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Physiology and Pharmacology of Nausea and Emesis Professor John Peters

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1 Physiology and Pharmacology of Nausea and Emesis Professor John Peters

2 Learning Objectives Following this lecture, students should be able to:  Provide a brief description of nausea  Describe the key events in vomiting  List the major consequences of severe vomiting  Describe the various triggers for vomiting  Be aware of the role of the chemoreceptor trigger zone (CTZ) and vomiting centre (VC) in vomiting  Know the major classes of antiemetic drugs, their clinical uses and be able to outline their proposed mechanisms of action 5-HT 3 receptor antagonists Muscarinic receptor antagonists Dopamine receptor antagonists Cannabinoids

3 Events in Vomiting  Vomiting (emesis) forceful propulsion of gastric contents out of the mouth  Is not due to stomach contraction – stomach, oesophagus and associated sphincters are relaxed  Vomiting is co-ordinated by the vomiting centre (VC) in the medulla oblogata of the brain stem Deep inhalationClosure of glottis and raising of soft palate Suspension of breathing Contraction of diaphragm and abdominal muscles compresses stomach Ejection of gastric contents Repeats of the cycle  Vomiting is frequently preceded by profuse salivation, sweating, elevated heart rate and the sensation of nausea

4 Nausea  Subjective, highly unpleasant, sensation – normally felt in throat and stomach as a ‘sinking’ sensation  Acute nausea interferes with mental and physical activity, often relieved by vomiting  Chronic nausea is greatly debilitating Movement of contents of upper jejunum, duodenum and pyloric region into the body and fundus of the stomach Contraction of upper small intestine, followed by contraction of pyloric sphincter and pyloric region of stomach Relaxed lower and upper eosophageal sphincters and oesophagus set the stage for retching and vomiting (which may, or may not, occur)  Nausea usually involves pallor, sweating and relaxation of the stomach and lower eosophagus resulting in tension in gastric and oesosphageal muscles triggering afferent nerve impulses: associated events are

5 Consequences of Severe Vomiting  Dehydration  Loss of gastric protons and chloride (causes hypochloreamic metabolic alkalosis, raising of blood pH)  Hypokalaemia. Mediated by the kidney, proton loss is accompanied by potassium excretion  Rarely, loss of duodenal bicarbonate may cause metabolic acidosis  Rarely, eosophageal damage (Mallory-Weiss tear)

6 VC = Vomiting centre CTZ = Chemoreceptor trigger zone (located in the area postrema, detects circulating emetic agents e.g. toxins, opiates, apomorphine) Triggers for Vomiting  Pain, repulsive sights, smells and emotional factors  Motion sickness and vestibular disorders  Endogenous toxins, numerous drugs, radiation  Stimuli from pharynx, G.I. tract and other viscera Medulla VC CTZ Output tovagusnerve and spinal motor neurones Medulla VC CTZ Output tovagusnerve and spinal motor neurones  Pregnancy  Intracranial pathology

7 Triggers for Vomiting VC CTZ NTS Motion (inner ear), signalling to vestibular nucleus Pain, repulsive sights, smells, emotional factors Retching, vomiting Endogenous toxins, drugs, vagal afferents Lacks blood brain barrier (BBB) Pharyngeal stimulation, gastric/duodenal distension, or irritation NTS = nucleus tractus solitarius

8 Drug- and Radiation-Induced Emesis Many classes of drug (or treatments) predictably cause nausea and vomiting  Cancer chemotherapy and radiotherapy (release of 5-HT from enterochromaffin cells in the gut)  Agents with dopamine agonist properties (e.g. used in Parkinson’s disease). Dopamine D 2 receptors are prevalent in the CTZ  Morphine and other opiate analgesics (tolerance develops)  Cardiac glycosides (e.g. digoxin)  Drugs enhancing 5-HT function (5-HT 3 receptors are prevalent in the CTZ)  Operations involving the administration of a general anaesthetic [post- operative nausea and vomiting (PONV)]

9 Major Classes of Antiemetic Drugs 5-HT 3 receptor antagonists (e.g. ondansetron)  Used to suppress chemotherapy- and radiation-induced emesis and post-operative nausea and vomiting  Block peripheral and central 5-HT 3 receptors AP (containing CTZ) and NTS Peripheral terminal in gut Central terminal AP = area postrema; NTS = nucleus tractus solitarius Vagal afferent Cytotoxic drug = 5-HT 3 receptor Vomiting centre Emesis Radiation 5-HT Circulating, or locally released 5-HT

10  Reduce acute nausea, retching and vomiting in cancer patients receiving emetogenic treatments (day 1)  Less effective during subsequent treatments (delayed phase) – improved by the addition of a corticosteroid (mechanism uncertain)  Generally well tolerated – most common unwanted effects are constipation and headaches  Not effective against motion sickness, or vomiting induced by agents increasing dopaminergic transmission

11 Muscarinic acetylcholine receptor antagonists (e.g. hyosine /scopolamine)  Used for prophylaxis and treatment of motion sickness (can be delivered by transdermal patch)  Probably block muscarinic acetylcholine receptors at multiple sites (e.g. vestibular nuclei, nucleus of the solitary tract, vomiting centre)  Direct inhibition of G.I. movements and relaxation of the G.I. tract may contribute (modestly) to anti-emetic effects  Have numerous unwanted effects resulting from blockade of the parasympathetic ANS (e.g. blurred vision, urinary retention, dry mouth) and centrally-mediated sedation

12 Histamine H 1 receptor antagonists (e.g. cyclizine + many others)  Used for prophylaxis and treatment of motion sickness and acute labyrinthitis N.b. many agents in this class also exert significant blockade of muscarinic receptors that probably contributes to their activity  Generally cause CNS depression and sedation – drowsiness may affect performance of skilled tasks  Action attributed to blockade of H 1 receptors in vestibular nuclei, nucleus of the solitary tract and area postrema

13 Dopamine receptor antagonists (e.g. domperidone and metoclopramide)  Used for drug-induced vomiting (e.g. cancer chemotherapy, treatment of Parkinson’s disease with agents stimulating dopaminergic transmission) and vomiting in gastrointestinal disorders. Use in children is restricted – consult BNF  Domperidone does not cross the blood brain barrier and is less likely to result in the many unwanted effects of metoclopramide (e.g. disorders of movement (extrapyramidal effects))  Complex mechanism of action Centrally block dopamine D 2 receptors in the CTZ Peripherally exert a prokinetic action on the oesophagus, stomach and intestine  Not effective against motion sickness Phenothiazines – which owe part of their action to dopamine D 2 blockade – are used for severe nausea and vomiting

14 Cannabinoids (e.g. nabilone)  Used ideally in in-patient setting for treatment of cytotoxic chemotherapy that is unresponsive to other anti-emetics  Decreases vomiting induced by agents stimulating the CTZ. Evidence suggests that opiate receptors are involved in drug effect  Numerous unwanted effects; drowsiness, dizziness, dry mouth, mood changes are common


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