Lecture 14: Pharmacology of Drug Treatment in the Liver Flashcards

1
Q

what do LFTs (liver profiles) measure

A

measure serum levels of liver enzymes

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2
Q

what does elevated ALP/GGT indicate

A

obstructive (cholestatic) condition e.g. PSC, PBC, biliary obstruction

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3
Q

what does elevated AST/ALT indicate

A

hepatitic condition i.e. hepatitis

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4
Q

what is the most common cause for isolated T. bilirubin

A

Gilbert’s disease

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5
Q

why might a very cirrhotic liver give a relatively normal liver profile

A

not enough hepatocytes to release any transaminases (enzymes) anymore

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6
Q

what liver functions are measured in a liver profile

A
  • protein formation of albumin

- prothrombin time/INR –> good measure of vit K activity of coagulation factors

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7
Q

name 3 reasons albumin levels might decrease

A
  • not enough in diet
  • losing albumin in gut and kidneys
  • liver not making enough albumin
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8
Q

what is the bioavailability of a drug

A

the fraction of the drug that makes it through the gut wall, through the portal system and into the liver, then eventually through to the SYSTEMIC SYSTEM

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9
Q

what is meant by phase 1 reactions? what is its purpose?

A

preparation reaction carried out by large isoenzyme family (74) of CYP450 monooxygenase –> catalyse redox or hydrolytic reactions to a molecule to form more chemically reactive products

  • may be pharmacologically active
  • may be toxic/carcinogenic

enables easy conjugation of a substituent group (phase 2 reaction) to make the molecule more water soluble and ready for excretion

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10
Q

name the enzyme enducers

A

PC BRAGS

  • phenytoin
  • carbamazepine/cigs
  • barbituates (brussel sprouts)
  • rifampicin
  • alcohol
  • glucocorticoids
  • St John’s Wort
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11
Q

how can water-soluble molecules be eliminated

A

in bile and urine

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12
Q

how do enzyme inducers work

A

work at a genetic level –> induce hepatocytes at a nuclear level to transcribe more CYP450s –> takes time to impact likewise takes time to calm down

  • more catalytic enzymes –> faster processing of molecules
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13
Q

what are phase 2 reactions

A

conjugation of water-soluble moiety to another molecule, making the original molecule change its shape, structures and function…it becomes more water soluble (polar)

  • tends to reduce activity of original parent compound
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14
Q

substitute groups conjugated in phase 2 reactions

A
  • glucuronyl
  • sulfate
  • methyl
  • acetyl
  • glycyl
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15
Q

what enzymes carry out conjugation reaction of phase 2

A

transferase enzymes

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16
Q

summarise liver drug metabolism

A
  • drugs undergo phase 1 and 2 reactions
  • phase 1 CYP450 monooxygenases create more reactive molecule
  • phase 2 conjugation sticks water soluble (polar) moiety onto molecule to enable excretion in bile or urine
17
Q

what enzymes do hepatotoxic drugs tend to affect most

A

transaminases ALT and AST

18
Q

name some common hepatotoxic drugs

A
  • alcohol
  • excessive paracetamol
  • statins
  • methotrexate
  • amiodarone
  • chlorpromazine (obstructive jaundice)
  • halothane (immune mediated)
  • isoniazid
19
Q

what is the most common cause of drug induced liver failure

A

paracetamols

20
Q

how does paracetamol cause liver failure

A

in excessive doses (overdose) usual conjugation pathways become overwhelmed and remaining paracetamol is oxidised into toxic metabolite NAPBQI (N-Acetyl-p-benzoquinoneimine)

  • normal doses safe
21
Q

manifestations of cirrhosis

A
  • ascites
  • encephalopathy
  • coagulation
  • spider nevi
  • hepatorenal syndrome
  • varices/ portal hypertension
22
Q

define ascites

A

build up of fluid in abdominal cavity

23
Q

name the system for determining how severe their cirrhosis is

A

Child-Turcotte-Pugh Scoring System

  • Child class A –> 5-6points
  • Child class B –> 7-9points
  • Child class C –> 10-15points
24
Q

name some non-pharmacological treatments for ascites

A
  • sodium restriction
  • paracentesis
  • bonnano catheter
  • transjugular intrahepatic portosystemic shunt (TIPS)
25
Q

name a pharmacological treatment for ascites

A

diuretics

26
Q

name two diuretics used for ascites treatment and their MoA

A
  • spironolactone –> blocks the aldosterone receptor in distal tubule
  • furosemide –> loop diuretic; inhibits Na/K/2Cl carrier in luminal membrane in Loop of Henle

work together very well

27
Q

outline some possibilities for hepatic encephalopathy

A
  • excess ammonia from bacteria in GIT not being converted to urea therefore making it into systemic circulation
  • excess GABA (neuroinhibitory substance) or neurosteroids building up in brain
28
Q

outline some treatment methods for hepatic encephalopathy

A
  • treat precipitant –> avoid high protein meals, avoid GI bleeding, avoid constipation (large doses of lactulose - reduce time bacteria has to make ammonia and inhibits formation of ammonia)
  • treat malnutrition –> high doses of thiamine, vit B and C to protect brain - Pabrinex
  • antibiotics –> if pain in abdomen and suspect spontaneous bacterial peritonitis
  • hepa merz (L-ornithine-L-aspartate) –> dietary supplement that promote urea reduction
29
Q

define cirrhosis-related coagulopathy

A

increased prothrombin time

30
Q

how is coagulopathy treated

A

treated w/ vit k (phytomenadione) or if bleeding give prothrombin complex (activated clotting factors)

31
Q

name on issue of hepatorenal syndrome

A

splanchnic vasodilatation (decreased vascular resistance) which increase portal hypertension, changing direction of blood flow away from kidneys

32
Q

outline a treatment for hepatorenal syndrome

A

can use ADH receptor selective vasoconstriction to redirect blood flow and reduce splanchnic vasodilatation