Midterm Section 3.3 - Protein/Body Comp Flashcards

1
Q

main functions of protein/AA

A

maintenance and regulation of body functions
growth
repair and response to injury
energy (converted to glucose, converted to fat or burned as fuel)

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2
Q

thyroid hormone requires which amino acid precursor?

A

tyrosine

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3
Q

definition of an essential nutrient

A

performs an identifiable biological function
abnormality results from lack of consumption
body cannot make it, or cannot make enough to satisfy demand

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4
Q

insulin peptides are held together with

A

disulfide bonds

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5
Q

enzymes and chemicals that break down proteins

A

HCl denatures protein structures
activated pepsin hydrolyzes peptide bonds
pancreatic bicarbonate denatures pepsin
pancreatic peptidases hydrolyze peptide bonds
dipeptidases on brush border

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6
Q

SNP

A

single nucleotide polymorphisms - single change of an amino acid in sequence can create disease state, such as sickle cell anemia
heterozygous genes for sickle cell have resistance to malaria

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7
Q

PKU

A

phenylketonuria - change of phenylalanine hydroxylase, needed to create enzyme to break down phenylalanine

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8
Q

nutritional genomics categories

A

nutritional genomics - interactions of food and genes, includes:
nutrigenetics - examines how genes influence activities of nutrients
nutrigenomics - include epigenetics, examines how nutrients affect expression of genes

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9
Q

how nutrients can affect gene expression

A

nutrients can turn on or off genes, or interacting with intermediates
protein synthesis up or down regulated which directly affects disease progression or prevention

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10
Q

protein turnover in a healthy adult

A

is in equilibrium: same amount synthesized, same amount broken down

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11
Q

does increased protein intake alone drive increase muscle mass?

A

no, requires weight training or increased protein requirements due to illness/injury/stage of life/poor absorption
30g in one sitting required to trigger protein synthesis

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12
Q

percent nitrogen in protein and nitrogen balance equation

A

16%
Nitrogen balance = N intake - N fecan - N urinary

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13
Q

how ammonia is never free in the body

A

it is toxic, transferred from one amino acid to another in intermediate keto acid form
delivered to liver for urea cycle

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14
Q

AA required for urea cycle

A

arginine, required for ammonia detoxification into urea

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15
Q

nephron definition and numbers

A

working unit of the kidney
more than 1 million nephrons in one kidney

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16
Q

nephron anatomy

A

blood flows into the glomerulus where fluid and substances are absorbed in the tubule
reabsorption of nutrients and fluid along the descending tubule

17
Q

adequacy of dietary protein (3)

A
  1. adequate energy intake, otherwise amino acids will be catabolized
  2. protein quantity: official RDA is .8g per kg/day, AMDR 10-35%
  3. quality - having all EAA in relative amounts similar to need
18
Q

usual intake of protein vs. RDA
athletes recommendation
unofficial recommendation

A

100g/day vs .8g per kg/day (~56g)
1.2-2 g per kg/day, 1.7g per kg/day for female athletes
unofficial recommendation is 1.2g per kg/day

19
Q

what is a limiting amino acid

A

AA present in the lowest amount, relative to the body’s need for it
all others are comparatively present in excess and must be degraded

20
Q

DIAAS

A

Digestible Indispensable Amino Acid Score
expressed as a percent of dietary requirement relative to .66g (EAR protein) of the test protein
test protein is lowest DIAAS score
above 100 is considered excellent

21
Q

homeostasis defition

A

dynamic processes maintain constant internal environment despite changing external environment (often relies on negative feedback)

22
Q

in energy production pathways, which intermediates have a one way arrow between them? meaning?

A

pyruvate to acetyl coA, ketogenic amino acids to acetyl coA
this means that ketogenic amino acids cannot produce glucose and an excess of acetyl coA will become ketone bodies

23
Q

cellular respiration pathway (basic)
glucogenic AA pathway for energy

A

glucose (or glycogen) –> pyruvate by pyruvate decarboxylase –> acetyl coA –> krebs cycle and ATP
AA –> pyruvate –> lactase to leave cell –> back to liver to convert into glucose

24
Q

postprandial

A

fed state

25
Q

excess proteins are metabolized into:

A

carbon skeleton stored as fat or glycogen
nitrogen lost as urea

26
Q

short term fasting pathways

A

glycogen stores converted to glucose for energy
fatty acids broken down by hormone sensitive lipase and used as energy via beta oxidation (acetyl coA)

27
Q

long term fasting pathways

A
  • body protein broken down into AA (glucogenic and ketogenic)
  • fat broken down by hormone sensitive lipase and used as energy via beta oxidation (acetyl coA) or into ketone bodies from build up of acetyl coA
  • Over time of continued fasting, the body adapts to reduce amino acid catabolism and increase fatty acid catabolism into ketones and ATP
28
Q

body mass index
BMI ranges

A

kg/m^2
healthy: 18.5-25
overweight: 25-30
obese: >30

29
Q

body composition analysis methods

A
  1. Hydro densitometry - under water weighing, fat is lighter than water adipose is less dense than lean tissue)
  2. Air displacement plethysmography
  3. DEXA - x ray absorptiometry, can also be used to measure bone density
  4. waist circumference (doesn’t differentiate visceral vs adipose)
    - >= 40” (M), 35” (F)
  5. skinfold testing
  6. BIA - bioelectrical impedance
30
Q

how to screen for visceral obesity

A

MRI, CT and waist circumference

31
Q

visceral adipose tissue metabolic activity

A

adipose tissue in the omentum that are metabolically active producing inflammatory signaling molecules
increases risk of type II

32
Q

BMI is

A

generalized screening tool to categorize people into weight related risk categories
Advantage: cheap, easy and available