Drug metabolism (1) Flashcards

1
Q

A perfect world

A
  • Patient takes their single drug regularl, takes no other drug, leads blameless healthy life
  • Theoretically patient/HCP can look forward to successful drug therapy for as long as is necessary
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2
Q

Therapeutic window

A
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3
Q

Patient life changes relevant to successful drug therapy

A
  • Greatest impact on drug therapy
  • Other drugs (practioniers idea’s)
  • Some supplements (patient’s mother’s idea)
  • Patient’s activities (patient’s idea)
  • Timeframe
  • How long do you have before a serious problem occurs
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4
Q

Deleterious drug interaction

A
  • 2 main reasons for drug therapies not working
    • PK- ADME reasons
    • PD- drug not working at receptor level
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5
Q

extremes of drug therapy

A
  • Failure of drug therapy => Anti-convulsant. Oral contraceptive
  • Drug (accumulation) toxicity => Cyclosporin renal toxicity, Terbinafine-cardiotoxicity
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6
Q

Therapeutic index

A
  • Therapeutic index = Toxic concentrations / Normal therapeutic range
  • Wide TI drugs: SSRI’s
  • Narrow TI: TCA, barbiturates, phenytoin
  • Changes in narrow TI drug concentrations are more serious
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7
Q

Clearance

A
  • Clearance is the removal of drug by all process from the biological systems (more about clearance of pharmacologically active marterial)
  • If clearance increase = Drug disappears
  • If clearance decrease = Drug accumulates
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8
Q

Clearance/Removal of drugs

Why does this happen

A
  • Drugs, toxin, food-borne chemicals, environmental chemicals threaten homeostasis
  • Even our own chemicals, that we made for ourselves, such as hormones, can threaten homeostasis
    • NB- aromatic A ring= estrogen
  • Control of cellular environment is not just everything, it is ONLY THING
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9
Q

Clearance / Removal of drug difficulties

A
  • Living systems struggle to clear Highly oil-soluble chemicals
  • In the kidney, the filtered oily agent will simply be reabsorbed
  • At the collecting tubule stage
  • The patient can only really clear water-soluble chemicals through urine and faeces
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10
Q

Threat from oil soluble agents

A
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11
Q

Threat posed by endobiotics

A
  • Hormones must be stable
  • Their stability means they are out of control
  • Some processes must be fine-tuned
  • Hormones must be inactivated quickly
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12
Q

The treat posed by xenobioitics

A
  • Membrane disruption
  • Resemble hormone
  • Environmental toxins are turning us all into girls
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13
Q

CLEARANCE/REMOVAL OF DRUGS/TOXINS

HOW DOES THIS HAPPEN

A
  • They must be made more water soluble (so the kidneys can remove them)
  • They must be made heavier (more routes of excretion)
  • Tasks carried out by the biotransformation organs: Liver, Gut, Kidneys
  • Pre-systemic metabolism/clearance
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14
Q
A
  • Liver has 2 inputs
    • Hepatic artery- from systemic blood supply
    • Hepatic portal vein- from GI tract
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15
Q

Process of drug clearance

A

*

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16
Q

How do CYP450 work?

A
  • Most biotransformation enzymes are found in the endoplasmic reticulum- P450’s
  • 60-70% of drugs are metabolised by CYP3A4
  • Fe is the key to this
  • It’s about gaining and losing electrons
  • P450 sits in the endoplasmic reticulum- which is very lipophilic- most drugs are lipophilic as well so when they’re taken up there more likely to go into the endoplasmic reticulum, so are chemically drawn to P450 sites
  • P450’s have a flexible active site can bind many shapes/functional groups (much like a hand), once bound the enzymes to draw the molecule to the Fe group in which it is then oxidised and its physicochemical properties change
17
Q

Main biotransformation human Cytochrome P450 isoforms

A
  • CYP2D6: SSRI’s, anti-psychotics, TCA, opiates
    • INDUCERS= rifampicin, Anti-convulsant
  • CYP3A4(5): Sterioids, Macrolides, Cyclosporine, Terfenadine, Statins, Methadone, Oestradiol
    • INDUCERS= Steroids, rifampicin, Anti-convulsant, St.Johns Wort
  • CYP2C: Warfarin, TCA’s, Fluoxetine, Anti-convulsant
    • INDUCERS= Rifampicin, Anti-convulsant
18
Q

Biotransformation and first pass

How much drugs into the system

A
  • Barriers: gut/liver metabolism
  • Liver/gut first pass depends on extraction ratio
19
Q

High extraction drugs

A
  • Changes in extraction has some impact on plasma levels
  • Examples
    • Pethidine, metoprolol, propranolol, lignocaine and verapamil
20
Q

Low extraction drugs

A
  • Changes in extraction has a large impact on plasma levels
  • Examples
    • Phenytoin, paracetamol, diazepam, naproxen and metronidazole
21
Q

Bioavailability (F)

A
  • How much drug reaches the plasma after an oral dose
  • F= (blood conc after IV dose - Blood Conc after oral dose) / Blood conc after IV dose
  • Depends on whether the drug is high or low extraction
  • 100mg dose and only 20 mg reaches plasma F=20%
  • If gut metabolism is prevented, F might increase to 50% so plasma levels more than double
  • If liver extraction increases, F might approach zero
22
Q

Biotransformation effects on drug therapy

A
  • Changes in biotransformation can massively influence patient welfare
  • Drug failure or drug toxicity
  • Next: How biotransformation adapts and fails to adapt to changing regimens