NSC 308 Chapter 9

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67 Terms

1
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Combining glucose to make the more complex molecule of glycogen is considered ______.

anabolic

2
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What is the name of the main form of energy (not nutrient) used directly by the body?

ATP

3
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Adenosine triphosphate, also known as _______, is the main form of energy used by the body.

ATP

4
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ATP consists of ______.

  • three phosphates

  • adenosine

5
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A substance is ______ when it loses 1 or more electrons.

oxidized

6
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Match the definition with the most appropriate term.

  • Anabolism ←———→Smaller, simpler compounds used to build larger, more complicated compounds

  • Catabolism ←———→ Breaking down compounds to small units

7
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______ functions as the coenzyme nicotinamide adenine dinucleotide during intense aerobic exercise.

Niacin

8
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Which is an example of a catabolic process?

production of ATP from fatty acids

9
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Catabolic pathways produce which of the following from the production of ATP?

  • Heat

  • Carbon dioxide

  • Water

10
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Choose the best definition of cellular respiration.

Removing electrons from food molecules to obtain energy

11
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Which of the following is true about ATP?

The bonds between the phosphate groups contain energy.

12
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A substance is ______ when it gains 1 or more electrons. For example, iron does this when it gains an electron.

reduced or reduce

13
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During glycolysis, glucose is converted to two units of ______.

pyruvate

14
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Which two of the following vitamins assist dehydrogenase enzymes and therefore play a role in transferring the hydrogens from energy-yielding compounds to oxygen in the metabolic pathways of the cell?

  • Riboflavin

  • Niacin

15
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The process of converting pyruvate into acetyl-CoA occurs in a process called ______.

the transition reaction

16
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Match the term with its best definition.

  • Cellular respiration ←———→ Removing electrons from food molecules to produce energy

  • Aerobic ←———→ Making ATP in the presence of oxygen

  • Anaerobic ←———→ Making ATP without oxygen

17
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What are other names for the citric acid cycle?

  • Krebs cycle

  • Tricarboxylic acid cycle

18
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What are two functions of glycolysis?

  • To produce energy

  • To provide building blocks for synthesizing other needed compounds

19
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The transition reaction also ______, which will eventually enter the electron transport chain.

reduces NAD

20
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What part of the cell is the electron transport chain located in?

Mitochondria

21
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How many turns of the citric acid cycle does it take to process one glucose molecule?

Two

22
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Why is oxygen essential to energy production?

Oxygen is the final acceptor of electrons and hydrogen ions.

23
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How do cells without mitochondria (such as red blood cells) produce ATP?

Anaerobic metabolism

24
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During anaerobic glycolysis, which compounds can regenerate or accumulate?

  • NAD+

  • lactate

25
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The final pathway of aerobic respiration is ______.

the electron transport chain

26
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The breakdown of triglycerides into free fatty acids and glycerol is called ______.

lipolysis

27
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What molecule is the final acceptor of electrons and hydrogen ions during aerobic respiration?

Oxygen

28
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Which process is considered more efficient at converting the energy in glucose to energy stored as ATP?

Aerobic metabolism

29
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Which yields the most ATP?

Fatty acid

30
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During high intensity exercise muscle cells rely heavily on ______ glycolysis to produce ATP.

anaerobic

31
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How does carbohydrate aid fatty acid oxidation?

By providing additional oxaloacetate

32
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What is produced when oxaloacetate production is limited and the TCA cycle activity decreases?

ketone bodies

33
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Match each term with its definition.

  • Carnitine ←———→ Carrier that shuttles fatty acids into the mitochondria

  • Fatty acid oxidation ←———→ The breakdown of fatty acids to produce ATP

  • Lipolysis ←———→ The breakdown of triglycerides into free fatty acids and glycerol

34
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What is another name for fatty acid oxidation?

Beta-oxidation

35
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Which of the following are true about how carbohydrates aid in fat metabolism? 

(More than one answer may be correct)

  • Pyruvate is produced by carbohydrate metabolism, which keeps the supply of oxaloacetate high.

  • Carbohydrate makes the entire pathway for fatty acid oxidation work better.

36
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What causes the formation of acetone, which eventually leaves the body through the lungs, causing breath with a fruity smell?

Ketosis

37
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Ketoacidosis occurs as a result of ______.

uncontrolled type I diabetes

38
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The breakdown of triglycerides into free fatty acids and glycerol is called ______.

lipolysis

39
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When a person is in a state of semistarvation, the amount of glucose in the body falls. As a result, insulin production ______.

decreases

40
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Where are the branched-chain amino acids (leucine, isoleucine, and valine) mainly metabolized?

Muscles

41
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Without sufficient ______, cells cannot readily utilize glucose, resulting in rapid lipolysis and the excess production of ketone bodies.

insulin

42
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In a state of semistarvation or fasting, a decrease in the hormone ______ causes fatty acids to flood into the bloodstream and eventually form ______ bodies in the liver.

  • insulin

  • ketone

43
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What is the name of the pathway that is used to produce glucose from amino acids?

Gluconeogenesis

44
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What are two options for acetyl-CoA once it has been produced?

  • Form ketones

  • Combine with oxaloacetate in the citric acid cycle

45
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Protein metabolism begins after proteins are degraded into ______ ______.

amino acids

46
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The use of amino acids as a fuel will result in the removal of the amino group from the amino acid. This amino group, which contains nitrogen, is converted to ______. This substance must be removed from the body as a buildup of it is toxic. This substance is removed from the body through urea, which is eventually excreted in urine.

ammonia

47
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Altered glucose metabolism by cancer cells allows these cells to grow ______.

rapidly

48
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During ______ alcohol intake the body uses the MEOS pathway.

  • moderate

  • excessive

49
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Where can gluconeogenesis occur?

  • Kidney cells

  • Liver cells

50
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What can happen when calorie supplies are insufficient or exceed needs?

  • The rate at which macronutrients are converted to energy changes.

  • The type of macronutrient used to generate energy changes.

51
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Typical fatty acids ______ converted into glucose.

cannot be

52
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To prolong survival during fasting, the body goes through which of the following adaptations?

  • Slowing of metabolic rate

  • Nervous system uses less glucose

  • Reduction in energy requirements

53
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What organ is responsible for the preparation of the amino groups for excretion in the urine through the urea cycle?

Liver

54
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Cancer cells use glycolysis and produce ______.

lactate

55
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Identify the consequences of feasting.

  • increased burning of glucose for energy

  • increased insulin production

  • fat accumulation

56
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The MEOS pathway is used during moderate to excessive alcohol consumption to prevent the toxic effects of ______.

  • alcohol

  • acetaldehyde

57
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Fasting and feasting ______ metabolism.

both affect

58
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Lean body mass that declines below 50% (catabolism) due to fasting will result in ______.

death

59
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The Advisory Committee on Heritable Disorders in Newborns and Children recommends ______.

screening for 36 core conditions

60
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The result of feasting is the accumulation of body ______.

fat

61
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People with PKU need to avoid foods containing high amounts of ______.

phenylalanine

62
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In galactosemia, a buildup of galactose in the blood can lead to ______.

  • intellectual disability

  • bacterial infections

  • cataracts

63
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What is the main purpose of newborn screenings?

Identify infants with genetic and metabolic disorders

64
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Which of the following foods should someone with PKU avoid?

  • Meats

  • Milk

  • Eggs

65
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The most common forms of glycogen storage disease lead to ______.

  • liver enlargement

  • poor physical growth

66
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The genetic disease which results in a reduction of the metabolism of galactose to glucose is called ______.

galactosemia

67
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The genetic disease in which the liver is unable to convert glycogen to glucose is called ______.

glycogen storage disease