Physiology and Pharmacology of Nausea and Emesis Flashcards

1
Q

nausea

A

subjective, highly unpleasant, sensation

normally felt in throat and stomach as a ‘sinking’ sensation

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2
Q

acute nausea

A

mental and physically activity often relieved by vomiting

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3
Q

chronic nausea

A

greatly debilitating

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4
Q

signs and symptoms of nausea

A

pallor
sweating
excessive salivation

relaxation of the stomach and lower oesophagus

upper intestinal contractions, forcing intestinal contents by reverse peristalsis into the stomach

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5
Q

nausea and vomiting

A

can occur in isolation

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6
Q

retching

A

rhythmic reverse peristalsis of the stomach and oesophagus

forceful, involuntary contraction of abdominal muscles and the diaphragm
cardiac portion of stomach pushed into the thorax

upper intestinal contractions, forcing intestinal contents by reverse peristalsis into the stomach

pallor, sweating, excessive salivation (protective against vomit)

‘dry’

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7
Q

vomiting = emesis

A

forceful expulsion of gastric/intestinal contents out of the mouth

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8
Q

overall events of vomiting

repeated

A

suspension of intestinal slow wave activity

retrograde contractions from ileum to stomach

suspension of breathing (closed glottis - prevents aspiration)

relaxation of LOS-contraction of diaphragm and abdominal muscles compresses stomach

ejection of gastric contents through open UOS

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9
Q

OS

A

oesophageal sphincter

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10
Q

coordination of vomiting

A

by the vomiting centre (VC) in the medulla oblongata of the brain stem

VC = group of interconnected neurones within the medulla that are driven by a central pattern generator (CPG) that in turn receives input from the NTS

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11
Q

stimuli inducing vomit

A

toxic materials in gut lumen

systemic toxins

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12
Q

enterochromaffin cells in mucosa

A

stimulated by stimuli

release mediators -
5-HT

causes depolarisation of sensory afferent terminals in mucosa -
via 5-HT3 receptor

acts on vagus nerve
action potential discharge in vagal afferents to brain stem

co-ordination of vomiting by the ‘vomiting centre’

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13
Q

vomiting reflect

A

important areas

chemoreceptor trigger zone within the area postrema

nucleus tractus solitarius

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14
Q

absorbed toxic materials and drugs in blood

A

stimulate

CTZ within the AP of brainstem (lacks an effective blood brain barrier (BBB))

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15
Q

mechanical stimuli

Pathological within the GI tract or other visceral organs

A

stimulate

vagal afferents to brainstem (CTZ and NTS)

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16
Q

vestibular system

motion sickness

A

signalling through …

vestibular nuclei

CTZ

17
Q

stimuli within the CNS

pain, repulsive sights and odours, fear anticipation, psychological factors

A

signalling through …

cerebral cortex, limbic system

medulla

18
Q

motor outputs in vomiting

A

located in the brainstem

19
Q

vagal efferents

A
oesophagus (shortening)
stomach (proximal relaxation)
small intestine (giant retrograde contraction)
20
Q

somatic motor neurons

A

anterior abdominal muscle (contraction)

diaphragm (contraction)

21
Q

autonomic/somatic effects

A

heart - increase rate and force
salivary glands - increased secretion
skin - pallor, sold sweating

sphincters of bladder and anus - constriction

22
Q

consequences of severe vomiting

A

dehydration

loss of gastric protons and chloride - causes hypochloraemic 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 oesophageal damage

23
Q

major classes of antiemetic drugs

A

5-HT3 receptor antagonists
(-setrons)

used to suppress chemotherapy and radiation induced emesis and post-operative nausea and vomiting

block peripheral and central 5-HT3 receptors

24
Q

miscarinic acetylcholine receptor antagonists

hyoscine/scopolamine

A

used for prophylaxis and treatment of motion sickness

probably block muscarinic acetylcholine receptors at multiple sites

direct inhibition of GI movements and relaxation fo the GI tract may contribute (modestly) to antiemetic effects

unwanted effects from blockage of the parasympathetic ANS
blurred vision, uriniary retention, dry mouth

25
Q

histamine H1 receptor antagonist

cyclizine

A

used for prophylaxis and treatment of motion sickness and acute labyrinthitis and nausea and vomiting caused by irritants in the stomach

less effective against substances that act directly on CTZ

action attributed to blockage of H1 receptors in vestibular nuclei and NTS

generally cause CNS depression and sedation - drowsiness may affect performance of skilled tasks