CB - Excretion Flashcards

1
Q

What are some features of CYTOCHROME-P450 enzyme? (6)

A
  1. Membrane-bound
  2. Part of the endoplasmic reticulum
  3. Occurs in phase 1 metabolism
  4. Haemoprotein containing Fe
  5. Catalyses oxidation of drug through binding with substrates O2 or CO
  6. Belongs to a class of enzymes called monooxygenases
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2
Q

What are compounds that induce (2) and inhibit (3) cytochrome P450 enzyme?

A

Inducible by:

  • DRUGS- Phenobarbitone
  • ENVIRONMENTALLY- Smoking

Inhibited by:

  • Cimetidine
  • Quinine
  • Grapefruit juice
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2
Q

What are examples of non-P450 oxidations? (2)

A
  • MAO
  • ALCOHOL DEHYDROGENASE
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3
Q

In which organs do P450-mediated reductions occur?

A

Mainly in the liver

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4
Q

What are examples of hydrolysis reactions in drug metabolism?

A

Hydrolysis of:

  • Esters
  • Amides
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5
Q

Explain the difference in metabolism between Procaine and Procainamide?

A

Procaine is acted upon by ESTERASES

  • Fast acting = rapid hydrolysis and short duration of action

Procainamide is acted upon by AMIDES

  • Slow acting = slow hydrolysis and longer duration of action
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6
Q

What are the three types of conjugation reactions in Phase 2 metabolism?

A
  1. Glucuronidation
  2. Sulphation
  3. Acetylation
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7
Q

What occurs in Glucuronidation?

A

Glucuronic acid C6H9O6 replaces the H in -OH, -COOH, -NH2, -SO2NH-, -SH to give water-soluble inactive products

Requires activation of carbohydrate (UDPGA)

UDP-glucuronyl transferase (UDPGT) acts

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8
Q

What occurs in Sulphation?

A

A sulphate group –SO3- replaces the H in R-OH, ArOH, ArNH2, ArNHOH to give very water-soluble inactive - usually - excretory products

Sulpho-transferase

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9
Q

What occurs in Acetylation?

A

Acetate CH3CO2- replaces the H in -NH2, -SO2NH2, -NHNH2 inactivates the functional group but no real increase in water solubility

Requires activation of acetate (AcetylCoA)

N-acetyl transferase transfers the acetate to the drug

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10
Q

What are 6 variables affecting metabolism?

A

SPECIES

rats and mice differ from humans

  • higher cardiac output
  • greater liver blood flow
  • higher rates of metabolism

GENETICS
Enzyme defects

ENVIRONMENT
Other drugs

ELDERLY
Size of liver and blood flow decreases with age

  • Reduced phase 1 metabolism

YOUNG
Drug metabolising enzymes are immature in the neonatal liver

  • First-pass metabolism is low

LIVER DISEASE
Anatomical changes that impair rapid uptake of lipid-soluble drugs

  • Intracellular enzyme activity is reduced
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11
Q

What are the 3 main routes of excretion?

A

Lungs

  • Volatile compounds only e.g. general anaesthetics, alcohol

Kidneys - urine

  • Low molecular weight (20kDa) + water soluble (glomerular F)
  • Active secretion + filtration of unbound (tubular secretion)
  • Reabsorption – affected by urine pH (reabsorption)

Bile

  • High molecular weight (>50kDa) – esp. conjugates
  • Biliary metabolites may be metabolised in gut lumen and reabsorbed - entero-hepatic circulation
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12
Q

What occurs in Glomerular Filtration? (2)

A
  1. Small molecules are filtered through pores 7-8nm diameter
  2. Protein-bound drug is not filtered, but some dissociates when water is reabsorbed from the tubule
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13
Q

What are features of pH-dependent reabsorption? (6)

A
  • All lipid-soluble compounds are reabsorbed from the tubule and returned to the circulation until they are metabolised to water-soluble products
  • Drug concentrates in the fluid in which it is most ionised (pH.partioning)
  • Weak acids can be reabsorbed into the plasma
  • Weak bases are excreted in the urine
  • NaHCO3 increases urine pH (alkalinases) and enhances elimination of acids
  • NH4Cl reduces urine pH (acidifies) and enhances elimination of bases
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14
Q

What are features of Renal Tubular Secretion? (3)

A
  • Different transporters for acids and bases
  • An active process that can strip a drug from protein-binding sites
  • Many drug conjugates are substrates for active secretion
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15
Q

What occurs in Biliary Excretion and Entero-hepatic circulation?

A

Biliary excretion
Drugs are eliminated in bile mixed with Bile salts

  • Large drugs or drug conjugates are eliminated in bile
  • Elimination depends on the release of bile from the gall-bladder (which is not present in the rat)

Entero-hepatic circulation

  • The drug may be reabsorbed from the intestine and carried back to the liver via the hepatic portal vein
  • A drug conjugate may be hydrolysed in the intestine back to the drug or an hydroxy- metabolite and then carried back to the liver via the hepatic portal vein