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DRUG METABOLISM
The liver is the major site of drug metabolism Drugs are converted from fat-soluble to water-soluble substances that can be excreted in the urine or bile Mediated by a group of mixed-function enzymes
DETOXIFICATION
Conjugation with glucuronide and sulphate Microsomal enzymes produce toxic derivatives that are immediately detoxified by conjugation with glutathione Saturation of the former and glutathione depletion in drug overdose produce hepatic damage
DRUG HEPATOTOXICITY
Damage to the liver by drugs is usually classified as Predictable (or dose-related) Non-predictable (not dose-related)
MECHANISMS
Disruption of intracellular calcium homeostasis Disruption of bile canalicular transport mechanisms Formation of non-functioning adducts (enzymedrug) Presentation on the surface of the hepatocyte as new immunogens (attacked by T cells) Induction of apoptosis Inhibition of mitochondrial function, which prevents fatty acid metabolism, and accumulation of both lactate and reactive oxygen species
CONTRIBUTING FACTORS
Chronic alcohol abusers (enzymeinducing effects) Starvation (Depletion of hepatic glutathione) Environmental factors Genetic effects
DIAGNOSIS
By exclusion of other causes. Most reactions occur within 3 months Monitoring liver biochemistry is advisable Suspected drug should be stopped immediately Liver biopsy is of limited help in confirming the diagnosis, but occasionally hepatic eosinophilia or granulomas may be seen Diagnostic challenge with subtherapeutic doses of the drug is sometimes required to confirm the diagnosis
Steatohepatitis
Fibrosis
Amiodarone,Synthetic oestrogens,Nifedipine
Methotrexate,Other cytotoxic agents,Arsenic,Vitamin A,Retinoids
Pelioses hepatis
Veno-occlusive
Hepatocanalicular Chlorpromazine, cholestasis Haloperidol, Erythromycin, Cimetidine/ranitidine, Nitrofurantoin, Imipramine, Azathioprine, Oral hypoglycaemics, Dextropropoxyphene
Hepatic tumours
Hepatocellular carcinoma
Penicillins NSAIDs
Antithyroid Quinine
Diltiazem
Anticonvulsants Phenytoin
PARACETAMOL
The toxic metabolite is N acetyl p benzoquinone It binds irreversibly to liver cell membranes In high doses paracetamol produces liver cell necrosis
HALOTHANE
Produces a hepatitis in patients having repeated exposures Mechanism is thought to be a hypersensitivity reaction Unexplained fever occurs about 10 days later Jaundice, typically with a hepatitic picture Most patients recover spontaneously High mortality in severe cases No chronic sequelae Risk is smaller with enflurane and isoflurane
STEROIDS
Cholestasis is caused by natural and synthetic oestrogens as well as methyltestosterone Interfere with canalicular biliary flow and cause a pure cholestasis Contraceptive pill is associated with gallstones, hepatic adenomas (rarely HCCs), the BuddChiari syndrome and peliosis hepatis Peliosis hepatis also occurs with anabolic steroids, consists of dilatation of the hepatic sinusoids to form blood-filled lakes
OTHER DRUGS
Phenothiazines -(e.g. chlorpromazine) can produce a cholestatic picture -Hypersensitivity reaction -Occurs within 4 weeks -Associated with fever,eosinophilia -Recovers on stopping the drug Amiodarone -steatohepatitis and liver failure
DRUG PRESCRIPTION
Removal of many drugs depends on liver blood flow and the integrity of the hepatocyte. Effect of drugs is prolonged by cholestasis Portosystemic shunting diminishes the firstpass extraction of drugs With hypoproteinaemia there is decreased protein binding of some drugs Bilirubin competes with many drugs for the binding sites on serum albumin Drugs with a central depressant action to be given cautiously in patients with portosystemic encephalopathy
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