GF - Nutrients & Drug absorption Flashcards

(30 cards)

1
Q

carbohydrates

A

Diet contains disaccharides and complex polymers (starch and sucrose)

All carbs are broken down into monosaccharides & absorbed in the small intestine

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2
Q

What breaks down glucose polymers to disaccharides?

A

amylase

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3
Q

What breaks down disaccharides to monosaccharides?

A

maltase, surcrase, lactose

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4
Q

examples of glucose polymers

A

starch, glycogen

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5
Q

disaccharides examples

A

Glucose + Glucose: Maltose
Glucose + Fructose: Sucrose
Glucose + Galactose: Lactose

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6
Q

monosaccharides examples

A

Glucose, Fructose, Galactose

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7
Q

name transporters that transport fructose, glucose and galactose through the intestinal fluid to the capillary:

A

SGLT2
GLUT5
GLUT2

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8
Q

Decreased lactase activity is associated with a condition known as ______ __________

A

lactose intolerance

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9
Q

what stops disaccharides from converting into monosaccharides?

A

Lactase

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10
Q

What are proteins broken down into and where are they absorbed?

A

di/tri peptide & absorbed in small intestine

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11
Q

Proteins > smaller peptides (what enzyme?)

A

endopeptidase

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12
Q

smaller proteins > di/tri peptides. amino acids (what enzyme?)

A

exopeptidase

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13
Q

transporters of protein that transports them into the intentinal fluid (aminoacids) and capillary (di/tri peptides)

A

a.a - sodium co-transporter

di/tri - H+- PepT

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14
Q

Most lipids are __________ and must be emulsified to facilitate digestion in the aqueous environment of the intestine

A

hydrophobic

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15
Q

how are micelles formed?

A

bile salts coat lipids to make emulsions

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16
Q

describe micelles

A

small disks with bile salts,
phospholipids, fatty acids, cholesterol,
and mono- and diglycerides

17
Q

nutrient digestion step by step

A
  1. micelles formed
  2. lipase and colipase digest triclycerides
18
Q

Nucleic acid polymers (DNA & RNA) digest into ????? by pancreatic and intestinal enzymes and are absorbed via active transporters.

A

amino bases and monosaccharides

19
Q

The fat-soluble vitamins

A

A, D, E, and K; are absorbed in the small intestine along with fats.

20
Q

The water-soluble vitamins

A

C and most B vitamins; are absorbed by mediated transport.

21
Q

B12 (seafood, milk, meat)

A

intestinal transporter for B12 is found only in the ileum and recognizes B12 only when the vitamin is complexed with a protein called intrinsic factor, secreted by the same gastric parietal cells that secrete acid)

22
Q

Electrolytes

A

Sodium, potassium, chloride and water are absorbed through various pathways

paracellular diffusion

23
Q

Drug absorption: 1. passive diffusion

A

FACTORS::

a) Rate of diffusion
-surface area
-thickness of the membrane
-molecular size & lipid solubility of the drug (diffusion constant)
what is rate of diffusion moving from GI tract to blood

b) Concentration of drug [D]/amount transfer
Transfer rate
Residence time at membrane

24
Q

drug absorption: 2. active diffusion

A

REQUIRE carrier

Low lipid soluble (hydrophilic) drugs use transporters

Organic anion transporters (OATs)
Organic cation transporters (OCTs)

25
What will cross lipid bilayers by PASSIVE DIFFUSION?
un-ionised drugs (weak acids or weak bases)
26
Factors affecting ionisation
pH (i.e. concentration of H+ ions) pKa of drug (pH at which 50% of molecules are in each state)
27
what is the pH i mouth stomach SI
7.4 1.5 5.3
28
factors influencing drug absorption
G.I. motility G.I. secretions & enzymes Drug-food/supplement interactions Differences in luminal pH along the GI tract Surface area per luminal volume Blood perfusion Presence of bile and mucus The nature of epithelial membranes
29
Advantages of G. I absorption (physiological)
Large surface area for passive diffusion Range of pH environments promotes the uptake of weak acids/bases Richly vascularised (high blood supply) Long tract and long dwell time Some active transport (e.g. Levodopa taken up by phenylalanine transporter) Small intestine is a major site for drug absorption
30
Kinetics of absorption (oral, intravenous, oral compromised) How well us drug absorbed in body?
Bioavailability (F): measure of proportion of dose absorbed, compared to I. V. (same) dose F= AUC of oral/AUC of I.V (for oral drug) Time to peak (tmax): time required to reach maximum drug concentration in plasma (is a measure of rate of absorption) tmax (oral)