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VOMITING
(Emesis)
Mechanism of vomiting
Three phases:
NAUSEA, RETCHING and VOMITING
Receptors and neurotransmitters involved in mediating vomiting:
Structures Receptors Agonists Antagonists
Area
postrema
CTZ
D2 Apomorphine
L-DOPA
Antidopaminergi
c drugs
Vestibular
nuclei
N. tractus
solitarius
M, H1 Cholinomimetics Scopolamine
Histamine Dramamine
Vomiting
center
M
(e.g.,
physostigmine)
Cholinomimetics Scopolamine
Vagal
sensory
nerve
endings
5-HT3 Serotonin Ondansetron
Granisetron
Tropisetron
Causes of Vomiting
Drug/treatment - induced Cancer chemotherapy
Opiates, Nicotine
Antibiotics, Radiotherapy
Labyrinth disorders
Endocrine causes
Infectious causes
Increased intracranial
ressure
Post-operative
CNS causes
Motion, Meniere's disease
Pregnancy
Gastroenteritis
Viral labyrinthitis
Haemorrhage, Meningitis
Anaesthetics, Analgesics
Procedural
Anticipatory
Migraine, Bulimia nervosa
Drugs causing emesis
a. Drugs acting on CTZ.
• apomorphine
• emetine (when given parenterally and only at
large doses)
• L-DOPA
• estrogens (morning sickness of pregnancy)
• ergot alkaloids
• cardiac glycosides
• opiates
• cancer chemotherapeutic agents
b. Drugs acting locally on the G-I tract.
• Activate enterochromaffin cells
• secrete serotonin
• acts on the 5-HT3 receptors
• at the nerve endings of the vagal sensory fibers.
• The afferent fibers transmit excitation to the N.
tractus solitarius,
• which in turn activates the VC.
• These drugs are traditionally called "local
irritants".
• Ipecac, zinc salts, copper sulfate,
Cancer chemotherapeutic agents and
radiation therapy
• produce free radicals
enterochromaffin cells
serotonin.
• also stimulate CTZ receptors
The management of
Nausea &Vomiting
• Identification and elimination of the
underlying cause if possible
• Control of the symptoms if it is not
possible to eliminate the underlying
cause
• Correction of electrolyte, fluid or
nutritional deficiencies
Antiemetics
Class Drug
Anti-cholinergic
Anti-histamine
Dopamine antagonists
nabiloneCannabinoid
Corticosteroid
Histamine analogue
5HT3-receptor antagonist
scopolamine (L-hyoscine)
cinnarizine
cyclizine
promethazine
metoclopramide
domperidone
droperidol (withdrawn 2001)
haloperidol
dexamethasone
betahistine
granisetron
ondansetron
tropisetron
Vomiting.3
Vomiting.3
Vomiting.3
Vomiting.3
Vomiting.3

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Vomiting.3

  • 2.
  • 3.
  • 4. Mechanism of vomiting Three phases: NAUSEA, RETCHING and VOMITING
  • 5.
  • 6.
  • 7.
  • 8. Receptors and neurotransmitters involved in mediating vomiting: Structures Receptors Agonists Antagonists Area postrema CTZ D2 Apomorphine L-DOPA Antidopaminergi c drugs Vestibular nuclei N. tractus solitarius M, H1 Cholinomimetics Scopolamine Histamine Dramamine Vomiting center M (e.g., physostigmine) Cholinomimetics Scopolamine Vagal sensory nerve endings 5-HT3 Serotonin Ondansetron Granisetron Tropisetron
  • 9.
  • 11. Drug/treatment - induced Cancer chemotherapy Opiates, Nicotine Antibiotics, Radiotherapy Labyrinth disorders Endocrine causes Infectious causes Increased intracranial ressure Post-operative CNS causes Motion, Meniere's disease Pregnancy Gastroenteritis Viral labyrinthitis Haemorrhage, Meningitis Anaesthetics, Analgesics Procedural Anticipatory Migraine, Bulimia nervosa
  • 12. Drugs causing emesis a. Drugs acting on CTZ. • apomorphine • emetine (when given parenterally and only at large doses) • L-DOPA • estrogens (morning sickness of pregnancy) • ergot alkaloids • cardiac glycosides • opiates • cancer chemotherapeutic agents
  • 13. b. Drugs acting locally on the G-I tract. • Activate enterochromaffin cells • secrete serotonin • acts on the 5-HT3 receptors • at the nerve endings of the vagal sensory fibers. • The afferent fibers transmit excitation to the N. tractus solitarius, • which in turn activates the VC. • These drugs are traditionally called "local irritants". • Ipecac, zinc salts, copper sulfate,
  • 14. Cancer chemotherapeutic agents and radiation therapy • produce free radicals enterochromaffin cells serotonin. • also stimulate CTZ receptors
  • 15.
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 23. • Identification and elimination of the underlying cause if possible • Control of the symptoms if it is not possible to eliminate the underlying cause • Correction of electrolyte, fluid or nutritional deficiencies
  • 25. Class Drug Anti-cholinergic Anti-histamine Dopamine antagonists nabiloneCannabinoid Corticosteroid Histamine analogue 5HT3-receptor antagonist scopolamine (L-hyoscine) cinnarizine cyclizine promethazine metoclopramide domperidone droperidol (withdrawn 2001) haloperidol dexamethasone betahistine granisetron ondansetron tropisetron