Ch 25 Flashcards

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1
Q

Define Metabolism

A

the sum of all body chemical reactions

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2
Q

Define Catabolism

A

is breaking down larger molecules into smaller molecules. Catabolic reactions provide more energy than they consume; they are exergonic – they liberate heat

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3
Q

Define Anabolism

A

is building up smaller molecules into larger molecules. Anabolic reactions consume more energy than they produce; they are endergonic – they consume heat

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4
Q

Metabolism and Nutrition

A
  • Metabolism is an energy-balancing act
    • ATP (adenosine triphosphate), is the energy currency unit that participates most often in living cells which couples energy-releasing catabolic reactions to energy-requiring anabolic reactions.
      • The exact reactions that occur depend on which enzymes are active in a particular cell at a particular time
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5
Q

Define nutrient

A

is a “food or liquid that supplies the body’s metabolic needs. Nutrients include: A necessary chemical (such as Na+ and other minerals) A substance that provides energy (such as lipids or carbohydrates like glucose) Something that helps in growth of new body components (such as vitamins) A substance that repairs or maintains body functions (such as proteins, or amino acids to make proteins)

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6
Q

ATP

A

ATP temporarily stores and transfers energy given off in catabolic reactions and transfers it to anabolic reactions that require energy.

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7
Q

How Do We Get Energy From ATP?

A

By breaking the high- energy bonds between the last two phosphates in ATP

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8
Q

Define Oxidation-reduction or redox reactions

A
  • Oxidation – removal of electrons
    • Decrease in potential energy
    • Dehydrogenation – removal of hydrogens
    • Liberated hydrogen transferred by coenzymes
      • Nicotinamide adenine dinucleotide (NAD)
      • Flavin adenine dinucleotide (FAD)
    • Glucose is oxidized
  • Reduction – addition of electrons
    • Increase in potential energy
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9
Q

REDOX Reactions

A
  • Chemical reactions in which a pair of electrons are exchanged as a means of transferring energy
    • Oxidation is the removal of electrons
    • Reduction is the addition of electrons
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10
Q

Oxidation Reduction Chemisty: Redox Chemistry

A
  • Oxidation and Reduction reactions always take place simultaneously.
  • Loss of electrons – oxidation
  • Gain of electrons - reduction
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11
Q

Carbohydrate Metabolism

A
  • Glucose (C6H12O6) is not just an example we happen to choose – it is indeed the body’s preferred source of fuel.
    • During digestion, polysaccharides and disaccharides are hydrolyzed into the monosaccharides glucose (80%), fructose, and galactose
    • These are absorbed into the villi of the small intestine and carried to the liver
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12
Q

Summary of Cellular Respiration

A
  • In the total oxidation of 1 molecule of glucose, 36-38 molecules of ATPs are generated, depending on the tissue.
    • Only 4 ATP are generated by substrate level phosphorylation (directly transferring a high energy phosphate from one organic molecule to another) in glycolysis and the Krebs cycle
    • Most of the ATP (either 32 or 34) is made by oxidative phosphorylation using the cytochromes of the electron transport chain and O2 as the final electron acceptor
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13
Q

Summary of Cellular Respiration

A
  • The location of events of cellular respiration are summarized in this graphic
    • Glycolysis is occurring in the cytoplasm
    • The Krebs cycle takes place in the mitochondrial matrix
    • The cytochrome proteins of the electron transport chain are embedded into the inner mitochondrial membrane
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14
Q

Cellular Respiration

A
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15
Q

Glucose Anabolism

A
  • GLYCOGENESIS - Glucose synthesized to GLYCOGEN
  • GLUCONEOGENESIS is the process of forming “new” glucose or its metabolites from fat or protein breakdown
  • GLYCOGENOLYSIS is break down of glycogen
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16
Q

Glucose storage - GLYCOGENESIS

A
  • Glucose stored as glycogen: glycogenesis
    • Polysaccharide that is the only stored carbohydrate in humans
    • Insulin stimulates hepatocytes and skeletal muscle cells to synthesize glycogen
    • 75% stored in skeletal muscle, 25% in liver
    • Glucose → G6P → G1P → Uridine diphosphate glucose →glycogen
  • and release into blood
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17
Q

Glucose release - GLYCOGENOLYSIS

A
  • Glucose release: glycogenolysis
    • Glycogen stored in hepatocytes broken down into glucose and release into blood
    • HEPATOCYTES: GLYCOGEN → G1P → G6P → GLUCOSE
    • MUSCLE: GLYCOGEN → G1P
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18
Q

Glycogenesis and glycogenolysis

A
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19
Q

Glucose formation - GLUCONEOGENESIS

A
  • No food, low glycogen stores in liver, EAT! OR
  • Triglycerides and Protein catabolism
  • Lactic acid, glycerol, amino acids converted to Pyruvic acid → glucose formation or Krebs cycle
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20
Q

Making Glucose

A
  • Gluconeogenesis is the process of forming “new” glucose or its metabolites from fat or protein (from non-carbohydrate sources). Gluconeogenesis is always taking place, but it occurs on a large scale during fasting, starving, or eating a low carbohydrate diet
  • Lactic acid, amino acids, and the glycerol portion of triglycerides are used to form glucose molecules or pyruvic acid to enter the Krebs cycle
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21
Q

Lipids

A
  • Although the word “fat” is commonly used to mean lipids, fats are, in fact, just one subgroup of lipids called triglycerides
    • Other lipids include waxes, sterols (steroid hormones), fat-soluble vitamins (such as vitamins A, D, E and K), monoglycerides, diglycerides, phospholipids, and others
      • For metabolic purposes, triglycerides are a condensed form of useable energy
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22
Q

Lipids

A
  • All triglycerides are composed of a glycerol backbone combined with 3 fatty acids
  • Fatty acids are anywhere from 4 to 24 carbons long,and they may have all single carbon-carbon bonds (saturated), or some double or triple bonds (making them unsaturated)
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23
Q

Triglycerides

A
  • are nonpolar, and therefore very hydrophobic molecules
    • To be transported in watery blood, they must first be made more water-soluble by combining them with carrier molecules called lipoproteins (produced in the liver)
      • Lipoproteins vary in their size, density, and the amount of cholesterol and protein in their make-up
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24
Q

Lipoproteins

A
  • In general, however, all lipoproteins have:
    • An outer shell that is made hydrophilic due to polar proteins (plus amphipathic phospholipid and cholesterol)
    • An inner core that is hydrophobic - a place where the triglycerides are transported
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25
Q

Lipoproteins – Docking proteins

A
  • APO C-2 (activates lipoprotein lipase)
  • APO E (hepatocyte docking protein)
  • APO B100 (docking protein for LDL to enter by receptor-mediated endocytosis)
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26
Q

Types of lipoproteins:

A
  1. Chylomicrons – transport of ingested lipids to adipose tissue for storage (APO C-2 & APO E)
  2. Very low-density lipoproteins (VLDL) – endogenous lipids, transport trigs made in liver to adipocytes for storage (APO C-2)
  3. Low-density lipoproteins (LDL) are used to transport lipids to repair cells throughout. Contain 75% of total cholesterol in blood (APO B100) (BAD)
  4. High-density lipoproteins (HDL) are used to transport excess cholesterol to the liver for elimination (GOOD)
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27
Q

Types of lipoproteins:

A
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28
Q

Sources of Cholesterol:

A

Ingestion

  • Fatty foods with or without cholesterol
  • Saturated fats (products from breaking saturated fats used by hepatocytes to make cholesterol)
                →Synthesis in hepatocytes
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29
Q

Lipid Metabolism

A
  • The term lipogenesis means fat synthesis, while lipolysis refers to the oxidation (catabolism) of lipids to yield glucose (which then yields ATP)
  • If the body has no immediate needs, lipids are stored in adipose tissue
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30
Q

Lipid Metabolism - Lipogenesis

A
  • Glucose and AAs used be liver and adipose cells to perform lipogenesis
  • If ATP needs are met, lipogenesis occurs
  • Lipogenesis stimulated by insulin
  • Excess carbohydrates, proteins, fats converted into triglycerides
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31
Q

Lipid Metabolism - Lipolysis

A

begins with separating the glycerol backbone of triglycerides from the 3 fatty acids

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32
Q

If ATP supply is LOW in cells…

A

If ATP supply is high in cells, Glyceraldehyde 3-P converted to glucose (gluconeogenesis)

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33
Q

Beta oxidation

A
  • is the process of cleaving off 2-carbon fragments from long fatty acid chains
  • The 2-carbon acetyl groups are joined to coenzyme A to form acetyl CoA for insertion into Krebs cycle
34
Q

Lipid Metabolism

A

The oxidation of triglycerides (specifically, the 3 carbon glycerol backbone), results in the formation of ketoacids, (ketone bodies) which must be eliminated by the kidneys in order to maintain homeostasis

35
Q

Ketogenesis

A
  • is a normal part of fat breakdown, but an excess will cause a metabolic acidosis
    • A mild ketoacidosis can occur even with a short 24 hour fast, and is responsible for the headaches and some of the other symptoms that are part of fasting
36
Q

Protein Metabolism

A
  • Proteins are not a primary source of energy; and unlike lipids and sugars, proteins are not stored
    • Yet a certain amount of protein catabolism occurs in the body each day as proteins from worn-out cells are broken down into amino acids
      • Some amino acids are converted into other amino acids, peptide bonds are re-formed, and new proteins are synthesized as part of the recycling process
37
Q

Protein Metabolism

A
  • In protein synthesis, transamination refers to the transfer of an amino group (NH2) to pyruvic acid or another acid in the Krebs cycle to form an amino acid
  • In protein catabolism, deamination refers to the removal of an amino group leaving the carbons of a carboxylic acid to be used to make ATP
    • Essential amino acids are the 10 amino acids that can’t be synthesized by the body
    • Non-essential amino acids are the others that can be synthesized by the body
38
Q

Metabolic Crossroads

A

Three pivotal molecules stand at the crossroads of many of the chemical reactions in carbohydrate, lipid, and protein metabolism: acetyl-CoA, glucose-6-phosphate, and pyruvic acid occupy these key entry points into, and out of the Krebs cycle

39
Q

Metabolic Adaptation:

During the Absorptive State

A

ingested nutrients enter the blood stream and glucose is readily available

40
Q

Metabolic Adaptation:

During the Postabsorptive state

A
  • absorption of nutrients from GI tract is complete and energy needs must be met by fuels in the body
    • Maintaining a steady blood glucose is critical because the nervous system and red blood cells depend solely on glucose as an energy source
      • The effects of insulin dominate
41
Q

The Absorptive State

A
  • Soon after a meal glucose, amino acids, and lipid nutrients enter the blood. Triglycerides enter the blood carried in large lipoproteins called chylomicrons. There are 2 metabolic hallmarks of this state:
    • Glucose is oxidized to produce ATP in all body cells
    • Any excess fuel molecules are stored in hepatocytes, adipocytes, and skeletal muscle cells
  • Pancreatic beta cells begin to release insulin to promote entry of glucose and amino acids into cells
42
Q

The Absorptive State

A

During the absorptive state, most body cells are concerned with producing ATP by oxidizing glucose

43
Q

The Postabsorptive State

A
  • About 4 hours after the last meal absorption in the small intestine is nearly complete and blood glucose levels start to fall. The main metabolic challenge at this point is to maintain normal blood glucose levels
    • As blood glucose levels decline, insulin secretion falls and glucagon secretion increases
      • Blood glucose levels are sustained by the breakdown of liver glycogen, lipolysis, and gluconeogenesis using lactic acid and/or amino acids
44
Q

The Postabsorptive State

A

The process is supported by sympathetic nerve endings that release norepinephrine, and by the adrenal medulla that releases epinephrine and norepinephrine directly into the blood

45
Q

Basal Metabolic Rate

A
  • The metabolic rate is the overall rate at which metabolic reactions use energy. Basal metabolic rate (BMR) is measured with the body in a quiet, fasting condition
    • Whatever the metabolic rate (other than death!), heat is a constant by-product of metabolic reactions, and can be expressed in calories
    • The BMR is 1200–1800 Cal/day in adults, or about 24 Cal/kg of body mass in adult males and 22 Cal/kg in adult females
46
Q

Body Temperature

A
  • Despite wide fluctuations in environmental temperatures, homeostatic mechanisms maintain a normal range for internal (core) body temperature at 37°C (98.6°F)
    • Peripheral tissues can be much cooler (“shell temperature 1-6°C lower)
      • Body temperature is maintained by hormonal regulation of the BMR, exercise, and sympathetic nervous system stimulation
47
Q

Heat and Energy Balance

A
  • Heat loss occurs through:
    • Conduction to solid materials in contact with the body, e.g. walking barefoot on the floor
    • Convection is the transfer of heat when a gas or liquid flows over an object, e.g. using a fan on a hot day
    • Thermal radiation is the transfer of heat in the form of electromagnetic energy (infrared, and encompassing visible light) between two bodies not in contact
    • Evaporation occurs when converting a liquid to a gas
48
Q

The Hypothalamic Thermostat

A
  • The control center that functions as the body’s thermostat is a group of neurons in the anterior part (preoptic area) of the hypothalamus that receives impulses from thermoreceptors scattered throughout the body
    • Neurons of the preoptic area generate nerve impulses at a higher frequency when blood temperature increases, and at a lower frequency when blood temperature decreases
49
Q

Thermoregulation

A
  • If the core temperature declines, skin blood vessels constrict and thyroid hormones and catecholamines (epinephrine and norepinephrine) are released. Cellular metabolism increases and shivering my ensue
  • If core body temperature rises, blood vessels of the skin dilate, sweat glands are stimulated, and the metabolic rate is lowered
50
Q

Nutrition

A
  • Nutrients are chemical substances in food that body cells use for growth, maintenance, and repair
    • There are 6 main types of nutrients
      • water , which is needed in the largest amount
      • carbohydrates
      • lipids
      • proteins
      • minerals
      • vitamins
51
Q

Nutrition

A
  • Guidelines for nutritious eating are not known with certainty. Different populations around the world eat radically different amounts and types of carbohydrates, fats and protein in their diets. Basic guidelines include:
    • Eat a variety of foods
    • Maintain a healthy weight
    • Choose foods low in fat, saturated fat and cholesterol
    • Eat plenty of vegetables, fruits and grain products
    • Use sugars in moderation only
52
Q

Nutrition:

**Essential minerals **

A
  • Essential minerals are those inorganic elements that occur naturally in the earth’s crust and are needed to maintain life. The major role of minerals is to help regulate enzymatic reactions and build bone
    • Recommendations are to eat foods that contain enough calcium, phosphorus, iron and iodine
      • Excess amounts of most minerals are excreted in urine and feces
53
Q

Nutrition:

Vitamins

A
  • Vitamins are organic nutrients required in small amounts to maintain growth and normal metabolism - they do not provide energy or serve as the body’s building materials
    • Most cannot be synthesized by us, and no single food contains all the required vitamins
    • They are divided into those that are water soluble (several B vitamins and vitamin C), and those that are fat soluble (A, D, E, K)
      • Most vitamins serve as coenzymes
54
Q

Vitamin Deficiencies

A
  • Vitamin A is needed to make the visual pigment retinal
    • Deficiency leads to night blindness and a weakened immune system
  • Vitamin D is needed for calcium absorption
    • Deficiency results in impaired bone mineralization, and leads to bone softening diseasess such as rickets in children and osteomalacia in adults
  • Vitamin K is needed to make clotting factors II, VII, and IX, X
    • A deficiency such as due to long-term antibiotic therapy or taking anticoagulant medications leads to delayed clotting times
  • Vitamin C is necessary for proper growth of connective tissues like collagen
    • Deficiency manifests as a disease called Scurvy
  • Niacin (B3) is a precursor to NAD (NADH), which plays essential metabolic roles in living cells
    • A deficiency (which is called Pellagra) results from an all corn diet, and manifests as dermatitis, diarrhea, and dementia
  • Thiamine (B1) is essential for neural function and carbohydrate metabolism
    • A deficiency (called Beriberi) results from a polished rice diet, and manifests with muscle wasting, and impaired reflexes
  • Folic Acid (vitamin B9) is needed to synthesize the bases used to replicate DNA
    • A deficiency manifests as a macrocytic anemia without nerve involvement
  • Cyanocobalamin (B12 ) is important for normal nerve function and for the formation of blood
    • A deficiency manifests as pernicious anemia, ataxia, memory loss, weakness, personality and mood changes
55
Q

Obesity

A
  • Obesity is defined as a body weight 10-20% (or more) above the desirable level because of excess fat
    • An explanation for the prevalence of obesity in our society is not universally agreed upon. In a complex interplay, many psychosocial and physiological issues appear to contribute
    • Obesity puts an individual at risk for a large number of diseases and conditions – cardiovascular disease predominant
56
Q

Factors of Obesity

A
  • Factors that are especially prevalent in western society include:
    • An abundance of good-tasting food
    • Working longer hours (less time preparing good food)
    • Fast-foods
    • Super-size portions
    • Sedentary jobs
    • Lack of Exercise
57
Q

The thermostat and food intake regulating center of the body is in the ________ of the brain.

A

Hypothalamus

58
Q

The three key molecules of metabolism are ________, ________, and ________

A
  1. glucose
  2. Pyruvic Acid
  3. Acetyl CoA
59
Q

**T or F: **Vitamins A, B, D, and K are fat‐soluble vitamins.

A

False

60
Q

T or F: Foods that we eat are used to supply energy for life processes, serve as building blocks for synthesis reactions, or are stored for future use.

A

True

61
Q

NAD+ and FAD (1) are both derivatives of B vitamins, (2) are used to carry hydrogen atoms released during oxidation reactions, (3) become NADH and FADH2 in their reduced forms, (4) act as coenzymes in the Krebs cycle, (5) are the final electron acceptors in the electron transport chain.

a. 1, 2, 3, 4, and 5
b. 2, 3, and 4
c. 2 and 4
d. 1, 2, and 3
e. 1, 2, 3, and 4
A

e. 1, 2, 3, and 4

62
Q

During glycolysis, (1) a 6‐carbon glucose is split into two 3‐carbon pyruvic acids, (2) there is a net gain of two ATP molecules, (3) two NADH molecules are oxidized, (4) moderately high levels of oxygen are needed, (5) the activity of phosphofructokinase determines the rate of the chemical reactions.

 a. 1, 2, and 3
 b. 1 and 2
 c. 1, 2, and 5
 d. 2, 3, 4, and 5
 e. 1, 2, 3, 4, and 5
A

c. 1, 2, and 5

63
Q

If glucose is not needed for immediate ATP production, it can be used for (1) vitamin synthesis, (2) amino acid synthesis, (3) gluconeogenesis, (4) glycogenesis, (5) lipogenesis.

a. 1, 3, and 5
 b. 2, 4, and 5
 c. 2, 3, 4, and 5
 d. 1, 2, and 3
 e. 2 and 5
A

b. 2, 4, and 5

64
Q

Which of the following is the correct sequence for the oxidation of glucose to produce ATP?

 a. electron transport chain, Krebs cycle, glycolysis, formation of acetyl CoA
 b. Krebs cycle, formation of acetyl CoA, electron transport chain, glycolysis
 c. glycolysis, electron transport chain, Krebs cycle, formation of acetyl CoA
 d. glycolysis, formation of acetyl CoA, Krebs cycle, electron transport chain
 e. formation of acetyl CoA, Krebs cycle, glycolysis, electron transport chain.
A

d. glycolysis, formation of acetyl CoA, Krebs cycle, electron transport chain

65
Q

Which of the following would you not expect to experience during fasting or starvation?

  a. decrease in plasma fatty acid levels
  b. increase in ketone body formation
  c. lipolysis
  d. increased use of ketones for ATP production in the brain
  e. depletion of glycogen
A

a. decrease in plasma fatty acid levels

66
Q

If core body temperature rises above normal, which of the follow‐ing would occur to cool the body? (1) dilation of vessels in the skin, (2) increased radiation and conduction of heat to the environment, (3) increased metabolic rate, (4) evaporation of perspiration, (5) increased secretion of thyroid hormones.

  a. 3, 4, and 5
  b. 1, 2, and 4
  c. 1, 2, and 5
  d. 1, 2, 3, 4 and 5
  e. 1, 2, 4, and 5
A

b. 1, 2, and 4

67
Q

In which of the following situations would the metabolic rate increase? (1) sleep, (2) after ingesting food, (3) increased secretion of thyroid hormones, (4) parasympathetic nervous system stimulation, (5) fever.

  a. 3 and 4
  b. 1, 3, and 5
  c. 2 and 3
  d. 2, 3, and 4
  e. 2, 3, and 5
A

e. 2, 3, and 5

68
Q

Which of the following are absorptive state reactions? (1) aerobic cellular respiration, (2) glycogenesis, (3) glycogenolysis, (4) gluconeogenesis using lactic acid, (5) lipolysis.

a. 1 and 2
b. 2 and 3
c. 3 and 4
d. 4 and 5
e. 1 and 5

A

b. 2 and 3

69
Q

Match the hormones with the reactions they regulate (answers may be used more than once; some reactions have more than one answer):

___ a.____gluconeogenesis

___ b.____glycogenesis

___ c.____glycogenolysis

___ d.____lipolysis

___ e.____lipogenesis

___ f.____protein catabolism

___ g.____protein anabolism

  1. insulin
  2. cortisol
  3. glucagon
  4. thyroid hormones
  5. epinephrine
  6. insulinlike growth factors
A

2,3 a.____gluconeogenesis

1 b.____glycogenesis

3,5 c.____glycogenolysis

2,4,5,6 d.____lipolysis

1 e.____lipogenesis

2 f.____protein catabolism

1,2,4,6 g.____protein anabolism

70
Q

Match the following:

___ a. ____deliver cholesterol to body cells for use in repair of membranes and synthesis of steroid hormones and bile salts

___ b. ____remove excess cholesterol from body cells and transport it to the liver for elimination

___ c. ____organic nutrients required in small amounts for growth and normal metabolism

___ d. ____the energy‐transferring molecule of the body

___ e. ____nutrient molecules that can be oxidized to produce ATP or stored in adipose tissue

___ f. ____transport endogenous lipids to adipocytes for storage

___ g.____the body’s preferred source for synthesizing ATP

___ h.____composed of amino acids and are the primary regulatory molecules in the body

___ i.____acetoacetic acid, beta‐hydroxybutyric acid, and acetone

___ j.____hormone secreted by adipocytes that acts to decrease total body‐fat mass

___ k.____neurotransmitter that stimulates food intake

___ l.____inorganic substances that perform many vital functions in the body

___ m.____carriers of electrons in the electron transport chain

  1. leptin
  2. minerals
  3. glucose
  4. lipids
  5. proteins
  6. neuropeptide Y
  7. cytochromes
  8. ketone bodies
  9. low‐density lipoproteins
  10. ATP
  11. vitamins
  12. high‐density lipoproteins
  13. very‐low‐density lipoproteins
A

Match the following:

9 a. ____deliver cholesterol to body cells for use in repair of membranes and synthesis of steroid hormones and bile salts

12 b. ____remove excess cholesterol from body cells and transport it to the liver for elimination

11 c. ____organic nutrients required in small amounts for growth and normal metabolism

10 d. ____the energy‐transferring molecule of the body

4 e. ____nutrient molecules that can be oxidized to produce ATP or stored in adipose tissue

13 f. ____transport endogenous lipids to adipocytes for storage

3 g.____the body’s preferred source for synthesizing ATP

5 h.____composed of amino acids and are the primary regulatory molecules in the body

8 i.____acetoacetic acid, beta‐hydroxybutyric acid, and acetone

1 j.____hormone secreted by adipocytes that acts to decrease total body‐fat mass

6 k.____neurotransmitter that stimulates food intake

2 l.____inorganic substances that perform many vital functions in the body

7 m.____carriers of electrons in the electron transport chain

71
Q

Match the following:

___ a.____the mechanism of ATP generation that links chemical reactions with pumping of hydrogen ions

___ b.____the removal of electrons from an atom or molecule resulting in a decrease in potential energy

___ c.____the transfer of an amino group from an amino acid to a substance such as pyruvic acid

___ d.____the formation of glucose from noncarbohydrate sources

___ e.____refers to all the chemical reactions in the body

___ f.____the oxidation of glucose to produce ATP

___ g.____the splitting of a triglyceride into glycerol and fatty acids

___ h.____the synthesis of lipids

___ i.____the addition of electrons to a molecule resulting in an increase in potential energy content of the molecule

___ j.____the formation of ketone bodies

___ k.____the breakdown of glycogen back to glucose

___ l.____exergonic chemical reactions that break down complex organic molecules into simpler ones

___ m.____overall rate at which metabolic reactions use energy

___ n.____the breakdown of glucose into two molecules of pyruvic acid

___ o.____removal of CO2 from a molecule

___ p.____endergonic chemical reactions that combine simple molecules and monomers to make more complex ones

___ q.____the addition of a phosphate group to a molecule

___ r.____the removal of the amino group from an amino acid

___ s.____the cleavage of one pair of carbon atoms at a time from a fatty acid

___ t.____the conversion of glucose into glycogen

  1. metabolism
  2. catabolism
  3. beta oxidation
  4. lipolysis
  5. phosphorylation
  6. glycolysis
  7. cellular respiration
  8. transamination
  9. anabolism
  10. lipogenesis
  11. glycogenolysis
  12. glycogenesis
  13. metabolic rate
  14. ketogenesis
  15. oxidation
  16. reduction
  17. chemiosmosis
  18. deamination
  19. gluconeogenesis
  20. decarboxylation
A

17 a.____the mechanism of ATP generation that links chemical reactions with pumping of hydrogen ions

15 b.____the removal of electrons from an atom or molecule resulting in a decrease in potential energy

8 c.____the transfer of an amino group from an amino acid to a substance such as pyruvic acid

19 d.____the formation of glucose from noncarbohydrate sources

1 e.____refers to all the chemical reactions in the body

7 f.____the oxidation of glucose to produce ATP

4 g.____the splitting of a triglyceride into glycerol and fatty acids

10 h.____the synthesis of lipids

16 i.____the addition of electrons to a molecule resulting in an increase in potential energy content of the molecule

14 j.____the formation of ketone bodies

11 k.____the breakdown of glycogen back to glucose

2 l.____exergonic chemical reactions that break down complex organic molecules into simpler ones

13 m.____overall rate at which metabolic reactions use energy

6 n.____the breakdown of glucose into two molecules of pyruvic acid

20 o.____removal of CO2 from a molecule

9 p.____endergonic chemical reactions that combine simple molecules and monomers to make more complex ones

5 q.____the addition of a phosphate group to a molecule

18 r.____the removal of the amino group from an amino acid

3 s.____the cleavage of one pair of carbon atoms at a time from a fatty acid

12 t.____the conversion of glucose into glycogen

72
Q

Before the nutrients in a cheeseburger can be absorbed in the small intestine, the complex carbohydrates, fats, and proteins contained in it must undergo

a. exergonic catabolic reactions
b. endergonic catabolic reactions
c. exergonic anabolic reactions
d. endergonic anabolic reactions
e. endergonic reactions which are both catabolic and anabolic.

A

a. exergonic catabolic reactions

73
Q

Glucose is stored in the liver and muscle in the form of

a. starch.
b. cellulose
c. triglycerides.
d. glycogen
e. glucagon

A

a. starch

74
Q

Which of the following places the events of glucose catabolism in the correct order?

a. glycolysis, formation of acetyl coA, Krebs cycle, electron transport chain reactions
b. glycolysis, Krebs cycle, formation of acetyl coA, electron transport chain reactions
c. glycolysis, anaerobic respiration, Krebs cycle, electron transport chain reactions
d. glycolysis, Krebs cycle, anaerobic respiration, electron transport chain reactions
e. formation of acetyl coA, glycolysis, electron transport chain reactions.

A

a. glycolysis, formation of acetyl coA, Krebs cycle, electron transport chain reactions

75
Q

High-density lipoproteins

a. remove excess cholesterol from the blood.
b. transport dietary lipids to adipose tissue for storage.
c. transport triglycerides to adipose tissue for storage.
d. remove fatty acids from chylomicron triglycerides.
e. deposit cholesterol in and around arteries.

A

a. remove excess cholesterol from the blood.

76
Q

Fatty acids may be converted to acetyl CoA through a process called ________.

a. dehydrogenation
b. gluconeogenesis
c. beta oxidation
d. ketogenesis
e. transamination

A

c. beta oxidation

77
Q

Essential amino acids

  1. are found in complete proteins.
  2. include phenylalanine and tryptophan.
  3. are found only in animal protein sources.

a. 1 only
b. 2 only
c. 3 only
d. 1 and 2 are correct.
1, 2, and 3 are correct.

A

d. 1 and 2 are correct.

78
Q

Which of the following may be used to produce ATP without utilizing glucose?

a. oxidation of fatty acids
b. oxidation of lactic acid
c. oxidation of amino acids
d. oxidation of ketone bodies
e. all of these choices

A

e. all of these choices

79
Q

The bulk of your total energy expenditure is due to your

a. voluntary exercise.
b. nonexercise activity thermogenesis.
c. basal metabolic rate.
d. food-induce thermogenesis.
e. energy homeostasis.

A

c. basal metabolic rate.

80
Q

Vitamins

a. serve as coenzymes
b. provide energy
c. serve as building materials within the body
d. serve as coenzymes and provide energy are correct
e. serve as coenzymes, provide energy, and serve as building materials within the body are correct

A

a. serve as coenzymes

81
Q

What is the role of oxygen in metabolism?

a. it provides energy to cells
b. it is needed in all oxidation reactions
c. it is a catalyst in the Krebs cycle
d. it is needed to produce ATP
e. it is the final electron acceptor in the electron transport system

A

e. it is the final electron acceptor in the electron transport system