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Manipulation of pH to increase the rate of elimination of a drug has a practical use in cases of overdose as shown by the following examples. Administration of sodium bicarbonate increases the alkalinity of the tubular filtrate therefore acidic drugs, for example aspirin and barbiturates become ionized and cannot diffuse back from the tubules to the plasma. Hence their rate of elimination is increased. This may be useful in the event of an overdose.

Binding of neurotransmitter with its receptor is very brief, but it brings about stimulation or inhibition of the post-synaptic neuron. See Figure transmission. The events that take place at a synapse, that is synthesis of neurotransmitter, storage in vesicles, release, interaction with receptors and eventual inactivation provide targets for drug action. Inactivation of a neurotransmitter can be by re-uptake into the neuron it was released from, or by the action of enzymes in the synaptic cleft.

Cells that produce glucagon are found peripherally in the islets while the predominant insulin producing cells are found in the centre. Insulin is essential for the metabolism of glucose and control of blood glucose levels, but it also has important effects on fat and protein metabolism. In the liver, insulin reduces glycogenolysis and gluconeogenesis (formation of glucose) and increases glycogen synthesis.

Mr Davies current medication is as follows: Lithium carbonate, Sodium valproate, Atenolol, Amlodipine Lisinopril, Chlorpromazine, Discuss this patient using the questions as a guide. Identify which of Mr Davies drugs are for hypertension and which are for bipolar disorder. Consider if there are likely to be any interactions between the many drugs that Mr Davies is taking.

Drugs that decrease the effectiveness of sulfonylureas include diuretics and corticosteroids. There are three other groups of drugs licensed in the United Kingdom for the treatment of NIDDM. Acarbose is an alpha glucosidase inhibitor. This intestinal enzyme is responsible for the breakdown of complex sugars into monosaccharides to enable absorption.

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Many well-established antiepileptic drugs (for example phenobarbital and benzodiaze pines) are known to facilitate the opening of GABA chloride ion channels at synapses. However, this is not the complete explanation as, for example phenobarbital is far more effective as an anticonvulsant than other barbiturates with the same enhancing effects on GABA.

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The neurotransmitter of this pathway is dopamine and loss of dopamine-containing neurons here causes Parkinsons disease. The hypothalamic-pituitary dopamine pathway inhibits the release of prolactin from the anterior pituitary gland.

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However, there is a high risk of teratogenesis and women must use adequate contraception and stop treatment for two years before conception.

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