March 13 Flashcards

1
Q

Before the 17th century, what was the key to restoring health if someone was unhealthy?

A
  1. Lifestyle (diet & exercise)
  2. Medication (herbs)
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2
Q

What principle guided treatments in pre-17th century medicine?

A

“Opposites cure opposites” (e.g. a cold remedy cures a hot illness)

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3
Q

How was illness understood before the 17th century?

A

As an internal disorder of the body, not caused by a specific agent like bacteria

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4
Q

Until when did the humoral vision of the body dominate in Europe?

A

Late seventeenth century

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5
Q

How was humoral medicine viewed by the Middle Ages?

A

It was seen as “quackery”

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6
Q

What new scientific approach replaced Aristotelian, qualitative, natural philosophy?

A

A mechanical, chemical, and mathematical vision of the world & body, developed by Galileo, Descartes, Newton, & Boyle

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7
Q

What are the three main functions of the circulatory system?

A
  1. Transportation (respiratory, nutritive, excretory)
  2. Regulation (hormonal, temperature)
  3. Protection (clotting, immune defense)
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8
Q

What substances does the circulatory system transport for cellular metabolism?

A

Respiratory: Oxygen & CO₂ via RBCs

Nutritive: Nutrients from digestion

Excretory: Waste removal

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9
Q

How does the circulatory system regulate body functions?

A
  • Hormonal regulation (transport of hormones)

Temperature regulation (heat distribution & dissipation)

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10
Q

How does the circulatory system protect the body?

A
  • Injury protection: Blood clotting

Pathogen protection: Immune response (white blood cells & antibodies)

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11
Q

What is hematopoiesis?

A

The formation of blood cells

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12
Q

Where do hematopoietic stem cells originate and migrate to?

A

They originate in the embryo and migrate to different tissues

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13
Q

What is the major hematopoietic organ of the fetus?

A

The liver

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14
Q

What is the major hematopoietic organ after birth?

A

The bone marrow

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15
Q

What role do cytokines play in hematopoiesis?

A

Cytokines play important roles in regulating and stimulating hematopoiesis.

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16
Q

What is the most abundant type of blood cell?

A

Red blood cells (RBCs)

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17
Q

What is the shape of red blood cells (RBCs)?

A

Biconcave disc shape

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18
Q

Where are red blood cells (RBCs) located in a blood sample after centrifugation?

A

Packed at the bottom

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19
Q

What forms the “buffy coat” in a blood sample after centrifugation?

A

White blood cells (WBCs) and platelets (thin, light interface)

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20
Q

Where is plasma located in a blood sample after centrifugation?

A

At the very top (fluid portion)

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21
Q

What is the process of erythropoiesis?

A

The formation of red blood cells (RBCs) from uncommitted stem cells through a series of stages in the bone marrow

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22
Q

What happens when the nucleus is expressed during erythropoiesis?

A

The cell forms a reticulocyte, which is released into circulation

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23
Q

What happens to the reticulocyte after it enters circulation?

A

It expels its nucleus and matures into a red blood cell (RBC)

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24
Q

Where does erythropoiesis occur?

A

In the bone marrow

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25
Q

What structure gives red blood cells (erythrocytes) their unique concave shape?

A

The cytoskeleton

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26
Q

How do red blood cells (RBCs) respond to changes in the tonicity of their environment?

A

They swell in hypotonic medium and shrink in hypertonic medium

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27
Q

What illness can affect the shape of red blood cells?

A

Sickle Cell Anemia

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28
Q

What is the primary function of erythrocytes (RBCs) and hemoglobin (Hb)?

A

To aid in oxygen delivery to tissues

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29
Q

Where is most of the oxygen found in the blood?

A

Most oxygen is bound to hemoglobin (Hb) in red blood cells (RBCs)

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30
Q

What gives blood its red color?

A

Hemoglobin (Hb)

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31
Q

What is the structure of hemoglobin in red blood cells?

A

Hemoglobin is made up of 4 globin proteins (2 alpha, 2 beta), each with a heme group that binds an iron molecule

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32
Q

How does heme iron interact with oxygen?

A

Heme iron combines with oxygen in the lungs and releases oxygen into tissues

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33
Q

How much oxygen can each red blood cell (RBC) carry?

A

Each RBC can carry over a billion molecules of oxygen (280 million hemoglobin molecules per RBC x 4 heme groups)

34
Q

How does the oxygen content change as blood moves from the arteries to the veins?

A

Blood entering tissues contains 200 mL O₂/L, and blood leaving tissues contains 155 mL O₂/L, meaning 45 mL O₂ is unloaded to tissues.

35
Q

What is the oxygen-hemoglobin saturation in systemic arteries and veins?

A

In systemic arteries, ~97% of hemoglobin is saturated with oxygen (oxyhemoglobin). In systemic veins, the saturation drops to ~75%, with about 22% of the oxygen unloaded to tissues.

36
Q

What physiologic factors can change hemoglobin (Hb) conformation and affect oxygen binding?

A

Factors like pH and temperature can change Hb conformation, influencing oxygen binding.

37
Q

How does a decrease in pH affect hemoglobin’s affinity for oxygen?

A

A decrease in pH decreases Hb’s affinity for oxygen, leading to more oxygen being offloaded into tissues. This occurs during exercise when muscle activity produces lactic acid (Bohr effect).

38
Q

How does an increase in temperature affect hemoglobin’s affinity for oxygen?

A

An increase in temperature decreases Hb’s affinity for oxygen, leading to more oxygen being offloaded into tissues.

39
Q

What is the Bohr effect?

A

The Bohr effect describes how a decrease in pH (e.g., due to lactic acid from muscle activity) reduces hemoglobin’s affinity for oxygen, enhancing oxygen delivery to tissues.

40
Q

How does temperature affect the bond between oxygen and hemoglobin?

A

Higher temperatures weaken the bond between oxygen and hemoglobin, promoting more oxygen offloading into tissues.

41
Q

What is the oxygen-hemoglobin dissociation curve?

A

It describes the relationship between the partial pressure of oxygen (pO₂) and the percentage of hemoglobin saturated with oxygen, indicating how oxygen is loaded into the blood and unloaded into tissues.

42
Q

How much does oxyhemoglobin decrease as blood passes from arteries to veins through the tissues?

A

Oxyhemoglobin decreases by ~22% as blood moves from arteries to veins.

43
Q

What is the oxygen reserve in venous blood?

A

The oxygen reserve is the oxyhemoglobin remaining in venous blood, which is enough to sustain the brain and heart for ~4-5 minutes without breathing or CPR. It can also be used when tissue oxygen requirements increase (e.g., during exercise).

44
Q

What happens to oxygen unloading in tissues during exercise?

A

Oxygen unloading increases (more oxygen is delivered to tissues) during exercise due to factors like increased temperature and decreased pH.

45
Q

How does oxygen unloading change under normal conditions?

A

Oxygen unloading decreases (less oxygen is offloaded to tissues) when conditions are such that hemoglobin’s affinity for oxygen is higher (e.g., higher pH, lower temperature).

46
Q

What structures do mature red blood cells (RBCs) lack?

A

Mature RBCs lack nuclei, mitochondria, and endoplasmic reticulum (ER).

47
Q

How do mature RBCs obtain energy?

A

RBCs obtain energy through anaerobic metabolism of glucose, as they cannot respire aerobically.

48
Q

What happens in the glycolytic pathway that leads to the production of 2,3-DPG?

A

A side reaction in the glycolytic pathway results in the production of 2,3-Diphosphoglyceric Acid (2,3-DPG).

49
Q

What enzyme produces 2,3-DPG, and how is it regulated?

A

The enzyme producing 2,3-DPG is inhibited by oxyhemoglobin. When oxyhemoglobin levels decrease (e.g., in hypoxia or anemia), 2,3-DPG production increases.

50
Q

How does increased 2,3-DPG concentration affect oxygen unloading?

A

Increased 2,3-DPG concentration enhances oxygen unloading by shifting the oxygen-hemoglobin dissociation curve to the right, facilitating more oxygen delivery to tissues.

51
Q

What happens as RBCs age?

A

RBCs become fragile and eventually are destroyed.

52
Q

What is the lifespan of a red blood cell (RBC)?

A

The lifespan of a RBC is 120 days.

53
Q

What is bilirubin, and how is it produced?

A

Bilirubin is produced when old RBCs are destroyed in the spleen, as a breakdown product of heme from hemoglobin (Hb).

54
Q

How is bilirubin processed in the body?

A

Liver enzymes bind bilirubin, and it is excreted into bile.

55
Q

How is bilirubin eliminated from the body?

A

Bilirubin circulates in bile and is eventually lost in urine and feces.

56
Q

What is jaundice and what causes it?

A

Jaundice is associated with high blood concentrations of bilirubin (hyperbilirubinemia) from the death of red blood cells (RBCs).

57
Q

Why do healthy newborns experience jaundice?

A

Healthy newborns experience a rapid decrease in blood hemoglobin (Hb) at birth, leading to increased bilirubin levels.

58
Q

Why are preemies more likely to experience jaundice?

A

Preemies often have inadequate amounts of liver enzymes needed to bind bilirubin, preventing its excretion in bile, making it toxic.

59
Q

What is alpha thalassemia?

A

Alpha thalassemia is characterized by decreased synthesis of alpha hemoglobin chains.

60
Q

What is beta thalassemia?

A

Beta thalassemia involves impaired synthesis of beta hemoglobin chains.

61
Q

What is sickle cell anemia and how is it inherited?

A

Sickle cell anemia is an inherited, recessive disease where two copies of the gene produce hemoglobin S (Hb-S) instead of normal hemoglobin A (Hb-A).

62
Q

What causes sickle cell anemia at the molecular level?

A

A single amino acid substitution in the beta globin chain of hemoglobin leads to polymerization of Hb-S into long fibers, causing red blood cells to take on a sickle shape and promoting hemolysis.

63
Q

What is the function of albumins in blood plasma?

A

Albumins provide osmotic pressure needed to draw water from surrounding tissue fluid into capillaries, helping maintain blood volume and pressure.

64
Q

Where are albumins produced and what percentage of plasma proteins do they account for?

A

Albumins are produced in the liver and account for most of the plasma proteins, making up 90% of plasma proteins when combined with 9 other proteins.

65
Q

What are globulins and their function in plasma?

A

Globulins are proteins in plasma; alpha and beta globulins transport lipids and fat-soluble vitamins, while gamma globulins (antibodies) are produced by lymphocytes and function in immunity.

66
Q

Where are fibrinogen proteins produced and what is their role in the body?

A

Fibrinogen is produced in the liver and is important for clot formation.

67
Q

agglutination

A
  • occurs when A-type RBCs are mixed with anti-A-type antibodies
  • occurs when B-type RBCs are mixed with anti-B-type antibodies
68
Q

What is the Rh factor and where is it found?

A

The Rh factor is a group of antigens found on red blood cells (RBCs).

69
Q

Can A/B antibodies cross the placenta?

A

No, A/B antibodies cannot cross the placenta, but Rh antibodies can.

70
Q

What can happen if an Rh-negative mother has an Rh-positive baby?

A

If an Rh-negative mother has an Rh-positive baby, it may cause issues during birth, as the mother could become sensitized and produce antibodies against the Rh antigen.

71
Q

What is Hemolytic Disease of the newborn?

A

Hemolytic Disease occurs when Rh antibodies from the mother cross the placenta in a subsequent pregnancy, causing RBC hemolysis in the fetus.

72
Q

what are the 3 steps of blood clotting

A
  1. vasocontraction
  2. formation of a platelet plug
  3. production of a web of fibrin proteins that penetrate & surround platelet plug
73
Q

What is the role of fibrinogen in blood clotting?

A

Fibrinogen is converted by thrombin into fibrin, which forms the clot.

74
Q

What pathway is involved in blood clotting in vivo (inside the body)?

A

The extrinsic pathway is involved in blood clotting in vivo.

75
Q

What pathway is involved in blood clotting in vitro (outside the body)?

A

The intrinsic pathway is involved in blood clotting in vitro.

76
Q

clot dissolution

A

plasminogen converted to
plasmin which digests
fibrin (promotes clot
dissolution)

77
Q

What is the initial treatment for heart attack patients to stop platelet clumping?

A

Heart attack patients are usually treated with chewable aspirin to stop platelet clumping before being evaluated for angioplasty or clot-dissolving drugs.

78
Q

What is a commonly used clot-dissolving medication in U.S. ER departments?

A

One of the most commonly used clot-dissolving medications in U.S. ER departments is tissue plasminogen activators (TPAs).

79
Q

What other medical conditions can tissue plasminogen activators (TPAs) be used for?

A

TPAs can also be used for stroke, blood clots, and other related conditions.

80
Q

What is STEMI?

A

ST Elevated Myocardial Infarction (STEMI) is the most severe type of heart attack, where the artery supplying blood to the heart becomes blocked.

81
Q

What class of drugs is preferred for treating STEMI, and why?

A

Fibrinolytic drugs are the preferred pharmacological class for STEMI treatment because they can achieve reperfusion, unlike drugs from other classes.

82
Q

How do fibrinolytic drugs work in STEMI treatment?

A

Fibrinolytics convert plasminogen to plasmin, which cleaves fibrin, leading to clot dissolution and restoration of blood flow to ischemic tissues.