A

A

32%

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330
Q

For the general US population, what % are: B

A

16%

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331
Q

For the general US population, what % are: AB

A

4%

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332
Q

What does idiopathic mean?

A

Of unknown origins

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333
Q

What does exacerbate vs ameliorate mean?

A

To make worse vs to make better

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334
Q

What is ablation?

A

To remove as with surgery

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335
Q

What is it called when you have elevated WBCs?

A

Leukocytosis

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336
Q

What is it called when you have reduced WBCs?

A

Leukocytopenia

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337
Q

What is it called when you have reduced levels of platelets?

A

Thrombocytopenia

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338
Q

What is pancytopenia?

A

Reduction of all blood cells

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339
Q

When is pancytopenia seen?

A

With bone marrow destruction from radiation

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340
Q

Reduction in RBCs vs WBCs cause what problems?

A

RBC: anemia
WBC: immuno suppressed

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341
Q

Reduction in platelets causes what problem?

A

Impaired blood clotting

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342
Q

What is an iatrogenic condition?

A

Caused by a clinician (ex. leaving forceps in the abdomen)

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343
Q

What is a nosocomial condition?

A

Contracted in the hospital

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344
Q

What is it called when there’s elevated RBCs?

A

Polycythemia

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345
Q

What color does the skin turn with polycythemia?

A

Pink

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346
Q

What causes polycythemia?

A

Respiratory diseases, long term anemias, smoking, living in high altitudes

347
Q

What is the most common form of hemophilia?

A

Hemophilia A

348
Q

What causes hemophilia A?

A

A mutation in the gene for clotting factor 8

349
Q

Is hemophilia A X or Y linked?

A

X

350
Q

What is it called when there’s too much iron stored as ferritin?

A

Hemosiderosis

351
Q

What is the medical term for iron overload?

A

Hemochromatosis

352
Q

What causes iron overload?

A

Genetics, hemolytic anemia, liver disease

353
Q

What are symptoms of hemochromatosis?

A

Damage to liver, heart, and pancreas

354
Q

What can damage to the pancreas from hemochromatosis lead to?

A

Diabetes mellitus (loss of insulin production)

355
Q

What color might the skin turn in iron overload?

A

Bronze

356
Q

What is the condition where there’s a decrease in RBCs or hemoglobin, or an abnormal oxygen carrying capacity?

A

Anemia

357
Q

What type of anemia is from vitamin B12 deficiency?

A

Pernicious Anemia (PA)

358
Q

Symptoms of pernicious anemia?

A

Weakness, sore tongue, tingling extremities, neuropathy

359
Q

What causes folate deficiency anemia?

A

Diet, alcohol abuse, infection, and drugs

360
Q

What are the symptoms of folate deficiency anemia?

A

Weight loss, intense weakness, tingling, skin lesions, hepatic disease

361
Q

What % of adults have iron deficiency anemia?

A

10-30%

362
Q

What causes iron deficiency anemia?

A

Diet and hemorrhage

363
Q

What are symptoms of iron deficiency anemia?

A

Weakness, sore tongue

364
Q

Where does sickle cell anemia take place in the hemoglobin chain?

A

The #6 amino acid of the beta hemoglobin chain

365
Q

What type of mutation occurs in sickle cell anemia?

A

Point mutation

366
Q

What is point mutation?

A

Only one base pair on the gene is switched

367
Q

What base pair is mutated in sickle cell anemia?

A

Glutamate is replaced by valine

368
Q

What deforms the RBCs in sickle cell anemia?

A

Hemoglobin S (when O2 is low) forms long fibrous polymers which deform the RBCs

369
Q

What is a complication in sickle cell anemia where there is blockage of small blood vessels?

A

Vaso-occlusive crisis

370
Q

What happens in sickle cell disease?

A

Episodes of hypoxic injury (ischemia), and infarction or necrosis

371
Q

What is one beneficial(?) outcome for sickle cell patients?

A

They are less likely to get malaria as they create a cellular environment that is unwelcoming to the virus

372
Q

What is seen in chronic hemolytic anemia?

A

Seizure, stroke, pallor of skin

373
Q

What disease is similar to sickle cell anemia?

A

Thalassemia

374
Q

Where does alpha thalassemia occur?

A

Asian nations

375
Q

Where does beta thalassemia occur?

A

Mediterranean nations

376
Q

What are symptoms of thalassemia?

A

Edema, ascites, CHF, hepato/cardio/spelomegaly

377
Q

What is aplastic anemia?

A

The inability to synthesize blood cells in bone marrow

378
Q

What causes aplastic anemia?

A

Toxins/drugs, radiation sickness

379
Q

What type of anemia is “bleeding out”?

A

Hemorrhagic anemia

380
Q

What type of anemia is from RBC ruptures (hemolysis)?

A

Hemolytic anemia

381
Q

What can cause hemolytic anemia?

A

Transfusion miss-match, toxins/drugs, radiation

382
Q

What is the “kissing disease”?

A

Mononucleosis

383
Q

What causes mono?

A

Epstein-Barr virus (EBV)

384
Q

What are symptoms of mono?

A

Enlarged lymphocytes, lethargy sore throat

385
Q

What is lymphadenopathy?

A

Swollen lymph nodes, especially around the neck

386
Q

What happens in disseminated intravascular coagulation (DIC)?

A

Widespread clotting, imminently life threatening

387
Q

What can cause DIC?

A

Septicemia, blood transfusion rejections

388
Q

What is erythroblastosis fetalis?

A

Hemolytic disease of the newborn, where the mother is Rh-, but the father and fetus are Rh+

389
Q

What happens in erythroblastosis fetalis?

A

The mother makes antibodies against Rh factor (which is in the baby’s blood)

390
Q

Is the fetus at risk in erythroblastosis fetalis?

A

No, as the antibodies are not formed for at least 6 weeks after exposure, which usually occurs during labor. It is the next fetus who is in danger

391
Q

What is the treatment for erythroblastosis fetalis?

A

Give the mother RhoGAM to prevent her immune system from attacking Rh+ cells

392
Q

What is leukemia?

A

Neoplasm of leukocytes, where there are increased #s and decreased immune function

393
Q

What causes leukemia?

A

Genetics, radiation, viruses, drugs

394
Q

How do you treat leukemia?

A

Chemo, bone marrow transplants, radiotherapy

395
Q

What is acute leukemia?

A

Undifferentiated cells never mature

396
Q

What is chronic leukemia?

A

Cells may mature, but remain dysfunctional

397
Q

Which form of leukemia has a poor prognosis?

A

Acute leukemia

398
Q

Which leukemia has a gradual onset of symptoms?

A

Chronic leukemia

399
Q

What is cachexia? When is it seen?

A

Wasting, as seen in acute leukemia

400
Q

Where does myelogenic leukemia come from?

A

Cells giving rise to neutrophils, basophils, and eosinophils

401
Q

What causes myelogenic leukemia?

A

Large doses of radiation

402
Q

What type of leukemia can come from high doses of chemotherapy?

A

Acute myelogenic leukemia

403
Q

What age group is chronic myelogenic leukemia usually seen in?

A

Adults

404
Q

What age group is acute lymphoblastic leukemia usually seen in?

A

Pediatrics

405
Q

What are symptoms of acute lymphoblastic leukemia?

A

Splenomegaly, hepatomegaly, lymphadenopathy

406
Q

What type of leukemia specifically occurs in adults over 50?

A

Chronic lymphoblastic leukemia

407
Q

What is a myeloma?

A

Neoplasm of plasma cells in bone marrow, where you can seen tumors in bone

408
Q

What is the most common symptom of myelomas?

A

Bone pain

409
Q

What causes myelomas?

A

Bone resorption and hypercalcemia

410
Q

What is the cancer of lymphocytes in lymphatic tissues?

A

Lymphomas

411
Q

What are symptoms of lymphomas?

A

Enlarged lymphatic tissues, painless masses, fever, weight loss, night sweats, compromised immune system

412
Q

What type of lymphoma has a malignancy of mature B cells?

A

Hodgkin’s lymphoma

413
Q

What are risk factors for Hodgkin’s lymphoma?

A

Epstein-Barr virus, genetics

414
Q

What % of lymphomas are non-Hodgkin’s?

A

90%

415
Q

What is malignant in non-Hodgkin’s lymphoma?

A

T or B lymphocytes

416
Q

What are risk factors for non-Hodgkin’s?

A

Autoimmune disorders, HIV, pesticides

417
Q

What a possible danger in non-Hodgkin’s?

A

Blood can become dangerously thickened/viscous

418
Q

What does the lymphatic system do?

A

Regulates fluid balance

419
Q

What % of ECM fluid do the lymphatic vessels take up?

A

10%

420
Q

Where do the lymphatic vessels return ECM to?

A

The blood stream

421
Q

What happens if lymphatic vessels are clogged?

A

Elephantiasis

422
Q

What is the largest lymphatic vessel collecting lymph from the body and returning it to the blood?

A

Thoracic duct

423
Q

Where does the thoracic duct return lymph via?

A

The left subclavian vein between the internal and external jugular veins

424
Q

What is lymph?

A

Lymphatic vessel fluid

425
Q

What are lymphoid tissues sites for?

A

Lymphocyte proliferation and maturation

426
Q

What do immune cells monitor for?

A

The presence of pathogens

427
Q

What are examples of lymphatic tissues?

A

Spleen, thymus, bone marrow, lymph nodes, tonsils

428
Q

What are diffuse lymphatic tissues?

A

Lymphatic tissues that are scattered throughout the body

429
Q

What are the principal lymphoid organs of the body?

A

Lymph nodes

430
Q

What do lymph nodes do?

A

Filter pathogens/infections in lymph that is being returned to the blood

431
Q

What are lymph nodes hooked up to?

A

Lymphatic vessels

432
Q

What are lymph nodes heavily populated by and why?

A

Macrophages that destroy and present antigens

433
Q

What do lymphocytes do in the lymph nodes?

A

Attack against antigens

434
Q

Do the lymph nodes recycle cells?

A

Yes

435
Q

What is the outer portion of the lymph node? What is the inner?

A

Outer: cortex
Inner: medulla

436
Q

What does the outer portion of the cortex contain?

A

Lymphoid follicles (round nodules)

437
Q

What does the outer portion of the lymphoid follicle contain?

A

T Lymphocytes

438
Q

What does the inner portion of the lymphoid follicle contain?

A

B lymphocytes, which become plasma cells that produce antibodies

439
Q

What do T lymphocytes do?

A

Process antigens/pathogens, microbes

440
Q

What is the inner portion of the lymphoid follicle called?

A

Germinal centers

441
Q

What does the medulla contain in lymph nodes?

A

B and T lymphocytes and plasma cells

442
Q

What are lymphatic tissues found in the walls of intestines (ex. protecting the body from pathogens that enter the body by mouth)

A

Peyer’s patches

443
Q

What is vermiform appendix?

A

An organ that is attached to the beginning of the colon that has abundant diffuse lymphatic tissues in its walls

444
Q

What is a major site for lymphocyte proliferation?

A

Spleen

445
Q

What is a major site for removal of dead/dying RBCs and WBCs?

A

Spleen

446
Q

What is the largest lymphoid organ?

A

Spleen

447
Q

What lymphatic structure is found in children, but regresses in adults?

A

Thymus

448
Q

What is the thymus important for?

A

Developing T Lymphocytes

449
Q

What tonsils are on either side of the posterior oral cavity?

A

Palatine tonsils

450
Q

Which are the largest tonsils that are most often infected?

A

Palatine tonsils

451
Q

What tonsils are at the base of the tongue?

A

Lingual tonsils

452
Q

What tonsils are at the posterior wall of the nasopharynx?

A

Pharyngeal tonsils

453
Q

What are the pharyngeal tonsils also known as?

A

Adenoids

454
Q

What does “Per Os”, or “per ostium” mean?

A

By mouth

455
Q

Do water soluble substances cross membranes easily?

A

No

456
Q

Do lipid soluble substances cross membranes easily?

A

Yes

457
Q

Where do both water soluble and lipid soluble substances start in their journey?

A

Intestines

458
Q

Where does water soluble substances go from the intestines?

A

Intestinal veins

459
Q

Where do lipid soluble substances go from the intestines?

A

Intestinal lacteals (lymphatics)

460
Q

What vein does the intestinal veins carry water soluble substances to?

A

Superior mesenteric vein

461
Q

Where do lipid soluble substances go from intestinal lacteals/lymphatics?

A

Thoracic duct

462
Q

What is the main lymphatic vessel?

A

Thoracic duct

463
Q

Where do water solubles go from superior mesenteric vein?

A

Hepatoportal vein (to the liver)

464
Q

Where do fat solubles go from the thoracic duct?

A

Left subclavian vein

465
Q

Where is the left subclavian vein? (What is it in between)

A

In between the external and internal jugular veins

466
Q

What in the liver detoxes water solubles?

A

Hepatic sinusoids

467
Q

What percent do hepatic sinusoids detox on first pass?

A

80-90%

468
Q

What compounds bypass the liver’s detox system on “first pass”?

A

Lipid/fat solubles

469
Q

Where do water solubles go from the hepatic sinusoids?

A

Central vein

470
Q

Where do water solubles go from the central vein?

A

Hepatic vein

471
Q

Where do water solubles go from the hepatic vein?

A

Inferior vena cava (then back into general circulation)

472
Q

Which immune system are you born with?

A

Nonspecific, or innate

473
Q

What is the first line of defense?

A

External or anatomical barriers

474
Q

What are examples of external barriers?

A

Skin, mucus, oil, sweat, tears, sloughed cells, saliva, wax, urine, gastric acid

475
Q

What is an enzyme in mucus, tears, and saliva that kills bacteria?

A

Lysozome

476
Q

What is the second line of defense?

A

Inflammation, fever, and cells getting to work

477
Q

What are leukocytes that phagocytize foreign materials including pathogens?

A

Phagocytes

478
Q

Which phagocytes contain bacteria-killing enzymes which make highly reactive Reactive Oxygen Species (ROS) or free radicals?

A

Neutrophils

479
Q

What are ROS or free radicals called?

A

Superoxide radicals

480
Q

What do superoxide radicals form?

A

Hydrogen peroxide

481
Q

What are proteins produced by neutrophils that digest holes in the membranes of microbes?

A

Defensins

482
Q

What phagocytes fight allergens and parasitic worms?

A

Eosinophils

483
Q

What do basophils release?

A

Heparin and histamine

484
Q

What does histamine do?

A

In response to allergens, causes allergic reactions

485
Q

What does heparin do?

A

Prevents clotting (anticoagulant)

486
Q

What are non-phagocytic lymphocytes that destroy our cells that become cancerous or contain viruses?

A

Natural killer (NK) cells

487
Q

What are enzymes that digest holes in cell membranes and cell walls of microbes? (As seen in NK cells)

A

Perforins

488
Q

What is genetically programmed cell death called?

A

Apoptosis

489
Q

When does apoptosis occur?

A

Cell completes its function
Mutations make dysfunction or cancer
Cell is stressed
Cell is infected

490
Q

What do monocytes do in the 2nd line of defense?

A

Become macrophages (powerful phagocytes)

491
Q

What cells roam looking for potentially dangerous antigens, then present them to the rest of the immune system for processing?

A

Monocytes

492
Q

What are macrophages of the liver?

A

Kupfer cells

493
Q

What cells are similar to macrophages, that are found throughout the body where there are external or internal surfaces?

A

Dendritic cells

494
Q

Where might you find dendritic cells?

A

Skin, mucosa of nose, lungs, stomach, intestines

495
Q

What do dendritic cells do?

A

Reach out from the protection of tissues to sample the surface for potential threats and present them to the rest of the immune system for processing

496
Q

What cells are newly described, similar to helper T, cytotoxic T, and NK cells?

A

Innate lymphoid cells

497
Q

What do innate lymphoid cells have an important role in?

A

Inflammation

498
Q

What can dysregulation of innate lymphoid cells do?

A

Cause allergies, asthma, and autoimmune diseases

499
Q

What cells regulate adipose function and metabolic homeostasis?

A

Innate lymphoid cells

500
Q

What are innate lymphoid cells classified based on?

A

Cytokine release (hormones) and transcription factors that control their development

501
Q

What is the process where a phagocyte engulfs particles such as cells?

A

Phagocytosis

502
Q

What is the organelle that is made when podocytes surround a particle and wrap it up in the cell membrane? (“undigested food”)

A

Phagosome

503
Q

What organelle is the cell’s digestive system?

A

Phagosomes

504
Q

What is the digestive hydrolytic enzymes in phagosomes?

A

Lysosome

505
Q

What is a phagosome fused with lysosome called?

A

Phagolysosome

506
Q

What is an organelle containing the undigested remains from phagocytosis called?

A

Residual bodies

507
Q

What is the process where the undigested remains are expelled from the cell?

A

Exocytosis

508
Q

What are toxic chemicals made by phagosomes with extra unpaired electrons that can destroy microbes and our own cells?

A

Reactive Oxygen Species (ROS) or free radicals

509
Q

What can ROS’s destroy?

A

Microbes as well as our own cells and tissues

510
Q

What is a reactive compound produced by our cells to combat pathogens?

A

H2O2

511
Q

Is H2O2 safe?

A

No, it is potentially damaging to cells and tissues so it must be broken down

512
Q

What enzymes break down H2O2 into water?

A

Peroxidase and catalase

513
Q

What enzyme breaks down the superoxide radical (ROS)?

A

Superoxide dismutase

514
Q

Where does superoxide dismutase get released from?

A

Neutrophils

515
Q

What turn ROS into H2O2?

A

Superoxide dismutase

516
Q

What turns H2O2 into water?

A

Peroxidase or catalase

517
Q

What movement is involved in inflammation?

A

Diapedesis

518
Q

What is the chemical attraction of WBC to various areas they are needed (such as inflammation, infected areas)?

A

Chemotaxis

519
Q

What produced by basophils can cause inflammation?

A

Bradykinin

520
Q

What isolates pathogens with an extravascular “clot” and cause inflammation?

A

Clotting proteins

521
Q

What hormone proteins regulate immune responses (and inflam.)?

A

Cytokines

522
Q

What cytokines from macrophages and lymphocytes stimulate many leukocyte immune responses?

A

Interleukins

523
Q

What cytokines are from anti-viral and anti-cancer compounds?

A

Interferons

524
Q

What are a series of proteins that destroy any pathogen marked by antibodies (and can sometimes attack pathogens without the antibodies)?

A

Complement

525
Q

What is released from basophils and mast cells that prevents blood clost?

A

Heparin

526
Q

Why is heparin released to prevent blood clots?

A

So WBCs can get to the area

527
Q

What is released from basophils and mast cells that cause inflam?

A

Histamine and leukotrienes

528
Q

What are active fatty acids from damaged cells that are hormone like?

A

Prostaglandins

529
Q

What produces prostaglandins?

A

An enzyme called cyclooxygenase

530
Q

What can inhibit cyclooxgenase?

A

NSAIDs

531
Q

What causes most headaches, uterine contractions, menstrual pain, etc?

A

Prostaglandins

532
Q

Do ROS and free radicals have a role in inflammation?

A

Yes

533
Q

What are characteristics of inflammation?

A

Redness, swelling, heat, pain

534
Q

What is leukocytosis?

A

An increase in the number of WBCs

535
Q

What does purulent/suppurative mean?

A

The condition of having pus

536
Q

Does pus indicate inflammation and infection?

A

Yes

537
Q

What causes vasodilation in inflammation?

A

Bradykinins, histamine, leukotrienes

538
Q

What is hyperemia?

A

Increased blood flow to the damaged area caused by vasodilation

539
Q

What can vasodilation cause?

A

Erythema or redness

540
Q

What can increased capillary permeability cause due to the fluid leaking from blood vessels to the ECM?

A

Edema or swelling

541
Q

What is exudate?

A

Fluid of edema or edematous fluid

542
Q

What type of exudate is a thick and gooey fluid composed of pus?

A

Purulent or suppurative exudate

543
Q

What is pus?

A

Cellular and microbial debris

544
Q

What type of exudate is thick and gooey and contains blood?

A

Hemorrhagic exudate

545
Q

What type of exudate is thick and gooey and contains fibrin or fibinogen?

A

Fibrous exudate

546
Q

What type of exudate is thin and watery, as in a blister?

A

Transudate or serous exudate

547
Q

What is urticaria?

A

Raised rash caused by histamine, as seen in jellyfish stings

548
Q

What is Pruritis?

A

Itching caused by histamine

549
Q

What causes increased mucus production?

A

Histamine

550
Q

What causes the pain in inflammation?

A

Bradykinin, histamine, prostaglandins

551
Q

What is febrile or pyrexia?

A

Having a fever caused by interleukin-1

552
Q

What is a pyrogen?

A

A compound that causes a fever

553
Q

Is interleukin-1 a pyrogen?

A

Yes

554
Q

Are cytokine storm and cytokine release syndrome life-threatening?

A

Yes

555
Q

What levels are elevated in cytokine storm?

A

Inflammatory cytokines and immune-cell hyperactivation

556
Q

What triggers cytokine storm?

A

Therapies, pathogens, cancer, autoimmune conditions, influenza, COVID

557
Q

What are symptoms of cytokine storm?

A

Cytokine induced tissue damage and multiple organ failure

558
Q

How do NSAIDs treat inflammation?

A

Reduce prostaglandins by inhibiting cyclooxygenase

559
Q

What are ibuprofen, aspirin, naproxen, and indomethacin examples of?

A

NSAIDs

560
Q

Is acetaminophen an NSAID?

A

No

561
Q

What are SAIDs?

A

Steroidal anti-a=inflammatory drugs

562
Q

How do SAIDs treat inflam?

A

Prevent lysosomes of WBCs from releasing enzymes

563
Q

How do decongestants treat inflammation?

A

Cause vasoconstriction (like epi or norepi) allowing lymphatic drainage to reduce swelling

564
Q

How do anti-histamines treat inflam?

A

Prevent the effects of histamines

565
Q

What is the immune system you are NOT born with?

A

Specific or adaptive immune system

566
Q

What is the third line of defense?

A

Specific or adaptive immune system

567
Q

What is the specific or adaptive immune system composed of?

A

Cells and antibodies (humoral immunity) and various T lymphocyte functions (cellular immunity)

568
Q

What is an antigen?

A

Foreign compounds that (usually) promote an immune response
They are “non self”

569
Q

What is an epitope or antigenic determinants?

A

The part of an antigen that stimulates the immune response

570
Q

Can an antigen have multiple epitopes?

A

Yes!

571
Q

What is hapten?

A

Not an antigenic by themselves, but when combined with other proteins, they become antigenic

572
Q

What are examples of hapten?

A

Penicillin, poison ivy, monosodium glutamate, animal dander

573
Q

What part of an antigen is presented to the MHC?

A

Epitopes or antigenic determinants

574
Q

Are antigen presenting cells innate or adaptive or both?

A

Both!
Macrophages and dendritic cells are innate
B lymphocytes are adaptive

575
Q

Where do antigen presenting cells present the partially digested antigen to?

A

The cell membrane so the whole rest of the immune system can see it

576
Q

What are major histocompatibility complex (MHC) and Human leukocyte antigens (HLA)?

A

Proteins on the cell membrane of the antigen presenting cells that help present the antigen and identify self vs non-self

577
Q

What do APCs phagocytize?

A

Antigens

578
Q

When APCs place part of the antigen on the membrane with the MHCs, what do they show it to?

A

Helper T lymphocytes

579
Q

Which MHC is found on every nucleated cell in the body and platelets?

A

MHC-1

580
Q

Which MHC presents intracellular or endogenous antigens?

A

MHC-1

581
Q

What are viruses and “neoantigens” produced by mutations in cancer cells examples of?

A

Endogenous antigens

582
Q

What cells recognize MHC-1?

A

CD8 cells (Cytotoxic T lymphocytes)

583
Q

Which MHC is found on APCs?

A

MHC-2

584
Q

Which MHC presents extracellular or exogenous antigens?

A

MHC-2

585
Q

What cells recognize MHC-2?

A

CD4 cells (Helper T lymphocytes)

586
Q

What do CD4 and CD8 refer to?

A

The type of receptor protein that can bind to or recognize the MHC

587
Q

Which T lymphocytes are involved in “specific resistance”?

A

Helper T lymphocytes CD4 cells

588
Q

What do the Helper T lymphocytes do once they’re “taught” the bad guy’s identity by the APC?

A

The Helper T clones itself thousands of times carrying the bad guy’s identity

589
Q

What is triggered when CD4 binds to the MHC-2 protein on an APC?

A

The CD4 triggers apoptosis to kill the infected cell

590
Q

What do cytotoxic T lymphocytes (CD8 cells) do once told be helper T cell the antigen’s identity?

A

They “seek and destroy” the antigen by docking with diseased cells and injecting lethal chemicals

591
Q

What do these chemicals released by cytotoxic T lymphocytes do?
Perforins

A

Punch holes in microbes

592
Q

What do these chemicals released by cytotoxic T lymphocytes do?
Lymphotoxin

A

Destroys the foreign target cell’s DNA

593
Q

What do these chemicals released by cytotoxic T lymphocytes do?
Tumor necrosis factor (TNF)

A

Destroys cancer cells

594
Q

What do these chemicals released by cytotoxic T lymphocytes do?
Interferon

A

Works against viruses

595
Q

What do these chemicals released by cytotoxic T lymphocytes do?
Interleukins

A

Induces fever

596
Q

What T lymphocytes are the “cheerleaders” that keep the system activated/fired up as long as the threat remains?

A

Inducer T lymphocytes

597
Q

What T lymphocytes turn the immune system OFF from the specific threat?

A

Regulator or suppressor T lymphocytes (T regs)

598
Q

What cells remember the identification of the antigen in case of future exposures and allow for a faster response? (Often before the patient feels sick!)

A

Memory cells

599
Q

What lymphocytes mature to become plasma cells that produce antibodies?

A

B lymphocytes

600
Q

What is the humoral immune response tasked with?

A

The production of antibodies

601
Q

Which antibody (immunoglobulin) is: found in secretions (milk, tears, sweat, etc.)

A

IgA

602
Q

Which antibody (immunoglobulin) is:
B cell receptors that bind to antigens…Lower concentrations found

A

IgD

603
Q

Which antibody (immunoglobulin) is:
Found in tonsils, skin, mucus membranes?

A

IgE

604
Q

Which antibody (immunoglobulin) causes basophils and mast cells to release histamine to cause an allergic reaction?

A

IgE

605
Q

Which antibody (immunoglobulin) is:
The first antibodies produced against pathogens and will be replaced by the IgG’s?

A

IgM

606
Q

Which antibody (immunoglobulin) is: the most abundant antibodies, the only antibodies that cross the placenta to bring mom’s immunity to the fetus and stimulates complement when bound to antigens?

A

IgG

607
Q

What is the marking of an antigen for destruction by the immune system called?

A

Opsonization

608
Q

What antibodies attach to pathogen, what destroys it?

A

Complement

609
Q

What is a tissue transfer within the same individual called?

A

Autograft/autotransplant

610
Q

What is a tissue transfer to an identical twin?

A

Isograft

611
Q

What is a tissue transfer to the same species?

A

Allograft/homograft

612
Q

What is a tissue transfer to different species?

A

Xenograft/heterograft

613
Q

Do isografts with identical twins usually have rejections?

A

No

614
Q

Do allografts with fraternal twins have rejections?

A

Sometimes, if the tissues are not matched

615
Q

What are drugs that lower the immune system to lower the risk of rejection of tissue transplant?

A

Immuno-supressants

616
Q

What is hypersensitivity in regards to the immune system?

A

A harmful immune reaction to antigens that do not usually cause this sort of reaction

617
Q

What happens in allergic reactions?

A

T lymphocytes cause B lymphocytes to produce IgEs, which cause mast cells and basophils to release histamine (and cause an allergic reaction)

618
Q

What is anaphylaxis?

A

Very fast and severe systemic reaction with swelling, mucus, bronchodilation, dyspnea, possible sudden death with heart attack

619
Q

What can treat anaphylaxis?

A

Epinephrine (adrenalin) injections

620
Q

What is delayed hypersensitivity?

A

Takes 12-72 hours to have a harmful immune reaction

621
Q

When might you see delayed hypersensitivity?

A

Poison ivy, transplant rejections

622
Q

What is the most common chronic illness of children?

A

Asthma

623
Q

What causes asthma?

A

Allergens cause plasma cells to produce IgEs, stimulating the mast cells to produce histamine

624
Q

Which disease is seen in children with severely suppressed immune systems (bubble boy)

A

Severe combined immunodeficiency disease

625
Q

What disease comes from a loss of helper T cells that results in a loss of immune system and death by opportunistic diseases?

A

AIDS

626
Q

What is a cancer of B lymphocytes resulting in immuno-compromised patients?

A

Hodgkin’s disease (lymphoma)

627
Q

How many types of autoimmune diseases are there?

A

Over 80

628
Q

Which autoimmune disease has:
antibodies against the ach receptors at the NMJ?

A

Myasthenia Gravis

629
Q

What type of paralysis is seen in Myasthenia Gravis?

A

Flaccid paralysis

630
Q

Which autoimmune disease has:
Antibodies against DNA/RNA and can effect many cell types

A

Systemic lupus erythematosus (SLE)

631
Q

Which autoimmune disease has:
antibodies against the myelin sheath destroying neurons

A

Multiple sclerosis

632
Q

Which autoimmune disease has:
Antibodies against the joint cartilages

A

Rheumatoid arthritis

633
Q

Which autoimmune disease has:
Hyperthyroidism

A

Graves disease

634
Q

Which autoimmune disease has:
Antibodies against beta cells that make insulin?

A

Diabetes mellitus type 1

635
Q

Which autoimmune disease has:
Antibodies against insulin receptors, therefore, insulin resistant

A

Diabetes mellitus type 2

636
Q

Which autoimmune disease has:
Chronic inflammation of small and large intestines

A

Inflammatory bowel diseases

637
Q

Which autoimmune disease has:
Reaction to gluten

A

Celiac disease

638
Q

What is the respiratory system lined with all the way down to the terminal bronchioles?

A

Pseudostratified ciliated columnar epithelium

639
Q

Does gas exchange occur with Pseudostratified ciliated columnar epi?

A

Nope

640
Q

What part of the respiratory tract contains the: nose, pharynx, larynx, trachea down to vocal folds

A

Upper respiratory tract

641
Q

What is the purpose of the upper respiratory tract?

A

Warm and moisten air, filter, olfaction, vocalization

642
Q

What part of the respiratory tract contains vocal folds to alveoli?

A

Lower respiratory tract

643
Q

What are the respiratory bronchioles to the alveoli lined with and why?

A

Simple squamous epi for gas exchange

644
Q

How do lungs: gas exhange

A

O2 in CO2 out

645
Q

Where does gas exchange occur in the lungs?

A

Respiratory bronchioles and alveoli

646
Q

How do lungs: buffer

A

lungs help regulate pH

647
Q

How do lungs: participate in the endocrine system

A

Produces angiotensin 2

648
Q

How do lungs: participate in allergic reactions?

A

Mast cells, like basophils, release histamine to cause reactions and asthma

649
Q

What are the phagocytic cells of the lungs?

A

Macrophages

650
Q

How big are alveoli?

A

0.2-0.5mm diameter
70m2 surface area

651
Q

What are type 1 cells in the lungs made of, %, and function?

A

Simple squamous, 95%, make up the walls

652
Q

What are type 2 cells in the lungs made of, %, and function?

A

Cuboidal, 5% of alveolar cells, produce surfactant

653
Q

What does surfactant do?

A

Reduces surface tension of water making it easier to inhale

654
Q

What are all the pleura made of?

A

Simple squamous epi

655
Q

Which pleura: lines the thoracic wall

A

Parietal pleura

656
Q

Which pleura: adheres to the lungs

A

Visceral pleura

657
Q

What is the space between two pleura?

A

Pleural cavity

658
Q

What kind of pressure in the pleural cavity allows you to inhale?

A

Negative pressure

659
Q

What is intrapulmonary pressure?

A

Pressure in the alveoli, close to atmospheric pressure

660
Q

What is intrapleural pressure?

A

Pressure within the pleural cavity

661
Q

Which is lower:
Intrapulmonary pressure or intrapleural pressure?

A

Intrapleural pressure is ALWAYS lower than intrapulmonary

662
Q

What is Boyle’s law?

A

With a constant temperature, volume and pressure vary inversely

663
Q

With Boyle’s law: if you increase volume, like when the diaphragm drops as it contracts, what does this do to pressure?

A

Pressure decreases

664
Q

Where does AP travel down in inhalation/exhalation?

A

Phrenic nerve

665
Q

When the diaphragm contracts, it pulls downwards to _____ volume of intrapleural space, causing a ____ in its pressure

A

When the diaphragm contracts, it pulls downwards to INCREASE volume of intrapleural space, causing a DROP in its pressure

666
Q

What is the major inspiratory muscle at rest?

A

The diaphragm

667
Q

What is quiet breathing?

A

Exhalation at rest, accomplished passively (no muscles work, the lungs just collapse)

668
Q

When are accessory muscles required for inhalation/exhalation?

A

Forced breathing (like during exercise)

669
Q

What is 1 atmosphere of pressure at sea level?

A

760 mm Hg

670
Q

With intrapulmonary or alveolar pressure, inspiration and expiration pressure changes are what?

A

Inspiration: -1 mm Hg
Exhalation: +1 mm Hg

671
Q

With Intrapleural pressure, inspiration and expiration pressure changes are what?

A

Inspiration: -6 mm Hg
Exhalation: -3 mm Hg

672
Q

Which is lower, especially during inspiration: intrapleural pressure or intrapulmonary pressure?

A

Intrapleural pressure is LOWER

673
Q

What does the volume of breath represent?

A

Tidal volume

674
Q

How thick is the respiratory membrane?

A

0.5 µm

675
Q

What is the combined surface area of the respiratory membrane’s capillaries?

A

100 m2

676
Q

What is the first layer of the respiratory membrane (closest to alveolus)?

A

Fluid lining alveoli

677
Q

What layer after the fluid lining alveoli?

A

Epithelium for alveoli (simple squamous)

678
Q

What layer after the epithelium?

A

Basement membrane for alveolar epi

679
Q

What layer after the basement membrane for alveolar epi?

A

Interstitum

680
Q

Is the interstitium thick or thin? What is it made out of?

A

Thin connective tissue

681
Q

What layer after the interstitium?

A

Basement membrane for capillary endothelium

682
Q

What layer after the basement membrane for the capillary endothelium?

A

Capillary endothelium

683
Q

What is the capillary endothelium made out of?

A

Simple squamous epi

684
Q

How much blood do the capillaries contain?

A

120 mL

685
Q

What happens if you decrease the # of capillaries in the lungs due to diseases such as cancer and emphysema?

A

You decrease the body’s ability to get O2 in and CO2 out

686
Q

What is the systemic circulatory system?

A

Sends blood from lungs to body and back

687
Q

What is the pulmonary circulatory system?

A

Blood enters the lungs to pick up O2 and release CO2, then back out to the systemic system

688
Q

What is the bronchial circulatory system?

A

Provides oxygenated blood to the tissues of the lungs

689
Q

Where does the bronchial circulatory system get blood from and return blood to?

A

Feeds from the aorta and returns blood to the pulmonary veins

690
Q

What proportion of collapsing forces is the elastic forces of the lungs?

A

1/3

691
Q

What proportion of the collapsing forces is the surface tension of water?

A

2/3

692
Q

What does the “collapsing forces of the lungs” mean?

A

What allows exhalation/expiration

693
Q

What does the inflating forces of the lungs mean?

A

Allows inhalation/inspiration

694
Q

Is surfactant like a detergent?

A

Yes

695
Q

What creates negative intrapleural pressure?

A

The contraction of the diaphragm and creating reduced intrapleural pressure

696
Q

What innervates the diaphragm?

A

The phrenic nerve

697
Q

What is measuring volumes and capacities via pulmonary function tests to see how the lungs are working?

A

Spirometry

698
Q

What is the tidal volume?

A

Amount in or out in 1 normal breath

699
Q

What is normal tidal volume?

A

500 mL

700
Q

What is inspiratory reserve volume (IRV)?

A

Max amount inhaled beyond tidal

701
Q

What is expiratory reserve volume (ERV)?

A

Max amount exhaled beyond tidal

702
Q

What is residual volume (RV)?

A

Amount in lungs after max exhalation

703
Q

What are respiratory capacities?

A

Two or more volumes combined

704
Q

What is vital capacity?

A

Max amount exhaled after max inhalation

705
Q

What is a normal vital capacity?

A

4800 mL

706
Q

What is inspiratory capacity?

A

Tidal + IRV (max amount inhaled after tidal expiration)

707
Q

What is functional residual capacity (FRC)?

A

Expiratory reserve volume + residual volume

708
Q

What is a normal total lung capacity?

A

6,000 mL

709
Q

What can increases in total lung capacity, functional residual capacity, and residual volume be cased by?

A

Hyperinflation due to chronic obstructive pulmonary diseases

710
Q

Tidal volume amount?

A

500 mL

711
Q

What is the respiratory or ventilation rate for adults?

A

12-18 breaths per minute

712
Q

What is the respiratory or ventilation rate for infants?

A

40-80 breaths per minute

713
Q

What is minute ventilation?

A

Amount air inhaled per minute

714
Q

What does minute ventilation determine?

A

Alveolar ventilation rate (AVR)

715
Q

What is forced vital capacity (FVC)?

A

Taking a deep breath, and forcibly exhaling maximally as much as possible

716
Q

What kind of forced vital capacity suggests restricted breathing?

A

Normal FVC at first, then low values

717
Q

What do low values of forced vital capacity indicate?

A

Obstructive disease

718
Q

What is forced expiratory volume?

A

% of vital capacity exhaled in 1 second

719
Q

What is normal forced expiratory volume?

A

75-85%

720
Q

What is the forced expiratory ratio?

A

(Forced Expiratory Volume/Forced Vital Capacity) x 100

721
Q

How do you calculate alveolar ventilation rate (AVR)?

A

Tidal volume - dead space

722
Q

What does alveolar ventilation rate indicate?

A

Ventilation effectiveness

723
Q

What is a normal alveolar ventilation rate?

A

4,200 mL/min

724
Q

What increases alveolar ventilation rate most efficiently: increasing volume or increasing rate?

A

Increasing VOLUME increases AVR more efficiently

725
Q

What demonstrates a marked decrease in alveolar ventilation rate?

A

Rapid, shallow breathing

726
Q

What is dead air/space?

A

Areas where no gas exchange occurs

727
Q

How much anatomical dead space is there?

A

~150 mL

728
Q

What is anatomical dead space lined with?

A

Pseudostratified ciliated columnar epi

729
Q

What is alveolar air?

A

Air that makes it to the alveoli for gas exhange

730
Q

How much air is alveolar? (Tidal - dead air = __)

A

500 mL - 150 mL = 350 mL alveolar

731
Q

What is alveolar dead space?

A

Physiological or function dead air space if the alveoli are clogged by mucus etc.

732
Q

What is Dalton’s law of partial pressure?

A

In a mix of gases, each gas contributes to total pressure or total pressure of mixture (sum = partial pressures of all gases)

733
Q

Amount of N2 in atmosphere?

A

78.6%

734
Q

Amount of O2 in atmo?

A

20.9%

735
Q

Amount of water in atmo?

A

0.46%

736
Q

Amount of CO2 in atmo?

A

0.04%

737
Q

What do higher levels of O2 increase the risk of?

A

Fire and explosion

738
Q

When do you see the first signs of hypoxia?

A

15-19% O2

739
Q

What % O2 do you see with exertion, associated with impaired coordination and judgement?

A

12-14%

740
Q

What % of O2 do you have abnormal fatigue and signs of cyanosis?

A

10-12%

741
Q

What % O2 will you lose consciousness without warning?

A

<12%

742
Q

What % O2 will you have mental failure?

A

8-10%

743
Q

What % O2 will you be unable to move, have a coma in 40 seconds, convulsions, and death?

A

<10%

744
Q

What is ventilation?

A

The amount of gas reaching the alveoli

745
Q

What is perfusion?

A

The amount of blood flow in the pulmonary capillaries

746
Q

What is autoregulation of vessel diameter?

A

Lungs are able to adjust their perfusion themselves

747
Q

What will the lungs do if ventilation is low (less O2, hypoxic conditions)?

A

Hypoxic pulmonary vasoconstriction

748
Q

If ventilation is low because of a pathology like emphysema, will arterioles constrict or dilate?

A

Constrict

749
Q

What will bronchioles do if CO2 is high? (How does it autoregulate)?

A

Bronchioles dilate to help eliminate CO2

750
Q

If low O2 and high CO2, what will the veins and bronchioles do?

A

Vasoconstriction
Bronchodilation

751
Q

What % of O2 is carried by hemoglobin?

A

98.5%

752
Q

What % of O2 is dissolved in plasma?

A

1.5%

753
Q

What % CO2 is carried by hemoglobin?

A

20%

754
Q

What % CO2 is dissolved in plasma?

A

7-10%

755
Q

What is the hemoglobin that carries CO2 called?

A

Carbaminohemoglobin

756
Q

How much CO2 is found in the form of carbonic acid or bicarbonate ions?

A

70%

757
Q

What enzymes cause CO2 to bind with H2O and is found in the erythrocytes and kidney tubules?

A

Carbonic anhydrase

758
Q

What is the chloride shift in TISSUES?

A

In the tissues, bicarb is exchanged for a chloride ion (Bicarb into plasma, Cl into RBC)

759
Q

What is the chloride shift in LUNGS?

A

In the lungs, bicarb is exchanged for a chloride ion (Bicarb into RBC, Cl back out to be exchanged into CO2 and H2O and to be dumped by lungs)

760
Q

What is Haldane effect?

A

O2 displaces CO2 from hemoglobin. The higher the PO2, the more O2 on hemoglobin, the less CO2 carried by hemoglobin

761
Q

What do you want in the lungs: more O2 on hemoglobin or CO2?

A

More O2, so release CO2

762
Q

What is the Bohr effect?

A

The more CO2 and H+, the less O2 carried by hemoglobin

763
Q

How does the Bohr effect relate to tissues?

A

In the tissues where there is more CO2 and H+, hemoglobin is more likely to release O2

764
Q

If O2 is influencing CO2 and H+, what effect is it?

A

Haldane

765
Q

If CO2 and H+ are influencing O2, what effect is it?

A

Bohr

766
Q

Does this condition cause hemoglobin to pick up/bind to O2?
Lungs: lower H+

A

PICK UP O2

767
Q

Does this condition cause hemoglobin to pick up/bind to O2?
Lungs: lower CO2

A

PICK UP O2

768
Q

Does this condition cause hemoglobin to pick up/bind to O2?
Lungs: lower temperature

A

PICK UP O2

769
Q

Does this condition cause hemoglobin to pick up/bind to O2?
Lungs: lower DPG or BPG)

A

PICK UP O2

770
Q

Does this condition cause hemoglobin to pick up/bind to O2?
In the fetus: higher levels of fetal hemoglobin

A

PICK UP O2 from mom

771
Q

Does this condition cause hemoglobin to release O2?
Tissues: higher H+

A

RELEASE O2

772
Q

Does this condition cause hemoglobin to release O2?
Tissues: higher CO2

A

RELEASE O2

773
Q

Does this condition cause hemoglobin to release O2?
Tissues: higher temperature

A

RELEASE O2

774
Q

Does this condition cause hemoglobin to release O2?
Tissues: DPG or BPG

A

RELEASE O2

775
Q

What causes the lungs to have hemoglobin RELEASE O2 rather than bind to it?

A

Smoking, lung diseases

776
Q

At the lungs the hemoglobin will be saturated at what %?

A

97%

777
Q

Once O2 is released in the tissues, hemoglobin returns to the heart/lungs in veins, but at rest it is about ___% saturated

A

75%

778
Q

What % of O2 is released to the tissues at rest?

A

22% (97%-75%)

779
Q

What does 22% O2 equate to in mL?

A

5 mL O2 per dL plasma

780
Q

What is the O2 still on the hemoglobin reserved for/what can triple the amount of O2 released?

A

Exercise

781
Q

What can exercise bring the O2 released level to?

A

66% or 15 mL O2/dL plasma

782
Q

What stimulates inhaling at rest?

A

Dorsal respiratory group (DRG)

783
Q

What stimulates forced inhalation and exhalation during exercise/forced respiration?

A

Ventral respiratory group (VRG)

784
Q

Where are the dorsal and ventral respiratory groups?

A

Medulla oblongata

785
Q

What type of neurons send AP along the phrenic nerve to the diaphragm?

A

Inspiratory neurons

786
Q

What type of neurons inhibit the inspiratory neurons to stop the AP from reaching the diaphragm?

A

Expiratory neurons

787
Q

What cuts off the dorsal respiratory group allowing us to exhale?

A

Pneumotaxic center or pontine respiratory center (PRC)

788
Q

What happens if the pontine respiratory center fails?

A

The patient inflates the lungs and can only do short expiratory puffs

789
Q

What controls respiration during vocalization, sleeping, and exercise?

A

Pontine respiratory center

790
Q

What keeps the pneumotaxic center functioning? (If this fails, the pneumotaxic center fails)

A

Apneustic center

791
Q

What is apneustic breathing?

A

Inability to fully exhale after damage to PRC

792
Q

Where are the pnumotaxic center and apneustic center?

A

Pons

793
Q

What has the GREATEST OVERALL effect on respiratory rate?

A

CO2

794
Q

What has the least significant effect on respiratory rate?

A

O2

795
Q

What has the GREATEST DIRECT effect on respiratory rate?

A

H+

796
Q

Hypercapnia has the most potent overall effect on _____ ventilation rate and depth

A

Increasing

797
Q

What compounds can easily cross the blood brain barrier via CO2?

A

Non-polar, fat soluable compounds

798
Q

Does the brain vasodilate or vasoconstrict when you hyperventilate (as seen in hypocapnia)?

A

Vasoconstriction

799
Q

About how much O2 has to be reduced before there is an effect on ventilation rate?

A

A significant reduction in O2, partial pressure of 60 mmHg or lower

800
Q

Increasing H+ does what to ventilation rate?

A

Increases ventilation rate

801
Q

Does H+ cross the blood brain barrier?

A

No

802
Q

Where are the central chemoreceptors found?

A

CNS

803
Q

Where are peripheral chemoreceptors found (specifically)?

A

Carotid bodies
Aortic bodies

804
Q

Where do the carotid bodies’ peripheral chemoreceptors send impulses to and by what nerve?

A

Medulla via glossopharyngeal nerve

805
Q

Where do the aortic bodies’ peripheral chemoreceptors send impulses to and by what nerve?

A

Medulla via vagus nerve

806
Q

What is the Hering-Breuer or inflation reflex?

A

If lungs overfill, stretch receptors in bronchial tree send inhibitory impulses to cut inspiration off

807
Q

What is the Hering-Breuer or inflation reflex normal in?

A

Infants

808
Q

What is the difference between obstructive and restrictive lung diseases?

A

Obstructive: harder to get air OUT
Restrictive: harder to get air IN

809
Q

Is COPD obstructive or restrictive?

A

Obstructive

810
Q

What causes restricted lung disease?

A

Obesity, fibrosis, ALS

811
Q

What is nitrogen narcosis?

A

Diving over 100ft increases pressure and forces N into plasma, becoming toxic

812
Q

What is the bends?

A

Diver comes up too fast, causing air embolisms to clog vessels

813
Q

What is pneumoconiosis?

A

Pathological change in lungs due to inhalation of particles

814
Q

Signs of pulmonary disease/pneymoconiosis?

A

Clubbing of finger tips, barrel chest

815
Q

What is pleurisy?

A

Inflamed pleura so fluid accumulates in pleural cavity

816
Q

What is empyema?

A

Pus in pleural cavity

817
Q

What is pulmonary hypertension?

A

Increased pulmonary blood pressure

818
Q

What ventricle works harder in pulmonary hypertension and can lead to Cor Pulmonale?

A

Right ventricle

819
Q

What is atelectasis?

A

Collapsed lung causes shortness of breath

820
Q

What is the treatment for atelectasis?

A

Deep breathing exercises

821
Q

What is compression atelectasis in the lungs?

A

Displacement of the pleural cavity by a tumor

822
Q

What is a compression in the pleural cavity by blood?

A

Hemothorax

823
Q

What is pneumothorax atelectasis?

A

Air in pleural cavity causes loss of negative interpleural pressure

824
Q

What is absorption or obstructive atelectasis?

A

Alveoli blocks the air and collapses

825
Q

What is patchy atelectasis caused by?

A

Pneumonia

826
Q

What is retrolental fibroplasia?

A

Behind the lens scarring (premature babies placed on O2 leading to blindness)

827
Q

What is a pulmonary embolism?

A

A foreign object getting lodged in the lungs from the blood

828
Q

What % of pulmonary embolisms are from femoral/calf venous thrombi?

A

90%

829
Q

What is cystic fibrosis?

A

Genetic mutation resulting in loss of Cl- channels (salty babies)

830
Q

What is 2nd to heart disease as cause of disability for adults under 65?

A

COPD

831
Q

What causes COPD?

A

Smoking, dust, chemical fumes, infection

832
Q

What is chronic bronchitis?

A

Inflam of bronchi causing obstruction

833
Q

What is emphysema?

A

Permanent enlargement of alveoli and loss of elasticity (lungs don’t collapse)

834
Q

What disease has “blue boaters”?

A

Chronic bronchitis

835
Q

What disease has “pink puffers”?

A

Emphysema

836
Q

What causes skin to have a pinkish color which may cause Cor Pulmonale?

A

Polycythemia

837
Q

What is an allergic inflammation with bronchospasms and mucus production?

A

Asthma

838
Q

What is the most common form of pneumonia?

A

Community acquired

839
Q

What % of community acquired pneumonia are gram positive streptococcus?

A

70%

840
Q

Does gram positive streptococcus have a high or low death rate?

A

Low

841
Q

What means hospital acquired?

A

Nosocomial infection

842
Q

What is the most common nosocomial infection that is often drug resistant?

A

Gram positive staph aureus

843
Q

What pneumonia has a poor prognosis with >50% mortality?

A

Gram negative bacteria

844
Q

Is viral pneumonia bad?

A

No, usually relatively mild/self limiting

845
Q

What causes TB?

A

Mycobacterium tuberculosis

846
Q

Is TB airborne, waterborne, etc?

A

Airborne

847
Q

What are the tubercles in TB filled with?

A

Caseous necrosis

848
Q

What is the most deadly single microbe in # of deaths?

A

TB

849
Q

What is the most common cancer cause of death?

A

Bronchogenic carcinomas

850
Q

Do men or women get bronchogenic carcinomas?

A

Both

851
Q

What increases risk of bronchogenic carcinomas?

A

Smoking, by 25x

852
Q

What % of lung cancers are squamous cell?

A

30%

853
Q

Where are the tumors in squamous cell carcinoma?

A

Near hilus (where things enter/leave lungs)

854
Q

What % of lung cancers are small (oat) cell?

A

20-25%

855
Q

Where are the tumors in small (oat) cell?

A

Central

856
Q

Which carcinoma has the highest correlation with smoking?

A

Small (oat) cell

857
Q

Which has the worst prognosis of lung cancers?

A

Small (oat) cell

858
Q

What % of individuals live past 2 years of small (oat) cell carcinoma?

A

<5%

859
Q

What % of lung cancers are adenocarcinomas?

A

30-35%

860
Q

Where are tumors in adenocarcinomas and what do they do?

A

The periphery, often asymptomatic or behave like glands producing hormones

861
Q

What % are large cell (undifferentiated) carcinomas?

A

10-15%

862
Q

Are large cell (undifferentiated) carcinomas responsive to therapy?

A

No

863
Q

What is a metastatic tumor?

A

Originates elsewhere in the body (ex. breast)