Food-Nutrient Interactions Pt. 1 Flashcards
define: drug-nutrient interaction
the results of the action between a drug and a nutrient that would not happen with the nutrient or drug alone
define: drug metabolism
may activate or inactivate a drug; more commonly drug metabolism means breakdown/inactivation
occurs in liver and intestines
define: first pass metabolism
when the drug is absorbed via portal vein and goes into the liver
define: absorption
movement from site of administration to blood stream
define: bioavailability
degree to which a drug or other substance reaches circulation and becomes available to the target organ or tissue
define: pharmacokinetics
movement of a drug through the body by absorption, distribution, metabolism, and excretion
define: pharmacodynamics
physiologic and biochemical effects of a drug or combination of drugs; the drug’s action
define: pharmacogenetics
genetically determined variations revealed solely by the effects of drugs
factors that influence drug absorption (4)
- drug solubility and other properties
- concentration/dose
- blood flow to the GI tract (less blood, less absorption)
- altered stomach pH
factors that influence drug distribution (7)
- 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.
factors that influence drug metabolism (2)
- general organ function (liver, intestines, kidney)
- cytochrome P-450 system (and other enzymes CYP3A4)
factors that influence drug excretion (6)
- 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.
differences in sex that impact drugs in the body (3)
- altered distribution (lower body weight + lean mass)
- altered clearance (lower GFR)
- decreased metabolism (decreased activities of certain enzymes - CYP3A4)
examples of pharmacogenomics that influence metabolism (3)
- 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
drug-nutrient interaction of: Fosamax
must be taken 30-60 mins before food
presence of anything in the stomach will decrease absorption to 0%
drug-nutrient interaction of: Levothyroxine
food and coffee decrease the absorption
what is a chelation reaction?
when two compounds bind together tightly so neither can be active
what does Fosamax do?
promotes bone health
what does Levothyroxine do?
replaces T4 in the body
drug-nutrient interaction of: entacapone (Comtan)
chelates with iron supplements
what does entacapone (Comtan) do?
Parkinson drug
drug-nutrient interaction of: tetracycline + ciprofloxacin
chelates with calcium-containing foods
what do tetracycline + ciprofloxacin do?
antibiotics
drug-nutrient interaction of: Levodopa
high protein intake (and B6) will decrease absorption
nutritional factors that influence drug absorption (4)
- 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
which amino acid is the precursor to dopamine?
tyrosine
nutritional factors that influence drug metabolism (2)
- 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
what is the active compound in grapefruit juice?
furanocoumarins
what determines if a drug is impacted by grapefruit juice?
drugs that are metabolized in the intestines will have a higher impact on their concentration than those not metabolized in the intestine
how does albumin contribute to the drug’s blood distribution?
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