NDFS 200 Flashcards

Chapter 9 (36 cards)

1
Q

vitamins synthesized

A

-cannot be synthesized by the body
-must be associated with a deficiency-related

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2
Q

stages of converting food to energy

A
  1. digestion: breakdown of complex molecules to their component building blocks
  2. conversion of building blocks to acetyl-CoA (or other simple intermediates)
  3. Metabolsims of acetyl-CoA to CO2 and formation of ATP
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3
Q

metabolism

A

all net reactions

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4
Q

anabolic

A

build larger molecules

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5
Q

catabolic

A

breaks down larger molecules

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6
Q

adenosine triphosphate (ATP)

A

-gnerally accepted energy storage molecule
-contains nucleotide base adenosine, ribose and three phosphates
-energy released by hydrolyzing phosphates

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7
Q

how much ATP is in the body?

A

-100 g
-body resynthesizes 40 kg/day

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8
Q

redox reactions

A

-carbohydrates, amino acids, and fats are oxidized to produce ATP

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9
Q

oxidation

A

when a molecule/atom loses one or more electrons

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10
Q

reduction

A

when a molecule/atom gains one or more electrons

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11
Q

what vitamins are key in biologic redox reactions?

A

niacin and riboflavin

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12
Q

what is produced by cellular respiration?

A

ATP

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13
Q

what does respiration remove from macronutrients?

A

electrons

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14
Q

carbohydrate catabolism overview

A

-glycolysis
-bridge reaction
-citric acid cycle
-electron transport chain

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15
Q

glycolysis

A

-glucose is converted to pyruvate
-requires 2 ATPs for a activation
-Produces 4 ATPs (Net 2 ATPs) and 2 NADH

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16
Q

bridge reaction

A

-pyruvate dehydrogenase
-this step is irreversible
-requires 4 B-vitamins
- Niacin
-Riboflavin
-thiamin
-pantothenic acid

17
Q

citric acid cycle

A

-acetyl CoA reacts with oxaloacetate to form citrate
-takes 2 turns to metabolize 1 molecule of glucose
-yeilds:
6 NADH
2FADH2
2 GTP (converted to a

18
Q

Electron transport chain

A

-90% of the ATP produced by glucose catabolism is by the ETC
-transfer electrons to pump hydrogens and form a proton gradient that can then be used to form ATP
-requires iron and copper
-ultimately oxygen accepts the electrons and is reduced to form water

19
Q

Anaerobic Respiration

A

-pyruvate is converted to lactate
-recycled NADH to NAD to enable further glycolysis

20
Q

Cori Cycle

A
  1. in the absence of oxygen, muscle produces lactate from pyruvate
  2. lactate leaves the muscle via blood and enters the liver
  3. liver enzymes convert lactate to glucose using ATP
  4. glucose returns to the muscle
21
Q

anaerobic metabolisms

A

-yeilds only 5% of potential ATP from glucose
-concentration of NAD drops
-to maintain glycolysis, NAD is regenerated
-pyruvate is converted to lactate (muscle fatigue)
-produces a net f 2 ATP, 2 NADH+H+

22
Q

aerobic metabolism

A

-yeilds 40% of potential energy from glucose
-requires sufficient oxygen, more ATP produced
-leads to pyruvate, then to TCA and ETS to CO2, H2O

23
Q

Sources of fatty acids

A

-dietary
-from adipose tissue
-hormone-sensitive lipase

24
Q

fatty acid transport

A

-into the cell through passive diffusion
-inot mitochondria by covalent linkage to carnitine

25
beta-oxidation
-activation of fatty acid by attaching CoA -hydrolyze ATP to AMP and pyrophosphate
26
beta oxidation overview
-oxidize -hydrate -oxidize -hydrolyze
27
how carbohydrates aid in fat
-compounds in the TCA cycle are used in other biosynthetic pathways -depeletion of TCA components slows down the reations -TCA components are replaced by carbohydrates (and amino acids)
28
ketone bodies
-often from a hormone imbalance (too little insulin-diabetes) -low carbohydrate diet -used by other tissue -fruity smell -blood can become acidic -fasting-decrease in insulin, increase in fat degradation
29
protein metabolsim
-takes place in the liver except branch chain amino acids (muscle) -starts with removal of amino group (deamination or trans animation-requires vitamin B6) -glucogenic amino acids (alanine, glycine, cysteine, serine, asparagine, histidine, glutamine, isoleucine, methionine, proline, valine, phenylalanine, and threonine) -ketogenic amino acids (leucine, lysine, isoleucine, tryptophan, tyrosine and phenylalanine)
30
urea cycle
-ammonia is toxic to the brain -urea cycle occurs in hepatic cells (liver) in Both the cytosol and mitochondria -NH3 + R-NH2 + CO2 -> Urea
31
gluconeogenesis
-occurs in kidney and liver -starts in mitochondria with the formation of oxaloacetate -not possible from fatty acids
32
regulation of energy metabolism
-ATP/ADP ratio -enzyme **expression level **activity -hormones **insulin, glucagon, etc. -vitamins and minerals
33
postprandial fasting (0-6 hours after eating)
-use glycogen -fatty acids from adipose -break down lean tissue to utilize glycogenic amino acids to make glucose for the brain
34
short term fasting (3-5 days)
-no carbohydrate left -lean muscle continues to be broken down-provides 90% of the glucose -10% of glucose comes from
35
long term fasting (5+ days)
-no carbohydrate left -metabolsim slows -brain uses more ketone bodies -less glucose -death occurs when lean body mass decreases below 50%
36