Food-Nutrient Interactions Pt. 1 Flashcards

1
Q

define: drug-nutrient interaction

A

the results of the action between a drug and a nutrient that would not happen with the nutrient or drug alone

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2
Q

define: drug metabolism

A

may activate or inactivate a drug; more commonly drug metabolism means breakdown/inactivation
occurs in liver and intestines

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3
Q

define: first pass metabolism

A

when the drug is absorbed via portal vein and goes into the liver

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4
Q

define: absorption

A

movement from site of administration to blood stream

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5
Q

define: bioavailability

A

degree to which a drug or other substance reaches circulation and becomes available to the target organ or tissue

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6
Q

define: pharmacokinetics

A

movement of a drug through the body by absorption, distribution, metabolism, and excretion

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7
Q

define: pharmacodynamics

A

physiologic and biochemical effects of a drug or combination of drugs; the drug’s action

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8
Q

define: pharmacogenetics

A

genetically determined variations revealed solely by the effects of drugs

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9
Q

factors that influence drug absorption (4)

A
  • drug solubility and other properties
  • concentration/dose
  • blood flow to the GI tract (less blood, less absorption)
  • altered stomach pH
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10
Q

factors that influence drug distribution (7)

A
  • volume distribution (dosage might be dependent on size of person)
  • blood flow and supply to target organ
  • drug transport (albumin in the body)
  • concentration/storage in adipose/other tissue
  • blood-brain barrier
  • inflammation (increases permeability)
  • pts body composition, age, sex, etc.
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11
Q

factors that influence drug metabolism (2)

A
  • general organ function (liver, intestines, kidney)
  • cytochrome P-450 system (and other enzymes CYP3A4)
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12
Q

factors that influence drug excretion (6)

A
  • if drug is eliminated as original compound or metabolite
  • renal excretion
  • fecal, enterohepatic circulation
  • drug doses assumes normal liver and kidney function
  • fluid status/electrolytes, urinary pH
  • pts body composition, age, sex, etc.
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13
Q

differences in sex that impact drugs in the body (3)

A
  • altered distribution (lower body weight + lean mass)
  • altered clearance (lower GFR)
  • decreased metabolism (decreased activities of certain enzymes - CYP3A4)
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14
Q

examples of pharmacogenomics that influence metabolism (3)

A
  • differences in cytochrome P450 enzymes (some higher + some lower) based on genes
  • altered activity of hepatic acetyl transferase (decreased acetylation -> increased half life; increased acetylation -> decreased half life)
  • glucose-6-phosphate dehydrogenase (G6PD) deficiency results in oxidative damage in response to certain drugs/nutrients
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15
Q

drug-nutrient interaction of: Fosamax

A

must be taken 30-60 mins before food
presence of anything in the stomach will decrease absorption to 0%

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16
Q

drug-nutrient interaction of: Levothyroxine

A

food and coffee decrease the absorption

17
Q

what is a chelation reaction?

A

when two compounds bind together tightly so neither can be active

18
Q

what does Fosamax do?

A

promotes bone health

19
Q

what does Levothyroxine do?

A

replaces T4 in the body

20
Q

drug-nutrient interaction of: entacapone (Comtan)

A

chelates with iron supplements

21
Q

what does entacapone (Comtan) do?

A

Parkinson drug

22
Q

drug-nutrient interaction of: tetracycline + ciprofloxacin

A

chelates with calcium-containing foods

23
Q

what do tetracycline + ciprofloxacin do?

A

antibiotics

24
Q

drug-nutrient interaction of: Levodopa

A

high protein intake (and B6) will decrease absorption

25
Q

nutritional factors that influence drug absorption (4)

A
  • food in GI tract (can increase or decrease, depending on the drug)
  • fiber and phytates decrease absorption
  • chelation reactions (iron and calcium) decrease absorption
  • high protein intake
25
Q

which amino acid is the precursor to dopamine?

A

tyrosine

25
Q

nutritional factors that influence drug metabolism (2)

A
  • grapefruit inhibits the cytochrome P-450 system; this increases the risk for toxicity because the drug is not inactivated
  • st john’s wort activates CYP3A4 production; this increases the risk for therapeutic failure because too much of the drug is inactivated
25
Q

what is the active compound in grapefruit juice?

A

furanocoumarins

26
Q

what determines if a drug is impacted by grapefruit juice?

A

drugs that are metabolized in the intestines will have a higher impact on their concentration than those not metabolized in the intestine

26
Q

how does albumin contribute to the drug’s blood distribution?

A

albumin binds to the drug in the blood rendering it inactive
if the pt has low albumin, the drug might have higher active concentration rates
examples: warfarin, phenytoin

27
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28
Q
A